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κ 阿片受体在发育中大鼠脑内的表达-提示围生期丁丙诺啡暴露的影响。

Expression of kappa opioid receptors in developing rat brain - Implications for perinatal buprenorphine exposure.

机构信息

School of Women's and Children's Health, Faculty of Medicine, University of New South Wales, Randwick, NSW 2031, Australia.

School of Women's and Children's Health, Faculty of Medicine, University of New South Wales, Randwick, NSW 2031, Australia; Westfield Research Laboratories, Sydney Children's Hospital, High Street, Randwick, NSW 2031, Australia.

出版信息

Reprod Toxicol. 2018 Jun;78:81-89. doi: 10.1016/j.reprotox.2018.04.006. Epub 2018 Apr 7.

Abstract

Buprenorphine, a mu opioid receptor partial agonist and kappa opioid receptor (KOR) antagonist, is an emerging therapeutic agent for maternal opioid dependence in pregnancy and neonatal abstinence syndrome. However, the endogenous opioid system plays a critical role in modulating neurodevelopment and perinatal buprenorphine exposure may detrimentally influence this. To identify aspects of neurodevelopment vulnerable to perinatal buprenorphine exposure, we defined KOR protein expression and its cellular associations in normal rat brain from embryonic day 16 to postnatal day 23 with double-labelling immunohistochemistry. KOR was expressed on neural stem and progenitor cells (NSPCs), choroid plexus epithelium, subpopulations of cortical neurones and oligodendrocytes, and NSPCs and subpopulations of neurones in postnatal hippocampus. These distinct patterns of KOR expression suggest several pathways vulnerable to perinatal buprenorphine exposure, including proliferation, neurogenesis and neurotransmission. We thus suggest the cautious use of buprenorphine in both mothers and infants until its impact on neurodevelopment is better defined.

摘要

丁丙诺啡是一种μ阿片受体部分激动剂和κ阿片受体(KOR)拮抗剂,是治疗妊娠中母体阿片类药物依赖和新生儿戒断综合征的一种新兴治疗药物。然而,内源性阿片系统在调节神经发育中起着关键作用,围产期丁丙诺啡暴露可能会对其产生不利影响。为了确定围产期丁丙诺啡暴露易受影响的神经发育方面,我们通过双重免疫组织化学方法定义了正常大鼠脑从胚胎第 16 天到出生后第 23 天的 KOR 蛋白表达及其细胞关联。KOR 表达在神经干细胞和祖细胞(NSPCs)、脉络丛上皮、皮质神经元亚群和少突胶质细胞以及海马体中的 NSPCs 和神经元亚群上。KOR 的这种独特表达模式表明存在几种易受围产期丁丙诺啡暴露影响的途径,包括增殖、神经发生和神经传递。因此,我们建议在母亲和婴儿中谨慎使用丁丙诺啡,直到其对神经发育的影响得到更好的定义。

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