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Review

Cucurbits Plants: A Key Emphasis to Its Pharmacological Potential

by
Bahare Salehi
1,
Esra Capanoglu
2,
Nabil Adrar
3,
Gizem Catalkaya
2,
Shabnum Shaheen
4,
Mehwish Jaffer
4,
Lalit Giri
5,
Renu Suyal
5,
Arun K Jugran
6,
Daniela Calina
7,
Anca Oana Docea
8,
Senem Kamiloglu
9,
Dorota Kregiel
10,
Hubert Antolak
10,
Ewelina Pawlikowska
10,
Surjit Sen
11,12,
Krishnendu Acharya
11,
Zeliha Selamoglu
13,
Javad Sharifi-Rad
14,*,
Miquel Martorell
15,*,
Célia F. Rodrigues
16,
Farukh Sharopov
17,
Natália Martins
18,19,* and
Raffaele Capasso
20,*add Show full author list remove Hide full author list
1
Student Research Committee, School of Medicine, Bam University of Medical Sciences, Bam 44340847, Iran
2
Faculty of Chemical & Metallurgical Engineering, Food Engineering Department, Istanbul Technical University, 34469 Maslak, Turkey
3
Laboratoire de Biotechnologie Végétale et d’Ethnobotanique, Faculté des Sciences de la Nature et de la Vie, Université de Bejaia, Bejaia 06000, Algérie
4
Department of Plant Sciences, LCWU, Lahore 54000, Pakistan
5
G.B. Pant National Institute of Himalayan Environment & Sustainable Development Kosi-Katarmal, Almora 263 643, India
6
G.B. Pant National Institute of Himalayan Environment & Sustainable Development Garhwal Regional Centre, Srinagar 246174, India
7
Department of Clinical Pharmacy, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania
8
Department of Toxicology, University of Medicine and Pharmacy of Craiova, 200349 Craiova, Romania
9
Mevsim Gida Sanayi ve Soguk Depo Ticaret A.S. (MVSM Foods), Turankoy, Kestel, 16540 Bursa, Turkey
10
Institute of Fermentation Technology and Microbiology, Lodz University of Technology, Wolczanska 171/173, 90-924 Lodz, Poland
11
Molecular and Applied Mycology and Plant Pathology Laboratory, Department of Botany, University of Calcutta, Kolkata 700019, India
12
Department of Botany, Fakir Chand College, Diamond Harbour, West Bengal 743331, India
13
Department of Medical Biology, Faculty of Medicine, Nigde Ömer Halisdemir University, Campus, 51240 Nigde, Turkey
14
Zabol Medicinal Plants Research Center, Zabol University of Medical Sciences, Zabol 61615-585, Iran
15
Department of Pharmacy, Faculty of Pharmacy, University of Concepcion, Concepcion 4070386, Chile
16
LEPABE, Department of Chemical Engineering, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, s/n, 4200-465 Porto, Portugal
17
Department of Pharmaceutical Technology, Avicenna Tajik State Medical University, Rudaki 139, Dushanbe 734003, Tajikistan
18
Faculty of Medicine, University of Porto, Alameda Prof. Hernâni Monteiro, 4200-319 Porto, Portugal
19
Institute for Research and Innovation in Health (i3S), University of Porto, 4200-135 Porto, Portugal
20
Department of Agricultural Sciences, University of Naples Federico II, 80055 Portici, Italy
 
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*
Authors to whom correspondence should be addressed.
Molecules 2019, 24(10), 1854; https://doi.org/10.3390/molecules24101854
Submission received: 2 April 2019 / Revised: 9 May 2019 / Accepted: 13 May 2019 / Published: 14 May 2019
(This article belongs to the Special Issue Plant Extracts: Biological and Pharmacological Activity)
Browse Figure
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Abstract

:
Cucurbita genus has received a renowned interest in the last years. This plant species, native to the Americas, has served worldwide folk medicine for treating gastrointestinal diseases and intestinal parasites, among other clinical conditions. These pharmacological effects have been increasingly correlated with their nutritional and phytochemical composition. Among those chemical constituents, carotenoids, tocopherols, phenols, terpenoids, saponins, sterols, fatty acids, and functional carbohydrates and polysaccharides are those occurring in higher abundance. However, more recently, a huge interest in a class of triterpenoids, cucurbitacins, has been stated, given its renowned biological attributes. In this sense, the present review aims to provide a detailed overview to the folk medicinal uses of Cucurbita plants, and even an in-depth insight on the latest advances with regards to its antimicrobial, antioxidant and anticancer effects. A special emphasis was also given to its clinical effectiveness in humans, specifically in blood glucose levels control in diabetic patients and pharmacotherapeutic effects in low urinary tract diseases.

