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在男性人类海洛因滥用者和海洛因自我给药雄性大鼠的内侧前额叶皮质中,μ阿片受体基因(OPRM1)的剪接变体 mRNA 表达失调。

Dysregulated expression of the alternatively spliced variant mRNAs of the mu opioid receptor gene, OPRM1, in the medial prefrontal cortex of male human heroin abusers and heroin self-administering male rats.

机构信息

Department of Neurology and the Molecular Pharmacology Program, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.

Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

出版信息

J Neurosci Res. 2022 Jan;100(1):35-47. doi: 10.1002/jnr.24640. Epub 2020 Jun 7.

DOI:10.1002/jnr.24640
PMID:32506472
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8143898/
Abstract

Heroin, a mu agonist, acts through the mu opioid receptor. The mu opioid receptor gene, OPRM1, undergoes extensive alternative splicing, creating an array of splice variants that are conserved from rodent to humans. Increasing evidence suggests that these OPRM1 splice variants are pharmacologically important in mediating various actions of mu opioids, including analgesia, tolerance, physical dependence, rewarding behavior, as well as addiction. In the present study, we examine expression of the OPRM1 splice variant mRNAs in the medial prefrontal cortex (mPFC), one of the major brain regions involved in decision-making and drug-seeking behaviors, of male human heroin abusers and male rats that developed stable heroin-seeking behavior using an intravenous heroin self-administration (SA) model. The results show similar expression profiles among multiple OPRM1 splice variants in both human control subjects and saline control rats, illustrating conservation of OPRM1 alternative splicing from rodent to humans. Moreover, the expressions of several OPRM1 splice variant mRNAs were dysregulated in the postmortem mPFCs from heroin abusers compared to the control subjects. Similar patterns were observed in the rat heroin SA model. These findings suggest potential roles of the OPRM1 splice variants in heroin addiction that could be mechanistically explored using the rat heroin SA model.

摘要

海洛因是一种μ阿片受体激动剂,通过μ阿片受体发挥作用。μ阿片受体基因(OPRM1)经过广泛的选择性剪接,产生了一系列从啮齿动物到人类都保守的剪接变体。越来越多的证据表明,这些 OPRM1 剪接变体在介导μ阿片类药物的各种作用方面具有重要的药理学意义,包括镇痛、耐受、身体依赖、奖赏行为以及成瘾。在本研究中,我们检查了雄性人类海洛因滥用者和使用静脉内海洛因自我给药(SA)模型形成稳定海洛因寻求行为的雄性大鼠的内侧前额叶皮质(mPFC)中 OPRM1 剪接变体 mRNAs 的表达,mPFC 是参与决策和觅药行为的主要大脑区域之一。结果表明,人类对照组和生理盐水对照组大鼠的多种 OPRM1 剪接变体具有相似的表达谱,说明从啮齿动物到人类,OPRM1 选择性剪接具有保守性。此外,与对照组相比,海洛因滥用者死后 mPFC 中的几种 OPRM1 剪接变体 mRNAs 的表达失调。在大鼠海洛因 SA 模型中也观察到了类似的模式。这些发现表明 OPRM1 剪接变体可能在海洛因成瘾中发挥作用,这可以通过大鼠海洛因 SA 模型在机制上进行探索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91cc/8143898/37b790074d50/nihms-1699817-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91cc/8143898/7523b6d67d4c/nihms-1699817-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91cc/8143898/b0e9044d4c50/nihms-1699817-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91cc/8143898/2caa1acc1123/nihms-1699817-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91cc/8143898/37b790074d50/nihms-1699817-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91cc/8143898/7523b6d67d4c/nihms-1699817-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91cc/8143898/b0e9044d4c50/nihms-1699817-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91cc/8143898/2caa1acc1123/nihms-1699817-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91cc/8143898/37b790074d50/nihms-1699817-f0004.jpg

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