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Review

Scorpions, Science and Folklore in Durango City

by
Eduardo Gonzalez-Ponce
1,†,
Sofia Rodríguez-Rangel
2,†,
Raymundo Martinez
1,
Adrian Alvarado
3,
Estela Ruiz-Baca
1,
Pablo Miranda
4,
Jorge E. Sánchez-Rodríguez
2,* and
Angelica Lopez-Rodriguez
1,*
1
Facultad de Ciencias Químicas, Universidad Juárez del Estado de Durango, Durango 34120, Mexico
2
Departamento de Física, Universidad de Guadalajara, Jalisco 44430, Mexico
3
Instituto de Investigación Científica, Universidad Juárez del Estado de Durango, Durango 34000, Mexico
4
National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA
*
Authors to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Diversity 2023, 15(6), 743; https://doi.org/10.3390/d15060743
Submission received: 5 April 2023 / Revised: 30 May 2023 / Accepted: 30 May 2023 / Published: 5 June 2023
(This article belongs to the Topic Arthropod Biodiversity: Ecological and Functional Aspects)
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Abstract

:
Scorpions are incredible venomous animals found on almost every continent. According to fossil data, these animals have been able to adapt to the different environments from the Cambrian period until today with minimal anatomical changes. Scorpions are mostly nocturnal animals, and their ability to detect and tolerate light stimuli seems to be an essential tool for their subsistence, homing and mating. Centruroides suffuses is the most predominant specie of scorpions in Durango City, Mexico. Interestingly, and despite their life-threatening venom, these predatory arthropod animals have been adopted by locals as part of the landscape and daily life, by including them as part of their folklore and their economic resources, and learning how to take advantage of their abundance. In addition, the venom of scorpions possesses potential for therapeutic uses, while the scorpions themselves represent a nutritional food resource rich in protein, which has been poorly explored so far. Therefore, they are an excellent model for exploring the interplay between light sensibilities, survival and therapeutic–medicinal uses. Here, we review some of the potential benefits of scorpions and share the ways people in Durango City, Mexico, use UV light devices to detect and avoid or catch them for business and research purposes.

1. Introduction

Fossil remains suggest that scorpions were among the first aquatic animals which adapted to be land-dwelling [1]. It is estimated that they have existed on our planet for more than 400 million years, and despite the multiple geographic and ecological modifications that have occurred since the Cambrian period, scorpion morphology has exhibited no major changes apart from size reduction. These kinds of arthropods have developed many mechanisms to defend themselves against predators, improved their skills to capture prey, and adapted to most ecosystems on Earth. Morphologically, scorpions possess an exoskeleton, which is an external structure that covers and protects their bodies, and it is fundamental for reducing water loss and sensing light stimuli [1,2]. These characteristics help them to camouflage themselves within the environment through exoskeleton ecomorphotype adaptations to mimic the color of the substrate on which they live [3,4]. However, the most well-known representative characteristic for which scorpions are so famous is probably their sting, which is the most common defense mechanism used when they feel threatened, and can sometimes be deadly. Their poisonous stinger is located in the tail.
The global distribution and diversity patterns of scorpions have been research topics for many scientific groups. To date, more than 2200 scorpion species, classified into 208 genera and 20 families, have been reported [5,6,7]. Scorpions are mainly distributed in tropical and subtropical regions around the world; however, they thrive in extreme climates, such as arid and semi-arid ecoregions. Mexico is a country with exquisite characteristics for scorpion proliferation, and therefore their diversity is continually increasing, as new phylogenetic and phylogenomic approaches allow changes in their classification. For instance, more than 281 species have been found in Mexico, representing more than 12% of the global diversity [7,8,9,10,11,12].

1.1. Durango Society Coexists with Scorpions

In the city of Victoria de Durango, commonly known as “the scorpion city” by locals, in the state of Durango, in the northwest of Mexico (Figure 1), scorpions represent an emblematic symbol because of their abundance. Finding a scorpion in Durango is not an exceptional event, and even less so is encountering Centruroides suffusus, the most abundant species of scorpions in the state and one of the most poisonous species in Mexico [7,13,14]. While scorpions can inflict a poisonous and painful sting, no deaths have been reported across health centers and hospitals [15]. This is due to the necessity that has emerged of the population managing and living with them, as well as the access to an antidote that counteracts the effects produced by their sting.
The folklore of Durango has been remarkably influenced by scorpions, better known locally as “alacranes”. From myths and legends to the local soccer team named “Los Alacranes”, scorpions represent an insignia for the city of Durango, as well as a significant economic resource. For instance, scorpions are marketed as souvenirs in keyrings, ashtrays, and napkin holders; suspended in alcoholic drinks such as mezcal; or used as ingredients in tacos, tostadas, desserts, sweet or spicy lollipops, and ice cream (Figure 2). Exotic delicatessens with scorpions have become prevalent tourist attractions, even when, considering all species on earth, scorpions might not be considered the most edible because of their poisonous tail sting. However, if the venom gland is removed, or the animal is cooked well, there appears to be no side-effects from eating scorpions. Although the nutritional value of scorpions has not yet been fully documented, one report from Androctonus australis indicated that, among other nutrients, scorpions contain approximately 50% protein, and 100 g of shredded product contains ~300 kilocalories [16]. Therefore, scorpions may be considered as a food resource in the future, given that they can be properly prepared to preserve the nutritional value without risk of poisoning or foodborne illness.
As a consequence of the increasing popularity of scorpions, jobs have been generated for scorpion hunters (better known in Spanish as “alacraneros”), who catch thousands of scorpions each summer to sell in local markets as souvenirs and satisfy tourist curiosity. Additionally, because of their medical importance, mostly related to venom compounds, scorpions are also bought for research purposes [7,17,18].
Scorpions are highly abundant in the Sierra Madre Occidental, situated to the west of Durango city, where they are predominantly collected by “alacraneros”. Using a hook, the “alacraneros” move stones and wood to find scorpions hiding from the sun during the daytime. However, as scorpions prefer hunting at night, some hunters prefer to catch them in the dark. Night-time hunters use common devices that produce green-blue lights instead of white lights, as scorpions are fluorescent under ultraviolet light, as well as to avoid scaring them away. This enables “alacraneros” to identify and catch scorpions easily, keeping themselves safe from being stung. Scorpions can crawl on most surfaces; thus, when caught, they are kept in a glass container with a pierced lid to allow the scorpion to breathe. Once scorpions are captured, buyers can then decide how they will be used: dead or alive. For instance, most of the scorpions used to make handcrafted souvenirs are killed by alcohol immersion, whereas it is better to keep them alive if used for gastronomic consumption or in biomedical research.

1.2. Scorpions’ Responses to Light

Scorpions usually build a burrow which serves as a shelter from predators and protection from adverse environmental conditions. From there, they navigate around, hunting, and then subsequently returning to their shelter [19,20]. This action may seem very simple; however, it is not when considering that scorpions have a very small brain, called a protocerebrum, which, working in tandem with a basic nervous system, can sense the surrounding environment and detect whether there are any predator or prey animals nearby [21,22]. Scorpions are nocturnal animals which exhibit negative phototaxis [23]; thus, scorpions prefer hiding or building their burrows under the cover of wood or stones.
Even when scorpions come out of their shelter during the day, they prefer to stay in darker areas away from bright light sources, as they have several light detection systems. The Durango scorpion has a pair of median eyes called ocelli, positioned in the top of the head, and three pairs of lateral eyes. These scorpions also have at least one other optical structure, called an eyespot, which is a very primitive visual organ, mainly composed of light-sensitive cells called photoreceptors. The eyespot can be classified as a simple eye [24] which enables some organisms to detect light, locate shadows, and identify colors.
Furthermore, studies have shown that scorpions may have 360° vision, giving them a complete panoramic perspective [23,25]. The median ocelli can detect images at low resolution, whereas the lateral ocelli are highly sensitive to light and cannot detect images [25]. Lateral and median ocelli are sensitive to green light (~500 nm), whereas lateral eyes have dichromatic vision with peaks of sensitivity corresponding to green light (~509 nm) and ultraviolet light (~371 nm) [26]. When scorpions are exposed to UV or green light, they move quickly and sporadically to escape to shelter. Apparently, scorpions perceive light at these wavelengths as danger signs [27]. On the other hand, it is unsurprising that infrared wavelengths do not bother them, because some animals, such as vipers and bats, are known to use this wavelength as a kind of thermal vision [28]. These differences between median and lateral eyes could be related to structural changes in the photoreceptor cells; in the median ocellus, these are discrete units, while cell clusters integrating a continuous cellular network are present in the lateral ocellus, suggesting a faster and direct signal transmission [24].
The phototransduction mechanisms by which light signals detected by the ocellus are converted into information in the scorpion protobrain are unknown. Similarly to other animals, the internal anatomy of scorpions shows interconnected ocular and nervous systems [29]. Figure 3 depicts a simplified view of the scorpion nervous system (SNC), where the cephalothoracic mass (protobrain) is connected to a ventral nerve cord (analogous to the spinal cord in vertebrates), nerves, and ganglia. The SNC also processes signals from hair-like structures called trichobothria, located mostly in the tail, pedipalps, and legs. Trichobothria detect air vibrations and other environmental factors, enabling scorpions to catch aerial prey, detect predators, navigate, and improve their homing abilities [30,31].
In addition to their ocular photosensitivity, scorpions may have non-retinal photoreceptors in their tails [32]. Moreover, all scorpions emit a unique glow in response to UV light irradiation [33,34,35]. This peculiar phenomenon is called scorpion fluorescence, and suggests that the exoskeleton is a photon collector which absorbs energy in the UV light range and emits part of this energy in the form of blue-green light.
Other wavelengths can be used to excite the exoskeleton. Figure 4 shows the representative fluorescence pattern of a Durango scorpion exposed to light at 475 nm and the detection of emissions above 505 nm. The image reveals some non-fluorescent body features. The stinger, median and lateral ocelli, eye spots, denticules either from mandible (located at chelicerae), or the fixed fingers (movable and immovable) on pedipalps did not fluoresce under 475 nm excitation. Interestingly, fixed fingers are an excellent source of taxonomic data, with size and dentition patterns used to distinguish animals [35,36,37]. Non-fluorescent denticles (or light-guiding denticles) have also been reported in shark species expressing regional skin biofluorescence and visually detectable biofluorescence [38].
Although autofluorescence is an intrinsic property of many animals, plants, and minerals, its biological function is not clear [39]; this characteristic may favor UV camouflage, protection, and animal communication [40,41,42]. Particularly in fish, biofluorescence is phylogenetically widespread and a phenotypically variable phenomenon [42], which clearly affects animal behavior, prey selection, mating, and other physical abilities [33,43].
Even though the molecular mechanisms which induce scorpion fluorescence remain unknown, it is clear that it depends on cuticle hardening [39]. This is evidenced by the fact that after ecdysis (molting), the remaining exoskeleton is still fluorescent, but the emerging exoskeleton only emits light 48 hours after molting [44,45], when the cuticle becomes thicker. The aromatic molecules beta carboline and 7-hydroxy-4-methylcoumarin [39,46] are involved in the hardening and tanning process of the scorpion exoskeleton, and are also experimentally associated with fluorescence [46]. Recently, a new fluorescent component from Liocheles australasiae was identified and classified as a macrocyclic diphthalate ester, which seems to be present in the scorpion cuticle [47].
In summary, some evidence suggests that scorpion fluorescence could have played an important role in their survival through the several environmental and biological changes that occurred over the past 400 million years. The physiological function of scorpion fluorescence deserves more in-depth examination. The molecular factors inducing biofluorescent targeting in specific scorpion body parts have been explored, as has the possibility of using this fluorescent pattern to improve scorpion typification; indeed, in Durango city, biofluorescence is suitable for identifying scorpions at night using a fluorescent blacklight UV lightbulb.

