Next Article in Journal
Responses of Tomato Plants under Saline Stress to Foliar Application of Copper Nanoparticles
Next Article in Special Issue
Inhibitory Activities of Momilactones A, B, E, and 7-Ketostigmasterol Isolated from Rice Husk on Paddy and Invasive Weeds
Previous Article in Journal / Special Issue
Myrica esculenta Buch.-Ham. ex D. Don: A Natural Source for Health Promotion and Disease Prevention
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Ethnopharmacological Properties and Medicinal Uses of Litsea cubeba

1
Department of Forestry, North Eastern Regional Institute of Science and Technology, Nirjuli 791109, India
2
School of Exercise and Nutrition Sciences, Deakin University, Burwood, VIC 3125, Australia
3
Molecular Genetics Lab, Department of Biotechnology, Yeungnam University, Gyeongsan, Gyeongbuk 38541, Korea
4
Department of Energy and Material Engineering, Dongguk University-Seoul, Seoul 04620, Korea
5
Stemforce, 302 Institute of Industrial Technology, Yeungnam University, Gyeongsan, Gyeongbuk 38541, Korea
*
Authors to whom correspondence should be addressed.
Plants 2019, 8(6), 150; https://doi.org/10.3390/plants8060150
Submission received: 8 May 2019 / Revised: 26 May 2019 / Accepted: 30 May 2019 / Published: 1 June 2019
(This article belongs to the Special Issue Plant Phytochemicals on Crop Protection and Biotechnology)

Abstract

:
The genus Litsea is predominant in tropical and subtropical regions of India, China, Taiwan, and Japan. The plant possesses medicinal properties and has been traditionally used for curing various gastro-intestinal ailments (e.g., diarrhea, stomachache, indigestion, and gastroenteritis) along with diabetes, edema, cold, arthritis, asthma, and traumatic injury. Besides its medicinal properties, Litsea is known for its essential oil, which has protective action against several bacteria, possesses antioxidant and antiparasitic properties, exerts acute and genetic toxicity as well as cytotoxicity, and can even prevent several cancers. Here we summarize the ethnopharmacological properties, essentials oil, medicinal uses, and health benefits of an indigenous plant of northeast India, emphasizing the profound research to uplift the core and immense potential present in the conventional medicine of the country. This review is intended to provide insights into the gaps in our knowledge that need immediate focus on in-situ conservation strategies of Litsea due to its non-domesticated and dioecious nature, which may be the most viable approach and intense research for the long-term benefits of society and local peoples.

Graphical Abstract

1. Introduction

Litsea cubeba Pers., Lauraceae, consists of more than 400 species [1] and is predominant in tropical and subtropical regions of India, Southeast Asia, southern China, Taiwan, and Japan. Litsea is evergreen, fast growing, and a rare deciduous tree or shrub that attains a height of about 8 m, growing spontaneously in the eastern Himalayas, Assam, Manipur, and Arunachal Pradesh up to an altitude of 2700 m from sea level [2]. In the Assam state of India, the tree is known as “mejankari”, while it is commonly called “May Chang” or “Chinese pepper” in China. Litsea plants are the primary source for traditional medicines but they also serve as a secondary source of food for muga silk worms (Antheraea assama) [3]. The muga silk (“mejankari pat”) produced from the Litsea plant is very attractive and more expensive than the silk produced from other plants [4]. The silk cocoons fed with Litsea produce high value silk, which is creamy, glossy, and five times more expensive than silk produced from a primary source of food plant, i.e., Machilus bombycina King [3].
Litsea cubeba is a pioneer herb traditionally utilized in medicine. Different extracts from its plant parts, such as bark, leaf, root, and fruits, have been utilized in traditional Chinese medicines for curing various diseases [5,6]. The fresh green fruit is used for culinary purposes like salad preparation, chutneys, pickles, etc. [7]. The L. cubeba essential oil (LEO) extracted from fresh fruits contains about 60–90% citral content [6], and is essential oil with volatile compounds having an intense lemon-like, fresh, sweet aroma, and insoluble in water. It was found effective against Vicia faba, and weevil (Bruchus rufimanus) [8]. China is the one of the largest producers and exporter of L. cubeba oil in the world. More than 4.4 million lb of LEO has been produced per year, and three quarters of that production is exported to England, United States, France, Germany, Holland, and other countries [9]. LEO is highly aromatic in nature and extracted from the fresh fruits to exploit as an enhancer of aroma in cosmetic products besides in foods. This is employed as raw material in the production of citral, vitamin A, E, and K, ionine and methylionine, and perfumes, and also to impart antimicrobial and insecticidal properties [10,11,12]. Additionally, LEO is also used as an antifungal agent and bio-insecticides in the storage of grains, foods, archival documents, and/or clothing. The dried fruits are used for several medicinal purposes such as carminative (relieves flatulence), diuretic (aids urine passage), expectorant (aids secretion of sputum), stimulant, stomach ache, antiasthmatic, sedative, antidysentric, and antiseptic [6,9,13]. Some recent studies described the functional properties of L. cubeba, such as its therapeutic [9], antimicrobial [14,15], antioxidant [12,16], anti-cancerous [17,18], anti-inflammatory [19], anti-diabetic [20,21,22], and anti-insecticidal activities [23,24,25] (Figure 1).

2. Ethnopharmacological Uses of Litsea Species

Different species of the genus Litsea have been used as traditional herbal medicines since 600 A.D. and as sources of important secondary metabolites [26,27,28]. Most Litsea species produces odor active compounds while the fruits contain biologically active components that are utilized in various foods as a source of natural ingredients and for flavor [9,29]. The ethnopharmacological properties and uses of Litsea species are briefly described in Table 1.

3. Essential Oils and Their Applications

Basically, the essential oils (EOs) are comprised of secondary metabolites intensely present in different parts of the Litsea cubeba, such as root, stem, leaf, flower, and fruits. The oils are usually extracted by steam distillation processes. The EOs are chemically a complex mixture of monoterpenes, phenols, and sesquiterpenes [23]. The chemical compounds of EO from different parts of the plant vary in composition, as revealed by different peak area percentage for these compounds in leaves [49], stem bark [50], and flowers [4]. It is important to note that citral rich essential oils are present in fruits while 1,8-cineole predominate the citral content in leaves [51]. The other compounds rich in EO oil from leaves are sabinene and α-pinene [51]. Similarly, Litsea EO collected from the different part of the plants from a northeast location of India and analyzed by GC–MS was reported to contain sabinene in maximum proportion in leaf oils (LC1 and LC2) along with other compounds like α-pinene, terpinen-4-ol, α-terpineol, 1,8-cineole, and myrcene. Citronellol and citronellal were dominant in fruit oils (LC3 and LC4) with their respective content of 70% and 10% of the total oil composition. Similarly, geranial (c. 44%) and neral (c. 40%) were also the important components but citronellal was only found to be around 3% in one of the fruit oil samples (LC5) [52].
The chemical composition of the EO of L. cubeba has been seen to vary from country to country [14,50]. Despite this, the different EOs possess similar properties and exert antimicrobial, antibacterial, antioxidant, and antiparasitic activity [14,53,54,55]. In addition to this, Litsea EO has a peculiar property of insecticidal activity and acts as a repellent against several insects, e.g., cabbage looper (Trichoplusia ni), Japanese termite (Reticulitermes speratus), mosquito (Aedes aegypti), maize weevil (Sitophilus zeamais), and red flour beetle (Tribolium castaneum), and also possesses nematicidal activity against the pine wood nematode (Bursaphelenchus xylophilus) [23,24,56,57].
Various agricultural food commodities are attacked by toxigenic fungi across the world [58,59], and pose a serious threat to food safety and security by causing huge crop damages and economic loss. Aspergillus flavus is major fungus producing aflatoxins (AFs) that affect several crops and exert carcinogenic, mutagenic, teratogenic, hepatotoxic, and immunosuppressive properties [60,61]. Therefore, the antifungal and antimicrobial effects of Litsea EO against several food pathogenic microbes such as F. verticillioides, F. graminearum and E. coli have been investigated by several researchers [15,62,63].