1. Introduction

Cucurbita plants have been applied in different cultures as traditional medication. For instance, Native Americans have used pumpkins for the treatment of intestinal worms and urinary ailments, this therapeutic strategy being approved by American doctors in the early nineteenth century as an anthelmintic for worms annihilating [1]. Seeds are used as an anthelmintic, to treat issues of the urinary framework, high blood pressure, to prevent the development of kidney stones, to ease prostate disorders and even to improve the erysipelas skin contamination [2]. In southeastern Europe, Cucurbita pepo L. (pumpkin) seeds have been applied to heal irritable bladder and prostate enlargement. Specifically, in Germany, the use of pumpkin seeds was adopted for application by the authority for irritated bladder conditions and micturition problems of prostate enlargement, although the monograph written in 1985 noted a lack of pharmacological studies that could confirm its effective clinical effects. On the other hand, in the USA, the purchase of all such non-prescription medications for the therapy of prostate enlargement was banned in 1990. In traditional Chinese medicine, Cucurbita moschata Duchesne seeds were also applied for handling the parasitic diseases caused by worms, while Mexican herbalists have used Cucurbita ficifolia Bouché as a remedy for reducing blood sugar levels [3,4,5,6,7].
Indeed, increasing evidence has shown that cucurbits’ medicinal properties depend upon the chemical compounds present, which produce a specific physiological effect in the human body [8,9,10]. Specifically, cucurbits fruits are found to be beneficial in blood cleansing, purification of toxic substances and good for digestion, besides giving the required energy to improve human health. These species possess a higher amount of proteins, phytosterols [11,12], unsaturated fatty acids [13,14], vitamins (like carotenoids, tocopherols) [15] and microelements (e.g., zinc) [16]. Fruits, seeds and leaves from various Cucurbita members (pumpkin, watermelon, melon, cucumber squash, gourds, etc.) possess different pharmacological effects [17,18], such as antidiabetic [19,20,21], antiulcer, analgesic, nephroprotective [22] and anticancer activities [18]. In this sense, this review provides a detailed overview to the folk medicinal uses of Cucurbita plants, an in-depth insight on the latest advances regarding its antimicrobial, antioxidant and anticancer effects, and lastly, a special emphasis to its clinical effectiveness in humans, specifically in blood glucose levels control and low urinary tract diseases (Figure 1).

2. Cucurbita Plants: A Brief Overview to Its Ethnopharmacological Uses

Recent ethnopharmacological studies showed that C. pepo and Cucurbita maxima Duchesne are among the most commonly used Cucurbita plants for traditional medicinal treatments. As shown in Table 1, many different components of Cucurbita plants are applied in diverse regions of the globe for handling different diseases.
In particular, the positive health effects of C. maxima seeds are well-documented [23,25,26,27,28]. Raw C. maxima seeds are orally administered for the treatment of digestive disorders, such as intestinal worms [23,25], constipation [23] and vomiting blood and blood bile [26] by the local people in the Iberian Peninsula, Argentina and India, respectively. Also, sun-dried seeds of C. maxima are ingested in Mauritius for the treatment of renal failure [27], whereas raw seeds are consumed to treat prostatitis in the Agro Nocerino Sarnese in Campania, Southern Italy [28]. C. maxima seeds, fruits, flowers and leaves are also used as traditional medicine [24,26,27,29,30,31], where the treatment of urinary disorders, blood pressure regulation and prevention of constipation can be achieved with oral consumption of C. maxima fruits, and the wound healing with dermal application [26,27,30]. In Mkuranga district in Tanzania, C. maxima leaves are used for healing anemia [24], and in the Ashanti region in Ghana, this plant part is orally consumed for lung and head cancer treatment [31]. Furthermore, in Mauritius, C. maxima fruits are compressed externally on eyes against cataract [27], while in India the same petals are used to treat osteosarcoma [29]. Nonetheless, and to the authors knowledge, much is needed to support both the in vitro and in vivo biological effects of this plant, since most of the efforts has been made towards its agro-industrial applications.
With regards to C. pepo seeds, they are mainly regarded as agro-industrial wastes, while in some parts of the globe they are used raw, roasted or cooked, at a domestic scale [40]. Accordingly, in a study carried out in Ghimbi District in Southwest Ethiopia [32], it was reported that oral administration of cultivated seed of C. pepo is used as a gonorrhea therapy. Moreover, C. pepo seeds are also used as an herbal remedy by breast cancer patients in West Bank in Palestine [36]. In another study, conducted in Nkonkobe municipality in Eastern Cape, South Africa [35], it was indicated that arthritis and blood booster are treated with orally taken C. pepo leaves. C. pepo leaves are also used for the treatment of malaria and dandruff in the local government area in south-eastern Nigeria and Ghimbi District in Southwest Ethiopia, respectively [37,38]. In the latter study, it was also pointed out that the fruits of C. pepo are consumed to treat gastritis and stomachache [37]. Topical use of C. pepo fruit as an external antiseptic was reported in Ripollès district, the Pyrenees in Catalonia and Iberian Peninsula, whereas in the same location the flowers of this plant are used for antigenic, antidermatitic, antiecchymotic, antiophidian, antipyretic and anti-toxic purposes [34]. C. pepo, as the whole plant, is also applied in the folk medicine of Mesoamerica and Caribbean for the therapy of fitness due to its pancreatic lipase inhibition activity [33]. In addition to the above, the decoction prepared from the Cucurbita galeottii Cogn. seeds is used against mucous discharge in Mauritius [39].