1.3. Venom Extraction and Preparation

Scorpion venom is used for multiple research purposes. Venom varies from species to species, and may differ in intensity due to the changes in composition according to environmental and genetic variations [48,49]. The process of obtaining venom can be a time-consuming and dangerous task, as the scorpions must be alive. For this process, commonly known as “scorpion milking”, different methods have been developed, such as manual extraction, electric stimulation, puncturing the abdominal gland of the scorpion, or telson maceration [50].
In Durango, as in many places around the world, milking scorpion venom via electrical stimulation is the preferred method. This procedure requires the following implements: (1) an electrical source (to induce a shock of ~5 to 7 volts) with two electrodes—the negative electrode clamped to long iron–steel forceps (partially covered with rubber for safety) and the positive electrode clamped to a metal plate or a metal wire; (2) long iron–steel forceps; (3) gloves to avoid electrical shocks and cross-contamination; (4) a micropipette to collect venom; and (5) a tube to store the venom.
With the scorpion resting on a metal plate, with one hand, one person holds the forceps connected to a negative electrode to clamp the tail of the scorpion between the mesosoma and metasoma; with the other hand, a second pair of forceps is used to clamp the end of the tail, very close to the telson gland. The second person can then collect venom with a micropipette and drop it into a tube (Figure 5). After receiving an electrical shock, the scorpion is stunned, but is still alive, and it will recover after a while. Extracted venom can be stored frozen (−20 °C) or lyophilized until use; however, diluting it in 0.1% BSA has been suggested to improve storage [51]. Approximately 2 µL of venom per animal can be collected with this method [52]; depending on the desired use, hundreds of scorpions may need to be processed.
Although milking scorpion venom via electrical stimulation is a widely used method, there is a risk of death or injury from scorpion stings, as well as suffering from electric shocks. To eliminate the chances of such accidents, recently, a robot designed to milk scorpions was patented by Moroccan scientists. Following a similar procedure, this machine holds down the tail of the animal and then, after electrical stimulation, droplets of venom are collected in a tube. This automated collection method makes the process easier and increases the efficiency of recollection [53]. However, this novel technology is not yet widely available.
Scorpion venom is a fascinating study object since it contains many chemical molecules (such as water, peptides, enzymes, amino acids, amines, mucopolysaccharides, and mucoproteins) which guarantee that venom will induce potent synergistic effects when it is injected into the prey. Thus, elucidating the biophysical, biochemical, and pharmacological properties and characteristics of scorpion venom represents a scientific challenge due to their complexity [54,55].
To preserve wildlife, many countries around the world have implemented species conservation programs. Mexico is no exception: The Ministry for the Environment and Natural Resources, SEMARNAT (Spanish abbreviation for “Secretaría de Medio Ambiente y Recursos Naturales”), in agreement with research institutions, civil societies, and native communities, protects scorpions by law. For research purposes, synthesizing the metabolite (or peptide) of interest has been suggested instead of using, and later killing, specimens [56].

1.4. Biophysical, Biochemical, and Pharmacological Importance of the Centruroides suffusus Venom for Voltage-Gated Ion Channels

In many cultures, scorpion body parts and venoms have been used by practitioners of medicine since ancient times [44,57,58,59]; in addition to using scorpions for mystical or pathological issues, crushed or fried scorpions have been applied as topical remedies to cure scorpion stings [60]. Antivenom therapies made from immunized animals are available around the world [55].
The first observations of interactions between scorpion venom and electrical signals triggered by nerve tissue were reported toward the end of the 1960s [61,62]. Since then, laboratories around the world have conducted exhaustive scientific research to understand their mechanisms of action [63,64,65,66,67]. These findings demonstrate that venom is composed of polypeptides as active components (toxins) that target voltage-gated ion channels such as sodium (NaV), potassium (KV), calcium (CaV), and chloride (CLC) channels [68,69,70]. These unique properties of toxins have been implemented as an important tool for structure–function relationship studies of ion channels [71,72,73,74]. The blocking effect of the crude venom of Centruroides suffusus (Durango scorpion) on NaV 1.4, Shaker KV from the larva of the fruit fly Drosophila melanogaster, expressed in oocytes of Xenopus laevis, was evidenced using the cut-open voltage clamp (COVC) technique [75,76]. The main effect of blocking venom from Centruroides scorpion species occurs mainly on the NaV and KV ion channels, supporting previous reports [77,78,79] (Figure 6).
At least nine peptides with toxic properties have been identified from Centruroides suffuses venom (CssI to CssIX) [81,82,83]. Several research groups around the world have reported that CssII, CssIV, CssVI, CssVIII, and CssIX bind NaV channels with high affinity. NaV channels are macro-molecules which are essential during the generation and propagation of electrical signals (action potentials) triggered by excitable cells, such as neurons [84,85,86,87]. The study of interactions between NaV channels and Centruroides suffuses toxins is of physiological relevance. Interestingly, the bioactivity of these neurotoxins exhibits a high level of specificity, which means that only some ion channels integrating the NaV family (NaV 1.1 to NaV 1.9) will be affected in a specific way by scorpion toxins; the CssII toxin is one of the most potent blocker toxins on NaV channels. Life-threatening conditions caused by scorpion stings are mostly related to the impairment of neurotransmission, which affects some vital functions and causes a wide range of conditions, including pain, anaphylactic reactions, severe local skin reactions, and neurologic, respiratory, and cardiovascular collapse, and can result in death as a consequence of venom toxins. In addition to the effect of CssII on the NaV ion channels for the CssII peptide, the inhibitory effect of γ-aminobutyric acid (GABA) uptake in neuronal cells has been reported [84].
Structurally, the CssII toxin comprises 66 amino acids, forming four disulfide bridges; it is the most abundant toxin present in the venom gland. CssII is also the most studied toxin from Centruroides suffuses; its three-dimensional structure was predicted by nuclear magnetic resonance spectroscopy [88]. Non-toxic and recombinant peptides of CssII have been used to produce antivenom against the Durango scorpion. Furthermore, several research groups around the world consider CssII as a “classical” β-type toxin affecting NaV channel activation [84,85,86,87]. The recombinant protein can be acquired commercially for scientific laboratory research purposes.
Css54 is a peptide also found in venom from Centruroides suffuses. It consists of 25 amino acid peptide residues, and has been predicted to form an alpha helix without sulfide bonds. Css54 was identified by testing the antibiotic activity of reverse-phase high-performance liquid chromatography (HPLC) fractions [83]. This product inhibits the active growth of Gram-positive and Gram-negative bacteria such as Staphylococcus aureus, Escherichia coli, Listeria monocytogenes, Streptococcus suis, Campylobacter jejuni, and Salmonella typhimurium, which frequently cause infections through contaminated water or food [89,90]. Therefore, Css54 peptides have been proposed to act as ‘host defense peptides’ [91], and may form part of the innate scorpion immune system to protect against bacteria and other pathogens [83]. Although antimicrobial activity has been evidenced in vitro and is not truly clear in mammalian models, we hope that it might be useful by itself or in combination with other molecules as an alternative to health treatment.
Despite the enormous progress in our understanding of the structure and function relationships of voltage-gated ion channels and the inhibitory properties of toxins from scorpion venoms, there are still many open questions that need to be addressed in this field. For instance, to gain further insight into the biophysical, biochemical, and pharmacological importance of Centruroides suffusus venom, it is vital to perform more exhaustive research with chromatography and functional methodologies in order to separate and identify new active components, peptides, and toxins that interact with ion channels to determine possible therapeutic and medical uses.
Multiple studies suggest that scorpions and their venom might have therapeutic applications (Table 1); however, thus far, chlorotoxin is the only scorpion toxin which has been evaluated in clinical medical trials [92]. Although various toxins and peptides from different scorpion species represent promising tools for scientific and biotechnological approaches, scorpions remain a key study topic, as they are fascinating survivors of multiple evolutionary events.