4. Pharmaceutical Compounds

Litsea cubeba encompasses a varied number of structurally diverse biologically active compounds, and their uses in traditional medicines and their various functions are listed in Table 2. The major groups of compounds include alkaloids, monoterpenes, sesquiterpenes, diterpenes, flavonoids, amides, lignans, steroids, and fatty acids. These compounds have anticancer, anti-inflammatory, antimicrobial, antioxidant, antidiabetic, and anti-HIV properties, and therefore have immense potential for treating various diseases [64,65].

4.1. Alkaloids

Around 63 alkaloid compounds have been identified in the genus Litsea (few are presented in Table 2). Most of the natural aporphine alkaloids have medicinal properties like antioxidant, antitumor, anticonvulsant, and antiplasmodial properties. These alkaloid compounds and their synthetic derivatives have the potential for curing various diseases [64].

4.2. Monoterpenes

The maximum proportion of essential oils from Litsea species are comprised of monoterpene compounds, i.e., approximately 90% of essential oils. To date, around 20 monoterpene compounds have been extracted from the EO of L. cubeba but with varying structures [29,62]. These compounds exhibit a wide range of functions like antioxidant, antifungal, antiasthmatic, and antianaphylactic properties [70]. The monoterpenes can be broadly classified into two categories: menthane and cineole. Menthane has been reported to occur in almost all species of Litsea except in L. coreana var. sinensis (Allen). Further, cineole is present in surplus amounts in L. mollis Hemsl. and L. lancilimaba.

4.3. Sesquiterpenes

Nearly 73 sesquiterpenoid compounds (few are shown in Table 2) have been extracted from different Litsea species. These compounds exhibit varying structures, namely aliphatic, monocyclic, bicyclic, and tricyclic sesquiterpenes, along with their oxygenated derivatives. Most of the sesquiterpenes and their derivatives exert natural anti-HIV properties [29].

4.4. Diterpenes

This group of compounds is rare in Litsea species. Recently, Trisonthi et al. [74] identified and isolated a new cytotoxic diterpene, known as cubelin (235), from the fruits of L. cubeba using methanol extract. No other compounds have been reported to exhibit a similar molecular structure as cubelin in L. cubeba or any other species of Litsea.

4.5. Flavonoids

Flavonoids are another important and major group of compounds present in Litsea species. Around 39 compounds have been identified, which include mainly flavones, flavanols, flavanones, flavanonols, anthocyanidins, chalcones, and flavan-3-ols (Table 2); and their glycosidic forms consisting of either glucose, galactose, or rhamnose [62,85]. These compounds are mainly present in L. coreana, Litsea glutinosa, and L. cubeba. However, some compounds like pinocembrinchalcone (271) and kaempferol 3,4′-di-O-L-rhamnopyranoside (258) were isolated from L. fruticosa (Hemsl.) [85]. Flavonoids have therapeutic properties and exhibit beneficial properties like anti-inflammatory, antioxidant, and hepatoprotective activities [11,77,78,79].

4.6. Amides

Approximately ten amide compounds have been identified from the genus Litsea, as shown in Table 2. The major Litsea species from where amides are obtained include L. acutivena, L. auriculata, L. hypophaea, L. greenmaniana, and L. cubeba. The application of amides as chemotaxonomic markers is, however, limited for individual species within the genus Litsea [12].

4.7. Lignans

Different types of lignans have been reported in Litsea species. To date, 35 lignans (few are shown in Table 2) have been extracted from various Litsea species: L. acutivena, L. costalis, L. cubeba, L. chinpingensis, L. euosma, L. glutinosa, L. greenmaniana, L. grandis, L. gracilipes, L. hypophaea, L. lancifolia, L. lii var. nunkao-tahangensis, L. turfosa, and L. verticillata [12].

4.8. Steroids

This group of compounds has limited structural diversity and only about seven steroid compounds have been reported to date from Litsea plants.

4.9. Fatty Acids

Fatty acids are predominant in Litsea species. Some of the major fatty acids present include cinnamic acid, canoic acid, octanoic acid, decenoic acid, dodecenoic acid, myristic acid, stearic acid, oleic acid, and linolenic acid [86].

5. Functions and Potential Mechanisms of Action

5.1. Anticancer Activity

The EO extracted from the L. cubeba fruit has been shown to have cytotoxic effects on human lung, liver, and oral cancer cells [17]. Furthermore, the fumes of oil compounds from L. cubeba seeds were detrimental to human NSCLC cells (A549) through the process of cell cycle arrest and apoptosis [18]. Zhang et al. [67] showed the in vitro cytotoxic effects of the alkaloids extracted from L. cubeba bark against various human cancer cells, like gastric carcinoma (BGC-823), hepatocellular carcinoma (HepG2), breast cancer (MCF-7), gastric adenocarcinoma (SGC-7901), human skin cancer (SK-MEL-2), and ovarian cancer (SK-OV-3) cells. It has been revealed that the nuclear erythroid-2 related factor (Nrf2) is responsible for controlling the expression of the antioxidant response element (ARE) gene. Therefore, the Nrf2/ARE pathway is supposed to be the potential molecular target to discover chemopreventive medicines [87]. Further, Shen et al. [88] experimented with the selection of EtOH extracts of L. glutinosa (ZK-06), L. monopetala (ZK-07), and L. garrettii (ZK-08), employing a stable ARE luciferase reporter cell line obtained from MDA-MB-231 cells (human breast cancer). It was revealed that the ZK-08 tripled the ARE luciferase activity in comparison to the control, while ZK-06 and ZK-07 showed moderate effects, i.e., two to three times increase in ARE luciferase activity.

5.2. Anti-Inflammatory Activity

The compound extracted from Litsea species has been shown to be effective against gastroenterologia, edema, and rheumatic arthritis, and mainly the species L. cubeba, L. glutinosa, L. akoensis, L. japonica, and L. guatemalensis have been tested for their anti-inflammatory properties [80,89,90]. The inflammatory mediators, nitric oxide (NO) and PGE2, are produced by inducible nitric oxide synthase (iNOS) and cyclooxygenase (COX)-2 enzymes, respectively. The over expression of these two mediators destroys the target tissue during an infection. However, it has been shown that iNOS and COX-2 are not regulated in macrophages, but induce the expression of other pro-inflammatory mediators like IL-6, COX-2, and iNOS for inflammatory response [91]. Therefore, restricting the biosynthesis of prostaglandin and production of NO could potentially treat cancer [92]. The MeOH extract (0.01 mg/mL) was able to prevent the formation of NO and PGE2 in LPS-activated RAW-264.7 macrophages and further declined the release of HOCl and O2 through myeloperoxidase-catalyzed oxidation of chloride [89].

5.3. Antimicrobial Activity

Several compounds extracted from Litsea species are effective against various pathogenic strains. The EO of L. cubeba leaves and fruits from northeast India have shown antimicrobial properties against S. aureus, L. monocytogenes, E. coli, P. aeruginosa, C. albicans, and A. niger. However, variation in their levels of inhibition was observed, which could be due to variation in the compounds present in the leaves and fruits of L. cubeba [52]. Further, antimicrobial activity of the EO from L. laevigata was tested in Gram-positive bacteria (S. aureus, B. subtilis, S. faecalis, S. albus); Gram-negative bacteria (E. coli, P. aeruginosa, P. vulgaris, and K. aerogenes), and fungi (C. albicans and A. niger). The EO was especially effective against Gram-positive bacteria (S. albus) and the fungus (A. niger) [71].