3. Cucurbita Plants Phytochemical Composition

Carotenoids are highly present in the fruit of these plants, namely α-carotene, β-carotene, ζ-carotene, neoxanthin, violaxanthin, lutein, zeaxanthin, taraxanthin, luteoxanthin, auroxanthine, neurosporene, flavoxanthin, 5,6,5′,6′-diepoxy-β-carotene, phytofluene, α-cryptoxanthin and β-cryptoxanthin [41]. Total carotenoid content varied between 234.21 μg/g to 404.98 μg/g in C. moschata fruit [42], and 171.9 μg/g to 461.9 μg/g in C. pepo fruit [43]. There are also several publications on the carotenoid content of a number of Cucurbita plants such as C. moschata, C. pepo [42] and C. maxima [44]. Edible Cucurbita seeds are also rich in vitamin E (49.49 μg/g to 92.59 µg/g), γ-tocopherol is more abundant than α-tocopherol and the fruit contains less [45].
The study of Yang et al. [46] showed no flavonoid content (below detection limit: 0.05 mg/100 g) in either the immature or the mature fruit of C. maxima. Only the shoots and buds showed positive results. Sreeramulu and Raghunath [47] reported that average total phenolic content of C. maxima was 46.43 mg gallic acid equivalent (GAE)/100 g. In another study, C. maxima was analyzed for its flavonoid content and kaempferol was found to be the only flavonoid in this species at a concentration of 371.0 mg/kg of dry weight [48].
C. pepo was found to be very weak in polyphenol content. Only 0.02 mg GAE/100 mg sample has been found in its fresh fruit by Mongkolsilp et al. [49]. However, Iswaldi et al. [50] have reported for the first time a list of 34 polyphenols including a variety of flavonoids in the fruit of C. pepo., in addition to other unknown polar compounds. Besides, the flowers of C. pepo may contain considerable amount of phenolic compounds. Andjelkovic et al. [51] studied the phenolic content of six pumpkin (C. pepo) seed oils and identified the following compounds: Tyrosol, vanillic acid, vanillin, ferulic acid and luteolin. Among them, tyrosol was the most abundant compound ranging from 1.6 mg/kg to 17.7 mg/kg.
Peričin et al. [52] studied the phenolic acid content of C. pepo seeds. p-Hydroxybenzoic acid was found to be the prevailing phenolic acid, with 34.72%, 67.38% and 51.80% of the total phenolic acid content in whole dehulled seed, kernels and hulls, respectively. Aside from p-hydroxybenzoic acid, the most dominant phenolic compounds can be listed in a decreasing order of quantity as follows: Caffeic, ferulic and vanillic acids in whole dehulled seeds. Trans-synapic and protocatechuic acids, and p-hydroxybenzaldehyde were the abundant phenolic acids presented in the kernels of hulled pumpkin variety; the hulls comprised p-hydroxybenzaldehyde, vanillic and protocatechuic acids with considerable amounts. Table 2 presents the main phenolic compounds found in the Cucurbita spp. and their structures.

4. Looking at Cucurbita Plants Biological Activity

4.1. Antimicrobial Activity of Cucurbita Plants

4.1.1. In Vitro Studies

Pumpkin extracts showed a positive activity towards bacterial and fungal infections. They were effective against gram-positive: Staphylococcus aureus, Bacillus subtilis, as well as gram-negative bacterium: Escherichia coli, Proteus vulgaris, Pseudomonas aeruginosa, Salmonella spp. or Klebsiella spp. Pumpkin extracts also showed antibacterial activity against water borne bacteria Vibrio cholerae as well as intestinal flagellated parasite Giardia lamblia, often isolated from surface water. Other studies documented that pumpkin extracts showed a wide range of antifungal activity against species from the Fusarium, Trichoderma, Aspergillus, Verticillium, Phytophora, Botrytis, Candida and Saccharomyces genera (Table 3). However, the mechanisms of antimicrobial activity of pumpkin extracts are still unknown, although it seems to exist a synergistic action between all extracted bioactive substances. It is well known that plant extracts exert biological effects more prominent than their isolated compounds. In fact, recent evidence has established that, in whole matrices, the major compounds interact with those in trace amounts to potentiate their own potential, to provide additional properties other than those often recommended and even to help counterbalance the side effects of these isolated compounds. In addition, and not the least important to emphasize, is that such minor compounds by strengthening the biological effects of a specific bioactive also reduces the dose required to achieve a similar effect.

4.1.2. In Vivo Studies

Not only pumpkin extracts, but also proteins and peptides isolated from Cucurbita spp. were identified and characterized in terms of antimicrobial activity. Three pumpkin proteins inhibited the growth of fungi Fusarium oxysporum, Verticillium dahliae and Saccharomyces cerevisiae [68]. The antifungal peptide—cucurmoschin—isolated from black pumpkin seeds also demonstrated inhibitory activity against mold growth: Botrytis cinerea, F. oxysporum and Mycosphaerella oxysporum [69]. The ribosome-inactivating protein extracted from C. moschata showed an antimicrobial effect towards phytopathogenic fungi Phytophora infestans as well as against bacteria Pseudomonas solanacearum and Erwinia amylovora [70]. Additionally, PR-5 protein isolated from leaves of pumpkin, demonstrated synergism with combination of nikkomycin, a chitin synthase inhibitor, towards to Candida albicans [71]. Protein Pr-1 isolated from pumpkin rind inhibited the growth of plant pathogenic fungi, namely B. cinerea, F. oxysporum, F. solani and Rhizoctonia solani, as well as the opportunistic pathogenic yeast C. albicans [72]. These results demonstrate that the proteins from pumpkin may be of importance to clinical microbiology with a wide range of therapeutic applications (Table 4). As the most prominent ones, and given the current evidence, namely regarding its ability to trigger fungal membranes damages and to improve the plasma membranes permeability, they can be effectively used to combat fungal infections and even to use in combination with current antifungal agents, both to improve its effectiveness and even to reduce its side effects.
Pumpkin pulp, due to its antimicrobial properties, is widely used to relieve intestinal inflammation or stomach disorders [73] (Table 5). Pumpkin and its seeds, in the traditional world medicine, are often employed as an anti-helminthic remedy and for supportive therapy in functional diseases of the bladder as well as in the case of digestion problems. The usage of an extract of C. pepo cortex towards urinary tract infections may correspond to a new source of antibiotics against bacterial urinary tract infections [57]. Other studies represented the importance of oil from seeds of a pumpkin as a hopeful drug for treating wounds in vivo [74]. The researchers demonstrated a premium quality of pumpkin oil with a high quantity of polyunsaturated fatty acids, tocopherols that were able to perform efficient wound healing [74]. Morphometric evaluation and histological evidence in rats showed healed biopsies from pumpkin oil and a complete re-epithelialization with a recurrence of skin appendages and well re-growing collagen fibers out of cells inflammation.
Pumpkin-based foodstuff is well recognized as a source of anti-inflammatory remedies, which can be useful in arthritis treatment [75]. Pumpkin seed oil notably prevent adjuvant-induced arthritis in rats, similar to indomethacin, a well-known anti-inflammatory substance. Its clinical applicability as an antioxidant was also assessed on rheumatoid arthritis [76] and recently confirmed by Dixon [77].