2. Conclusions

Scorpions may seem threatening to some, but this is not the case for the citizens of Durango, who have adopted them into their nature, folklore, and economy. The multiple uses for scorpions include basic scientific, clinical, and biological applications and beyond. Venoms are deadly; however, for some conditions, the cure might be found within them. In addition to the therapeutic potential of scorpions, many biotechnological applications may emerge by taking advantage of the biodiversity of venoms and their intrinsic nutritional factors, or by understanding the physiological relevance of exoskeleton fluorescence and their ability to survive, among other unexplored qualities. Thus, sustainable production systems, including agriculture, animal breeding, organic food production, and many other bio-based economical resources, can be positively influenced by increasing our knowledge of scorpions.

Author Contributions

Conceptualization, A.L.-R., E.G.-P., P.M., E.R.-B. and J.E.S.-R.; bibliographical investigation, E.G.-P., R.M., A.A. and S.R.-R.; resources, A.L.-R., P.M. and E.R.-B.; writing—original draft preparation, E.G.-P., A.A. and S.R.-R.; writing—E.G.-P., S.R.-R., R.M., P.M., A.A., E.R.-B., A.L.-R. and J.E.S.-R. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

This review did not require ethical approval for scorpion manipulation. Protocols involving Xenopus laevis frogs were approved by the Institutional Review Board of “Comité Institucional del Cuidado y Uso de Animales en el Laboratorio” (protocol code: CUCEI/CINV/CICUAL-03/2023, 02/01/2023) in accordance with relevant guidelines and regulations of the “Norma Oficial Mexicana-NOM-062-ZOO-1999”.

Data Availability Statement

No new data were generated or analyzed during this review.

