QCM-4 a novel 5-HT3 antagonist attenuates the behavioral and biochemical alterations on chronic unpredictable mild stress model of depression in Swiss albino mice

Yeshwant Kurhe, Mahesh Radhakrishnan, Deepali Gupta, Thangaraj Devadoss

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

Objectives The inconsistent therapeutic outcome necessitates identifying novel compounds for the treatment of depression. Therefore, the present study is aimed at evaluating the antidepressant-like effects of a novel 5-HT3 receptor antagonist 3-methoxy-N-p-tolylquinoxalin-2-carboxamide (QCM-4) on chronic unpredictable mild stress (CUMS) induced behavioral and biochemical alterations in mice. Methods Animals were subjected to different stressors for a period of 28 days. Thereafter, battery tests like locomotor score, sucrose preference test, forced swim test (FST), tail suspension test (TST), elevated plus maze (EPM) and open field test (OFT) were performed. Biochemical assays like lipid peroxidation, nitrite levels, reduced glutathione (GSH), catalase and superoxide dismutase (SOD) were assessed in brain homogenate. Key findings QCM-4 dose dependently reversed the CUMS induced behavioral and biochemical alterations by increasing the sucrose consumption, reducing the immobility time in FST and TST, increasing the percent time in open arm in EPM and increasing the ambulation along with the rearings and decreased number of fecal pellets in OFT. Further, biochemical alterations were attenuated by QCM-4 as indicated by reduced lipid peroxidation and nitrite levels and elevated antioxidant enzyme levels like GSH, catalase and SOD. Conclusions QCM-4 attenuated the behavioral and biochemical derangements induced by CUMS in mice, indicating antidepressant behavior of the novel compound.

Original languageEnglish (US)
Pages (from-to)122-132
Number of pages11
JournalJournal of Pharmacy and Pharmacology
Volume66
Issue number1
DOIs
StatePublished - Jan 2014
Externally publishedYes

Keywords

  • 5-HT antagonist
  • CUMS
  • immobility time
  • lipid peroxidation
  • sucrose preference

ASJC Scopus subject areas

  • Pharmacology
  • Pharmaceutical Science

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