Regulation of rat MOR-1 gene expression after chronic intracerebroventricular administration of morphine

Mol Med Rep. 2012 Feb;5(2):513-6. doi: 10.3892/mmr.2011.677. Epub 2011 Nov 15.

Abstract

The µ-opioid receptor is the primary site for the action of morphine. In the present study, we investigated the regulation of the µ-opioid receptor mRNA levels in the locus ceruleus, ventral tegmental area, nucleus accumbens and hypothalamus of the rat brain following intracerebroventricular administration of morphine for 7 days. The isolated mRNA from these regions was subjected to real-time quantitative RT-PCR to determine the regulation of µ-opioid receptor gene expression. It was observed that 7 days of treatment with morphine significantly down-regulated the µ-opioid receptor mRNA levels in the hypothalamus of the brain in comparison to the control group. However, the µ-opioid receptor levels in the locus ceruleus, ventral tegmental area and nucleus accumbens regions remained the same as the control levels. Down-regulation of µ-opioid receptor mRNA levels in the hypothalamus region of the brain indicates the probable role of opioids to influence neuroendocrine function. The results further indicate that cellular adaptation for morphine tolerance is tissue-specific. These findings help us to understand the mechanism of morphine tolerance in various regions of the brain.

Keywords: μ-opioid receptor; real-time RT-PCR; rat brain; morphine; tolerance.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Gene Expression Regulation / drug effects*
  • Hypothalamus / drug effects
  • Hypothalamus / metabolism
  • Infusions, Intraventricular
  • Male
  • Morphine / administration & dosage
  • Morphine / pharmacology*
  • Narcotics / administration & dosage
  • Narcotics / pharmacology*
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Opioid, mu / genetics
  • Receptors, Opioid, mu / metabolism*

Substances

  • Narcotics
  • Oprm1 protein, rat
  • RNA, Messenger
  • Receptors, Opioid, mu
  • Morphine