Acknowledgments

We express our gratitude to the people working at Mercado Gomez Palacios in Durango City for being kind and participative and to Hascibe Mijares Andrade and Itzel Nájera Ibarra for reading and discussing this paper.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Wendru, A.J.; Babcock, L.E.; Wirkner, C.S.; Kluessendorf, J.; Mikulic, D.G. Open A Silurian ancestral scorpion with fossilised internal anatomy illustrating a pathway to arachnid terrestrialisation. Sci. Rep. 2020, 10, 14. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Kellersztein, I.; Cohen, S.R.; Bar-on, B.; Wagner, H.D. Acta Biomaterialia The exoskeleton of scorpions pincers: Structure and micro-mechanical properties. Acta Biomater. 2019, 94, 565–573. [Google Scholar] [CrossRef] [PubMed]
  3. Lourenco, W.R.; Cloudsley-Thompson, J.L. The evolutionary significance of colour, colour patterns and fluorescence in scorpions. Rev. Suisse Zool. Hors Ser. 1996, 2, 449–458. [Google Scholar]
  4. Williams, S.C. Scorpion bionomics. Annu. Rev. Entomol. 1987, 32, 275–295. [Google Scholar] [CrossRef]
  5. Prendini, L. Order Scorpiones C.L. Koch, 1850. In: Zhang, Z.-Q. (Ed.) Animal biodiversity: An outline of higher-level classification and survey of taxonomic richness. Zootaxa 2011, 1850, 2005–2007. [Google Scholar] [CrossRef]
  6. Rein, J.O. The Scorpion Files. Norwegian University of Science and Technology. 2009. Available online: Http://www.Ub.Ntnu.No/Scorpion-Files (accessed on 9 January 2022).
  7. Santibáñez-lópez, C.E.; Francke, O.F.; Ureta, C.; Possani, L.D. Scorpions from Mexico: From Species Diversity to Venom Complexity. Toxins 2015, 8, 2. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Francke, O.F. Biodiversity of Arthropoda (Chelicerata: Arachnida ex Acari) in Mexico. Rev. Mex. Biodivers. 2014, 85, 408–418. [Google Scholar] [CrossRef] [Green Version]
  9. González-Santillán, E. Catálogo de Escorpiones de la Colección Nacional de Arácnidos (CNAN). Ph.D. Thesis, Facultad de Ciencias, Universidad Nacional Autónoma de México, Ciudad de México, Mexico, 2001. [Google Scholar]
  10. Lourenço, W.R.; Sissom, W.D. Scorpiones. Biodiversidad, Taxonomía y Biogeografía de Artrópodos de México: Hacia Una Síntesis de Su Conocimiento. Conabio 2000, 2, 115–135. [Google Scholar]
  11. Ponce-Saavedra, J.; Moreno-Barajas, R.J. El género Centruroides Marx 1890 (Scorpiones: Buthidae) en México. Biológicas 2005, 7, 42–51. [Google Scholar]
  12. Santibáñez-López, C.E.; Ponce-Saavedra, J. A new species of Centruroides (Scorpiones: Buthidae) from the northern mountain range of Oaxaca, Mexico. Rev. Mex. Biodivers. 2009, 80, 321–331. [Google Scholar]
  13. Jover, E.; Couraud, F.; Rochat, H. Two types of scorpion neurotoxins characterized by their binding to two separate receptor sites on rat brain synaptosomes. Biochem. Biophys. Res. Commun. 1980, 95, 1607–1614. [Google Scholar] [CrossRef] [PubMed]
  14. Rochat, H.; Bernard, P.; Couraud, F. Scorpion toxins: Chemistry and mode of action. Adv. Cytopharmacol. 1979, 3, 325–334. [Google Scholar] [PubMed]
  15. Chippaux, J.P.; Celis, A.; Boyer, L.; Alagón, A. Factors involved in the resilience of incidence and decrease of mortality from scorpion stings in Mexico. Toxicon 2020, 188, 65–75. [Google Scholar] [CrossRef] [PubMed]
  16. Abulude, F.O.; Ogunkoya, M.O.; Esiet, E.E.; Kayode, B.O.; Oni, J.O. Studies on Scorpion (Androctonus australis): Nutritional and Anti-nutritional Factors. J. Entomol. 2006, 3, 156–160. [Google Scholar] [CrossRef] [Green Version]
  17. Goudarzi, H.R.; Salehi Najafabadi, Z.; Movahedi, A.; Noofeli, M. Bradykinin-Potentiating Factors of Venom from Iranian Medically Important Scorpions. Arch. Razi Inst. 2019, 74, 385–394. [Google Scholar]
  18. Martins, J.G.; Santos, G.C.; Procópio, R.E.D.L.; Arantes, E.C.; Bordon, K.D.C.F. Scorpion species of medical importance in the Brazilian Amazon: A review to identify knowledge gaps. J. Venom. Anim. Toxins Incl. Trop. Dis. 2021, 27, e20210012. [Google Scholar] [CrossRef]
  19. Adams, A.M.; Marais, E.; Turner, J.S.; Prendini, L.; Pinshow, B. Similar burrow architecture of three arid-zone scorpion species implies similar ecological function. Sci. Nat. 2016, 103, 56. [Google Scholar] [CrossRef]
  20. Gaffin, D.D.; Muñoz, M.G.; Hoefnagels, M.H. Evidence of learning walks related to scorpion home burrow navigation. J. Exp. Biol. 2022, 225, jeb243947. [Google Scholar] [CrossRef]
  21. Smarandache-Wellmann, C.R. Arthropod neurons and nervous system. Curr. Biol. 2016, 26, R960–R965. [Google Scholar] [CrossRef] [Green Version]
  22. Tanaka, G.; Hou, X.; Ma, X.; Edgecombe, G.D.; Strausfeld, N.J. Chelicerate neural ground pattern in a Cambrian great appendage arthropod. Nature 2013, 502, 364–367. [Google Scholar] [CrossRef]
  23. Prévost, E.D.; Stemme, T. Non-visual homing and the current status of navigation in scorpions. Anim. Cogn. 2020, 23, 1215–1234. [Google Scholar] [CrossRef]
  24. Loria, S.F.; Prendini, L. Homology of the lateral eyes of scorpiones: A six-ocellus model. PLoS ONE 2014, 9, e112913. [Google Scholar] [CrossRef] [PubMed]
  25. Locket, A. Scorpion Biology and Research; Brownell, P., Polis, G., Eds.; Oxford University Press: Oxford, UK, 2001; pp. 79–106. [Google Scholar]
  26. Fleissner, G.; Fleissner, G. Night Vision in Desert Scorpions. In Scorpions 2001: In Memoriam Gary a Polis; British Arachnological Society: Burnham Beeches, UK, 2001; pp. 317–324. [Google Scholar]
  27. Giambelluca, F.L.; Osio, J.; Giambelluca, L.A.; Cappelletti, M.A. Novel scorpion detection system combining computer vision and fluorescence. arXiv 2021, arXiv:2108.04177. [Google Scholar]
  28. Darbaniyan, F.; Liu, L.; Sharma, F. Soft Matter Mechanics and the Mechanisms Underpinning the Infrared Vision of Snakes. 2020. Available online: https://ssrn.com/abstract=3606795 (accessed on 18 October 2022).
  29. Horn, A.C.M.; Chaval, A. The gross anatomy of the nervous system of Bothriurus bonariensis (L. C. KOCH, 1842) (Scorpiones, Bothriuridae). Braz. J. Biol. 2002, 62, 253–262. [Google Scholar] [CrossRef] [Green Version]
  30. Ashfford, K.; Blankenship, R.; Carpenter, W.; Wheeler, I.; Gaffin, D. Response of the eastern sand scorpion, Paruroctonus utahensis, to air movement from a moth analog. J. Arachnol. 2018, 46, 226–230. [Google Scholar] [CrossRef]
  31. Pimenta Murayama, G.L.; Hirata Willemart, R. Are trichobothria used in terrestrial prey capture by the yellow scorpion Tityus serrulatus Lutz, Mello, 1922 (Buthidae)? Arachnology 2019, 18, 287–290. [Google Scholar] [CrossRef]
  32. Geethabali, K.P.R. A Metasomatic Neural Photoreceptor in the Scorpion. J. Exp. Biol. 1973, 58, 189–196. [Google Scholar]
  33. Lawrence, R.F. Fluorescence in Arthropoda. J. Entomol. Soc. S. Afr. 1954, 17, 167–170. [Google Scholar]
  34. Pavan, M. Studi sugli Scorpioni: I.-Una nuova caratteristica tipica del tegumento degli Scorpioni. Ital. J. Zool. 1954, 21, 283–291. [Google Scholar] [CrossRef]
  35. Graham, M.R. Malformed pedipalp finger dentition of the scorpion Superstitionia donensis (Scorpiones: Superstitioniidae). Euscorpius 2006, 42, 1–4. [Google Scholar] [CrossRef]
  36. Stahnke, H.L. Scorpion Nomenclature And Mensuration. Entomol. News 1970, 81, 297–316. [Google Scholar]
  37. Williams, S.C. Developmental anomalies in scorpion centruroides-sculpturatus (Scorpionida-buthidae). Pan-Pac. Entomol. 1971, 47, 76. [Google Scholar]
  38. Park, H.B.; Lam, Y.C.; Gaffney, J.P.; Weaver, J.C.; Krivoshik, S.R.; Hamchand, R.; Pieribone, V.; Gruber, D.F.; Crawford, J.M. Bright Green Biofluorescence in Sharks Derives from Bromo-Kynurenine Metabolism. IScience 2019, 19, 1291–1336. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  39. Stachel, S.J.; Stockwell, S.A.; Van Vranken, D.L. The fluorescence of scorpions and cataractogenesis. Chem. Biol. 1999, 6, 531–539. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  40. Kloock, C.T.; Kubli, A.; Reynolds, R. Ultraviolet light detection: A function of scorpion fluorescence. J. Arachnol. 2010, 38, 441–445. [Google Scholar] [CrossRef]
  41. Lim, M.L.M.; Land, M.F.; Li, D. Sex-specific UV and fluorescence signals in jumping spiders. Science 2007, 315, 481. [Google Scholar] [CrossRef] [Green Version]
  42. Sparks, J.S.; Schelly, R.C.; Smith, W.L.; Davis, M.P.; Tchernov, D.; Pieribone, V.A.; Gruber, D.F. The Covert World of Fish Biofluorescence: A Phylogenetically Widespread and Phenotypically Variable Phenomenon. PLoS ONE 2014, 9, e83259. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Welch, V.L.; Van Hooijdonk, E.; Intrater, N.; Vigneron, J.P. Fluorescence in Insects. The Nature of Light: Light in Nature. Photo-Optical Instrumentation Engineers Photo-optical Instrumentation. Engineers 2012, 8480, 848004. [Google Scholar] [CrossRef]
  44. Chen, Y.J.; Chiu, P.J.; Lee, C.C. Fluorescence and multilayer structure of the scorpion cuticle. In Optical Systems Design 2015: Illumination Optics IV; SPIE Press: Bellingham, WA, USA, 2015; Volume 9629, pp. 108–111. [Google Scholar]
  45. Cloudsley-Thompson, J.L.; Constantinou, C. Biological clocks in desert beetles (Tenebrionidae), with special reference to Erodius octocostatus Peyerimhof in Kuwait. J. Univ. Kuwait (Sci.) 1985, 12, 237–243. [Google Scholar]
  46. Frost, L.M.; Butler, D.R.; O’Dell, B.; Fet, V.A. A Coumarin as a Fluorescent Compound in Scorpion Cuticle. In Scorpions, In Memoriam Gary A. Polis; Fet, V., Selden, P.A., Eds.; British Arachnological Society: Burnham Beeches, UK, 2001; pp. 365–368. [Google Scholar]
