Evaluation of ethanolic extract of Piper methysticum leaves on anxiolytic activity of mice

Authors

  • Dr Shallvi Department of Pharmacology, St. Soldier Institute of Pharmacy, Lidhran Campus, Behind NIT (R.E.C.), Jalandhar –Amritsar by pass, NH-1, Jalandhar -144011, Punjab, India.
  • Meenakshi Malhotra Department of Pharmacology, St. Soldier Institute of Pharmacy, Lidhran Campus, Behind NIT (R.E.C.), Jalandhar –Amritsar by pass, NH-1, Jalandhar -144011, Punjab, India. https://orcid.org/0000-0002-0080-1479
  • Dr Saruchi Department of Pharmacology, St. Soldier Institute of Pharmacy, Lidhran Campus, Behind NIT (R.E.C.), Jalandhar –Amritsar by pass, NH-1, Jalandhar -144011, Punjab, India.
  • Ajeet Pal Singh Department of Pharmacology, St. Soldier Institute of Pharmacy, Lidhran Campus, Behind NIT (R.E.C.), Jalandhar –Amritsar by pass, NH-1, Jalandhar -144011, Punjab, India. https://orcid.org/0000-0002-1212-5770
  • Amar Pal Singh Department of Pharmacology, St. Soldier Institute of Pharmacy, Lidhran Campus, Behind NIT (R.E.C.), Jalandhar –Amritsar by pass, NH-1, Jalandhar -144011, Punjab, India. https://orcid.org/0000-0003-0027-2869

Abstract

The ethanol extract of Piper methysticum, commonly known as kava, has shown promising results in reducing anxiety. Studies suggest it may have anxiolytic effects, potentially offering a natural alternative to conventional anxiety treatments. The ethanolic extract of Piper methysticum can increase the duration of action. It can also increase the time spent in open arm, entry in open arm (in elevated plus model) as well as increase the time spent in light field (in Light Dark field) thus we can conclude that it can also possesses Anxiolytic action. The ethanolic extract of Piper methysticum possesses an anxiolytic like activity without sedative side effect. The corticosterone level in mice is increased when they got anxiety.  So when the plasma corticosterone level of mice is checked in control group its turn out to be 10.28±0.52. It gets decreased with increase in doses. When treated with low dose of Aqueous extract is 7.28±1.44 is less effective than low dose of Ethanolic extract that is 6.22±1.28. Same as that high dose of extract shows the corticosterone level was 6.24±2.28 which was also less effective than high dose of ethanolic extract which was 5.52±0.32. Most effectively stress was decreased when treated with the Standard drug (Alprazolam) which shows plasma corticosterone level was 1.24±0.36. The mice of Piper methysticum extract (300 &600 mg/kg/ p.o.) treated group showed significantly (p<0.05) increased in body water intake as compared to the control group. Results showed that synthesized extract is very effective for the treatment of anxiety.

Keywords: Piper methysticum; anxiolytic activity; Anthraquinones; Light Dark model

Keywords:

Piper methysticum, Anxiolytic activity, Anthraquinones, Light Dark model

DOI

https://doi.org/10.22270/jddt.v14i11.6636

Author Biographies

Dr Shallvi, Department of Pharmacology, St. Soldier Institute of Pharmacy, Lidhran Campus, Behind NIT (R.E.C.), Jalandhar –Amritsar by pass, NH-1, Jalandhar -144011, Punjab, India.

Department of Pharmacology, St. Soldier Institute of Pharmacy, Lidhran Campus, Behind NIT (R.E.C.), Jalandhar –Amritsar by pass, NH-1, Jalandhar -144011, Punjab, India.

Meenakshi Malhotra, Department of Pharmacology, St. Soldier Institute of Pharmacy, Lidhran Campus, Behind NIT (R.E.C.), Jalandhar –Amritsar by pass, NH-1, Jalandhar -144011, Punjab, India.

Department of Pharmacology, St. Soldier Institute of Pharmacy, Lidhran Campus, Behind NIT (R.E.C.), Jalandhar –Amritsar by pass, NH-1, Jalandhar -144011, Punjab, India.

Dr Saruchi, Department of Pharmacology, St. Soldier Institute of Pharmacy, Lidhran Campus, Behind NIT (R.E.C.), Jalandhar –Amritsar by pass, NH-1, Jalandhar -144011, Punjab, India.