5.4. Antioxidant Activity

The antioxidant activity of three flavonoids, viz., kaempferol, querctin-3-O-β-D-glucopyranoside, and kaempferol-3-O-β-D-glucopyranoside extracted from L. coreana leaves revealed that the kaempferol had the highest activity while kaempferol-3-O-β-D-glucopyranoside showed the least effect [93]. Further, the antioxidant activity from leaf and bark of four different Litsea species from India, namely L. glutinosa, L. monopetala, L. assamica, and L. laeta showed that the bark extract of L. glutinosa and L. laeta had higher metal chelating activity with IC50 of 15.25 and 16.14 mg/mL, respectively [94]. Furthermore, the MeOH extracts of the root and stem of L. elliptica and L. resinosa depicted enhanced antioxidant activity for DPPH (2,2-Diphenyl-1-picrylhydrazyl) radicals with EC50 values of 23.99, 41.69, 11.22, and 33.48 mg/L, respectively, against the standard butylated hydroxyl toluene (BHT) [95].

5.5. Antidiabetic Activity

The efficacy of total flavonoids of Litsea coreana (TFLC) was investigated for their mechanism to reduce the level of blood glucose in diabetic rats. TFLC was observed to decrease the glucose and lipid levels in the blood and relieved the liver from oxidation stress. In addition, TFLC masked the expression of PTP1B in liver, which resulted in improving the insulin signaling pathway [20]. Similarly, TFLC was further observed to increase the insulin sensitivity, and high-density lipoprotein cholesterol (HDL-C) and superoxide dismutase (SOD) activities. On the other hand, bodyweight, serum free fatty acid, total cholesterol, triglyceride, and low-density lipoprotein cholesterol (LDL-C) content were decreased [12].

5.6. Anti-HIV Activity

Several compounds extracted from L. verticillata, namely litseachromolaevane B (15-epi-eudesm-4(15)-ene-1β,6β-diol(13), litseagermacrane(14), litseaverticillols A–H (16–23), isolitseaneB(24),1,2,3,4-tetrahydro-2,5-dimethyl-8-(1-methylethy)-l,2-naphthalenediol(25), oxyphyllenodiol B (26), verticillatol (15), hydroxydihydrobovolide (28), 3-epilitsenolide D2 (29), 4-hydroxy-2-methylbut-2-enolide (30), litseabutenolide (31), (+)-epiexcelsin(36), and (+)-5ʹ-demethoxyepiexcelsin (37), have potential anti-HIV activity. These compounds showed growth inhibition of HIV in HOG.R5 cells with IC50 values ranging from 2.0 to 34.5 μg/mL [73,96,97], thus providing potential leads to discover medicines for HIV.

6. Conservation Strategies

The suitable growth and conservation of Litsea plants are constrained at different stages of life. Seedling development is vital to predict the survival of plants and also to influence the forest regeneration process [14]. Litsea seeds possess a long dormancy phase and have the potential to form long-lived seed reserves. Therefore, seed propagation is an inefficient method of propagation and needs involvement of biotechnological interventions for this potentially important medicinal plant for long-term genetic conservation.
The ecosystem studies have shown that the regeneration of forests depends mainly on two factors, namely the seed rain and the soil seed bank [98,99,100,101]. Seed rain is the result of seed production from several plants within the same community as well as addition of seeds from other neighboring communities [102]. Therefore, seed rain has a significant role in generating new plants and determining the structure, dynamics, and regeneration of any forest community [101,103,104]. The soil seed bank, on the other hand, represents the current and past plant community. It prevents the extinction of local species and aids in the regeneration of the forest [105,106]. Furthermore, the soil seed bank functions as a source of colonizing species and accelerates the process of forest succession [107,108]. In addition, the concept of in situ conservation includes the establishment of different types of nature protection areas. These valuable plants can be conserved in the form of ex situ conservation by creating botanical gardens and arboretums. As an alternative, the germplasm resources storehouse could be restored for the long-term preservation of seeds, pollen, and/or asexual propagules [109]. A rapid clonal propagation system for the conservation of various explant sources (shoot tip, node, leaf, and petiole) of Litsea cubeba was developed [110]. Furthermore, in-vitro rooting without growth-regulator is possible and over 100 plantlets have been successfully developed in the glasshouse.

7. Conclusions and Future Prospects

The present review has discussed the ethnopharmacological properties of Litsea cubeba compounds having the potential to cure various ailments because of inherent anticancer, antimicrobial, anti-inflammatory, antioxidant, antidiabetic, and anti-HIV properties. However, the underlying mechanism and their mode of action are not well researched and established. Further in vitro and in vivo genotoxic experiments of Litsea need to be evaluated to entitle its ethnomedical values. The in-depth exploration of Litsea cubeba for its various withstanding pharmacological properties can potentially be employed as an initiative to discover new drugs to treat serious diseases like cancer and HIV. Furthermore, it is also considered high time to combine biological research activity with clinical applications to gain insights into the mechanisms of action, drug reactions, and other health related issues associated with the consumption of crude extracts of the plant. Therefore, research involving clinical evaluation along with conservation strategies is imperative for long term benefits to society.

Author Contributions

P.K. and M.K. conceived and designed the paper. D.K.M. and P.K. wrote the paper. K.E.L. and M.K. helped during the writing of manuscript. P.R.G. assisted in the identification of plants. V.K.B., K.S.G., and P.K. critically reviewed the manuscript and did the required editing.

Funding

Author (K.E.L.) was supported by the NRF-2017R1A6A3A01011299) funded by the Korea government (MSIT). Author (S.G.K.) was supported by the National Research Foundation of Korea (NRF-213R1A1A2013248) funded by the Korea government (MSIT).

Acknowledgments

Authors M.K. and P.K. would like to acknowledge the support of the Department of Biotechnology, Government of India (ref. BT/PR24741/NER/95/836/2017) and IERP-GBPH, Government of India (ref. GBPI/IERP/17-18/58).

Conflicts of Interest

The authors declare that there is no conflict of interest.

