CRHR1 antagonist alleviates LPS-induced depression-like behaviour in mice

BMC Psychiatry. 2023 Jan 9;23(1):17. doi: 10.1186/s12888-023-04519-z.

Abstract

Background: Maladaptation of the HPA (hypothalamic-pituitary-adrenal) axis plays an important role in depression-like behaviour, but the specific molecular mechanisms are unknown. Here, we determined the roles of CRHR1 (corticotrophin releasing hormone receptor 1) and nectin3 in LPS (lipopolysaccharide)-induced depression-like behaviour in mice.

Methods: C57BL/6 male mice were intraperitoneally injected with LPS (0.83 g/kg), and the open field, novelty-suppressed feeding, forced swimming, and tail suspension tests were performed after intraperitoneal injections of saline or antalarmin (20 mg/kg). The hippocampal mRNA levels of CRHR1 and nectin3 were determined by quantitative reverse transcription-PCR. The hippocampal protein levels of CRHR1, nectin3, and calbindin were measured by western blotting. The CORT (corticosterone) levels in the blood were measured by ELISA kits.

Results: Antalarmin alleviated LPS-induced depression-like behaviour in male mice. Furthermore, antalarmin significantly inhibited changes in CRHR1, nectin3 and calbindin levels in the hippocampus and reduced the increase in CORT levels in LPS-treated mice.

Conclusion: CRHR1antagonist showed antidepressant effects in LPS-induced depressive mice, and CRHR1/nectin3 signalling may play a crucial role in this process.

Keywords: CRHR1; Depression-like behaviour; HPA; Stress; nectin3.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antidepressive Agents / pharmacology
  • Antidepressive Agents / therapeutic use
  • Depression* / chemically induced
  • Depression* / drug therapy
  • Disease Models, Animal
  • Hippocampus
  • Hypothalamo-Hypophyseal System / metabolism
  • Lipopolysaccharides
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Pituitary-Adrenal System / metabolism
  • Receptors, Corticotropin-Releasing Hormone* / antagonists & inhibitors

Substances

  • Antidepressive Agents
  • Lipopolysaccharides
  • CRF receptor type 1
  • Receptors, Corticotropin-Releasing Hormone