Orexin type-1 receptor inhibition in the rat lateral paragigantocellularis nucleus attenuates development of morphine dependence

Neurosci Lett. 2020 Apr 17:724:134875. doi: 10.1016/j.neulet.2020.134875. Epub 2020 Feb 27.

Abstract

Orexin neuropeptides are involved in opiate-induced physical dependence and expression of withdrawal signs following drug abstinence. Orexin type-1 receptors (OXR1) are expressed throughout the rostroventrolateral medulla (RVLM), particularly in the lateral paragigantocellularis (LPGi) nucleus. The present study examined whether blocking OXR1 in LPGi region could affect the development of morphine dependence and so behavioral manifestations induced by morphine withdrawal in rats. Male Wistar rats weighing 250-300 g were used. In order to induce drug dependence, morphine was injected subcutaneously (s.c.) (6, 16, 26, 36, 46, 56, and 66 mg/kg, 2 ml/kg) at an interval of 24 h for 7 days. Animals were divided into experimental groups in which the orexin type-1 receptor antagonist, SB-334867 (0.2 μl, 3 mM), or its vehicle were injected into the LPGi nucleus for 7 days before each morphine injection. On day 8, naloxone (2.5 mg/kg, i.p.) was administered and morphine withdrawal behaviors were monitored for 25 min. Our results indicated that the inhibition of OXR1 in LPGi nucleus significantly reduces the development of morphine dependence and behavioral signs elicited by the administration of naloxone in morphine-dependent rats.

Keywords: LPGi; Morphine dependent rat; Morphine withdrawal; Orexin type-1 receptor; SB-334867.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Male
  • Medulla Oblongata / drug effects
  • Medulla Oblongata / physiology*
  • Microinjections / methods
  • Mitochondrial Proteins / antagonists & inhibitors*
  • Mitochondrial Proteins / physiology*
  • Morphine / administration & dosage
  • Morphine / adverse effects*
  • Morphine Dependence / physiopathology
  • Morphine Dependence / prevention & control*
  • Orexin Receptor Antagonists / administration & dosage*
  • Rats
  • Rats, Wistar

Substances

  • Mitochondrial Proteins
  • Orexin Receptor Antagonists
  • Oxr1 protein, rat
  • Morphine