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腹侧被盖区中食欲素能系统在下丘脑外侧刺激诱导的吗啡敏化形成中的作用

Role of the Orexinergic System Within the Ventral Tegmental Area in the Development of Sensitization to Morphine Induced by Lateral Hypothalamus Stimulation.

作者信息

Haghparast Amir, Rashvand Mina

机构信息

School of Dentistry, International Branch of Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Neuroscience Research Center, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

Basic Clin Neurosci. 2022 Jan-Feb;13(1):97-106. doi: 10.32598/bcn.2021.2946.1. Epub 2022 Jan 1.

Abstract

INTRODUCTION

The Lateral Hypothalamus (LH) has long been known to implicate the addictive behaviors of drug abuse. The Ventral Tegmental Area (VTA) is a major area of the mesolimbic system that is strongly involved in developing morphine sensitization. The current study aimed to examine the role of intra-VTA orexin receptors in the LH stimulation-induced sensitization to the antinociceptive response of morphine.

METHODS

A total of 114 adult male Wistar rats underwent unilateral implantation of two separate cannulae in the LH and VTA using the stereotaxic apparatus. Intra-VTA administration of the Orexin-1 (OX1) and Orexin-2 (OX2) receptor antagonists, SB334867 and TCS OX2 29 (1, 3, and 10 nM/0.3 μL DMSO), respectively, was performed 5 min before concurrent microinjection of carbachol (250 nM/0.5 μL saline) into the LH and an ineffective dose of morphine (0.5 mg/kg; SC) during a 3-day sensitization period. After a 5-day free drug period, on the ninth day, for assessing the morphine sensitization, the nociceptive response was measured before and after morphine injection (1 mg/kg; SC) using the tail-flick test.

RESULTS

The results revealed that the concurrent administration of carbachol (250 nM) and an ineffective dose of morphine significantly induced morphine sensitization. Besides, the blockade of OX1 and OX2 receptors within the VTA before intra-LH carbachol injection attenuated morphine sensitization.

CONCLUSION

These findings suggest that LH stimulation potentiates the sensitization to morphine antinociceptive responses via affecting orexin receptors located in the VTA. However, OX1 receptors contribute more than OX2 receptors in the VTA to morphine sensitization in rats.

HIGHLIGHTS

LH stimulation enhances sensitization to the ineffective dose of morphineIntra-VTA OX1 receptor involves in morphine sensitization-induced by LH stimulationIntra-VTA OX2 receptor involves in morphine sensitization-induced by LH stimulation.

PLAIN LANGUAGE SUMMARY

Behavioral sensitization, such as sensitization to the antinociceptive response of drugs, which defines as an enhanced systemic reaction to the same dose of addictive drugs, occurs in response to continuous and intermittent administration of these drugs. The Lateral Hypothalamus (LH) sends the orexinergic projections to the various regions of the brain and stimulation of LH induces sensitization to the antinociceptive response of morphine. The Ventral tegmental area (VTA) is a region of the brain that is strongly involved in developing morphine sensitization and receives orexinergic projections of LH. The current study aimed to examine the role of orexin receptors within the VTA in the LH stimulation-induced sensitization to the antinociceptive response of morphine in rats. In this study orexin-1 (OX1) and orexin-2 (OX2) receptors within the VTA region were blocked using their antagonists. After five minutes chemical stimulation of LH was done using carbachol microinjection into this area and ineffective dose of morphine was injected subcutaneously. These interventions were done for three consecutive days as sensitization period. After a 5-day free drug period, on the ninth day, for assessing the morphine sensitization, the nociceptive response was measured. The results revealed that the concurrent administration of LH stimulation and an ineffective dose of morphine significantly induced morphine sensitization. Besides, the blockade of OX1 and OX2 receptors within the VTA before LH stimulation attenuated sensitization to the antinociceptive response of morphine. Therefore, the orexinergic system plays an important role in morphine sensitization and can be considered as one of the potential targets to increase the analgesic effect of morphine.

摘要

引言

长期以来,人们一直认为外侧下丘脑(LH)与药物滥用的成瘾行为有关。腹侧被盖区(VTA)是中脑边缘系统的一个主要区域,在吗啡敏化的形成中起着重要作用。本研究旨在探讨VTA内食欲素受体在LH刺激诱导的吗啡镇痛反应敏化中的作用。

方法

总共114只成年雄性Wistar大鼠使用立体定位仪在LH和VTA中单侧植入两根独立的套管。在为期3天的敏化期内,在向LH同时微量注射卡巴胆碱(250 nM/0.5 μL生理盐水)和无效剂量的吗啡(0.5 mg/kg;皮下注射)前5分钟,分别向VTA内注射食欲素-1(OX1)和食欲素-2(OX2)受体拮抗剂SB334867和TCS OX2 29(1、3和10 nM/0.3 μL二甲基亚砜)。在5天的停药期后,在第9天,为评估吗啡敏化,使用甩尾试验在注射吗啡(1 mg/kg;皮下注射)前后测量伤害性反应。

结果

结果显示,同时给予卡巴胆碱(250 nM)和无效剂量的吗啡可显著诱导吗啡敏化。此外,在LH内注射卡巴胆碱前阻断VTA内的OX1和OX2受体会减弱吗啡敏化。

结论

这些发现表明,LH刺激通过影响VTA中的食欲素受体增强对吗啡镇痛反应的敏化。然而,在大鼠中,VTA内的OX1受体比OX2受体对吗啡敏化的作用更大。

要点

LH刺激增强对无效剂量吗啡的敏化VTA内的OX1受体参与LH刺激诱导的吗啡敏化VTA内的OX2受体参与LH刺激诱导的吗啡敏化。

通俗易懂的总结

行为敏化,如对药物镇痛反应的敏化,被定义为对相同剂量成瘾药物的全身反应增强,是在持续和间歇给予这些药物后发生的。外侧下丘脑(LH)向大脑的各个区域发送食欲素能投射,刺激LH会诱导对吗啡镇痛反应的敏化。腹侧被盖区(VTA)是大脑中一个在吗啡敏化形成中起重要作用的区域,并接受LH的食欲素能投射。本研究旨在探讨VTA内食欲素受体在LH刺激诱导的大鼠对吗啡镇痛反应敏化中的作用。在本研究中,使用拮抗剂阻断VTA区域内的食欲素-1(OX1)和食欲素-2(OX2)受体。在向该区域微量注射卡巴胆碱对LH进行化学刺激并皮下注射无效剂量的吗啡后五分钟。这些干预连续进行三天作为敏化期。在5天停药期后,在第9天,为评估吗啡敏化,测量伤害性反应。结果显示,同时给予LH刺激和无效剂量的吗啡可显著诱导吗啡敏化。此外,在LH刺激前阻断VTA内的OX1和OX2受体会减弱对吗啡镇痛反应的敏化。因此,食欲素能系统在吗啡敏化中起重要作用,可被视为增强吗啡镇痛作用的潜在靶点之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1916/9790096/31806850a05a/BCN-13-97-g002.jpg

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