‬The expression of purinergic P2X4 and P2X7 receptors in selected mesolimbic structures during morphine withdrawal in rats

Brain Res. 2019 Sep 15:1719:49-56. doi: 10.1016/j.brainres.2019.05.025. Epub 2019 May 20.

Abstract

Morphine is one of the most potent analgesics used in medicine and it's long-term use is associated with the risk of the state of dependence. The cessation of chronic morphine administration leads to withdrawal signs which are associated with neurotransmitter dysregulations within mesolimbic system. Adenosine 5'-triphosphate (ATP) and purinergic system play an important role in the activity of central nervous system (CNS). Purinergic receptors are widely distributed in neurons and glial cells throughout the CNS taking part in integration of functional activity between neurons, glial and vascular cells. In the present study the mRNA and protein expression of purinergic P2X4 and P2X7 receptors in selected mesolimbic structures (striatum, hippocampus and prefrontal cortex) during morphine withdrawal in rats was investigated by RT-PCR and Western Blot analysis. Two experimental models of morphine withdrawal were studied: single and repeated morphine withdrawal. We demonstrated that expression of P2X4 and P2X7 receptors was altered during morphine withdrawal period in rats. These alterations were varied in particular mesolimbic areas depending on the scheme of morphine administration. Our results extend the current knowledge on morphine withdrawal and for the first time high-light interactions between purinergic system and morphine withdrawal. It seems, the purinergic system may be a new, valuable tool in searching for a new strategy of management of opioid dependence.

Keywords: Addiction; Inflammation; Morphine; P2X4 receptors; P2X7 receptors; Purinergic receptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Brain / metabolism
  • Corpus Striatum / metabolism
  • Gene Expression / genetics
  • Gene Expression Regulation / drug effects
  • Hippocampus / metabolism
  • Male
  • Morphine / metabolism
  • Morphine Dependence / genetics
  • Morphine Dependence / physiopathology
  • Neuroglia / metabolism
  • Neurons / metabolism
  • Prefrontal Cortex / metabolism
  • RNA, Messenger
  • Rats
  • Rats, Wistar
  • Receptors, Purinergic P2X4 / genetics*
  • Receptors, Purinergic P2X4 / metabolism
  • Receptors, Purinergic P2X7 / genetics*
  • Receptors, Purinergic P2X7 / metabolism
  • Substance Withdrawal Syndrome / genetics
  • Substance Withdrawal Syndrome / metabolism*

Substances

  • RNA, Messenger
  • Receptors, Purinergic P2X4
  • Receptors, Purinergic P2X7
  • Morphine
  • Adenosine Triphosphate