Department of Pharmacology, St. Soldier Institute of Pharmacy, Lidhran Campus, Behind NIT (R.E.C.), Jalandhar –Amritsar by pass, NH-1, Jalandhar -144011, Punjab, India.

Ajeet Pal Singh, Department of Pharmacology, St. Soldier Institute of Pharmacy, Lidhran Campus, Behind NIT (R.E.C.), Jalandhar –Amritsar by pass, NH-1, Jalandhar -144011, Punjab, India.

Department of Pharmacology, St. Soldier Institute of Pharmacy, Lidhran Campus, Behind NIT (R.E.C.), Jalandhar –Amritsar by pass, NH-1, Jalandhar -144011, Punjab, India.

Amar Pal Singh, Department of Pharmacology, St. Soldier Institute of Pharmacy, Lidhran Campus, Behind NIT (R.E.C.), Jalandhar –Amritsar by pass, NH-1, Jalandhar -144011, Punjab, India.

Department of Pharmacology, St. Soldier Institute of Pharmacy, Lidhran Campus, Behind NIT (R.E.C.), Jalandhar –Amritsar by pass, NH-1, Jalandhar -144011, Punjab, India.

References

1. Abid M, Hrishikeshavan HJ, and Asad M.Pharmacological evaluation of Pachyrrhizus erosus Linn. seeds for central nervous system depressant activity. Indian J Physiol Pharmacol. 2006; 50(2): 143-151.

2. Adefunmilayo E. Taiwo, Franco B. Leite, Anxiolytic and antidepressant-like effects of Melissaofficinalis (lemon balm) extract in rats: Influence of administration and gender, Indian J Pharmacol. 2012 Mar-Apr; 44(2): 189-192. https://doi.org/10.4103/0253-7613.93846

3. Adnaik RS, Pai PT, Sapakal VD, Naikwade NS, Magdum CS. Anxiolytic activity of Vitex negundo Linn. in experimental models of anxiety in mice. Int J Green Pharm. 2009; 3(3): 243-247. https://doi.org/10.4103/0973-8258.56284

4. Ali A, Rao VM, Shalam M, Gouda ST, Babu JM, Shantakumar S. Anxiolytic activity of seed extract of Caesalpinia Bonducella (Roxb) in laboratory animals. Internet J Pharmacol. 2008; 5: No.2. https://doi.org/10.5580/2438

5. Ambavade SD, Mhetre NA, Tate VD, Bodhankar SL. Pharmacological evaluation of the extracts of Sphaeranthus indicus flowers on anxiolytic activity in mice. Indian J Pharmacol. 2006; 38(4): 254-259. https://doi.org/10.4103/0253-7613.27021

6. Dhakar RC, Maurya SD, Pooniya BK, Bairwa N, Gupta M, Moringa: The Herbal Gold To Combat Malnutrition, Chronicles of Young Scientists, 2011;2(3):119-125. https://doi.org/10.4103/2229-5186.90887

7. Showman A.F., Baker J.D., Linares C., Naeole C.K., Borris R., Johnston E., Konanui J., Turner H.Contemporary Pacific and Western perspectives on kawa (Piper methysticum)toxicology. Fitoterapia. 2015;100:56-67. https://doi.org/10.1016/j.fitote.2014.11.012

8. Bian T., Corral P., Wang Y., Botello J., Kingston R., Daniels T., Salloum R., Johnston E., Huo Z., Lu J., et al. Kava as a Clinical Nutrient: Promises and Challenges. Nutrients. 2020;12:3044. https://doi.org/10.3390/nu12103044

9. Baker J.D. Tradition and toxicity: Evidential cultures in the kava safety debate. Soc. Stud.Sci. 2011;41:361-384. https://doi.org/10.1177/0306312710395341

10. Dave P., Addressing Stress Among Healthcare Workers Using Mindfulness-Based Interventions. Asian Journal of Dental and Health Sciences, 2024:4(2):56-60 https://doi.org/10.22270/ajdhs.v4i2.89

