Azizbeigi R, Farzinpour Z, Haghparast A. Role of Orexin-1 Receptor Within the Ventral Tegmental Area in Mediating Stress- and Morphine Priming-induced Reinstatement of Conditioned Place Preference in Rats. BCN 2019; 10 (4) :373-382
URL:
http://bcn.iums.ac.ir/article-1-1107-en.html
1- Department of Physiology, Faculty of Veterinary Medicine, Sanandaj Branch, Islamic Azad University, Sanandaj, Iran.
2- CAS Key Laboratory of Brain Function and Disease, School of Life Sciences, University of Science and Technology of China, Hefei, Anhui, China.
3- Neuroscience Research Center, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Abstract:
Introduction: Orexin-containing neurons exist in the lateral hypothalamic region, sending their projections toward mesolimbic regions such as the Ventral Tegmental Area (VTA).
Methods: In the current study, a Reinstatement model is used to examine the effects of intra-VTA administration of SB334867 as an Orexin-1 Receptor (OX1R) antagonist on drug priming- and Forced Swim Stress (FSS)-induced reinstatement of morphine. Eighty-eight male adult albino Wistar rats, weighing 200-280 g, were bilaterally implanted by cannulas into the VTA. We induced the Conditioned Place Preference (CPP) by Subcutaneous (SC) injection of morphine (5 mg/kg) daily in three days. Then, the CPP score was calculated. After a 24-h “off” period following achievement of extinction criterion, the rats were tested for drug priming-induced reinstatement by a priming dose of morphine (1 mg/kg, SC) and for FSS-induced reinstatement 10 min after FSS. In the next experiments, the animals received different doses of intra-VTA administration of SB334867 (0.3, 3, and 1 nM/0.3 µL 12% DMSO per side) and bilaterally were subsequently tested for FSS- and morphine priming-induced reinstatement.
Results: Our findings indicated that the FSS could induce the reinstatement of seeking behaviors. Furthermore, intra-VTA administration of OX1R antagonists suppressed FSS- and drug priming-induced reinstatement dose-dependently.
Conclusion: It is concluded that FSS and drug priming-induced reinstatement might be mediated, at least in part, by stimulation of orexin receptors in the VTA.
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Highlights
• Forced swim stress (FSS) induced the reinstatement of morphine seeking in rats.
• Orexin-1 receptor blockade in the intra-ventral tegmental area reduced morphine-induced reinstatement.
• Orexin-1 receptor blockade in the intra-ventral tegmental area reduced FSS-induced reinstatement.
Plain Language Summary
We designed this study to investigate effects of intra-VTA (ventral tegmental area) administration of SB334867 as an orexin-1 receptor (OX1R) antagonist on drug priming- and forced swim stress (FSS)-induced reinstatement of morphine. The conditioned place preference (CPP) was induced by injecting morphine and the reinstatement by the administration of effective priming dose of morphine. The extinguished rats received an intra-VTA injection of SB334867 before effective priming dose injection of morphine. In others, the extinguished rats were given intra-VTA administration of SB334867 bilaterally and were subsequently tested for FSS- and morphine priming- induced reinstatement. Our results indicated that intra-VTA administration of SB334867 could inhibit morphine priming - and FSS-induced reinstatement of extinguished morphine seeking in the rats. It seems that OX1R in the VTA may be involved in the reward system and could play an important role in the effect of stress on reinstatement of morphine-seeking behaviors in this area.
Type of Study:
Original |
Subject:
Behavioral Neuroscience Received: 2018/01/8 | Accepted: 2018/09/24 | Published: 2019/07/1