Evaluation of Antidepressant Activity of Ethanol Leaf Extract of <i>Entada africana</i> Guill. & Perr. (Fabaceae) in Mice
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Abstract
Depression remains the major cause of global disease burden and affects individuals in all communities around the world. More than 300 million individuals worldwide suffer from depression. The objective of the present study was to evaluate the antidepressant activity of ethanol leaf extract of Entada africana (ELEEA) in mice. Preliminary phytochemical screening and acute toxicity studies of the extract were carried out using standard methods. Antidepressant activity screening of the extract was conducted using Tail Suspension Test (TST), Forced Swim Test (FST), and Open Field Test (OFT) in mice. Phytochemical screening shows the presence of terpenoids, steroids, cardiac glycosides, tannins, saponins, flavonoids and carbohydrates in the extract. The result of the acute toxicity studies revealed an LD50 value of 28.3 mg/kg body weight in mice. ELEEA at all the tested doses significantly (p < 0.05) reduced the duration of immobility of mice in TST compared to the normal saline (control) group. In the FST, the extract at doses of 2, 4 and 8 mg/kg body weight exhibited significant (p < 0.01) reduction in the immobility time when compared to the control group. However, in the OFT, ELEEA at doses of 2, 4 and 8 mg/kg body weight and diazepam (0.5 mg/kg) had no significant effect (p > 0.05) on the number of lines crossed by the mice compared to the control group. The results of our study suggest that the ethanol leaf extract of Entada africana has potential for use as an antidepressant agent.
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References
World Health Organization.What Causes Depression, 'What Is Depression?' WHO, 2012.
Abelaira HM, Réus GZ, Quevedo J. Animal models as tools to study the pathophysiology of depression. Braz J Psychiatr. 2013; 35:S112-S120.
Luduvico KP, Spohr L, Soares MSP, Teixeira FC, de Farias AS, Bona NP, Stefanello FM. Antidepressant effect and modulation of the redox system mediated by tannic acid on lipopolysaccharide-induced depressive and inflammatory changes in mice. Neurochem Res. 2020; 45:2032-2043.
Benazzi F. Various forms of depression. Dialogues Clin Neurosci. 2006; 8(2):151-161
Swartz CM and Shorter E. Psychotic depression: Cambridge University Press. 2007.
Adediwura FJA and Bola OA. Antidepressant activities of the methanol extract, petroleum ether and ethyl acetate fractions of Morus mesozygia stem bark. Pharmacol Pharm. 2013; 4(01):100-103.
Otte C, Gold SM, Penninx BW, Pariante CM, Etkin A, Fava M, Schatzberg AF. Major depressive disorder. Nat Rev Dis Prim. 2016; 2(1):1-20.
World Health Organization. Depression [fact sheet no. 369]. Geneva: WHO, 2012.
World Health Organization. Depression and other common mental disorders. Global health estimates. WHO, 2017.
Ferrari AJ, Charlson FJ, Norman RE, Patten SB, Freedman G, Murray CJ, Whiteford HA. Burden of depressive disorders by country, sex, age, and year: findings from the global burden of disease study 2010. PLoS Med. 2013; 10(11):e1001547.
World Health Organization. Depression and other common mental disorders. Global health estimates. WHO, 2017.
Hao Y, Ge H, Sun M, Gao Y. Selecting an appropriate animal model of depression. Int J Mol Sci. 2019; 20(19):4827.
World Health Organization. Public health action for the prevention of suicide: a framework. WHO, 2012.
Gu X, Zhou Y, Wu X, Wang F, Zhang C-Y, Du C, Liu C. Antidepressant-like effects of auraptenol in mice. Sci Rep. 2014; 4(1):4433.
Burkill HM. The useful plants of west tropical Africa (2 ed.), Royal Botanic Gardens, Kew, UK, 1995; 1-3.
Owona BA, Njayou NF, Laufer S, Moundipa PF, Schluesener HJ. A fraction of stem bark extract of Entada africana suppresses lipopolysaccharide-induced inflammation in RAW 264.7 cells. J Ethnopharmacol. 2013; 149(1):162-168.
Keay RWJ. Trees of Nigeria: Clarendon Press. 1989.
Orwa C, Mutua A, Kindt R, Jamnadass R, Simons A. Agroforestree Database: a tree reference and selection guide. Version 4. Agroforestree Database: a tree reference and selection guide. Version 4. 2009.
Burkill HM. Families AD. In: The Useful Plants of West Tropical Africa. Royal Botanic Gardens, Kew, UK, 1985.