11. Narayanapillai S.C., Balbo S., Leitzman P., Grill A.E., Upadhyaya P., Shaik A.A., Zhou B., O'Sullivan M.G., Peterson L.A., Lu J., et al. Dihydromethysticin from kava blocks tobacco carcinogen 4- (methylnitrosamino)-1-(3-pyridyl)-1-butanone-induced lung tumorigenesis and differentially reduces. DNA damage in A/J mice. Carcinogenesis. 2014;35:2365-2372. https://doi.org/10.1093/carcin/bgu149

12. Shaver J.H., Sosis R. How Does Male Ritual Behavior Vary Across the Lifespan?: An Examination of Fijian Kava Cere-monies. Hum. Nat. 2014;25:136-160. https://doi.org/10.1007/s12110-014-9191-6

13. Singh Y.N., Singh N.N. Therapeutic Potential of Kava in the Treatment of Anxiety Disorders. CNS Drugs. 2002;16:731-743. https://doi.org/10.2165/00023210-200216110-00002

14. Nosa V., Ofanoa M. The social, cultural and medicinal use of kava for twelve Tongan born men living in Auckland, New Zealand. Pac. Health Dialog. 2009;15:96-102.

15. Kuchta K., Schmidt M., Nahrstedt A. German Kava Ban Lifted by Court: The Alleged Hepatotoxicity of Kava (Piper methysticum) as a Case of Ill-Defined Herbal Drug Identity, Lacking Quality Control, and Misguided Regulatory Politics. Planta Medica. 2015;81:1647-1653. https://doi.org/10.1055/s-0035-1558295

16. Bilia A.R., Scalise L., Bergonzi M.C., Vincieri F.F. Analysis of kavalactones from Pipermethysticum (kava-kava) Anal. Technol. Biomed. Life Sci. 2004;812:203-214. https://doi.org/10.1016/S1570-0232(04)00644-0

17. Celentano A., Tran A., Testa C., Thayanantha K., Tan-Orders W., Tan S., Syamal M., McCullough M.J., Yap T. The protective effects of Kava (Piper methysticum) constituents in cancers: A systematic review. J. Oral Pathol. Med. 2019;48:510-529. https://doi.org/10.1111/jop.12900

18. Sarris J., LaPorte E., Schweitzer I. Kava: A Comprehensive Review of Efficacy, Safety, andPsychopharmacology. Aust. N. Z. J. Psychiatry. 2011;45:27-35. https://doi.org/10.3109/00048674.2010.522554

19. Hegazy N.H., Breitinger H.-G., Breitinger U. Kavalactones from Kava (Piper methysticum) root extract as modulators of recombinant human glycine receptors. Biol. Chem. 2019;400:1205-1215. https://doi.org/10.1515/hsz-2019-0112

20. Kong Y., Gao X., Wang C., Ning C., Liu K., Liu Z., Sun H., Ma X., Sun P., Meng Q. Protective effects of yangonin from an edible botanical Kava against lithocholic acid-induced cholestasis and hepatotoxicity. Eur. J. Pharmacol. 2018;824:64-71. https://doi.org/10.1016/j.ejphar.2018.02.002

21. Tang Y., Fields C. A UHPLC-UV Method Development and Validation for Determining Kavalactones and Flavokavains in Piper methysticum (Kava) Molecules. 2019;24:1245. https://doi.org/10.3390/molecules24071245

22. Liu Y., Lund J.A., Murch S.J., Brown P.N. Single-Lab Validation for Determination of Kavalactones and Flavokavains in Piper methysticum (Kava) Planta Medica. 2018;84:1213-1218. https://doi.org/10.1055/a-0637-2400

23. Teschke R., Sarris J., Lebot V. Kava hepatotoxicity solution: A six-point plan for new kavastandardization. Phytomedicine. 2011;18:96-103. https://doi.org/10.1016/j.phymed.2010.10.002

24. Dinh L.D., Simmen U., Bueter K.B., Bueter B., Lundstrom K., Schaffner W. Interaction ofVarious Piper methysticum Cultivars with CNS Receptors in vitro. Planta Medica. 2001;67:306-311. https://doi.org/10.1055/s-2001-14334

25. Lebot V., Do T., Legendre L. Detection of flavokavins (A, B, C) in cultivars of kava (Pipermethysticum) using high performance thin layer chromatography (HPTLC) Food Chem. 2014;151:554-560. https://doi.org/10.1016/j.foodchem.2013.11.120

26. Kuchta K., de Nicola P., Schmidt M. Randomized, dose-controlled double-blind trial: Efficacy of an ethanolic kava (Piper methysticum rhizome) extract for the treatment of anxiety in elderlypatients. Tradit. Kamp Med. 2017;5:3-10. https://doi.org/10.1002/tkm2.1079

27. Sarris J., Kavanagh D.J., Byrne G., Bone K.M., Adams J., Deed G. The Kava Anxiety Depression Spectrum Study (KADSS): A randomized, placebo-controlled crossover trial using an aqueous extract of Piper methysticum. Psychopharmacology. 2009;205:399-407. https://doi.org/10.1007/s00213-009-1549-9

28. Zhao X., Su C., Ren R., Zhang B., Wang Y., Su X., Lu F., Zong R., Yang L., Zhang W., et al.Simultaneous determination of both kavalactone and flavokawain constituents by different single- marker methods in kava. J. Sep. Sci. 2021;44:2705-2716. https://doi.org/10.1002/jssc.202100198

29. Ferreira J.V., Pierotte I.C., Pianetti G.A., César I.C. Simultaneous quantitation of kavalactones in kava dry extracts: Comparison of multi-standards and single standard validation approaches. Phytochem. Anal. 2021;32:740-748. https://doi.org/10.1002/pca.3019

30. Fu P.P., Xia Q., Guo L., Yu H., Chan P.-C. Toxicity of Kava Kava. J. Environ. Sci. Health PartC. 2008;26:89-112. https://doi.org/10.1080/10590500801907407

31. Pantano F., Tittarelli R., Mannocchi G., Zaami S., Ricci S., Giorgetti R., Terranova D., Busardò F.P., Marinelli E. Hepatotoxicity Induced by "the 3Ks": Kava, Kratom and Khat. Int. J. Mol.Sci. 2016;17:580. https://doi.org/10.3390/ijms17040580

32. Clayton N.P., Yoshizawa K., Kissling G.E., Burka L.T., Chan P.-C., Nyska A. Immunohistochemical analysis of expressions of hepatic cytochrome P450 in F344 rats following oral treatment with kava extract. Exp. Toxicol. Pathol. 2007;58:223-236. https://doi.org/10.1016/j.etp.2006.08.002

33. Li Y., Mei H., Wu Q., Zhang S., Fang J.-L., Shi L., Guo L. Methysticin and 7,8-Dihydromethysticin are Two Major Kavalactones in Kava Extract to Induce CYP1A1. Toxicol. Sci. 2011;124:388-399. https://doi.org/10.1093/toxsci/kfr235

34. da Silva Córneo E., Machado-de-Ávila R.A., Boligon A.A., Fachinetto R. Kava decreases thestereotyped behavior induced by amphetamine in mice. J. Ethnopharmacol. 2021;265:113293. https://doi.org/10.1016/j.jep.2020.113293

35. Krum B.N., de Freitas C.M., Busanello A., Schaffer L.F., Fachinetto R. Ex vivo and in vitro inhibitorypotential of Kava extract on monoamine oxidase B activity in mice. J. Tradit. Complement.Med. 2022;12:115-122. https://doi.org/10.1016/j.jtcme.2021.07.002

36. Prakash Pawan et al: Role of natural polymers in sustained release drug delivery system: application and recent approach. International research journal pharmacy 2011; 2(9):6-11

Published

15-11-2024
Statistics
Abstract Display: 69
PDF Downloads: 105
PDF Downloads: 12

How to Cite

1.
Shallvi D, Malhotra M, Saruchi D, Singh AP, Singh AP. Evaluation of ethanolic extract of Piper methysticum leaves on anxiolytic activity of mice. J. Drug Delivery Ther. [Internet]. 2024 Nov. 15 [cited 2024 Dec. 6];14(11):1-9. Available from: https://jddtonline.info/index.php/jddt/article/view/6636

How to Cite

1.
Shallvi D, Malhotra M, Saruchi D, Singh AP, Singh AP. Evaluation of ethanolic extract of Piper methysticum leaves on anxiolytic activity of mice. J. Drug Delivery Ther. [Internet]. 2024 Nov. 15 [cited 2024 Dec. 6];14(11):1-9. Available from: https://jddtonline.info/index.php/jddt/article/view/6636