Evaluations of antidepressant activity of Anacyclus pyrethrum root extract
DOI:
https://doi.org/10.22377/ijgp.v4i2.124Abstract
The present study was designed to screen antidepressant activity of Anacyclus pyrethrum (AP) root extract. An experiment was designed by different method such as Locomotor activity, Haloperidol-induced catalepsy, Forced swim test (FST), Tail suspension test (TST), Clonidine-induced hypothermia and Reserpine-induced hypothermia on Swiss male albino mice. Standard root extract of Anacyclus pyrethrum (AP root extract) showed an increase in ambulatory behaviour indicating a stimulant effect of the photoactometer. AP rootextract produces a significant antidepressant effect in both FST and TST as they reduced the immobility. AP root extract was found to be effective in reversing hypothermia produced by clonidine and reserpine. In our study, we found that AP root extract inhibited haloperidol-induced catalepsy. These study suggest that AP root extract might produce antidepressant effect by interaction with adrenergic and dopamine receptor thereby increasing the level of noradrenaline and dopamine in brains of mice.
Key words: Anacyclus pyrethrum, antidepressant activity, forced swim test and tail suspension test
Downloads
References
Stahl SM. Essential Psychopharmacology: Neuroscientific Basis
and Practical: Applications. Cambridge University Press; 1998.
Rechelson E. Pharmacology of Antidepressants. Mayo Clin Proc
;65:1227-36.
Rechelson E. Pharmacology of Antidepressants. Mayo Clin Proc
;76:516-27.
Tripathi KD. Essential of Medical Pharmacology. 5th ed. New Delhi,
India: Medical Publishers Pvt. Ltd; 2005. p. 168-72.
Hardman JG, Limbird LE, Goodman Gilman A. Goodman and
Gilman’s: The Pharmacological Basis of Therapeutics. 10th ed.
New York: The McGraw Hill Companies, Inc; 2001. p. 825-8.
Shalam MD, Shantakumar SM, Laxmi Narasu M. Pharmacological
and Biochemical evidence for the antidepressant effect f the herbal
preparation Trans-01. Indian Journal Pharmacology 200739:231-4.
Nadkarni AK. Indian Materica Medica. 3rd ed. Vol. 1. Mumbai:
Popular Publication; 2000. p. 97-8.
Bendjeddou D, Lalaoui K and Satta D. Immumostimulating
activity of the hot water soluble polysacharrides extract of
Anacyclus pyrethrum, Alpinia galanga and Citeullus colocynthis.
J Ethnopharmacol 2003;88:155-60.
Muller JB, Breu W, Probstle A, Redi K, Greger H, Bauer R. In vitro
inhibition of cyclooxygenase and 5-lipoxygenase by alkamides
from Echinacea and Achillea species. Planta Medica 1994;60:37-40.
Kulkarni SK. Handbook of Experimental Pharmacology.
New Delhi: Vallabh Prakashan; 3rd ed. 1999. p. 115-7.
Dantzer R, O’Connor JC, Freund GG, Johnson RW, Kelley KW.
From inflammation to sickness and depression: When the immune
system subjugates the brain. Nat Rev Neurosci 2008;9:46-56.
Stephani U. The natural history of myoclonic astatic epilepsy
the natural history of myoclonic astatic epilepsy. Epilepsia
;47:S53‑5.
Sanberg PR. Haloperidol induced catalepsy is mediated by post
synaptic dopamine receptor. Nature 1980;24:93-11.
Porsolt RD, Le Pichnon M, Jalfre M. Depression: A new animal
model sensitive to antidepressant treatment. Nature of Science
;266:730-2.
Steru L, Chermat R, Thierry B, Simon P. The tail suspension
test: A new method for screening antidepressant in mice.
Psychopharmacology (Berl) 1985;85:367-70.
Rojas-Corrales R, Esther B, Juan GR, Juan AM. Antidepressant
like effect of tramodol and its enantiomers in reserpinized mice:
Comparative study with desipramine, fluvaxamine, Venlafaxine
and opiates. Psychopharmacol 2004;18:404-11.
Drew GM, Grower AJ, Marnott AS. Pharmacological
characterization of alpha adrenoreceptor, which mediate, clonidine
induced sedation. British Journal of Pharmacol 1979;63:468-14.