Diallo D, Paulsen BS, Liljebäck TH, Michaelsen TE. Polysaccharides from the roots of Entada africana Guill. et Perr., Mimosaceae, with complement fixing activity. J Ethnopharmacol. 2001; 74(2):159-171.
Sanogo R, Germano M, D'Angelo V, Guglielmo M, De Pasquale R. Antihepatotoxic properties of Entada africana (Mimosaceae). Phytother Res. 1998; 12(S1):S157-S159.
Guissou IP, Nacoulma GO, Faso B. Evaluation of antioxidant activity, total phenolic and flavonoid contents of Entada africana Guill. et Perr.(Mimosaceae) organ extracts. Res J Med Sci. 2010; 4:81-87.
Baidoo MF, Mensah AY, Ossei PPS, Asante-Kwatia E, Amponsah IK. Wound healing, antimicrobial and antioxidant properties of the leaf and stem bark of Entada africana Guill. & Perr. South Afr J Bot. 2021; 137:52-59.
Abubakar AR, Sani IH, Chiroma SS, Malami S, Yaro AH. Ethno-botanical survey of medicinal plants used traditionally in the treatment of mental disorders in Kano, Nigeria. Trop J Pharm Res. 2022; 21(5):1009-1017.
Steru L, Chermat R, Thierry B, Simon P. The tail suspension test: a new method for screening antidepressants in mice. Psychopharmacol. 1985; 85:367-370.
Nakamura K and Tanaka Y. Antidepressant-like effects of aniracetam in aged rats and its mode of action. Psychopharmacol. 2001; 158:205-212.
Seibenhener ML and Wooten MC. Use of the open field maze to measure locomotor and anxiety-like behavior in mice. J Vis Exp. 2015; 96:e52434.
Bethesda M. Guide for the care and use of laboratory animals. National Institute of Health. Public Health Service. DHEW Publication no: NIH, 1985, 80-23p.
Yusuf AJ and Abdullahi M. The phytochemical and pharmacological actions of Entada africana Guill. & Perr. Heliyon. 2019; 5(9):e02332.
Bahramsoltani R, Farzaei MH, Farahani MS, Rahimi R. Phytochemical constituents as future antidepressants: a comprehensive review. Rev Neurosci. 2015; 26(6):699-719.
Hamid HA, Ramli AN, Yusoff MM. Indole alkaloids from plants as potential leads for antidepressant drugs: A mini review. Front Pharmacol. 2017; 8:96.
Porsolt R, Bertin A, Jalfre M. Behavioral despair in mice: a primary screening test for antidepressants. Arch Int Pharmacodyn Ther. 1977; 229(2):327-336.
Willner P. Validity, reliability and utility of the chronic mild stress model of depression: a 10-year review and evaluation. Psychopharmacol. 1997; 134:319-329.
Yankelevitch-Yahav R, Franko M, Huly A, Doron R. The forced swim test as a model of depressive-like behavior. J Vis Exp. 2015; 97:e52587.
Koob GF. Encyclopedia of behavioral neuroscience: Elsevier. 2010.
Thierry B, Steru L, Simon P, Porsolt R. The tail suspension test: ethical considerations. Psychopharmacol. 1986; 90:284-285.
Kang S, Kim H-J, Kim HJ, Shin SK, Choi S-H, Lee M-S, Shin K-H. Effects of reboxetine and citalopram pretreatment on changes in cocaine and amphetamine regulated transcript (CART) expression in rat brain induced by the forced swimming test. Eur J Pharmacol. 2010; 647(1-3):110-116.
Brian H and Francois N. New Insights on Antidepressant Discontinuation Syndrome. Pharmacol Theory. 2015; 59:67-70.
Ya’u J, Malami S, Abugi M, Ngura H. Antidepressant activity of ethanol extract and residual aqueous fraction of Carissa edulis (Apocynaceae) root bark in mice. Trop J Nat Prod Res. 2017; 1(3):129-132.
Hritcu L, Ionita R, Postu P, Gupta G, Turkez H, Lima T. Antidepressant flavonoids and their relationship with oxidative stress. Oxid Med Cell Longev. 2017; 2017:5762172.
Shi Y and Wang H. Antidepressant activity of extract of Hypericum perforatum with enriched flavonoids. Trad Chin Drug Res Clin Pharmacol. 1993;
Sinclair A, Begg D, Mathai M, Weisinger R. Omega 3 fatty acids and the brain: Rev Stud Depress. 2007;
Xiang H, Liu Y, Zhang B, Huang J, Li Y, Yang B, Zhang H. The antidepressant effects and mechanism of action of total saponins from the caudexes and leaves of Panax notoginseng in animal models of depression. Phytomed. 2011; 18(8-9):731-738.