4.2. Anticancer Activities of Cucurbita Plants

Cucurbitacins are a unique gathering of triterpenoids that containing a cucurbitane basic structure skeleton, and an extensive variety of natural exercises is related with their substance basic multifaceted nature. Cucurbitacins have been accounted for the most secondary metabolites in the Cucurbitaceae. They have the biogenetically 10α-cucurbit-5-ene [19(10→19β) abeo-10α-lanostane skeleton, which is related to their cytotoxicity. A few reports credited in vitro and in vivo cytotoxic exercises to the cucurbitacins [79,80]. Jayaprakasam et al. [81] exhibited the anticancer properties of cucurbitacins B, D, E and I, confined from the products of Cucurbita andreana Naudin, towards colon, bosom, lung and focal sensory system disease cell lines. Cucurbitacin B is the most considered and keeping in mind that few investigations exhibited its viability in various models of malignant growth, incorporating into vivo tumor xenografts [82,83,84,85], there is a contradiction concerning the components hidden its anticancer action. Concealment of the oncogene STAT 3 (signal transducer and activator of transcription 3) has all the earmarks of being identified with tumor restraint [86], which does not prohibit elective. A malignant growth is in charge of 12% of the global impermanence. Medications incorporate chemotherapy medical procedure and radiation therapy. Be that as it may, chemotherapy endures constraints of medication obstruction, poisonous quality, reactions and lacking explicitness toward tumor cells [87]. Consequently, there is a solid enthusiasm for the utilization of plants as a promising wellspring of increasingly productive anticancer medications.

In Vitro Anticancer/Antitumor Effects

Presently over forty cucurbitacins have been isolated from the Cucurbitaceae family and different types of the herbs. The apoptotic impacts of cucurbitacins are expected of their capacity to change the qualities, transcriptional exercises using atomic components and mitochondrial trans-film potential and their ability to initiate or hinder ace or hostile to apoptotic proteins. Cucurbitacins are specific inhibitors of the JAK/STAT pathways; likewise, different instruments are involved in their apoptotic impacts, for example, PARP cleavage, MAPK pathway, articulation of dynamic caspase-3, diminished JAK3 and pSTAT3 levels and also diminishes in different downstream STAT3 targets, for example, Bcl-2, Mcl-1, cyclin D3 and BclxL, which are all embroiled in the cell cycle control [88].
C. pepo alcohol extract demonstrated cytotoxicity towards HepG2 and CT26 cell lines with IC50 values 132.6 μg/mL and 167.2 μg/mL, individually. The ethanol extract of C. pepo was displayed a huge portion subordinate inhibitory impact towards HeLa cell development [89].
Cucurbita glycosides A and B isolated from C. pepo ethanol extract demonstrated cytotoxic action in vitro towards HeLa cells with IC50 17.2 μg/mL and 28.5 μg/mL, individually [90]. Cucurbitacin B and E isolated from C. pepo cv dayangua demonstrated an antiproliferative in MCF-7, HCT-116, SF-268, A549 and NCI-H460 cell lines [81].
The antiproliferative impact of 23,24-dihydrocucurbitacin F, on human PCa cells may jump out at the enlistment of the cofilin-actin pole development and actin collection delivering to cell cytokinesis disappointment, hindered cell development cycle capture at G2/M stage and apoptosis [91]. Likewise, 23,24-dihydrocucurbitacin F has an inhibitory effect on Epstein-Barr infection actuation initiated by the tumor advertiser, 12-O-tetradecanoyl-phorbol-13-acetic acid derivation and furthermore, shows altogether hostile to tumor-advancement action on mouse skin tumor advancement [88].
Treatment with cucurbitacins B and E resulted in apoptosis and cell cycle capture of MDAMB-231 and MCF-7 breast cancer cell lines. Additionally, they tweaked the outflow of proteins associated with cell-cycle control in both of the estrogen-autonomous (MDA-MB-231) and estrogen-subordinate (MCF-7) in human bosom malignant growth cell lines. Growth hindrance and cytotoxic impact of cucurbitacin B on bosom disease cell lines SKBR-3 and MCF-7 were credited to G2/M stage capture and apoptosis. Cucurbitacin B treatment repressed Cyclin D1, c-Myc and β-catenin articulation levels, translocation to the core of β-catenin and galectin-3. Western smear investigation demonstrated expanded PARP cleavage proposing actuated caspase action and diminished mitogenic Wnt-related flagging particles galectin-3, β-catenin, c-Myc and cyclin D1 with changes in phosphorylated GSK-3β levels [92].
Cucurbitacin E caused disturbance of the cytoskeleton structure of actin and vimentin inhibiting the multiplication of prostate disease cells. Cucurbitacins also additionally hindered the expansion of endothelial cells joined by an interruption of the F-actin and tubulin microfilaments cytoskeleton, typical mitogen-prompted T-lymphocytes and lessened cell motility recommend an enemy of angiogenesis and hostile to the metastasis job for cucurbitacins. It is also fit for instigating and keeping up high multiplication rates in lymphocytes [93].
The literature has indicated that secondary metabolites of C. pepo have the potential anticancer activity, which represents great interest for the development of new chemotherapeutic agents for preventive growth of the tumor.