References

  1. Mabberley, D.J. The Plant-Book: A Portable Dictionary of the Higher Plants; Cambridge University Press: Cambridge, UK, 1993; Volume 581. [Google Scholar]
  2. Kapoor, L. Handbook of Ayurvedic Medicinal Plants: Herbal Reference Library; Routledge: London, UK, 2017. [Google Scholar]
  3. Yadav, G.; Goswami, B. Studies on the foliar constituents of food plants of muga silkworm (Antheraea assama Westwood). J. Ecobiol. 1990, 2, 222–228. [Google Scholar]
  4. Choudhury, S.; Ahmed, R.; Barthel, A.; Leclercq, P.A. Composition of the stem, flower and fruit oils of Litsea cubeba Pers. from two locations of Assam, India. J. Essent. Oil Res. 1998, 10, 381–386. [Google Scholar] [CrossRef]
  5. Duke, J.A.; Ayensu, E.S. Medicinal Plants of China; Reference Publications: Cambridge, MA, USA, 1985; Volume 2. [Google Scholar]
  6. Chen, Z.; Bi, H.; Fan, C.; Bao, C. Chemical constituents from the branch of Litsea cubeba (Lour.) Pers. Chem. Ind. For. Prod. 2013, 33, 133–136. [Google Scholar]
  7. Mao, A. Preliminary report on the folklore botany of Mao Nagas of Manipur India. Ethnobotany 1993, 5, 143–147. [Google Scholar]
  8. Yao, K.; Yang, C. Using pheasant pepper seed oil for controlling the broad bean weevil Bruchus rufimanus. Acta Ecol. Sin. 1984, 27, 173–181. [Google Scholar]
  9. Chen, S.-L.; Yu, H.; Luo, H.-M.; Wu, Q.; Li, C.-F.; Steinmetz, A. Conservation and sustainable use of medicinal plants: Problems, progress, and prospects. Chin. Med. 2016, 11, 37. [Google Scholar] [CrossRef]
  10. Budavari, S.; O’Neil, M.J.; Smith, A.; Heckelman, P.E. The Merck Index; Merck: Rahway, NJ, USA, 1989; Volume 11. [Google Scholar]
  11. Wang, J.-Q.; Li, J.; Zou, Y.-H.; Cheng, W.-M.; Lu, C.; Zhang, L.; Ge, J.-F.; Huang, C.; Jin, Y.; Lv, X.-W. Preventive effects of total flavonoids of Litsea coreana leve on hepatic steatosis in rats fed with high fat diet. J. Ethnopharmacol. 2009, 121, 54–60. [Google Scholar] [CrossRef] [PubMed]
  12. Wang, Y.-S.; Wen, Z.-Q.; Li, B.-T.; Zhang, H.-B.; Yang, J.-H. Ethnobotany, phytochemistry, and pharmacology of the genus Litsea: An update. J. Ethnopharmacol. 2016, 181, 66–107. [Google Scholar] [CrossRef] [PubMed]
  13. Feng, T.; Zhang, R.-T.; Tan, Q.-G.; Liu, Y.-P.; Cai, X.-H.; Luo, X.-D. Two new isoquinoline alkaloids from Litsea cubeba. Z. Naturforsch. B 2009, 64, 871–874. [Google Scholar] [CrossRef]
  14. Wang, H.; Liu, Y. Chemical composition and antibacterial activity of essential oils from different parts of Litsea cubeba. Chem. Biodivers. 2010, 7, 229–235. [Google Scholar] [CrossRef]
  15. Liu, T.-T.; Yang, T.-S. Antimicrobial impact of the components of essential oil of Litsea cubeba from Taiwan and antimicrobial activity of the oil in food systems. Int. J. Food Microbiol. 2012, 156, 68–75. [Google Scholar] [CrossRef]
  16. Hwang, J.-K.; Choi, E.-M.; Lee, J.H. Antioxidant activity of Litsea cubeba. Fitoterapia 2005, 76, 684–686. [Google Scholar] [CrossRef] [PubMed]
  17. Ho, C.-L.; Jie-Ping, O.; Liu, Y.-C.; Hung, C.-P.; Tsai, M.-C.; Liao, P.-C.; Wang, E.I.-C.; Chen, Y.-L.; Su, Y.-C. Compositions and in vitro anticancer activities of the leaf and fruit oils of Litsea cubeba from Taiwan. Nat. Prod. Commun. 2010, 5, 617–620. [Google Scholar] [CrossRef]
  18. Seal, S.; Chatterjee, P.; Bhattacharya, S.; Pal, D.; Dasgupta, S.; Kundu, R.; Mukherjee, S.; Bhattacharya, S.; Bhuyan, M.; Bhattacharyya, P.R. Vapor of volatile oils from Litsea cubeba seed induces apoptosis and causes cell cycle arrest in lung cancer cells. PLoS ONE 2012, 7, 47014. [Google Scholar] [CrossRef]
  19. Liao, P.-C.; Yang, T.-S.; Chou, J.-C.; Chen, J.; Lee, S.-C.; Kuo, Y.-H.; Ho, C.-L.; Chao, L.K.-P. Anti-inflammatory activity of neral and geranial isolated from fruits of Litsea cubeba Lour. J. Funct. Foods 2015, 19, 248–258. [Google Scholar] [CrossRef]
  20. Sun, Y.-X.; Lu, Y.-X.; Wang, L.-Y. Study on the mechanism of action of total flavonoids of Litsea coreana for reducing blood glucose level in rat with type 2 diabetes mellitus. Chin. J. Integr. Med. 2010, 30, 617–621. [Google Scholar]
  21. Chhetri, D.; Parajuli, P.; Subba, G. Antidiabetic plants used by Sikkim and Darjeeling Himalayan tribes, India. J. Ethnopharmacol. 2005, 99, 199–202. [Google Scholar] [CrossRef]
  22. Yadav, M. Herbal drugs and phytoconstituents useful for the management of diabetes. Int. J. Green Pharm. 2017, 11, S21. [Google Scholar]
  23. Jiang, Z.; Akhtar, Y.; Bradbury, R.; Zhang, X.; Isman, M.B. Comparative toxicity of essential oils of Litsea pungens and Litsea cubeba and blends of their major constituents against the cabbage looper, Trichoplusia ni. J. Agric. Food Chem. 2009, 57, 4833–4837. [Google Scholar] [CrossRef]
  24. Seo, S.-M.; Kim, J.; Lee, S.-G.; Shin, C.-H.; Shin, S.-C.; Park, I.-K. Fumigant antitermitic activity of plant essential oils and components from ajowan (Trachyspermum ammi), allspice (Pimenta dioica), caraway (Carum carvi), dill (Anethum graveolens), geranium (Pelargonium graveolens), and litsea (Litsea cubeba) oils against Japanese termite (Reticulitermes speratus Kolbe). J. Agric. Food Chem. 2009, 57, 6596–6602. [Google Scholar]
  25. Zhang, H.J.; Zheng, L.H.; Zhao, K.; Chen, Y.; Yi, Z. Insecticidal activities of constituents of Litsea cubeba fruit extracts effective against the maize weevil (Coleoptera: Curculionidae). J. Insect Sci. 2017, 17, 103. [Google Scholar] [CrossRef]
  26. Mohanan, N.; Kumar, E.S. A new species of Litsea (Lauraceae) from India. Nord. J. Bot. 2003, 23, 611–613. [Google Scholar] [CrossRef]
  27. Guzmán-Gutiérrez, S.; Gómez-Cansino, R.; García-Zebadúa, J.; Jiménez-Pérez, N.; Reyes-Chilpa, R. Antidepressant activity of Litsea glaucescens essential oil: Identification of β-pinene and linalool as active principles. J. Ethnopharmacol. 2012, 143, 673–679. [Google Scholar] [CrossRef] [PubMed]
  28. Kong, D.-G.; Zhao, Y.; Li, G.-H.; Chen, B.-J.; Wang, X.-N.; Zhou, H.-L.; Lou, H.-X.; Ren, D.-M.; Shen, T. The genus Litsea in traditional Chinese medicine: An ethnomedical, phytochemical and pharmacological review. J. Ethnopharmacol. 2015, 164, 256–264. [Google Scholar] [CrossRef]
  29. Agrawal, N.; Choudhary, A.S.; Sharma, M.C.; Dobhal, M.P. Chemical constituents of plants from the genus Litsea. Chem. Biodivers. 2011, 8, 223–243. [Google Scholar] [CrossRef]
