Molecular Genetics Section, National Institute of Dental and Craniofacial Research/NIH, Bethesda, MD, USA.
Handb Exp Pharmacol. 2022;271:255-274. doi: 10.1007/164_2020_397.
The opioid peptides and their receptors have been linked to multiple key biological processes in the nervous system. Here we review the functions of the kappa opioid receptor (KOR) and its endogenous agonists dynorphins (Goldstein A, Tachibana S, Lowney LI, Hunkapiller M, Hood L, Proc Natl Acad Sci U S A 76:6666-6670, 1979) in modulating itch and pain (nociception). Specifically, we discuss their roles relative to recent findings that tell us more about the cells and circuits which are impacted by this opioid and its receptor and present reanalysis of single-cell sequencing data showing the expression profiles of these molecules. Since the KOR is relatively specifically activated by peptides derived from the prodynorphin gene and other opioid peptides that show lower affinities, this will be the only interactions we consider (Chavkin C, Goldstein A, Nature 291:591-593, 1981; Chavkin C, James IF, Goldstein A, Science 215:413-415, 1982), although it was noted that at higher doses peptides other than dynorphins might stimulate KOR (Lai J, Luo MC, Chen Q, Ma S, Gardell LR, Ossipov MH, Porreca F, Nat Neurosci 9:1534-1540, 2006). This review has been organized based on anatomy with each section describing the effect of the kappa opioid system in a specific location but let us not forget that most of these circuits are interconnected and are therefore interdependent.
阿片肽及其受体与神经系统中的多个关键生物学过程有关。在这里,我们回顾了κ阿片受体(KOR)及其内源性激动剂强啡肽(Goldstein A、Tachibana S、Lowney LI、Hunkapiller M、Hood L,Proc Natl Acad Sci U S A 76:6666-6670, 1979)在调节瘙痒和疼痛(痛觉)中的作用。具体来说,我们讨论了它们的作用,以及最近的发现,这些发现告诉我们更多关于受这种阿片类药物及其受体影响的细胞和回路的信息,并重新分析了单细胞测序数据,显示了这些分子的表达谱。由于 KOR 相对特异性地被来自前强啡肽基因的肽和其他显示出较低亲和力的阿片肽激活,这将是我们唯一考虑的相互作用(Chavkin C、Goldstein A,Nature 291:591-593, 1981;Chavkin C、James IF、Goldstein A,Science 215:413-415, 1982),尽管有人指出,在较高剂量下,除强啡肽以外的肽可能会刺激 KOR(Lai J、Luo MC、Chen Q、Ma S、Gardell LR、Ossipov MH、Porreca F、Nat Neurosci 9:1534-1540, 2006)。本综述是基于解剖结构组织的,每一节描述了κ阿片系统在特定位置的作用,但不要忘记,这些回路中的大多数都是相互连接的,因此是相互依存的。