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抑制食欲素受体 1 通过减弱 cAMP 反应元件结合蛋白和磷脂酶 Cβ 促进吗啡依赖的发展。

Inhibition of orexin receptor 1 contributes to the development of morphine dependence via attenuation of cAMP response element-binding protein and phospholipase Cβ.

机构信息

Department of Neuroscience, School of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran; Department of Physiology, School of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

Department of Physiology, School of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

出版信息

J Chem Neuroanat. 2020 Oct;108:101801. doi: 10.1016/j.jchemneu.2020.101801. Epub 2020 May 11.

Abstract

Noradrenergic neurons of the locus coeruleus (LC) receive projection from hypothalamus orexinergic neurons and express orexin 1 receptor (Orx). Orx in the locus coeruleus nucleus is involved in the development of morphine dependence. The downstream signaling of Orx contribution to the development of morphine dependence in LC neurons of morphine-dependent rats was studied. Therefore, we evaluated cyclic adenosine monophosphate (cAMP), cAMP response element-binding protein (CREB) and phospholipase Cβ (PLCβ) levels by the application of immunohistochemistry. Results showed that cAMP, CREB and PLCβ levels were suppressed by the application of SB-334867 (as a selective Orx antagonist) in morphine-dependent rats. Our results unraveled that Orx blockade is involved in the development of morphine dependency through diminution of a variety of intracellular events including the cAMP, CREB and PLCβ levels in morphine-dependent rats. Furthermore, the Orx blockade could decrease the percentage of tyrosine hydroxylase (TH)/CREB and TH/PLCβ neurons in LC of morphine-treated rats. It is concluded that the activation of Orx in LC nucleus might be involved in some intracellular changes in morphine dependent rats.

摘要

蓝斑核(LC)的去甲肾上腺素能神经元接收下丘脑食欲素能神经元的投射,并表达食欲素 1 受体(Orx)。LC 核中的 Orx 参与吗啡依赖的发展。研究了 LC 神经元中 Orx 对吗啡依赖大鼠中吗啡依赖发展的下游信号转导。因此,我们通过免疫组织化学评估了环磷酸腺苷(cAMP)、cAMP 反应元件结合蛋白(CREB)和磷脂酶 Cβ(PLCβ)的水平。结果表明,在吗啡依赖大鼠中,SB-334867(作为选择性 Orx 拮抗剂)的应用抑制了 cAMP、CREB 和 PLCβ 的水平。我们的结果表明,通过减少包括吗啡依赖大鼠中的 cAMP、CREB 和 PLCβ 水平在内的各种细胞内事件,Orx 阻断参与了吗啡依赖的发展。此外,Orx 阻断可降低吗啡处理大鼠 LC 中酪氨酸羟化酶(TH)/CREB 和 TH/PLCβ 神经元的百分比。结论是,LC 核中 Orx 的激活可能参与了吗啡依赖大鼠中的一些细胞内变化。

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