  30. Ho, C.-L.; Lin, C.-Y.; Wang, E.I.-C.; Su, Y.-C. Composition, antioxidant and antimicrobial activities of leaf and twig essential oils of Litsea akoensis from Taiwan. Nat. Prod. Commun. 2011, 6, 901–904. [Google Scholar] [CrossRef]
  31. Cheng, H.-I.; Lin, W.-Y.; Duh, C.-Y.; Lee, K.-H.; Tsai, I.-L.; Chen, I.-S. New cytotoxic butanolides from Litsea acutivena. J. Nat. Prod. 2001, 64, 1502–1505. [Google Scholar] [CrossRef]
  32. Normile, D. The new face of traditional Chinese medicine. Science 2003, 299, 188–190. [Google Scholar] [CrossRef]
  33. Xie, Z.; Yu, Y. The Guide of National Chinese Herbal Medicine (I); People’s Medical Publishing House: Beijing, China, 1996. [Google Scholar]
  34. Kumar, P.B.; Kannan, M.M.; Quine, S.D. Litsea deccanensis ameliorates myocardial infarction in wistar rats: Evidence from biochemical histological studies. J. Young Pharm. 2011, 3, 287–296. [Google Scholar] [CrossRef]
  35. Ageel, A.; Islam, M.; Ginawi, O.; Al-Yahya, M. Evaluation of the aphrodisiac activity of Litsea chinensis (Lauraceae) and Orchis malculata (Orchidaceae) extracts in rats. Phytother. Res. 1994, 8, 103–105. [Google Scholar] [CrossRef]
  36. Hassan, S.H.A.; Fry, J.R.; Bakar, M.F.A. Antioxidant and phytochemical study on pengolaban (Litsea garciae), an edible underutilized fruit endemic to Borneo. Food Sci. Biotechnol. 2013, 22, 1–7. [Google Scholar] [CrossRef]
  37. Min, B.S.; Lee, S.Y.; Kim, J.H.; Kwon, O.K.; Park, B.Y.; An, R.B.; Lee, J.K.; Moon, H.I.; Kim, T.J.; Kim, Y.H. Lactones from the Leaves of Litsea j aponica and Their Anti-complement Activity. J. Nat. Prod. 2003, 66, 1388–1390. [Google Scholar] [CrossRef] [PubMed]
  38. Yoon, W.-J.; Kang, S.C.; Ham, Y.-M.; Kim, K.-N.; Yang, W.H.; Kim, H.-J.; Park, S.-Y.; Jung, Y.-H. Antioxidative and anti-inflammatory activities of Litsea japonica leaves. J. Korean Soc. Appl. Biol. 2010, 53, 27–32. [Google Scholar] [CrossRef]
  39. Bhatt, B.; Lemtur, M.; Changkija, S.; Sarkar, B. Fuelwood characteristics of important trees and shrubs of Eastern Himalaya. Energ. Sources Part A Recovery Util. Environ. Eff. 2017, 39, 47–50. [Google Scholar] [CrossRef]
  40. Baul, T.K.; Hossain, M.M.; Mezbahuddin, M.; Mohiuddin, M. Vegetative propagation of Litsea monopetala, a wild tropical medicinal plant: Effects of indole-3-butyric acid (IBA) on stem cuttings. J. For. Res. 2011, 22, 409–416. [Google Scholar] [CrossRef]
  41. Hua, H.; Xing, F.; Selvaraj, J.N.; Wang, Y.; Zhao, Y.; Zhou, L.; Liu, X.; Liu, Y. Inhibitory effect of essential oils on Aspergillus ochraceus growth and ochratoxin A production. PLoS ONE 2014, 9, 108285. [Google Scholar] [CrossRef]
  42. Rana, M.P.; Sohel, M.S.I.; Akhter, S.; Islam, M.J. Ethno-medicinal plants use by the Manipuri tribal community in Bangladesh. J. For. Res. 2010, 2, 85–92. [Google Scholar] [CrossRef]
  43. Ho, C.-L.; Wang, E.I.-C.; Hsu, K.-P.; Lee, P.-Y.; Su, Y.-C. Composition and antimicrobial activity of the leaf essential oil of Litsea kostermansii from Taiwan. Nat. Prod. Commun. 2009, 4, 1123–1236. [Google Scholar] [CrossRef]
  44. Nawawi, A.A.; Nakamura, N.; Hattori, M.; Kurokawa, M.; Shiraki, K. Inhibitory effects of Indonesian medicinal plants on the infection of herpes simplex virus type 1. Phytother. Res. 1999, 13, 37–41. [Google Scholar] [CrossRef]
  45. Ghosh, M.; Sinha, B. GC-MS studies on the bark extracts of Litsea polyantha Juss. Middle East J. Sci. Res. 2010, 5, 441–444. [Google Scholar]
  46. Delectis Florae Reipublicae Popularis Sinicae agendae. In Flora Reipublicae Popularis Sinicae; Academiae Sinicae (Ed.) Science Press: Beijing, China, 1999; Volume 77, pp. 1977–1999. [Google Scholar]
  47. Kala, C.P. Ethnomedicinal botany of the Apatani in the Eastern Himalayan region of India. J. Ethnobiol. Ethnomed. 2005, 1, 11. [Google Scholar] [CrossRef]
  48. Holloway, D.M.; Scheinmann, F. Co-occurrence of aporphine and biphenyl constituents in Litsea turfosa. Phytochemistry 1973, 12, 1503–1505. [Google Scholar] [CrossRef]
  49. Bighelli, A.; Muselli, A.; Casanova, J.; Tam, N.T.; Van Anh, V.; Bessière, J.-M. Chemical variability of Litsea cubeba leaf oil from Vietnam. J. Essent. Oil Res. 2005, 17, 86–88. [Google Scholar] [CrossRef]
  50. Si, L.; Chen, Y.; Han, X.; Zhan, Z.; Tian, S.; Cui, Q.; Wang, Y. Chemical composition of essential oils of Litsea cubeba harvested from its distribution areas in China. Molecules 2012, 17, 7057–7066. [Google Scholar] [CrossRef]
  51. Thielmann, J.; Muranyi, P. Review on the chemical composition of Litsea cubeba essential oils and the bioactivity of its major constituents citral and limonene. J. Essent. Oil Res. 2019, 1–18. [Google Scholar] [CrossRef]
  52. Saikia, A.K.; Chetia, D.; D’Arrigo, M.; Smeriglio, A.; Strano, T.; Ruberto, G. Screening of fruit and leaf essential oils of Litsea cubeba Pers. from north-east India–chemical composition and antimicrobial activity. J. Essent. Oil Res. 2013, 25, 330–338. [Google Scholar] [CrossRef]
  53. Luo, M.; Jiang, L.-K.; Zou, G.-L. Acute and genetic toxicity of essential oil extracted from Litsea cubeba (Lour.) Pers. J. Food Prot. 2005, 68, 581–588. [Google Scholar] [CrossRef]
  54. Wang, Y.-S.; Liao, Z.; Zhu, H.-K.; Feng, X.-F.; Huang, R.; Zhu, N.; Yang, J.-H. Megastigmane O-glucopyranosides from Litsea glutinosa. Chem. Nat. Compd. 2012, 48, 346–349. [Google Scholar] [CrossRef]
  55. Huang, X.-W.; Feng, Y.-C.; Huang, Y.; Li, H.-L. Potential cosmetic application of essential oil extracted from Litsea cubeba fruits from China. J. Essent. Oil Res. 2013, 25, 112–119. [Google Scholar] [CrossRef]
  56. Noosidum, A.; Prabaripai, A.; Chareonviriyaphap, T.; Chandrapatya, A. Excito-repellency properties of essential oils from Melaleuca leucadendron L. Litsea cubeba (Lour.) Persoon, and Litsea salicifolia (Nees) on Aedes aegypti (L.) mosquitoes. J. Vector Ecol. 2008, 33, 305–313. [Google Scholar] [CrossRef]
  57. Ko, K.; Juntarajumnong, W.; Chandrapatya, A. Repellency, fumigant and contact toxicities of Litsea cubeba (Lour.) Persoon against Sitophilus zeamais Motschulsky and Tribolium castaneum (Herbst). Kasetsart J. 2009, 43, 56–63. [Google Scholar]