5. Clinical Effectiveness of Cucurbita Plants in Humans

5.1. Control of Blood Glucose Level in Diabetic Patients

Diabetes mellitus is a chronic disease characterized by changes in saccharide, lipid and protein metabolism resulting from a deficiency in insulin secretion from the pancreas, insulin resistance or both. The main clinical symptom is represented by increased blood sugar levels (hyperglycemia) that uncontrolled lead in time to a wide spectrum of complications [94]. Natural therapeutic alternatives to allopathic treatment always attracted the researchers to the intention of finding new drugs with fewer side effects [95,96,97,98,99,100]. Thus, the hypoglycemic effect of Cucurbita species (Table 6) is known and used for long traditional medicine in many countries, like China, India, Iran and Mexico [101,102,103,104].
Mahmoodpoor et al. [106] in a recent study performed on patients with severe diabetes from the Intensive Care Unit showed the hypoglycemic effect of C. maxima pulp. The subjects received five grams of C. maxima powder per 12 h for three consecutive days. After the treatment, it was observed a decrease of serum glucose levels from 214.9 mg/dL to 214.9 mg/dL associated with a reduction of insulin doses from 48.05 IU to 39.5 IU [106]. C. ficifolia also showed a good hypoglycemic effect when the extract was administered in doses of 4 mL/kg to patients with type 2 diabetes and moderately elevated blood glucose level [105]. Five hours after administration, the mean of serum glucose level decreased from 217.2 mg/dL to 150.8 mg/dL [105].
The most important hypoglycemic active substances in pumpkin are non-pectines polysaccharides and pectines from pulp, proteins and oil obtained from seeds [107,108,109]. Alenazi et al. [118] reported a clinical case of a 12-year-old Asian diabetic patient that ate every day for four months 200 g of pumpkin. After two months of daily pumpkin consumption, a decrease of glycosylated hemoglobin (HbA1C) from 10.8% to 8.5% was observed [118]. The same positive hypoglycemic effect was also revealed in another study by Jain et al. [119]. Fourteen patients diagnosed with type 2 diabetes received C. ficifolia juice for 40 days, and glycosylated hemoglobin decreased with 22.5% [119]. Shi et al. [120] investigated the antidiabetic activity of pumpkin carbohydrate granules in patients with type 2 diabetes compared to a control placebo group. After one month of treatment, both blood and urine glucose levels were significantly decreased compared with the placebo control group [120]. The results of a randomized, placebo-controlled trial conducted showed that a rich diet in pumpkin (C. maxima) seeds significantly reduced postprandial blood glucose of adults with normal glycaemia [121]. This study included 25 normoglycemic adults who consumed daily 65 g of pumpkin seeds [121]. Possible mechanisms of antihyperglycemic action of Cucurbita species are not fully understood but several studies investigated this subject in the last decades. Zhang et al. [122] demonstrated that C. moschata heteropolysaccharides regenerate pancreatic islets by stimulating proliferation of pancreatic β-cells. Quanhong et al. [123] showed that polysaccharides bounded by protein (polysaccharide 41.21% and protein 10.13%) increase glucose tolerance level and reduce hyperglycemia. In the light of these results, supplements with natural extracts from Cucurbita plants can be considered as alternative hypoglycemic products and further multicenter randomized studies can confirm these results.

5.2. Pharmacotherapeutic Effects in Low Urinary Tract Diseases

Benign prostatic hyperplasia (BPH) represents an increase in the volume of the prostate under the influence of androgenic hormones, and 70% of aging men suffer from this condition. Since clinical evolution of urinary signs is slow, prevention of BPH is useful, phytotherapy being an alternative way [124]. For example, oil obtained from C. pepo seeds is traditionally used to treat urinary symptoms in BPH as the daily frequency of urination, nycturia, time of the bladder emptying and residual volume [110,111]. The main mechanism through which these effects are obtained is represented by the inhibition of 5-α-reductase. This enzyme is required to convert testosterone to dihydrotestosterone, which has a higher affinity than testosterone for androgen receptors. As a result, protein synthesis increases the volume of the prostate implicitly [113].
In a multicenter clinical trial, thousands of patients diagnosed with BPH were treated with capsules containing 500 mg of C. pepo seeds extracts. Their quality of life has been significantly improved by reducing the urinary symptoms of BPH [125].
Other modern studies have shown pharmacotherapeutic synergism in BPH when C. Pepo is administrated simultaneously with other plants. Thus, the combination with Serenoa repens (W. Bartram) Small significantly improved the urinary symptoms of BPH and decreased blood dihydrotestosterone levels [111]. Hong et al. [112] obtained similar results on urinary symptoms in Korean men with BPH treated with 320 mg of C. pepo plus 320 mg of S. repens. They also observed a decrease in prostatic antigen levels after the treatment, but without changes in prostate volume [112]. In a randomized Phase II clinical trial carried out by Coulson et al. [126] the efficacy of the ProstateEZE Max formulation obtained from a mixture of plants traditionally used in treating BPH was evaluated. ProstateEZE is a natural formulation containing C. pepo, S. repens, Pygeum africanum Hook.f., E. parviflorum Schreb. and lycopene. Fifty-seven male patients diagnosed with BPH were selected in the study. Thirty-two of them received a capsule of ProstateEZE Max daily for three consecutive months, and 25 patients were treated with a placebo. In patients treated with Prostate EZE, the clinical symptoms of BPH decreased by 35.9% compared with only 8.3% for the placebo. The frequency of nocturnal urination was reduced with 39.3% in subjects treated for three months with ProstateEZE compared to the placebo group [126].
Due to these beneficial therapeutic effects of Cucurbita plants in BPH, the European Medicines Agency approved the use of C. pepo for both BPH and other bladder disorders, such as urinary stress incontinence in women [127].
Urinary stress incontinence occurs when pelvic muscles that support the bladder and the sphincter muscle, which controls the urinary flow, are weakened. This disorder is associated with aging in women. The main symptom is urinary incontinence [115]. The seeds extract of C. pepo have a therapeutic effect in this condition through a double mechanism. Directly by relaxing the bladder muscles leading to a decrease in nycturia and indirectly through a hormonal mechanism by inhibiting 5-α reductase. This inhibition determines the anabolic effects that strengthen the bladder sphincter muscles [115,127]. The main chemical compounds in the pumpkin seeds that explain these effects are sterols (sitosterol, spinasterol) and fatty oil, which contain oleic, linoleic, palmitic acids and tocopherol) [114]. Gažová et al. [128] demonstrated these effects in a study of 86 women with urinary incontinence stress who were treated for twelve weeks with the preparation of a plant mix: C. pepo, Equisetum arvense L. and Linum usitatissimum L. Episodes of urinary incontinence during the day were reduced to 35% and nocturnal urinary frequency to 54% [128].
Overactive bladder syndrome (OAB) is characterized by the frequent urge to urinate during the day and night, followed by an involuntary loss of urine [116]. A human clinical trial conducted by Shim et al. (2014) investigated the efficacy and utility of Cucuflavone (tablets with a mixture of plant extracts 87.5% C. pepo seeds and 12.5% soy) in reducing OAB symptoms [116]. The active compounds of Cucuflavone are phenols (pyrogallol) and isoflavones (genistein, daidzin). One hundred and twenty patients were included in the study, divided into two groups: The Cucuflavone group and the placebo group. Patients from Cucuflavone group received two tablets twice a day (a total of 875 mg of C. pepo seed extract and 125 mg of soy extract daily) for twelve weeks. The final results of the investigation showed that urinary incontinence, the frequency of daily and nocturnal urination was statistically significantly reduced compared to the initial parameters [116]. In a recent investigation, Nishimura et al. obtained similar results. They confirmed the efficacy of C. maxima seeds oil on urinary disorders in OAB. Forty-five subjects with OAB were included and treated daily with 10 g of C. maxima seed oil for twelve weeks. At the end of the investigation, the frequency of average daily urination was reduced from 10.96 to 8.00 [117].

