Carvacrol alleviates CUMS-induced depressive-like behaviors and cognitive impairment by reducing oxidative stress and neuroinflammation in mice

Behav Brain Res. 2024 Aug 24:472:115135. doi: 10.1016/j.bbr.2024.115135. Epub 2024 Jul 2.

Abstract

The present study aimed to evaluate the protective potential of carvacrol against depressive-like behavior and cognitive impairment prompted by chronic unpredictable mild stress (CUMS) in mice. The animals were divided into six groups: Control (non-stressed), CARV (carvacrol at 50 mg/kg, p.o.), FLU (fluoxetine at 10 mg/kg, p.o.), CUMS (stressed), CUMS + CARV and CUMS + FLU, and the groups with CUMS were subjected to different stressors for 28 days. After treatment, mice underwent behavioral testing (open field, forced swimming, sucrose preference, social interaction, novel object recognition and Y-maze) and brain areas were removed for oxidative stress (MDA, nitrite/nitrate and GSH levels) and cytokine (IL-1β and TNF-α) content assays. The results revealed that CARV administration reversed depressive-like behavior and significantly ameliorated the cognitive deficit induced by CUMS, as well as was able to attenuate oxidative stress (decreased MDA and nitrite/nitrate levels and increased GSH levels). In addition, a significant reduction in hippocampal IL-1β and TNF-α levels was observed, demonstrating a potential anti-neuroinflammatory activity. Taken together, the antioxidant and anti-inflammatory activities observed in this study indicate that CARV is a promising drug for antidepressant treatment.

Keywords: Carvacrol; Chronic stress; Depression; Inflammation; Oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antidepressive Agents / administration & dosage
  • Antidepressive Agents / pharmacology
  • Antioxidants / pharmacology
  • Behavior, Animal* / drug effects
  • Cognitive Dysfunction* / drug therapy
  • Cognitive Dysfunction* / etiology
  • Cognitive Dysfunction* / metabolism
  • Cymenes* / administration & dosage
  • Cymenes* / pharmacology
  • Depression* / drug therapy
  • Depression* / etiology
  • Depression* / metabolism
  • Disease Models, Animal*
  • Fluoxetine / administration & dosage
  • Fluoxetine / pharmacology
  • Hippocampus / drug effects
  • Hippocampus / metabolism
  • Interleukin-1beta / metabolism
  • Male
  • Mice
  • Neuroinflammatory Diseases* / drug therapy
  • Neuroinflammatory Diseases* / metabolism
  • Oxidative Stress* / drug effects
  • Stress, Psychological* / complications
  • Stress, Psychological* / drug therapy
  • Stress, Psychological* / metabolism

Substances

  • carvacrol
  • Cymenes
  • Antidepressive Agents
  • Antioxidants
  • Fluoxetine
  • Interleukin-1beta