  58. Zhou, S.; Kong, W.; Cao, J.; Logrieco, A.; Yang, S.; Yang, M. Effect of Aspergillus flavus contamination on the inherent quality of Glycyrrhiza uralensis. World Mycotoxin J. 2014, 7, 83–89. [Google Scholar] [CrossRef]
  59. Guerra, I.C.D.; de Oliveira, P.D.L.; de Souza Pontes, A.L.; Lúcio, A.S.S.C.; Tavares, J.F.; Barbosa-Filho, J.M.; Madruga, M.S.; de Souza, E.L. Coatings comprising chitosan and Mentha piperita L. or Mentha × villosa Huds essential oils to prevent common postharvest mold infections and maintain the quality of cherry tomato fruit. Int. J. Food Microbiol. 2015, 214, 168–178. [Google Scholar] [CrossRef] [PubMed]
  60. Ellis, W.; Smith, J.; Simpson, B.; Oldham, J.; Scott, P.M. Aflatoxins in food: Occurrence, biosynthesis, effects on organisms, detection, and methods of control. Crit. Rev. Food Sci. Nutr. 1991, 30, 403–439. [Google Scholar] [CrossRef]
  61. Kumar, P.; Mahato, D.K.; Kamle, M.; Mohanta, T.K.; Kang, S.G. Aflatoxins: A global concern for food safety, human health and their management. Front. Microbiol. 2017, 7, 2170. [Google Scholar] [CrossRef] [PubMed]
  62. Yang, Y.; Jiang, J.; Qimei, L.; Yan, X.; Zhao, J.; Yuan, H.; Qin, Z.; Wang, M. The fungicidal terpenoids and essential oil from Litsea cubeba in Tibet. Molecules 2010, 15, 7075–7082. [Google Scholar] [CrossRef]
  63. Li, W.-R.; Shi, Q.-S.; Liang, Q.; Xie, X.-B.; Huang, X.-M.; Chen, Y.-B. Antibacterial activity and kinetics of Litsea cubeba oil on Escherichia coli. PLoS ONE 2014, 9, 110983. [Google Scholar] [CrossRef] [PubMed]
  64. Zhang, A.; Zhang, Y.; Branfman, A.R.; Baldessarini, R.J.; Neumeyer, J.L. Advances in development of dopaminergic aporphinoids. J. Med. Chem. 2007, 50, 171–181. [Google Scholar] [CrossRef]
  65. Custodio, D.L.; da Veiga Junior, V.F. Lauraceae alkaloids. RSC Adv. 2014, 4, 21864–21890. [Google Scholar] [CrossRef]
  66. Lee, S.-S.; Chen, C.-K.; Huang, F.-M.; Chen, C.-H. Two dibenzopyrrocoline alkaloids from Litsea cubeba. J. Nat. Prod. 1996, 59, 80–82. [Google Scholar] [CrossRef]
  67. Zhang, W.; Hu, J.-F.; Lv, W.-W.; Zhao, Q.-C.; Shi, G.-B. Antibacterial, antifungal and cytotoxic isoquinoline alkaloids from Litsea cubeba. Molecules 2012, 17, 12950–12960. [Google Scholar] [CrossRef]
  68. Tanaka, H.; Yatsuhashi, S.; Yasuda, T.; Sato, M.; Sakai, E.; Xiao, C.; Murata, H.; Murata, J. A new amide from the leaves and twigs of Litsea auriculata. J. Nat. Med. 2009, 63, 331–334. [Google Scholar] [CrossRef] [PubMed]
  69. Huang, C.-H.; Huang, W.-J.; Wang, S.-J.; Wu, P.-H.; Wu, W.-B. Litebamine, a phenanthrene alkaloid from the wood of Litsea cubeba, inhibits rat smooth muscle cell adhesion and migration on collagen. Eur. J. Pharmacol. 2008, 596, 25–31. [Google Scholar] [CrossRef] [PubMed]
  70. Chen, C.-J.; Tseng, Y.-H.; Chu, F.-H.; Wen, T.-Y.; Cheng, W.-W.; Chen, Y.-T.; Tsao, N.-W.; Wang, S.-Y. Neuropharmacological activities of fruit essential oil from Litsea cubeba Persoon. J. Wood Sci. 2012, 58, 538–543. [Google Scholar] [CrossRef]
  71. Muhammed, A.M.; Subbu, R.M.; Jirovetz, L.; Mohamed, S.P. Composition and antimicrobial analysis of the essential oil of Litsea Laevigata nees (Lauraceae). Nat. Prod. Commun. 2008, 3, 1069–1072. [Google Scholar] [CrossRef]
  72. Ahmad, F.B.; bin Jantan, I.; Bakar, B.A.; Ahmad, A.S.B. A comparative study of the composition of the leaf oils of three Litsea species from Borneo. J. Essent. Oil Res. 2005, 17, 323–326. [Google Scholar] [CrossRef]
  73. Zhang, H.-J.; Van Hung, N.; Cuong, N.M.; Soejarto, D.D.; Pezzuto, J.M.; Fong, H.H.; Tan, G.T. Sesquiterpenes and butenolides, natural anti-HIV constituents from Litsea verticillata. Planta Med. 2005, 71, 452–457. [Google Scholar] [CrossRef] [PubMed]
  74. Trisonthi, P.; Sato, A.; Nishiwaki, H.; Tamura, H. A new diterpene from Litsea cubeba fruits: Structure elucidation and capability to induce apoptosis in HeLa cells. Molecules 2014, 19, 6838–6850. [Google Scholar] [CrossRef]
  75. Cheng, M.-J.; Wang, T.-A.; Lee, S.-J.; Chen, I.-S. A new butanolide and a new secobutanolide from Litsea lii var. nunkao-tahangensis. Nat. Prod. Res. 2010, 24, 647–656. [Google Scholar] [CrossRef]
  76. Chowdhury, J.U.; Bhuiyan, M.N.I.; Nandi, N.C. Aromatic plants of Bangladesh: Essential oils of leaves and fruits of Litsea glutinosa (Lour.) CB Robinson. Bangladesh J. Bot. 2008, 37, 81–83. [Google Scholar] [CrossRef]
  77. Chen, L.; Cheng, W.; Hu, C.; Jin, Y.; Li, R.; Li, J. Study on anti-inflammatory effects of total flavonoids of Litsea coreana Leve. Var. Anhui Nongye Daxue Xuebao 2004, 39, 439–442. [Google Scholar]
  78. Ye, H.; Jin, L.; Yu, J.; Wu, J. Research on the mechanism of antioxidation of flavoniods from leaves of Litsea coreana. J. Wenzhou Med. Coll. 2006, 36, 424–427. [Google Scholar]
  79. Tang, W.J.; Zhang, Y.L.; Xiao, Q.P.; Huang, C.; Jin, Y.; Li, J. Four flavanocoumarins from the leaves of Litsea coreana LEVL. Chem. Biodivers. 2013, 10, 1128–1132. [Google Scholar] [CrossRef] [PubMed]
  80. Guo, Q.; Zeng, K.; Gao, X.; Zhu, Z.; Zhang, S.; Chai, X.; Tu, P. Chemical constituents with NO production inhibitory and cytotoxic activities from Litsea cubeba. J. Nat. Med. 2015, 69, 94–99. [Google Scholar] [CrossRef] [PubMed]
  81. Chen, J.; Zhu, C.; Xu, H.; Ni, X.; Yang, P. Study on chemical constituents of the root of Litsea cubeba II chloroform portion and ethyl acetate portion from methanol extract. Chin. J. Pharm. 2010, 7, 504–508. [Google Scholar]
  82. Agrawal, N.; Pareek, D.; Dobhal, S.; Sharma, M.C.; Joshi, Y.C.; Dobhal, M.P. Butanolides from methanolic extract of Litsea glutinosa. Chem. Biodivers. 2013, 10, 394–400. [Google Scholar] [CrossRef]
  83. Tsai, I.L.; Cheng, M.J.; Hung, H.W.; Cheng, H.I.; Chen, I.S. Chemical constituents from the leaves of Litsea acutivena. J. Chin. Chem. Soc. 2007, 54, 503–506. [Google Scholar] [CrossRef]
  84. Hata, T. Studies on the formosan plant seed oils XVI oil of Litsea cubeba pers. Nippon Kagaku Kaishi 1939, 60, 122–125. [Google Scholar] [CrossRef]
  85. Liu, R.; Zhang, H.-C.; Zhou, F.; Wang, R.-M.; Tu, Q.; Wang, J.-Y. Flavonoids and alkaloids from the leaves of Litsea fruticosa. Biochem. Syst. Ecol. 2013, 50, 293–295. [Google Scholar] [CrossRef]
