Evaluation of costus speciosus in experimental models of depression in Albino mice

Zahoor Ahmad Rather, M. Nateshprabhu, D. S. Sushma, Kb Rakesh, Sunil Pai, D. Ullal Sheetal

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Abstract

Introduction: Despite theavailability of numerous antidepressant drugs the therapy of depression is far from satisfactory. Two of the many reasons for this are the delay in onset of effect and the adverse effects associated with most of the antidepressants. Costus speciosus rhizome has shown adaptogenic activity. Objective: To evaluate the antidepressant activity of50% aqueous-ethanol extract of Costus speciosus (CS) leaves in experimental models of depression. Materials and Methods: Male albino mice were randomly assigned to five groups of six each. We studied three doses of the leaf extract (100, 200 and 400 mg/kg) on two models of depression - forced swim test and tail suspension test. Imipramine was used as the standard control. Both acute and chronic effects were studied. Drugs (test drug, standard control and vehicle) were administeredorally, one hour before the experiment in the acute study and daily for 14 days for the chronic study. Results: Imipramine showed significant antidepressant activity as demonstrated by a reduction in duration of immobility in both acute and chronic studies of forced swim test and tail suspension test. CS showed a dose dependent antidepressant activity. CS-100 demonstrated an antide-pressant effect only in the acute forced swim test. CS-200 demonstrated an antidepressant activity in both acute and chronic forced swim test but not in tail suspension test. CS-400 showed maximum antidepressant activity in both acute and chronic studies, which was comparable to that of the standard drug imipramine. Conclusion: CS showed dose dependent antidepressant activity with CS-400 mg/kg showing maximum effect.

Original languageEnglish
Pages (from-to)483-486
Number of pages4
JournalPharmacognosy Journal
Volume8
Issue number5
DOIs
Publication statusPublished - 01-01-2016

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All Science Journal Classification (ASJC) codes

  • Pharmacology
  • Drug Discovery

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