Hippocampal AMPARs involve the central sensitization of rats with irritable bowel syndrome

Brain Behav. 2017 Feb 22;7(3):e00650. doi: 10.1002/brb3.650. eCollection 2017 Mar.

Abstract

Objective: The roles of hippocampal AMPARs were investigated in irritable bowel syndrome (IBS)-like rats to clarify the central sensitization mechanisms.

Methods: IBS model was induced by neonatal maternal separation. The effects of AMPARs on visceral hypersensitivity were examined by the responses of abdominal muscle to colorectal distension after the bilateral intrahippocampal injections of CNQX (an AMPAR inhibitor). The expressions of hippocampal AMPARs (GluR1 and GluR2) were determined by Western blot.

Results: The IBS-like rats showed visceral hypersensitivity when compared with controls. Bilateral intrahippocampal injections of CNQX alleviated the visceral pain in IBS-like rats. The maximal effect appeared at the time point of 30 min, and the duration lasted for 90 min after CNQX application, under 40 and 60 mmHg CRD. The expressions of hippocampal GluR2 significantly increased in IBS-like rats when compared with controls (p < .05). However, the levels of hippocampal GluR1 had no significant differences in rats. Hippocampal LTP induced by HFS was significantly enhanced when compared with controls (p < .05). The expressions of GluR2 significantly increased in the control and IBS-like rats after 60 min LTP of recordings (p < .05), but not GluR1.

Conclusion: Neonatal maternal separation enhances the expression of GluR2 and facilitates the LTP in the hippocampus, which could lead to the formation of visceral hypersensitivity when grown up.

Keywords: AMPARs; hippocampus; irritable bowel syndrome; long‐term potentiation; visceral hypersensitivity.

MeSH terms

  • Animals
  • Central Nervous System Sensitization / physiology*
  • Disease Models, Animal
  • Hippocampus* / metabolism
  • Hippocampus* / physiopathology
  • Irritable Bowel Syndrome* / etiology
  • Irritable Bowel Syndrome* / metabolism
  • Irritable Bowel Syndrome* / physiopathology
  • Long-Term Potentiation / physiology*
  • Male
  • Maternal Deprivation*
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, AMPA / metabolism*

Substances

  • Receptors, AMPA
  • glutamate receptor ionotropic, AMPA 2
  • glutamate receptor ionotropic, AMPA 1