6. Conclusions and Future Perspectives

In short, the use of Cucurbita species and their active constituents in various clinical and pharmacological studies revealed the presence of multiple, effective and useful compounds, which provide the opportunity for further production of antidiabetic, analgesic, anti-inflammatory and cardioprotective drugs and foods. Indeed, the use of Cucurbita plants in the treatment of several diseases, including gastrointestinal disorders, intestinal parasites and hypertension, dates from a long time ago. The antimicrobial and antioxidant properties of these species have triggered a huge interest for multiple applications. First of all, free radicals are generated through various metabolic activities in the body, ultimately resulting in various deleterious diseases [99]. These diseases can be treated by supplementation of cucurbits as activities of some cucurbits are comparable with commercially available antibiotics. The present review markedly highlights that Cucurbita species have preventive and therapeutic abilities for treatment of different diseases. The presence of active phytochemicals in Cucurbita species further strengthens the opportunity for their application as an upcoming anticancer, antidiabetic, analgesic, anti-inflammatory and cardioprotective drugs, as well as foods. Finally, and not the least important, the application of Cucurbitaceae members in public health, as nutraceuticals is associated with great availability and a good safety profile.

Author Contributions

All authors contributed equally to this work. J.S.-R., M.M., N.M., and R.C., critically reviewed the manuscript. All the authors read and approved the final manuscript.

Funding

This research received no external funding.

Acknowledgments

This work was supported by CONICYT PIA/APOYO CCTE AFB170007. N. Martins would like to thank the Portuguese Foundation for Science and Technology (FCT-Portugal) for the Strategic project ref. UID/BIM/04293/2013 and “NORTE2020—Northern Regional Operational Program” (NORTE-01-0145-FEDER-000012) and C.F.R. for the project UID/EQU/00511/2019—Laboratory for Process Engineering, Environment, Biotechnology, and Energy—LEPABE funded by national funds through FCT/MCTES (PIDDAC).

Conflicts of Interest

The authors declare no conflict of interest.