  47. Yoshimoto, Y.; Tanaka, M.; Miyashita, M.; Abdel-Wahab, M.; Megaly, A.M.A.; Nakagawa, Y.; Miyagawa, H. A Fluorescent Compound from the Exuviae of the Scorpion, Liocheles australasiae. J. Nat. Prod. 2020, 83, 542–546. [Google Scholar] [CrossRef]
  48. Rodríguez-Ravelo, R.; Coronas, F.I.; Zamudio, F.Z.; González-Morales, L.; López, G.E.; Urquiola, A.R.; Possani, L.D. The Cuban scorpion Rhopalurus junceus (Scorpiones, Buthidae): Component variations in venom samples collected in different geographical areas. J. Venom. Anim. Toxins Incl. Trop. Dis. 2013, 19, 13. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  49. Pucca, M.B.; Amorim, F.G.; Cerni, F.A.; de Castro Figueiredo Bordon, K.; Cardoso, I.A.; Anjolette, F.A.P.; Arantes, E.C. Influence of post-starvation extraction time and prey-specific diet in Tityus serrulatus scorpion venom composition and hyaluronidase activity. Toxicon 2014, 90, 326–336. [Google Scholar] [CrossRef] [PubMed]
  50. Gopalakrishnakone, P.; Cheah, J. Gwee MCE Black scorpion (Heterometrus longimanus) as a laboratory animal: Maintenance of a colony of scorpion for milking of venom for research, using a restraining device. Lab Anim. 1995, 29, 456–458. [Google Scholar] [CrossRef]
  51. van Cann, M.; Kuzmenkov, A.; Isensee, J.; Andreev-Andrievskiy, A.; Peigneur, S.; Khusainov, G.; Berkut, A.; Tytgat, J.; Vassilevski, A.; Hucho, T. Scorpion toxin MeuNaTxα-1 sensitizes primary nociceptors by selective modulation of voltage-gated sodium channels. Fed. Eur. Biochem. Soc. 2021, 288, 2418–2435. [Google Scholar] [CrossRef]
  52. Tobassum, S.; Tahir, H.M.; Zahid, M.T.; Gardner, Q.A.; Ahsan, M.M. Effect of Milking Method, Diet, and Temperature on Venom Production in Scorpions. J. Insect Sci. 2018, 18, 19. [Google Scholar] [CrossRef] [Green Version]
  53. Kamel, M.; Saile, R.; Tanane, O.; Kettani, A. The robotic scorpion venom extraction system. Rev. Rev. ’entrepreneuriat Et L’innovation 2022, IV, V4N14A2022. [Google Scholar]
  54. Ferreira, M.G.; Duarte, C.G.; Oliveira, M.S.; Castro, K.L.; Teixeira, M.S.; Reis, L.P.; Zambrano, J.A.; Kalapothakis, E.; Michel, A.F.; Soto-Blanco, B.; et al. Toxicity of crude and detoxified Tityus serrulatus venom in anti-venom-producing sheep. J. Vet. Sci. 2016, 17, 467–477. [Google Scholar] [CrossRef] [PubMed]
  55. Al-Asmari, A.K.; Kunnathodi, F.; Al Saadon, K.; Idris, M.M. Elemental analysis of scorpion venoms. J. Venom Res. 2016, 7, 16–20. [Google Scholar]
  56. Norma Oficial Mexicana NOM-062-ZOO-1999, Especificaciones Técnicas para la Producción, Cuidado y uso de los Animales de Laboratorio. Available online: http://www.sagarpa.gob.mx/Dgg/NOM/062zoo.pdf (accessed on 2 October 2022).
  57. Dehghani, R. Scorpions and Scorpion Sting (Biology, Ecology and Control of Them); Esfahan Beautiful Arts; Publications of Kashan University of Medical Sciences: Esfahan, Iran, 2006; p. 334. [Google Scholar]
  58. Dehghani, R.; Arani, M.G. Scorpion sting prevention and treatment in ancient Iran. J. Tradit. Complement. Med. 2015, 5, 75–80. [Google Scholar] [CrossRef] [Green Version]
  59. Najmabadi, M. History of Medicine in Iran, 2nd ed.; Tehran University Press: Tehran, Iran, 1992. [Google Scholar]
  60. González, J.A.; Vallejo, J.R. The scorpion in Spanish folk medicine: A review of traditional remedies for stings and its use as a therapeutic resource. J. Ethnopharmacol. 2013, 146, 62–74. [Google Scholar] [CrossRef]
  61. Koppenhofer, E.; Schmidt, H. Incomplete sodium inactivation in nodes of ranvier treated with scorpion venom. Experientia 1967, 24, 41–43. [Google Scholar] [CrossRef] [PubMed]
  62. Koppenhöfer, E.; Schmidt, H. Die Wirkung von Skorpiongift auf die Ionenströme des Ranvierschen Schnürrings. II. Unvollständiage Natrium-Inaktivierung Effect of scorpion venom on ionic currents of the node of Ranvier. II. Incomplete sodium inactivation. Pflug. Arch. 1968, 303, 150–161. [Google Scholar] [CrossRef] [PubMed]
  63. Patterson, R.A. Physiological action of scorpion venom. Am. J. Trop. Med. Hyg. 1960, 9, 410–414. [Google Scholar] [CrossRef] [PubMed]
  64. d’Ajello, V.; Zlotkin, E.; Miranda, F.; Lissitzky, S.; Bettini, S. The effect of scorpion venom and pure toxins on the cockroach central nervous system. Toxicon 1972, 10, 399–404. [Google Scholar] [CrossRef] [PubMed]
  65. Fletcher, P.L.; Fletcher, M.; Fainter, L.K.; Terrian, D.M. Action of new world scorpion venom and its neurotoxins in secretion. Toxicon 1996, 34, 1399–1411. [Google Scholar] [CrossRef]
  66. Gwee, M.C.; Nirthanan, S.; Khoo, H.E.; Gopalakrishnakone, P.; Kini, R.M.; Cheah, L.S. Autonomic effects of some scorpion venoms and toxins. Clin. Exp. Pharmacol. Physiol. 2002, 29, 795–801. [Google Scholar] [CrossRef]
  67. Nencioni, A.L.A.; Beraldo Neto, E.; Freitas, L.A.D.; Dorce, V.A.C. Effects of Brazilian scorpion venoms on the central nervous system. J. Venom. Anim. Toxins Incl. Trop. Dis. 2018, 24, 3. [Google Scholar] [CrossRef] [Green Version]
  68. Possani, L.D.; Merino, E.; Corona, M.; Bolivar, F.; Becerril, B. Peptides and genes coding for scorpion toxins that affect ion-channels. Biochimie 2000, 82, 861–868. [Google Scholar] [CrossRef]
  69. Quintero-Hernández, V.; Jiménez-Vargas, J.M.; Gurrola, G.B.; Valdivia, H.H.; Possani, L. Scorpion venom components that affect ion-channels function. Toxicon 2013, 76, 328–342. [Google Scholar] [CrossRef] [Green Version]
  70. Almaaytah, A.; Albalas, Q. Scorpion venom peptides with no disulfide bridges: A review. Peptides 2014, 51, 35–45. [Google Scholar] [CrossRef]
  71. Lecomte, C.; Sabatier, J.M.; Van Rietschoten, J.; Rochat, H. Synthetic peptides as tools to investigate the structure and pharmacology of potassium channel-acting short-chain scorpion toxins. Biochimie 1998, 80, 151–154. [Google Scholar] [CrossRef] [PubMed]
  72. MacKinnon, R.; Reinhart, P.H.; White, M.M. Charybdotoxin block of Shaker K+ channels suggests that different types of K+ channels share common structural features. Neuron 1988, 10, 997–1001. [Google Scholar] [CrossRef] [PubMed]
  73. Possani, L.D.; Becerril, B.; Delepierre, M.; Tytgat, J. Scorpion toxins specific for Na+-channels. Eur. J. Biochem. 1999, 264, 287–300. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  74. Cestèle, S.; Yarov-Yarovoy, V.; Qu, Y.; Sampieri, F.; Scheuer, T.; Catterall, W.A. Structure and function of the voltage sensor of sodium channels probed by a beta-scorpion toxin. J. Biol. Chem. 2006, 281, 21332–21344. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  75. Bezanilla, F.; Stefani, E. Gating currents. Methods Enzym. 1998, 293, 331–352. [Google Scholar] [CrossRef] [Green Version]
  76. Stefani, E.; Bezanilla, F. Cut-open oocyte voltage-clamp technique. Methods Enzym. 1998, 293, 300–318. [Google Scholar]
  77. Carbone, E.; Wanke, E.; Prestipino, G.; Possani, L.D.; Maelicke, A. Selective blockage of voltage-dependent K+ channels by a novel scorpion toxin. Nature 1982, 296, 90–91. [Google Scholar] [CrossRef]
  78. Olamendi-Portugal, T.; Restano-Cassulini, R.; Riaño-Umbarila, L.; Becerril, B.; Possani, L.D. Functional and immuno-reactive characterization of a previously undescribed peptide from the venom of the scorpion Centruroides limpidus. Peptides 2017, 87, 34–40. [Google Scholar] [CrossRef]
  79. García-Guerrero, I.A.; Cárcamo-Noriega, E.; Gómez-Lagunas, F.; González-Santillán, E.; Zamudio, F.Z.; Gurrola, G.B.; Possani, L.D. Biochemical characterization of the venom from the Mexican scorpion Centruroides ornatus, a dangerous species to humans. Toxicon 2020, 173, 27–38. [Google Scholar] [CrossRef]
  80. Rodríguez-Rangel, S.; Bravin, A.D.; Ramos-Torres, K.M.; Brugarolas, P.; Sánchez-Rodríguez, J.E. Structure-activity relationship studies of four novel 4-aminopyridine K+ channel blockers. Sci. Rep. 2020, 10, 52. [Google Scholar] [CrossRef] [Green Version]
  81. Martin, M.F.; Garcia y Perez, L.G.; el Ayeb, M.; Kopeyan, C.; Bechis, G.; Jover, E.; Rochat, H. Purification and chemical and biological characterizations of seven toxins from the Mexican scorpion, Centruroides suffusus suffusus. J. Biol. Chem. 1987, 262, 4452–4459. [Google Scholar] [CrossRef] [PubMed]
  82. Espino-Solis, G.P.; Estrada, G.; Olamendi-Portugal, T.; Villegas, E.; Zamudio, F.; Cestele, S.; Possani, L.D.; Corzo, G. Isolation and molecular cloning of beta-neurotoxins from the venom of the scorpion Centruroides suffusus suffusus. Toxicon 2011, 57, 739–746. [Google Scholar] [CrossRef] [PubMed]
  83. Garcia, F.; Villegas, E.; Espino-Solis, G.P.; Rodriguez, A.; Paniagua-Solis, J.F.; Sandoval-Lopez, G.; Possani, L.D.; Corzo, G. Antimicrobial peptides from arachnid venoms and their microbicidal activity in the presence of commercial antibiotics. J. Antibiot. 2013, 66, 3–10. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  84. Johnson, T.M.; Quick, M.W.; Sakai, T.T.; Krishna, N.R. Expression of functional recombinant scorpion beta-neurotoxin Css II in, E. coli. Peptides 2000, 21, 767–772. [Google Scholar] [CrossRef]
  85. Smith, J.J.; Alphy, S.; Seibert, A.L.; Blumenthal, K.M. Differential phospholipid binding by site 3 and site 4 toxins. Implications for structural variability between voltage-sensitive sodium channel domains. J. Biol. Chem. 2005, 280, 11127–11133. [Google Scholar] [CrossRef] [Green Version]
  86. Bosmans, F.; Martin-Eauclaire, M.-F.; Tytgat, J. Differential effects of five ‘classical’ scorpion β-toxins on rNav1.2a and DmNav1 provide clues on species-selectivity. Toxicol. Appl. Pharmacol. 2007, 218, 45–51. [Google Scholar] [CrossRef] [Green Version]
  87. Schiavon, E.; Pedraza-Escalona, M.; Gurrola, G.B.; Olamendi-Portugal, T.; Corzo, G.; Wanke, E.; Possani, L.D. Negative-shift activation, current reduction and resurgent currents induced by β-toxins from Centruroides scorpions in sodium channels. Toxicon 2012, 59, 283–293. [Google Scholar] [CrossRef]