  86. Yan, X.; Wei, X.; Xie, H.; Liu, M.; Zhang, F. Aporphine alkaloids of Litsea rotundifolia and L. rotundifolia var. oblongifolia. J. Trop. Subtrop. Bot. 2000, 8, 324–328. [Google Scholar]
  87. Jeong, W.-S.; Jun, M.; Kong, A.-N.T. Nrf2: A potential molecular target for cancer chemoprevention by natural compounds. Antioxid. Redox Signal. 2006, 8, 99–106. [Google Scholar] [CrossRef] [PubMed]
  88. Shen, T.; Chen, X.-M.; Harder, B.; Long, M.; Wang, X.-N.; Lou, H.-X.; Wondrak, G.T.; Ren, D.-M.; Zhang, D.D. Plant extracts of the family Lauraceae: A potential resource for chemopreventive agents that activate the nuclear factor-erythroid 2-related factor 2/antioxidant response element pathway. Planta Med. 2014, 80, 426–434. [Google Scholar] [PubMed]
  89. Choi, E.-M.; Hwang, J.-K. Effects of methanolic extract and fractions from Litsea cubeba bark on the production of inflammatory mediators in RAW264. 7 cells. Fitoterapia 2004, 75, 141–148. [Google Scholar] [CrossRef]
  90. Gogoi, D.; Bezbaruah, R.L.; Bordoloi, M.; Sarmah, R.; Bora, T.C. Insights from the docking analysis of biologically active compounds from plant Litsea Genus as potential COX-2 inhibitors. Bioinformation 2012, 8, 812. [Google Scholar] [CrossRef] [PubMed]
  91. Kim, S.S.; Oh, O.-J.; Min, H.-Y.; Park, E.-J.; Kim, Y.; Park, H.J.; Han, Y.N.; Lee, S.K. Eugenol suppresses cyclooxygenase-2 expression in lipopolysaccharide-stimulated mouse macrophage RAW264. 7 cells. Life Sci. 2003, 73, 337–348. [Google Scholar] [CrossRef]
  92. Hong, C.H.; Hur, S.K.; Oh, O.-J.; Kim, S.S.; Nam, K.A.; Lee, S.K. Evaluation of natural products on inhibition of inducible cyclooxygenase (COX-2) and nitric oxide synthase (iNOS) in cultured mouse macrophage cells. J. Ethnopharmacol. 2002, 83, 153–159. [Google Scholar] [CrossRef]
  93. Ye, H.; Yu, J. The preliminary studies on antioxidation of three kinds of flavoniods from Litsea coreana. Zhong Yao Cai 2004, 27, 113–115. [Google Scholar] [PubMed]
  94. Choudhury, D.; Ghosal, M.; Das, A.P.; Mandal, P. In vitro antioxidant activity of methanolic leaves and barks extracts of four Litsea plants. Asian J. Plant Sci. Res. 2013, 3, 99–107. [Google Scholar]
  95. Wong, M.-H.; Lim, L.-F.; bin Ahmad, F.; bin Assim, Z. Antioxidant and antimicrobial properties of Litsea elliptica Blume and Litsea resinosa Blume (Lauraceae). Asian Pac. J. Trop. Biomed. 2014, 4, 386–392. [Google Scholar] [CrossRef] [PubMed]
  96. Hoang, V.D.; Tan, G.T.; Zhang, H.-J.; Tamez, P.A.; Van Hung, N.; Cuong, N.M.; Soejarto, D.D.; Fong, H.H.; Pezzuto, J.M. Natural anti-HIV agents—Part I:(+)-demethoxyepiexcelsin and verticillatol from Litsea verticillata. Phytochemistry 2002, 59, 325–329. [Google Scholar] [CrossRef]
  97. Zhang, H.-J.; Tan, G.T.; Hoang, V.D.; Van Hung, N.; Cuong, N.M.; Soejarto, D.D.; Pezzuto, J.M.; Fong, H.H. Natural anti-HIV agents. Part 3: Litseaverticillols A–H, novel sesquiterpenes from Litsea verticillata. Tetrahedron 2003, 59, 141–148. [Google Scholar] [CrossRef]
  98. McClanahan, T.R. The effect of a seed source on primary succession in a forest ecosystem. Vegetatio 1986, 65, 175–178. [Google Scholar] [CrossRef]
  99. Urbanska, K.M.; Erdt, S.; Fattorini, M. Seed rain in natural grassland and adjacent ski run in the Swiss Alps: A preliminary report. Restor. Ecol. 1998, 6, 159–165. [Google Scholar] [CrossRef]
  100. Bossuyt, B.; Hermy, M. Seed bank assembly follows vegetation succession in dune slacks. J. Veg. Sci. 2004, 15, 449–456. [Google Scholar] [CrossRef]
  101. Pakeman, R.; Small, J. The role of the seed bank, seed rain and the timing of disturbance in gap regeneration. J. Veg. Sci. 2005, 16, 121–130. [Google Scholar] [CrossRef]
  102. Booth, B.D.; Larson, D.W. The role of seed rain in determining the assembly of a cliff community. J. Veg. Sci. 1998, 9, 657–668. [Google Scholar] [CrossRef]
  103. Fuller, R.; Del Moral, R. The role of refugia and dispersal in primary succession on Mount St. Helens, Washington. J. Veg. Sci. 2003, 14, 637–644. [Google Scholar] [CrossRef]
  104. Tackenberg, O.; Stöcklin, J. Wind dispersal of alpine plant species: A comparison with lowland species. J. Veg. Sci. 2008, 19, 109–118. [Google Scholar] [CrossRef]
  105. Olano, J.; Caballero, I.; Laskurain, N.; Loidi, J.; Escudero, A. Seed bank spatial pattern in a temperate secondary forest. J. Veg. Sci. 2002, 13, 775–784. [Google Scholar] [CrossRef]
  106. Auld, T.D.; Denham, A.J.; Turner, K. Dispersal and recruitment dynamics in the fleshy-fruited Persoonia lanceolata (Proteaceae). J. Veg. Sci. 2007, 18, 903–910. [Google Scholar] [CrossRef]
  107. Augusto, L.; Dupouey, J.-L.; Picard, J.-F.; Ranger, J. Potential contribution of the seed bank in coniferous plantations to the restoration of native deciduous forest vegetation. Acta Oecol. 2001, 22, 87–98. [Google Scholar] [CrossRef]
  108. Luzuriaga, A.L.; Escudero, A.; Olano, J.M.; Loidi, J. Regenerative role of seed banks following an intense soil disturbance. Acta Oecol. 2005, 27, 57–66. [Google Scholar] [CrossRef]
  109. Xie, G.; Li, X.; Li, L.; Jiang, Y.; Zheng, Y.; Wang, W. Wild Energy Plant Resources, Conservation and Sustainable Use of Sanqingshan in Eastern China. IERI Procedia 2013, 5, 10–13. [Google Scholar] [CrossRef] [Green Version]
  110. Mao, A.; Wetten, A.; Fay, M.; Caligari, P. In vitro propagation of Litsea cubeba (Lours.) Pers., a multipurpose tree. Plant Cell Rep. 2000, 19, 263–267. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Various ethnopharmacological applications and uses of essential oil of Litsea cubeba.
Figure 1. Various ethnopharmacological applications and uses of essential oil of Litsea cubeba.
Plants 08 00150 g001
Table 1. Ethnopharmacological properties of Litsea species and their uses.
Table 1. Ethnopharmacological properties of Litsea species and their uses.
CountrySpeciesPlant PartsEthnopharmacological PropertiesSolvent/Ratio/Dose AdministeredReference
TaiwanL. akoensis HayataStem barkCytotoxicity, antimicrobial activity15–30 μL of the oil dissolved in dimethylsulfoxide (DMSO) inoculated to plates with test microorganisms[30]
China, Taiwan, IndochinaL. acutivena HayataLeaves and twigsOil for antimicrobial50 μL of 1 mg/mL MTT administered against A549 and HT-29 cells[31]