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Molecules 24 01854 g001 550
Figure 1. Most pronounced and investigated biological effects of Cucurbita spp.
Figure 1. Most pronounced and investigated biological effects of Cucurbita spp.
Molecules 24 01854 g001
Table
Table 1. Cucurbita plants traditionally applied in the cures of different diseases in diverse regions of the world.
Table 1. Cucurbita plants traditionally applied in the cures of different diseases in diverse regions of the world.
Scientific Name (Common Name)LocationLocal NameParts UsedAdministrationDisease(s) TreatmentReferences
Cucurbita maxima Duchesne (Squash)Basque Country, Iberian PeninsulaKalabazeaSeedsOralDigestive (Intestinal worms, Constipation)[23]
Mkuranga District, TanzaniaMabogaLeavesOralAnemia[24]
Polish people in Misiones, ArgentinaZapalloSeedsOralIntestinal parasites[25]
Nelliyampathy hills of Kerala, IndiaParangiSeedsOralVomiting blood, Blood bile[26]
FruitsOralUrinal disorders
MauritiusGiromonFlowersDermalCataract[27]
SeedsOralRenal failure
FruitsDermalWound
Agro Nocerino Sarnese, Campania, Southern ItalyCocozzaSeedsOralProstatitis[28]
IndiaUNSPFlowersUNSPOsteosarcoma[29]
Pakistani descent in Copenhagen, DenmarkKadooFruitsOralBlood pressure, constipation[30]
Ashanti region, GhanaUNSPLeavesOralCancer (lung, head)[31]
Cucurbita pepo L. (Pumpkin)Ghimbi District, Southwest EthiopiaBuqqeeSeedsOralGonorrhea[32]
Mexico, Central America, CaribbeanCalabazaWhole plantOralObesity[33]
Ripollès district, Pyrenees, Catalonia, Iberian PeninsulaCarbassaFlowersDermalAcne, Dermatitis, Ecchymosis, Fever, Toxicity, Wound[34]
FruitsDermalInfection
Nkonkobe Municipality, Eastern Cape, South AfricaImithwaneLeavesOralArthritis, Blood booster[35]
West Bank, PalestineKare’aSeedsOralBreast cancer[36]
Delanta, Northwestern Wello, Northern EthiopiaUNSPFruitsOralGastritis, Stomachache[37]
LeavesDermalDandruff
Local Government Area,
south-eastern Nigeria		OkeuguLeavesOralMalaria[38]
Cucurbita galeottii Cogn. (Pumpkin)MauritiusGiraumonSeedsOralMucous discharge[39]
UNSP: Unspecified.
Table
Table 2. Main chemical structures of the phenolic compounds found in the Cucurbita spp.*.
Table 2. Main chemical structures of the phenolic compounds found in the Cucurbita spp.*.
Compound NameSynonym(s)Empirical FormulaStructureReferences
Protocatechuic acid3,4-Dihydroxybenzoic acidC7H6O4 Molecules 24 01854 i001[52]
http://phenol-explorer.eu/compounds/412
p-Hydroxybenzoic acid4-Hydroxybenzoic acidC7H6O3 Molecules 24 01854 i002[52]
http://phenol-explorer.eu/compounds/418
p-Hydroxybenzaldehyde4-HydroxybenzaldehydeC7H6O2 Molecules 24 01854 i003[52]
http://phenol-explorer.eu/compounds/725
Vanillic acid4-Hydroxy-3-methoxybenzoic acid; p-Vanillic acidC8H8O4 Molecules 24 01854 i004[52]
http://phenol-explorer.eu/compounds/414
Caffeic acid3,4-Dihydroxycinnamic acidC9H8O4 Molecules 24 01854 i005[52]
http://phenol-explorer.eu/compounds/457
Syringic acid3,5-Dimethoxy-4-hydroxybenzoic acidC9H10O5 Molecules 24 01854 i006[52]
http://phenol-explorer.eu/metabolites/420
trans-p-coumaric acidtrans-4-Hydroxycinnamic acidC9H8O3 Molecules 24 01854 i007[52]
http://phenol-explorer.eu/compounds/454
Ferulic acid3-Methoxy-4-Hydroxycinnamic acid; 3-Methylcaffeic acid; Coniferic acidC10H10O4 Molecules 24 01854 i008[52]
http://phenol-explorer.eu/compounds/459
trans-sinapic acidtrans-4-Hydroxy-3,5-dimethoxy-cinnamic acid; trans-Sinapinic acidC11H12O5 Molecules 24 01854 i009[52]
http://phenol-explorer.eu/compounds/464
Tyrosolp-HPEA; 4-(2-Hydroxyethyl)phenol; 2-(4-Hydroxyphenyl)ethanol; 2,4-Hydroxyphenyl-ethyl-alcohol; 4-HydroxyphenylethanolC8H10O2 Molecules 24 01854 i010[52]
http://phenol-explorer.eu/compounds/673
Vanillin4-Hydroxy-3-methoxy-benzoic aldehyde; Methylprotocatechuic aldehyde; Vanillic aldehyde; p-VanillinC8H8O3 Molecules 24 01854 i011[52]
http://phenol-explorer.eu/compounds/724
Luteolin5,7,3′,4′-TetrahydroxyflavoneC15H10O6 Molecules 24 01854 i012[52]
http://phenol-explorer.eu/compounds/229
Kaempferol3,5,7,4′-TetrahydroxyflavoneC15H10O6 Molecules 24 01854 i013[52]
http://phenol-explorer.eu/compounds/290
* The data were collected from the Phenol-Explorer database, which is an online comprehensive database on polyphenol contents in foods, http://phenol-explorer.eu/ (Accessed on 09.12.2018).
Table
Table 3. Antimicrobial activity of Cucurbita spp. extracts evaluated in vitro.
Table 3. Antimicrobial activity of Cucurbita spp. extracts evaluated in vitro.
Cucurbita spp./Plant PartExtractMicrobialReferences
Cucurbita pepo L.
fruits		WaterEscherichia coli[53]
Cucurbita pepo L.
fruits		MethanolBacillus cereus
Bacillus subtilis
Escherichia coli
Enterobacter aerogenes
Enterobacter agglomerans
Salmonella enteritidis
Salmonella choleraesuis
Staphylococcus aureus
Pseudomonas aeruginosa
Enterobacter faecalis
Klebsiella pneumoniae
Bacillus sphericus
Bacillus thruengenesis
Cryptococcus meningitis
Penicillium chrysogenum		[54]
Cucurbita pepo L.Phosphate buffered saline (PBS)Serratia marcescens
Escherichia coli