  88. Saucedo, A.L.; del Rio-Portilla, F.; Picco, C.; Estrada, G.; Prestipino, G.; Possani, L.D.; Delepierre, M.; Corzo, G. Solution structure of native and recombinant expressed toxin CssII from the venom of the scorpion Centruroides suffusus suffusus, and their effects on Nav1.5 sodium channels. Biochim. Et Biophys. Acta 2012, 1824, 478–487. [Google Scholar] [CrossRef]
  89. Park, J.; Oh, J.H.; Kang, H.K.; Choi, M.C.; Seo, C.H.; Park, Y. Scorpion-Venom-Derived Antimicrobial Peptide Css54 Exerts Potent Antimicrobial Activity by Disrupting Bacterial Membrane of Zoonotic Bacteria. Antibiotics 2020, 9, 831. [Google Scholar] [CrossRef]
  90. Tuxpan-Pérez, A.; Ibarra-Valencia, M.A.; Estrada, B.E.; Clement, H.; Corrales-García, L.L.; Espino-Solis, G.P.; Corzo, G. Antimicrobial and Immunomodulatory Effects of Selected Chemokine and Antimicrobial Peptide on Cytokine Profile during Salmonella Typhimurium Infection in Mouse. Antibiotics 2022, 11, 607. [Google Scholar] [CrossRef]
  91. Dai, C.; Ma, Y.; Zhao, Z.; Zhao, R.; Wang, Q.; Wu, Y.; Cao, Z.; Li, W. Mucroporin, the first cationic host defense peptide from the venom of Lychas mucronatus. Antimicrob. Agents Chemother. 2008, 52, 3967–3972. [Google Scholar] [CrossRef] [Green Version]
  92. 131-I-TM-601 Study in Adults with Recurrent High-Grade Glioma—Phase 2. Available online: https://clinicaltrials.gov/ct2/show/NCT00114309 (accessed on 26 March 2023).
  93. King, J.V.L.; Emrick, J.J.; Kelly, M.J.S.; Herzig, V.; King, G.F.; Medzihradszky, K.F.; Julius, D. A Cell-Penetrating Scorpion Toxin Enables Mode-Specific Modulation of TRPA1 and Pain. Cell 2019, 178, 1362–1374.e16. [Google Scholar] [CrossRef]
  94. Hakim, M.A.; Jiang, W.; Luo, L.; Li, B.; Yang, S.; Song, Y.; Lai, R. Scorpion Toxin, BmP01, Induces Pain by Targeting TRPV1 Channel. Toxins 2015, 7, 3671–3687. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  95. Cao, Z.Y.; Mi, Z.M.; Cheng, G.F.; Shen, W.Q.; Xiao, X.; Liu, X.M.; Liang, X.T.; Yu, D.Q. Purification and characterization of a new peptide with analgesic effect from the scorpion Buthus martensi Karch. J. Pept. Res. 2004, 64, 33–41. [Google Scholar] [CrossRef]
  96. Guan, R.J.; Wang, C.G.; Wang, M.; Wang, D.C. A depressant insect toxin with a novel analgesic effect from scorpion Buthus martensii Karsch. Biochim. Et Biophys. Acta Protein Struct. Mol. Enzymol. 2001, 1549, 9–18. [Google Scholar] [CrossRef]
  97. Zeng, X.C.; Wang, S.X.; Zhu, Y.; Zhu, S.Y.; Li, W.X. Identification and functional characterization of novel scorpion venom peptides with no disulfide bridge from Buthus martensii. Peptides 2004, 25, 143–150. [Google Scholar] [CrossRef]
  98. Cao, Z.; Di, Z.; Wu, Y.; Li, W. Overview of scorpion species from china and their toxins. Toxins 2014, 6, 796–815. [Google Scholar] [CrossRef] [Green Version]
  99. Harrison, P.L.; Abdel-Rahman, M.A.; Miller, K.; Strong, P.N. Antimicrobial peptides from scorpion venoms. Toxicon 2014, 88, 115–137. [Google Scholar] [CrossRef]
  100. Fan, Z.; Cao, L.; He, Y.; Hu, J.; Di, Z.; Wu, Y.; Li, W.; Cao, Z. Ctriporin, a new anti–methicillin–resistant Staphylococcus aureus peptide from the venom of the scorpion Chaerilus tricostatus. Antimicrob. Agents Chemother. 2011, 55, 5220–5229. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  101. Roger, S.; Rollin, J.; Barascu, A.; Besson, P.; Raynal, P.I.; Iochmann, S.; Lei, M.; Bougnoux, P.; Gruel, Y.; Le Guennec, J.Y. Voltage-gated sodium channels potentiate the invasive capacities of human non-small-cell lung cancer cell lines. Int. J. Biochem. Cell Biol. 2007, 39, 774–786. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  102. Roger, S.; Rollin, J.; Barascu, A.; Besson, P.; Raynal, P.I.; Iochmann, S.; Lei, M.; Bougnoux, P.; Gruel, Y.; Le Guennec, J.Y. A drug repositioning approach identifies tricyclic antidepressants as inhibitors of small cell lung cancer and other neuroendocrine tumors. Cancer Discov. 2013, 3, 1364–1377. [Google Scholar]
  103. Bechohra, L.; Laraba-Djebari, F.; Hammoudi-Triki, D. Cytotoxic activity of Androctonus australis venom and its toxic fractions on human lung cancer cell line. J. Venom. Anim. Toxins Incl. Trop. Dis. 2016, 22, 29. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  104. Tong-ngam, P.; Roytrakul, S.; Sritanaudomchai, H. BmKn-2 scorpion venom peptide for killing oral cancer cells by apoptosis. Asian Pacific journal of cancer preven tion. Asian Pac. J. Cancer Prev. 2015, 16, 2807–2811. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  105. Dardevet, L.; Rani, D.; Aziz, T.A.; Bazin, I.; Sabatier, J.M.; Fadl, M.; Brambilla, E.; De Waard, M. Chlorotoxin: A helpful natural scorpion peptide to diagnose glioma and fight tumor invasion. Toxins 2015, 7, 1079–1101. [Google Scholar] [CrossRef] [Green Version]
  106. BenAissa, R.; Othman, H.; Villard, C.; Peigneur, S.; Mlayah-Bellalouna, S.; Abdelkafi-Koubaa, Z.; Marrakchi, N.; Essafi-Benkhadir, K.; Tytgat, J.; Luis, J. Srairi-Abid N AaHIV a sodium channel scorpion toxin inhibits the proliferation of DU145 prostate cancer cells. Biochem. Biophys. Res. Commun. 2019, 521, 340–346. [Google Scholar] [CrossRef]
  107. Shao, J.H.; Cui, Y.; Zhao, M.Y.; Wu, C.F.; Liu, Y.F.; Zhang, J.H. Purification, characterization, and bioactivity of a new analgesic-antitumor peptide from Chinese scorpion Buthus martensii Karsch. Peptides 2014, 53, 89–96. [Google Scholar] [CrossRef]
  108. Satitmanwiwat, S.; Changsangfa, C.; Khanuengthong, A.; Promthep, K.; Roytrakul, S.; Arpornsuwan, T.; Saikhun, K.; Sritanaudomchai, H. The scorpion venom peptide BmKn2 induces apoptosis in cancerous but not in normal human oral cells. Biochem. Biophys. Res. Commun. 2016, 84, 1042–1050. [Google Scholar] [CrossRef]
  109. Khamessi, O.; Ben Mabrouk, H.; ElFessi-Magouri, R.; Kharrat, R. RK1, the first very short peptide from Buthus occitanus tunetanus inhibits tumor cell migration, proliferation and angiogenesis. Biochem. Biophys. Res. Commun. 2018, 499, 1–7. [Google Scholar] [CrossRef] [PubMed]
  110. Lansu, K.; Gentile, S. Potassium channel activation inhibits proliferation of breast cancer cells by activating a senescence program. Cell Death Dis. 2013, 4, e652. [Google Scholar] [CrossRef] [Green Version]
  111. Perez-Neut, M.; Rao, V.R.; Gentile, S. hERG1/Kv11.1 activation stimulates transcription of p21waf/cip in breast cancer cells via a calcineurin-dependent mechanism. Oncotarget 2016, 7, 58893–58902. [Google Scholar] [CrossRef] [Green Version]
  112. Wang, X.; Wang, G. Insights into Antimicrobial Peptides from Spiders and Scorpions. Protein Pept. Lett. Publ. Lett. 2016, 23, 707–721. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  113. de Melo, E.T.; Estrela, A.B.; Santos, E.C.; Machado, P.R.; Farias, K.J.; Torres, T.M.; Carvalho, E.; Lima, J.P.; Silva-Júnior, A.A.; Barbosa, E.G.; et al. Structural characterization of a novel peptide with antimicrobial activity from the venom gland of the scorpion Tityus stigmurus: Stigmurin. Peptides 2015, 68, 3–10. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  114. Du, Q.; Hou, X.; Wang, L.; Zhang, Y.; Xi, X.; Wang, H.; Zhou, M.; Duan, J.; Wei, M.; Chen, T.; et al. AaeAP1 and AaeAP2: Novel Antimicrobial Peptides from the Venom of the Scorpion, Androctonus aeneas: Structural Characterisation, Molecular Cloning of Biosynthetic Precursor-Encoding cDNAs and Engineering of Analogues with Enhanced Antimicrobial and Anticancer Activities. Toxins 2015, 7, 219–237. [Google Scholar] [PubMed] [Green Version]
  115. Machado, R.J.A.; Estrela, A.B.; Nascimento, A.K.L.; Melo, M.M.A.; Torres-Rêgo, M.; Lima, E.O.; Rocha, H.A.O.; Carvalho, E.; Silva-Junior, A.A.; Fernandes-Pedrosa, M.F. Characterization of TistH, a multifunctional peptide from the scorpion Tityus stigmurus: Structure, cytotoxicity and antimicrobial activity. Toxicon 2016, 119, 362–370. [Google Scholar] [CrossRef]
  116. Guilhelmelli, F.; Vilela, N.; Smidt, K.S.; de Oliveira, M.A.; da Cunha Morales Álvares, A.; Rigonatto, M.C.L.; da Silva Costa, P.H.; Tavares, A.H.; de Freitas, S.M.; Nicola, A.M. Activity of Scorpion Venom-Derived Antifungal Peptides against Planktonic Cells of Candida spp. and Cryptococcus neoformans and Candida albicans Biofilms. Front. Microbiol. 2016, 7, 1844. [Google Scholar] [CrossRef] [Green Version]
  117. Santussi, W.M.; Bordon, K.C.F.; Rodrigues Alves, A.P.N.; Cologna, C.T.; Said, S.; Arantes, E.C. Antifungal Activity against Filamentous Fungi of Ts1, a Multifunctional Toxin from Tityus serrulatus Scorpion Venom. Front. Microbiol. 2017, 8, 984. [Google Scholar] [CrossRef] [Green Version]
  118. Conde, R.; Zamudio, F.Z.; Rodríguez, M.H.; Possani, D. Scorpine, an anti-malaria and anti-bacterial agent purified from scorpion venom. FEBS Lett. 2000, 471, 165–168. [Google Scholar] [CrossRef] [Green Version]
  119. Carballar-Lejarazú, R.; Rodríguez, M.H.; de la Cruz Hernández-Hernández, F.; Ramos-Castañeda, J.; Possani, L.D.; Zurita-Ortega, M.; Reynaud-Garza, E.; Hernández-Rivas, R.; Loukeris, T.; Lycett, G.; et al. Recombinant scorpine: A multifunctional antimicrobial peptide with activity against different pathogens. Cell. Mol. Life Sci. 2008, 65, 3081–3092. [Google Scholar] [CrossRef]
  120. Gao, B.; Xu, J.; Rodriguez, M.d.C.; Lanz-Mendoza, H.; Hernández-Rivas, R.; Du, W.; Zhu, S. Characterization of two linear cationic antimalarial peptides in the scorpion Mesobuthus eupeus. Biochimie 2010, 92, 350–359. [Google Scholar] [CrossRef]
