Chemical stimulation of the lateral hypothalamus induced seeking behaviors in rats: Involvement of orexin receptors in the ventral tegmental area

Eur J Pharmacol. 2020 Nov 5:886:173433. doi: 10.1016/j.ejphar.2020.173433. Epub 2020 Aug 4.

Abstract

Orexinergic projections originated from the lateral hypothalamus (LH) to the ventral tegmental area (VTA) play essential role in reward-related behaviors. Our previous studies show that intra-LH injection of carbachol, as a cholinergic agonist, induces conditioned place preference (CPP) in rats. This study aimed to determine whether chemical stimulation of the LH alone can induce reinstatement or not, and whether intra-VTA orexin receptors are involved in the reinstatement of intra-LH carbachol-induced CPP in the rats. The animals were unilaterally treated by carbachol (250 nM) in the LH during 3-day conditioning phase. Then, they underwent an extinction phase without receiving carbachol, and on the reinstatement day, animals received a different priming dose of carbachol in the separate groups. Extinguished animals unilaterally received intra-VTA administration of SB334867 or TCS OX2 29 as orexin-1 or orexin-2 receptor antagonists to evaluate the role of orexin receptors before effective priming dose of carbachol on the reinstatement day. Findings showed that intra-LH microinjection of a priming dose of carbachol (25 and 50 nM) induced the reinstatement of LH chemical stimulation-induced CPP. Moreover, it was indicated that, intra-VTA administration of either SB334867 or TCS OX2 29 (10 and 30 nM) before to intra-LH injection of the priming dose of carbachol (50 nM) dose-dependently inhibited the reinstatement of intra-LH carbachol-induced CPP. Also, the orexin-2 receptor antagonist was a little more effective than orexin-1 receptor antagonist for inhibiting the reinstatement of LH chemical stimulation-induced CPP. The consequences propose that both orexin receptors in the VTA play roles in the reinstatement of intra-LH carbachol-induced CPP.

Keywords: Extinction; Lateral hypothalamus; Orexin system; Reinstatement; Reward; Ventral tegmental area.

MeSH terms

  • Animals
  • Behavior, Animal
  • Benzoxazoles / pharmacology
  • Carbachol / pharmacology
  • Conditioning, Operant / drug effects
  • Dose-Response Relationship, Drug
  • Exploratory Behavior / drug effects*
  • Extinction, Psychological / drug effects
  • Hypothalamic Area, Lateral / drug effects*
  • Isoquinolines / pharmacology
  • Male
  • Microinjections
  • Muscarinic Agonists / pharmacology
  • Naphthyridines / pharmacology
  • Orexin Receptors / drug effects*
  • Pyridines / pharmacology
  • Rats
  • Rats, Wistar
  • Reward
  • Stimulation, Chemical
  • Urea / analogs & derivatives
  • Urea / pharmacology
  • Ventral Tegmental Area / drug effects*

Substances

  • 1-(2-methylbenzoxazol-6-yl)-3-(1,5)naphthyridin-4-yl urea
  • 1-(3,4-dihydro-6,7-dimethoxy-2(1H)-isoquinolinyl)-3,3-dimethyl-2-((4-pyridinylmethyl)amino)-1-butanone
  • Benzoxazoles
  • Isoquinolines
  • Muscarinic Agonists
  • Naphthyridines
  • Orexin Receptors
  • Pyridines
  • Urea
  • Carbachol