Streptococcus thermophilous
Fusarium oxysporium
Trichoderma reesei
Aspergillus niger		[55]
Cucurbita pepo L.
fruits		Ethanol extractHeligmosoides bakeri (worm)[56]
Cucurbita pepo L.
cortex		Water, methanolStaphylococcus aureus
Escherichia coli
Proteus mirabilis
Klebsiella pneumoniae		[57]
Cucurbita pepo L.
seeds, backpeel		Methanol,
ethanol		Staphylococcus aureus
Salmonella typhi		[58]
Cucurbita pepo L.
leaves		EthanolSerratia sp.
Escherichia coli
Klebsiella pneumoniae
Bacillus subtilis		[59]
Cucurbita pepo L.
leaves		MethanolProvidencia stuartii
Pseudomonas aeruginosa
Klebsiella pneumoniae
Escherichia coli
Enterobacter aerogenes
Enterobacter cloacae		[60]
Cucurbita pepo L.
leaves		Ethyl acetate, n-butanol, waterBacillus subtilis
Pseudomonas aeruginosa
Staphylococcus aureus		[61]
Cucurbita moschata Duchesne
seeds oil extract		MethanolCandida albicans
Rhodotorula rubra
Trichoderma viride
Penicillium chrysogenum
Rhizopus oligosporus		[62]
Cucurbita moschata Duchesne
crude protein from rinds, seeds and pulp		AcetoneAspergillus fumigatus
Aspergillus parasiticus
Aspergillus niger
Staphylococcus aureus
Bacillus subtilis
Klebsiella pneumoniae
Pseudomonas aeruginosa
Escherichia coli		[62]
Cucurbita maxima Duchesne
fruit		Petroleum ether and methanolGiardia lamblia[63]
Cucurbita maxima Duchesne
flowers		AlcoholSalmonella typhi,
Escherichia coli
Enterobacter faecalis,
Bacillus cereus
Curvularia lunata
Candida albicans		[64]
Cucurbita maxima Duchesne
peels		WaterEscherichia coli
Pseudomonas sp.
Vibrio cholerae		[65]
Cucurbita maxima Duchesne
seeds		EthanolEntamoeba histolytica
Staphylococcus aureus
Bacillus subtilis
Pseudomonas aeruginosa
Escherichia coli
Candida albicans
Aspergillus niger		[66]
Cucurbita maxima Duchesne
seeds 		EthanolStaphylococcus aureus
Bacillus subtilis
Staphylococcus werneri
Pseudomonas putida
Pseudomonas aeruginosa
Proteus mirabilis
Escherichia coli
Kleibsella pneumoniae		[67]
Table
Table 4. In vitro antimicrobial activity of Cucurbita spp. proteins.
Table 4. In vitro antimicrobial activity of Cucurbita spp. proteins.
Cucurbita spp. ProteinsMicrobialReferences
Cucurbita maxima Duchesne seeds proteinsFusarium oxysporum,
Verticillium dahliae
Saccharomyces cerevisiae		[68]
Cucurbita maxima Duchesne seeds protein RIPPhytophora infestans,
Erwinia amylovora,
Pseudomonas solanacearum		[70]
Pumpkin leaves protein PR-5 Candida albicans[71]
Pumpkin rind protein Pr-1Botrytis cinerea,
Fusarium oxysporum,
Fusarium solani
Rhizoctonia solani,
Candida albicans		[72]
Black pumpkin seeds protein cucurmoschinBotrytis cinerea,
Fusarium oxysporum
Mycosphaerella oxysporum		[69]
Table
Table 5. Antimicrobial property of Cucurbita spp. and its importance in vivo.
Table 5. Antimicrobial property of Cucurbita spp. and its importance in vivo.
Antimicrobial PropertyReferences
Cucurbita pepo L. seedsWounds healing[74]
Pumpkin seeds Anthelmintic, treatment of bladder functional disorders [78]
Pumpkin seed oil Arthritis prevention[75]
Pumpkin fruitsControl of gastrointestinal nematode infections[56]
Cucurbita pepo L. cortex extractEffective treatment of bacterial urinary tract infections[57]
Table
Table 6. Pharmacotherapeutic effects of Cucurbita plants in human clinical studies.
Table 6. Pharmacotherapeutic effects of Cucurbita plants in human clinical studies.
Part of the Plant with Active CompoundsCucurbita spp.References
HypoglycemicPolysaccharides from pulp fruitCucurbita maxima Duchesne
Cucurbita ficifolia Bouché		[105,106]
Non-pectines polysaccharides and pectines from pulp; proteins and oil from seedsCucurbita ficifolia Bouché[107,108,109]
Reduced clinical symptoms of benign prostatic hyperplasiaΔ5-Δ7-Δ8-Phytosterols, unsaturated fatty acids from seeds extracts, lignansCucurbita pepo L.[110,111,112,113]
Positive effects in stress urinary incontinence in femaleOil, sterols from seedsCucurbita pepo L.[114,115]
Improved urinary symptoms in human overactive bladderSeeds oil (sterols) blended with soy germ extract (phenols, isoflavones)Cucurbita pepo L.[116]
Cucurbita maxima Duchesne[117]

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Salehi, B.; Capanoglu, E.; Adrar, N.; Catalkaya, G.; Shaheen, S.; Jaffer, M.; Giri, L.; Suyal, R.; Jugran, A.K.; Calina, D.; et al. Cucurbits Plants: A Key Emphasis to Its Pharmacological Potential. Molecules 2019, 24, 1854. https://doi.org/10.3390/molecules24101854

AMA Style

Salehi B, Capanoglu E, Adrar N, Catalkaya G, Shaheen S, Jaffer M, Giri L, Suyal R, Jugran AK, Calina D, et al. Cucurbits Plants: A Key Emphasis to Its Pharmacological Potential. Molecules. 2019; 24(10):1854. https://doi.org/10.3390/molecules24101854

Chicago/Turabian Style

Salehi, Bahare, Esra Capanoglu, Nabil Adrar, Gizem Catalkaya, Shabnum Shaheen, Mehwish Jaffer, Lalit Giri, Renu Suyal, Arun K Jugran, Daniela Calina, and et al. 2019. "Cucurbits Plants: A Key Emphasis to Its Pharmacological Potential" Molecules 24, no. 10: 1854. https://doi.org/10.3390/molecules24101854

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