  121. Flores-Solis, D.; Toledano, Y.; Rodríguez-Lima, O.; Cano-Sánchez, P.; Ramírez-Cordero, B.E.; Landa, A.; de la Vega, R.C.R.; del Rio-Portilla, F. Solution structure and antiparasitic activity of scorpine-like peptides from Hoffmannihadrurus gertschi. FEBS Lett. 2016, 590, 2286–2296. [Google Scholar] [CrossRef]
  122. Borges, A.; Silva, S.; Op den Camp, H.J.M.; Velasco, E.; Alvarez, M.; Alfonzo, M.J.M.; Jorquera, A.; De Sousa, L.; Delgado, O. In vitro leishmanicidal activity of Tityus discrepans scorpion venom. Parasitol. Res. 2006, 99, 167–173. [Google Scholar] [CrossRef] [PubMed]
  123. Scholl, U.I.; Goh, G.; Stölting, G.; de Oliveira, R.C.; Choi, M.; Overton, J.D.; Fonseca, A.L.; Korah, R.; Starker, L.F.; Kunstman, J.W.; et al. Somatic and germline CACNA1D cal cium channel mutations in aldosterone-producing adeno mas and primary aldosteronism. Nat. Genet. 2013, 45, 1050–1054. [Google Scholar] [CrossRef] [PubMed]
  124. Cheng, Y.; Zhao, J.; Qiao, W.; Chen, K. Recent advances in diagnosis and treatment of gliomas using chlorotoxin-based bioconjugates. Am. J. Nucl. Med. Mol. Imaging 2014, 4, 385–405. [Google Scholar] [PubMed]
  125. Diss, J.K.; Stewart, D.; Pani, F.; Foster, C.S.; Walker, M.M.; Patel, A.; Djamgoz, M.B. A potential novel marker for human prostate cancer: Voltage-gated sodium channel expression in vivo. Prostate Cancer Prostatic Dis. 2005, 8, 266–273. [Google Scholar] [CrossRef] [Green Version]
  126. Nakajima, T.; Kubota, N.; Tsutsumi, T.; Oguri, A.; Imuta, H.; Jo, T.; Oonuma, H.; Soma, M.; Meguro, K.; Takano, H.; et al. Eicosapentaenoic acid inhibits volt age gated sodium channels and invasiveness in prostate cancer cells. Br. J. Pharmacol. 2009, 156, 420–431. [Google Scholar] [CrossRef] [Green Version]
  127. Al-Asmari, A.K.; Islam, M.; Al-Zahrani, A.M. In vitro analysis of the anticancer properties of scorpion venom in colorectal and breast cancer cell lines. Oncol. Lett. 2016, 11, 1256–1262. [Google Scholar] [CrossRef] [Green Version]
  128. El-Ghlban, S.; Kasai, T.; Shigehiro, T.; Yin, H.X.; Sekhar, S.; Ida, M.; Sanchez, A.; Mizutani, A.; Kudoh, T.; Murakami, H.; et al. Chlorotoxin-Fc fusion inhibits release of MMP-2 from pancreatic cancer cells. BioMed Res. Int. 2014, 2014, 152659. [Google Scholar] [CrossRef] [Green Version]
  129. Li, Q.; Zhao, Z.; Zhou, D.; Chen, Y.; Hong, W.; Cao, L.; Yang, J.; Zhang, Y.; Shi, W.; Cao, Z.; et al. Virucidal activity of a scorpion venom peptide variant mucroporin-M1 against measles, SARS-CoV and influenza H5N1 viruses. Peptides 2011, 32, 1518–1525. [Google Scholar] [CrossRef]
  130. Zhao, Z.; Hong, W.; Zeng, Z.; Wu, Y.; Hu, K.; Tian, X.; Li, W.; Cao, Z. Mucroporin-M1 Inhibits Hepatitis B Virus Replication by Activating the Mitogen-activated Protein Kinase (MAPK) Pathway and Down-regulating HNF4α in Vitro and in Vivo. J. Biol. Chem. 2012, 287, 30181–30190. [Google Scholar] [CrossRef] [Green Version]
  131. Li, B.; Lyu, P.; Xi, X.; Ge, L.; Mahadevappa, R.; Shaw, C.; Kwok, H.F. Triggering of cancer cell cycle arrest by a novel scorpion venom-derived peptide—Gonearrestide. J. Cell. Mol. Med. 2018, 22, 4460–4473. [Google Scholar] [CrossRef] [Green Version]
  132. Zeng, Z.; Zhang, R.; Hong, W.; Cheng, Y.; Wang, H.; Lang, Y.; Ji, Z.; Wu, Y.; Li, W.; Xie, Y. Histidine-rich Modification of a Scorpion-derived Peptide Improves Bioavailability and Inhibitory Activity against HSV-1. Theranostics 2018, 8, 199–211. [Google Scholar] [CrossRef] [PubMed]
  133. Yu, Y.; Deng, Y.Q.; Zou, P.; Wang, Q.; Dai, Y.; Yu, F.; Du, L.; Zhang, N.N.; Tian, M.; Hao, J.N.; et al. A peptide-based viral inactivator inhibits Zika virus infection in pregnant mice and fetuses. Nat. Commun. 2017, 8, 1–12. [Google Scholar] [CrossRef]
  134. Ji, Z.; Li, F.; Xia, Z.; Guo, X.; Gao, M.; Sun, F.; Cheng, Y.; Wu, Y.; Li, W.; Ali, S.A.; et al. The Scorpion Venom Peptide Smp76 Inhibits Viral Infection by Regulating Type-I Interferon Response. Virol. Sin. 2018, 33, 545–556. [Google Scholar] [CrossRef]
  135. El-Bitar, A.M.; Sarhan, M.M.; Aoki, C.; Takahara, Y.; Komoto, M.; Deng, L.; Moustafa, M.A.; Hotta, H. Virocidal activity of Egyptian scorpion venoms against hepatitis C virus. Virol. J. 2015, 12, 47. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  136. Zabihollahi, R.; Pooshang Bagheri, K.; Keshavarz, Z.; Motevalli, F.; Bahramali, G.; Siadat, S.D.; Momen, S.B.; Shahbazzadeh, D.; Aghasadeghi, M.R. Venom components of Iranian scorpion Hemiscorpius lepturus inhibit the growth and replication of human immunodeficiency virus 1 (HIV-1). Iran. Biomed. J. 2016, 20, 259–265. [Google Scholar]
  137. Deng, S.Q.; Chen, J.T.; Li, W.W.; Chen, M.; Peng, H.J. Application of the Scorpion Neurotoxin AaIT against Insect Pests. Int. J. Mol. Sci. 2019, 20, 3467. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  138. Gordon, D. A new approach to insect-pest control—combination of neurotoxins interacting with voltage sensitive sodium channels to increase selectivity and specificity. Invertebr. Neurosci. 1997, 3, 103–116. [Google Scholar] [CrossRef]
  139. Attarde, S.S.; Pandit, S.V. Scorpion venom as therapeutic agent-current perspective. Int. J. Curr. Pharm. Res. 2016, 7, 59–72. [Google Scholar]
  140. Crest, M. Kaliotoxin, a novel peptidyl inhibitor of neur onal BK-type Ca(2þ)-activated K þ channels characterized from Androctonus mauretanicus mauretanicus venom. J. Biol. Chem. 1992, 267, 1640–1647. [Google Scholar] [CrossRef]
  141. Chen, R.; Chung, S.H. Engineering a potent and specific blocker of voltage-gated potassium channel Kv1.3, a target for autoimmune diseases. Biochemistry 2012, 51, 1976–1982. [Google Scholar] [CrossRef]
  142. Adi-Bessalem, S.; Hammoudi-Triki, D.; Laraba-Djebari, F. Pathophysiological effects of Androctonus australis hector scorpion venom: Tissue damages and inflammatory response. Exp. Toxicol. Pathol. 2008, 60, 373–380. [Google Scholar] [CrossRef]
  143. Adi-Bessalem, S.; Hammoudi-Triki, D.; Laraba-Djebari, F. Scorpion Venom Interactions with the Immune System; Gopalakrishnakone, P., Possani, L.D.F., Schwartz, E., Rodríguez de la Vega, R.C., Eds.; Scorpion Venoms; Springer: Dordrecht, The Netherlands, 2015; pp. 87–107. [Google Scholar]
  144. Pucca, M.B.; Cerni, F.A.; Cordeiro, F.A.; Peigneur, S.; Cunha, T.M.; Tytgat, J.; Arantes, E.C. Ts8 scorpion toxin inhibits the Kv4.2 channel and produces nociception in vivo. Toxicon 2016, 119, 244–252. [Google Scholar] [CrossRef]
  145. Hmed, B.N.; Serria, H.T.; Mounir, Z.K. Scorpion peptides: Potential use for new drug development. J. Toxicol. 2013, 2013, 958797. [Google Scholar] [CrossRef]
  146. Lu, X.; Lu, D.; Scully, M.F.; Kakkar, V.V. Integrins in drug targeting-RGD templates in toxins. Curr. Pharm. Des. 2006, 12, 2749–2769. [Google Scholar] [CrossRef] [PubMed]
  147. McLane, M.A.; Joerger T Mahmoud, A. Disintegrins in health and disease. Front. Biosci. A J. Virtual Libr. 2008, 13, 6617–6637. [Google Scholar] [CrossRef] [PubMed]
  148. Hasan, H.F.; Radwan, R.R.; Galal, S.M. Bradykinin-potentiating factor isolated from Leiurus quinquestriatus scorpion venom alleviates cardiomyopathy in irradiated rats via remodelling of the RAAS pathway. Clin. Exp. Pharmacol. Physiol. 2020, 47, 263–273. [Google Scholar] [CrossRef]
  149. Rocha-Resende, C.; Leão, N.M.; de Lima, M.E.; Santos, R.A.; Pimenta, A.M.C.; Verano-Braga, T. Moving pieces in a cryptomic puzzle: Cryptide from Tityus serrulatus Ts3 Nav toxin as potential agonist of muscarinic receptors. Peptides 2017, 98, 70–77. [Google Scholar] [CrossRef] [PubMed]
  150. Xiong, Y.M.; Lan, Z.D.; Wang, M.; Liu, B.; Liu, X.Q.; Fei, H.; Xu, L.G.; Xia, Q.C.; Wang, C.G.; Wang, D.C.; et al. Molecular characterization of a new excitatory insect neurotoxin with an analgesic effect on mice from the scorpion Buthus martensi Karsch. Toxicon 1999, 37, 1165–1180. [Google Scholar] [CrossRef] [PubMed]
  151. Chen, B.; Ji, Y. Antihyperalgesia effect of BmK AS, a scorpion toxin, in rat by intraplantar injection. Brain Res. 2002, 952, 322–326. [Google Scholar] [CrossRef]
  152. Joseph, B.; George, J. Scorpion toxins and its applications. Int. J. Toxicol. Pharmacol. Res. 2012, 4, 57–61. [Google Scholar]
  153. Xie, J.; Herbert, T.P. The role of mammalian target of rapamycin (mTOR) in the regulation of pancreatic b-cellmass: Implications in the development of type-2 diabetes. Cell. Mol. Life Sci. CMLS 2012, 69, 1289–1304. [Google Scholar] [CrossRef] [PubMed]
  154. Bouafir, Y.; Ait-Lounis, A.; Laraba-Djebari, F. Improvement of function and survival of pancreatic betacells in streptozotocin-induced diabetic model by the scorpion venom fraction F1. Toxin Rev. 2016, 36, 1–8. [Google Scholar]
  155. Elshater, A.-E.; Salman, M.; Abd-Elhady, A. Physiological studies on the effect of a bradykinin potentiating factor (BPF) isolated from scorpion venom on the burnt skin of alloxan-induced diabetic Guinea pigs. Egypt. Acad. J. Biol. Sci. C Physiol. Mol. Biol. 2011, 3, 5–15. [Google Scholar] [CrossRef]
  156. Wang, C.G.; He, X.L.; Shao, F.; Liu, W.; Ling, M.H.; Wang, D.C.; Chi, C.W. Molecular characterization of an anti-epilepsy peptide from the scorpion Buthus martensi (Karsch). Eur. J. Biochem. 2001, 268, 2480–2485. [Google Scholar] [CrossRef] [Green Version]
  157. Villetti, G.; Bregola, G.; Bassani, F.; Bergamaschi, M.; Rondelli, I.; Pietra, C.; Simonato, M. Preclinical evaluation of CHF3381 as novel antiepileptic agent. Neuropharmacology 2001, 40, 866–878. [Google Scholar] [CrossRef]
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Figure 1. Worldwide scorpion distribution. Representative geographical distribution of scorpions. Durango State in Mexico is highlighted in red. The area in green illustrates where scorpions have been reported worldwide.
Figure 1. Worldwide scorpion distribution. Representative geographical distribution of scorpions. Durango State in Mexico is highlighted in red. The area in green illustrates where scorpions have been reported worldwide.
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Figure 2. Scorpions as an economic resource in Durango: (A) sold as souvenirs and included in alcoholic drinks, (B) used in desserts, and (C) as meals.
Figure 2. Scorpions as an economic resource in Durango: (A) sold as souvenirs and included in alcoholic drinks, (B) used in desserts, and (C) as meals.
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Figure 3. Scorpion nervous system. Graphic representation of a scorpion, where the silhouette is marked in gray and the protobrain connected to a ventral nerve cord, which runs along the length of the body, is highlighted in green. The nerves and ganglia that extend from this cord to the different bodily segments are also shown.
Figure 3. Scorpion nervous system. Graphic representation of a scorpion, where the silhouette is marked in gray and the protobrain connected to a ventral nerve cord, which runs along the length of the body, is highlighted in green. The nerves and ganglia that extend from this cord to the different bodily segments are also shown.
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Figure 4. Scorpion body fluorescence. A 16-megapixel camera was used to photograph a Durango scorpion’s full body, exposed to a blacklight blue fluorescent lamp (Wildfire SableLux® BLB lamp with a peak wavelength of 368 nm). To obtain a better resolution of nonresponsive body parts, the animal was exposed to a light beam of 475/505 nm (λex/λem), and multiple sequential images were taken, using the 5× objective of an epifluorescent-inverted microscope (Nikon ECLIPSE TS2) coupled with a digital camera (Infinity 3 Lumenera); then, a panorama collection was assembled with PTGui 12.13 software. Circles show: (A) the stinger at the end of tail; (B) median ocelli on the middle of the head; (C) lateral ocelli and eye spot (shown as a little black spot above the left ocellus); (D,E) the fingers on the pedipalps, and (F) mandibular teeth. Scorpion body segments are indicated as follows: prosoma (head), mesosoma (abdomen) and metasoma (tail).
Figure 4. Scorpion body fluorescence. A 16-megapixel camera was used to photograph a Durango scorpion’s full body, exposed to a blacklight blue fluorescent lamp (Wildfire SableLux® BLB lamp with a peak wavelength of 368 nm). To obtain a better resolution of nonresponsive body parts, the animal was exposed to a light beam of 475/505 nm (λex/λem), and multiple sequential images were taken, using the 5× objective of an epifluorescent-inverted microscope (Nikon ECLIPSE TS2) coupled with a digital camera (Infinity 3 Lumenera); then, a panorama collection was assembled with PTGui 12.13 software. Circles show: (A) the stinger at the end of tail; (B) median ocelli on the middle of the head; (C) lateral ocelli and eye spot (shown as a little black spot above the left ocellus); (D,E) the fingers on the pedipalps, and (F) mandibular teeth. Scorpion body segments are indicated as follows: prosoma (head), mesosoma (abdomen) and metasoma (tail).
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Figure 5. Electrical extraction of venom. Two people work together to milk fresh venom. Collecting the droplets that dribble from the venom gland is a dangerous task, as the scorpion is alive.
Figure 5. Electrical extraction of venom. Two people work together to milk fresh venom. Collecting the droplets that dribble from the venom gland is a dangerous task, as the scorpion is alive.
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Figure 6. Venom from Centruroides suffusus scorpions interacts with sodium and potassium voltage−gated ion channels. (A) Cartoon of the COVC electrophysiology technique setup. An oocyte (green-brown sphere) that heterologously expresses a voltage-gated ion channel is placed into the recording chamber, where it is electrically separated into three regions, the top, middle and bottom, leaving exposed a fraction of the membrane where the voltage stimulus is imposed and controlled (top chamber) by the feedback of the capacitance and resistance process. In response to the stimulus, the ion channels produce a macroscopic current due the passive flux of ions through its aqueous pores. Then, the ion current is amplified and recorded by an acquisition system controlled by a computer (see Stefani and Bezanilla (1998) [76] for more details). Because this methodology provides access to the interior (and exterior) of the cell, it is possible to perform studies of ion channels under physiological environment conditions. Representative records elicited from two different oocytes expressing (B) Mouse NaV 1.4 sodium ion channel and (C) Shaker KV ion channel from Drosophila melanogaster. Ion currents were elicited via a voltage pulse stimulus, shown on the top of each recording first in the absence of venom (black) and then in the presence of a 103 (a thousand)-fold dilution of venom (red). Dashed lines represent a zero level of current. Vertical and horizontal bars represent the current amplitude and temporal pulse duration scale for each recording. The chemical reagents used for these representative recordings were acquired from Sigma-Aldrich (Sigma−Aldrich Co., St. Louis, MO, USA). Each electrophysiological experiment was repeated at least three times in order to verify the trend observed. More detailed information regarding the electrophysiology methods and heterologous expression of ion channels in Xenopus oocytes can be found in Rodriguez-Rangel et al., (2020) [80].
Figure 6. Venom from Centruroides suffusus scorpions interacts with sodium and potassium voltage−gated ion channels. (A) Cartoon of the COVC electrophysiology technique setup. An oocyte (green-brown sphere) that heterologously expresses a voltage-gated ion channel is placed into the recording chamber, where it is electrically separated into three regions, the top, middle and bottom, leaving exposed a fraction of the membrane where the voltage stimulus is imposed and controlled (top chamber) by the feedback of the capacitance and resistance process. In response to the stimulus, the ion channels produce a macroscopic current due the passive flux of ions through its aqueous pores. Then, the ion current is amplified and recorded by an acquisition system controlled by a computer (see Stefani and Bezanilla (1998) [76] for more details). Because this methodology provides access to the interior (and exterior) of the cell, it is possible to perform studies of ion channels under physiological environment conditions. Representative records elicited from two different oocytes expressing (B) Mouse NaV 1.4 sodium ion channel and (C) Shaker KV ion channel from Drosophila melanogaster. Ion currents were elicited via a voltage pulse stimulus, shown on the top of each recording first in the absence of venom (black) and then in the presence of a 103 (a thousand)-fold dilution of venom (red). Dashed lines represent a zero level of current. Vertical and horizontal bars represent the current amplitude and temporal pulse duration scale for each recording. The chemical reagents used for these representative recordings were acquired from Sigma-Aldrich (Sigma−Aldrich Co., St. Louis, MO, USA). Each electrophysiological experiment was repeated at least three times in order to verify the trend observed. More detailed information regarding the electrophysiology methods and heterologous expression of ion channels in Xenopus oocytes can be found in Rodriguez-Rangel et al., (2020) [80].
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Table
Table 1. Insight into the potential application of scorpion venom.
Table 1. Insight into the potential application of scorpion venom.
UsesReferences
Analgesic[93,94,95,96,97,98]
Antibacterial[83,89,90,99,100]
Anticancer[101,102,103,104,105,106,107,108,109,110,111]
Antifungal[112,113,114,115,116,117]
Antiparasitic[118,119,120,121,122]
Antitumoral[123,124,125,126,127,128]
Antiviral[129,130,131,132,133,134,135,136]
Insect pests[137,138]
Treatment for autoimmune diseases[139,140,141,142,143,144]
Treatment for cardiovascular diseases[145,146,147,148]
Treatment for chronic pain[149,150,151,152]
Treatment for diabetes[153,154,155]
Treatment for epilepsy[156,157]
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Gonzalez-Ponce, E.; Rodríguez-Rangel, S.; Martinez, R.; Alvarado, A.; Ruiz-Baca, E.; Miranda, P.; Sánchez-Rodríguez, J.E.; Lopez-Rodriguez, A. Scorpions, Science and Folklore in Durango City. Diversity 2023, 15, 743. https://doi.org/10.3390/d15060743

AMA Style

Gonzalez-Ponce E, Rodríguez-Rangel S, Martinez R, Alvarado A, Ruiz-Baca E, Miranda P, Sánchez-Rodríguez JE, Lopez-Rodriguez A. Scorpions, Science and Folklore in Durango City. Diversity. 2023; 15(6):743. https://doi.org/10.3390/d15060743

Chicago/Turabian Style

Gonzalez-Ponce, Eduardo, Sofia Rodríguez-Rangel, Raymundo Martinez, Adrian Alvarado, Estela Ruiz-Baca, Pablo Miranda, Jorge E. Sánchez-Rodríguez, and Angelica Lopez-Rodriguez. 2023. "Scorpions, Science and Folklore in Durango City" Diversity 15, no. 6: 743. https://doi.org/10.3390/d15060743

APA Style

Gonzalez-Ponce, E., Rodríguez-Rangel, S., Martinez, R., Alvarado, A., Ruiz-Baca, E., Miranda, P., Sánchez-Rodríguez, J. E., & Lopez-Rodriguez, A. (2023). Scorpions, Science and Folklore in Durango City. Diversity, 15(6), 743. https://doi.org/10.3390/d15060743

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