India, China, Taiwan, Indonesia, and other parts of Southeast AsiaL. cubeba (Lour.) Pers.FruitsPain reliever, promotes blood circulation, relieves stomach distension, asthma, demesia, diarrhea, turbid urine, and traumatic injury-[28,32,33,34]
RootsRelieves cold, stomachache, headache, dermatophytosis, and arthralgia-
LeavesPromotes blood circulation, cures mammitis, heals hemostasis, sores furuncle, insect and snake bites, cures myocardial infarction in Wistar rats100 to 200 mg/kg of extract daily for a period of 21 days in rats
IndiaL. chinensis (Gaertn.) Sonner.Fruit, leaves, stemActivates sexual behavior500 mg/kg of extract to male rats[35]
Malaysia, Indonesia, Philippines, TaiwanL. garciae S. VidalFruitsAntifungal, antioxidant Samples (0.1 g) extracted for 2 h with 80% methanol[36]
Southern Korea, JapanL. japonica (Thunb.) JussieuLeavesAntioxidative, anti-inflammatoryAssay with IC50 values of 149 and 58 μM[37,38]
India (Eastern Himalaya)L. laeta (Nees) Hook. f.LeavesFuelwood -[39]
Nepal, India, Bangladesh, Burma, ChinaL. monopetala (Roxb.) PersBarks, leaves, roots, trunkCures gonorrhea, skin diseases, boil, diarrhea, and dislocation, antimicrobialFungal growth inhibition at 150–250 µL/L with fumigation[40,41,42]
TaiwanL. nakaii HayataLeavesAntimicrobial15–30 μL of the oil in DMSO applied to microbial plates[43]
IndonesiaL. odorifera Val.LeavesAnti HSV-1-[44]
IndiaL. polyantha Juss.Barks and rootsEffective in pains, bruises, fractures, diarrhea-[45]
ChinaL. rotundifolia Hemsl.RootsTreating rheumatic pain-[33]
India, Nepal, Bhutan, Vietnam, Bangladesh, Myanmar, ChinaL. salicifolia (J. Roxb. ex Nees) Hook. f.-Fruits for bone fracture, stomach disorder-[46,47]
Malaysia (Sarawak)L. turfusa Kosterm.Ground barksAntifungal, antitumor-[48]
Table 2. Compounds isolated from Litsea cubeba and their properties.
Table 2. Compounds isolated from Litsea cubeba and their properties.
CompoundsFunctionReference
Alkaloids
(–)-8-O-Methyloblongine; (–)-Litcubine; (–)-Litcubinine; (–)-Magnocurarine; (–)-Oblongine; (+)-Isoboldine β-N-oxide;(+)-8-Methoxyisolaurenine-N-oxide; (+)-N-(Methoxycarbonyl)-N-(norboldine/norglaucine/norlauroscholtzine/norglaucine/norbulbodione/nordicentrin/norisocorydione/norpredicentrine); Actinodaphnine; Isoboldine; Atheroline; Boldine; Cassameridine; Cassythicine; Coclaurine; Corydine; Corytuberine; Dicentrine; Dicentrinone; Glaucine; Glaziovine; Isocorydine; Isodomesticine; Juziphine; Laetanine; Laetine; Lancifoliaine; Laurelliptine; Laurolitsine; Laurotetanine; Lindcarpine; Litebamine; Litsedine; Litseferine; Litseglutine B; Magnoflorine; N,O-Dimethylharnovine; N-Acetyllaurolitsine; N-Allyllaurolitsine; N-Methylcoclaurine; N-Methyllaurotetanine; N-Methyllindcarpine; Norcorydine; Nordicentrine; Norisoboldine; Norisocorydine; Norjuziphine; Oxoushinsunine; Pallidine; Phanostenine; Predicentrine; Reticuline; Sebiferine; Ushinsunine; Xanthoplanine; Butanolides and ButenolactoneAntioxidant, antiplatelet, antitumor, anticonvulsant, and antiplasmodial effects[12,13,66,67,68,69]
Monoterpenes
Camphene; Bornylacetate; DL-Carvone; 1,8-Cineole; Citronellal; Citronellol; p-Cymene; Geranial; Geranyl acetate; Geraniol; Limonene; Linalool; β-Myrcene; Neral; Nerol; Neryl acetate; (E)-β-Ocimene; (Z)-β-Ocimene; β-Phellandrene; α-Pinene; β-Pinene; α-a-Isopulegol; Sabinene; cis-Sabinene hydrate; α-Terpineol; Terpinen-4-ol; Terpinolene; α-Terpinylacetate; Litseacubebic acidAntibacterial activity[29,62,70]
Sesquiterpenes
α-Amorphene; Aphanamol II; Aromadendrene; Bulnesol; α-Cadinene; β-Cadinene; γ-Cadinene; δ-Cadinene; α-Cadinol; β-Caryophyllene; Chromolaevanedione; α-Copaene; Isocurcumol; Elemol; β-Elemene; γ-Elemene; α-Eudesmol; β-Eudesmol; γ-Eudesmol; Germacrene; α-Humulene; Humulene oxide; Indonesiol; LedeneDefensive roles[29,71,72,73]
Diterpenes
Cubelin ((þ)-6-(4-hydroxy-4-methyl-2-pentenoyl)-4,6-dimethyl-5-(3-methyl 2-butenyl)-1,3-cyclohexadienecarbaldehyde);trans-PhytolAntioxidative, antifungal, antiasthmatic, anti-anaphylactic properties[74,75,76]
Flavonoids
Flavones; flavanols; flavanones; flavanonols; anthocyanidins; chalcones; flavan-3-olsAnti-inflammatory, antioxidant, and hepatoprotective activities[11,77,78,79]
Amides
cis-N-Feruloyl-3-methoxytyramine; N-Feruloyl-3-methoxytyramine; 3-Methoxy-N-sinapoyltyramine; N-trans-3,4-methylenecinnamoyl-3-methoxytyramine; Cubebamine A; 1,2-dihydro-6,8-dimethoxy-7-1-(3,5-dimethoxy-4-hydroxyphenyl)-N1,N2-bis-(2-(4-hydroxyphenyl)ethyl)-2,3-naphthalene dicarboxamide; N-cis-3,4-methylenedioxycinnamoyl-3-methoxytyramineAnticancer effects[6,68,80,81]
Lignans
Eugenol; syringaresinol; 9,9′-O-di-(E)-feruloyl-(+)-secoisolariciresinol; 9,9′-O-di-(E)-feruloyl-5,5′-(+)-dimethoxysecoisolariciresinol; balanophonin B; (+)-medioresinol; Lancifolin A; cyclolignan; Dehydrodieugenol; Dehydrodiisougenol; Grandisin; (+)-Eudesmin; (+)-Epiexcelsin; Biseugenol A, B; syringaresinol; Glochidioboside Antioxidant and anticancer effects[80,82]
Steroids
β-sitostenone; Daucosterol; β-Sitosterol; Sepesteonol, 5,6-Epoxystigmastan-3-ol; Stigmasterol; 6-O-Palmitoyl-β-sitosteryl-D-glucoside [6,83]
Fatty acids
Capric acid; cis-Dec-4-enoic acid; cis-Dodec-4-enoic acid (Linderic acid); cis-Tetradec-4-enoic acid (Tsuzuic acid); Hexadecenoic acid; Lignoceric acid; Lauric acid; Linoleic acid; Myristic acid; Oleic acid; Palmitic acid; Ethyl palmitate; Stearic acid; Ethyl stearate; Litseacubebic acid; 2,6-Dimethyl-6-hydroxy-2E,4E-hepta-2,4-dienal; 6,7-Dihydroxy-3,7-dimethyl-oct-2-enoic acidAntidiabetic effects[62,81,84]

Share and Cite

MDPI and ACS Style

Kamle, M.; Mahato, D.K.; Lee, K.E.; Bajpai, V.K.; Gajurel, P.R.; Gu, K.S.; Kumar, P. Ethnopharmacological Properties and Medicinal Uses of Litsea cubeba. Plants 2019, 8, 150. https://doi.org/10.3390/plants8060150

AMA Style

Kamle M, Mahato DK, Lee KE, Bajpai VK, Gajurel PR, Gu KS, Kumar P. Ethnopharmacological Properties and Medicinal Uses of Litsea cubeba. Plants. 2019; 8(6):150. https://doi.org/10.3390/plants8060150

Chicago/Turabian Style

Kamle, Madhu, Dipendra K. Mahato, Kyung Eun Lee, Vivek K. Bajpai, Padam Raj Gajurel, Kang Sang Gu, and Pradeep Kumar. 2019. "Ethnopharmacological Properties and Medicinal Uses of Litsea cubeba" Plants 8, no. 6: 150. https://doi.org/10.3390/plants8060150

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop