Assessment of antidepressant and sedative-hypnotic activities of methanolic crude extracts of<i> Stephania japonica</i> (Thunb.) Miers. whole plants
PDF

Keywords

Antidepressant
edative-hypnotic
forced swimming,
tail suspension,
open field
hole-board

Abstract

In this study, methanolic crude extracts ofStephania japonica(Thunb.) Miers. (MESJ) whole plants were examined for possible antidepressant and sedative-hypnotic activities. Herein, the forced swimming test and tail suspension test were conducted to explore the antidepressant activity. In addition, the open field test and hole-board test were performed to evaluate the sedative-hypnotic activities. In the acute toxicity test, the MESJ ensured safety up to a dose of 2000 mg/kg, p.o. The experimental doses were 100 and 200 mg/kg p.o.
In both the forced swimming test and tail suspension test, the extract significantly (p<0.01 and p<0.05) inhibited immobility time in a dose dependent manner compared to the control. These results (13.56-26.46% inhibition) indicate the mild antidepressant activity of MESJ compared to nortriptyline (60.4-64.6% inhibition). The open field test and hole-board test demonstrated the dose dependent significant (p<0.001, p<0.01 and p<0.05) and moderate sedative-hypnotic activities of the extract compared to diazepam. However, these activities were found to gradually decrease after 60 min in the open field test and must be considered as short-term activities, compared to diazepam. It can be claimed that the methanolic crude extract ofStephania japonicapossesses mild antidepressant and moderate but short-term sedative-hypnotic activities.

PDF

References

1. Moussavi S, Chatterji S, Verdes E, Tandon A, Patel V, Ustun B. Depression, chronic diseases, and decrements in health: results from the World Health Surveys. The Lancet. 2007;370(9590):851-8.

2. Murray CJ, Lopez A. The global burden of disease. Harvard School of Public Health: Harvard University Press;1996:1:201-46.

3. Cassano P, Fava M. Depression and public health: an overview. J Psychosom Res. 2002;53(4):849-57.

4. Cassileth BR, Lusk EJ, Strouse TB, Miller DS, Brown LL, Cross PA, et al. Psychosocial status in chronic illness: A comparative analysis of six diagnostic groups. N Engl J Med. 1984;311(8):506-11.

5. Noël PH, Williams JW, Unützer J, Worchel J, Lee S, Cornell J, et al. Depression and comorbid illness in elderly primary care patients: impact on multiple domains of health status and well-being. Ann Fam Med. 2004;2(6):555-62.

6. Chapman DP, Perry GS, Strine TW. The vital link between chronic disease and depressive disorders. Prev Chronic Dis. 2005;2(1):A14.

7. Angst F, Stassen HH, Clayton PJ, Angst J. Mortality of patients with mood disorders: follow-up over 34-38 years. J Affect Disord. 2002;68(2-3):167-81.

8. Stark C, Hall D, O’Brien F, Smith H. Suicide after discharge from psychiatric hospitals in Scotland. BMJ. 1995;311(7016):1368.

9. Mann JJ, Currier D, Quiroz JA, Manji HK. Neurobiology of severe mood and anxiety disorders. InBasic Neurochemistry. Academic Press;2012:1021-36.

10. Milak MS, Parsey RV, Keilp J, Oquendo MA, Malone KM, Mann JJ. Neuroanatomic correlates of psychopathologic components of major depressive disorder. Arch Gen Psychiatry. 2005;62(4):397-408.

11. Dhawan K, Dhawan S, Chhabra S. Attenuation of benzodiazepine dependence in mice by a tri-substituted benzoflavone moiety of Passiflora incarnata Linneaus: a non-habit forming anxiolytic. J Pharm Pharm Sci. 2003;6(2):215-2.

12. Kripke DF, Garfinkel L, Wingard DL, Klauber MR, Marler MR. Mortality associated with sleep duration and insomnia. Arch G Psychiatry. 2002;59(2):131-6.

13. Spielberger CD. State‐Trait anxiety inventory. The Corsini Encyclopedia of Psychology; 2010:1-1.

14. Tobler I, Kopp C, Deboer T, Rudolph U. Diazepam-induced changes in sleep: role of the α1 GABAA receptor subtype. PNAS. 2001;98(11):6464-9.

15. Semwal DK, Badoni R, Semwal R, Kothiyal SK, Singh GJ, Rawat U. The genus Stephania (Menispermaceae): Chemical and pharmacological perspectives. J Ethnopharmacol. 2010;132(2):369-83.

16. Rahman MH, Alam MB, Chowdhury NS, Jha MK, Hasan M, Khan MM, et al.Antioxidant, analgesic and toxic potentiality of Stephania japonica (Thunb.) Miers. Leaf. Int J Pharmacol. 2011;7(2):257-62.

17. Cowan MM. Plant products as antimicrobial agents. CMR. 1999;12(4):564-82.

18. Singh H, Kapoor VK, Piozzi F, Passannanti S. Paternostro M. Pharm Phytochem. 1978;17:154.

19. Adinolfi M, Corsaro MM, Lanzetta R, Parrilli M, Folkard G, Grant W, et al. Composition of the coagulant polysaccharide fraction from Strychnos potatorum seeds. Carbohydrate Res. 1994;263(1):103-10.

20. Singh H, Kapoor VK, Phillipson JD, Bisset NG. Pharm Phytochem. 1975;14:587.

21. Massiot G, Thepenier P, Jacquier MJ, Le Men-Olivier L, Delaude C. Alkaloids from roots of Strychnos potatorum. Phytochem. 1992;31(8):2873-6.

22. Gani A. Medicinal plants of Bangladesh: Chemical constituents and uses. Dhaka: Asiatic Society of Bangladesh; 2003:434-55.

23. Gamble JS. The flora of Presidency of Madras. Vol. II. Botanical survey of India;1958.

24. Seetharam YN, Kotresh K, Upalaonkar SB. Flora of Gulbarga district. Gulbarga: Gulbarga University;2000:27-31.

25. Hossan S, Agarwala B, Sarwar S, Karim M, Jahan R, Rahmatullah M. Traditional use of medicinal plants in Bangladesh to treat urinary tract infections and sexually transmitted diseases. Ethnob Res App. 2010;8:61-74.

26. Chopra RN, Chopra IC, Handa KL, Kapur LD. Chopra’s Indigenous Drugs of India. 2nd ed. Calcutta, India: Char UN and Sons, Ltd.;1958:412.

27. Kirtikar KR., Basu BD. Indian Medicinal Plants. vol. 1, 2nd ed. India: L.M. Basu, Allahabad;2004:94.

28. Achike FI, Kwan CY. Characterization of a novel tetrandrine-induced contraction in rat tail artery. APS. 2002;23:698-704.

29. Rafe MR, Ahsan M, Hasan CM, Masud MM. Chemical and biological studies of leaf extract of Dendrophthoe falcata Linn. Dhaka Univ J Pharm Sci. 2017;16(2):215-9.

30. Nasri H. Toxicity and safety of medicinal plants. J HerbMed Pharmacol. 2013;2.

31. Haq I. Safety of medicinal plants. Pak J Med Res. 2004;43(4):203-10.

32. Litchfield JJ, Wilcoxon F. A simplified method of evaluating dose-effect experiments. JPET. 1949;96(2):99-113.

33. Porsolt RD, Bertin A, Jalfre M. “Behavioural despair” in rats and mice: strain differences and the effects of imipramine. Eur J Pharmacol. 1978;51(3):291-4.

34. Steru L, Chermat R, Thierry B, Simon P. The tail suspension test: a new method for screening antidepressants in mice. Psychopharmacol. 1985;85(3):367-70.

35. Gupta BD, Dandiya PC, Gupta ML. A psycho-pharmacological analysis of behaviour in rats. Jap J Pharmacol. 1971;21(3):293-8.

36. Öztürk Y, Aydin S, Beis R, Başer KH, Berberoĝlu H. Effects of Hypericum perforatum L. and Hypericum calycinum L. extracts on the central nervous system in mice. Phytomed. 1996;3(2):139-46.

37. Jebin R, Molla MI, Chowdhury SM, Rafe MR. Antidepressant and sedative-hypnotic activities of methanolic extract of grewia asiatica Linn. Leaves in Mice. Bangladesh Pharmaceutical J. 2019:22(2):185-91.

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 Unported License.

Copyright (c) 2020 Autors

Downloads

Download data is not yet available.