Department of Psychology, Developmental Exposure Alcohol Research Center, Center for Developmental and Behavioral Neuroscience, Binghamton University - SUNY, 4400 Vestal Parkway East, Binghamton, NY 13902, USA.
Department of Pharmaceutical and Administrative Sciences, St. Louis College of Pharmacy, Department of Anesthesiology Washington University in St. Louis, Center for Clinical Pharmacology, Washington University School of Medicine & St. Louis College of Pharmacy 660 S.Euclid, Box 8054, St. Louis, MO 63110, USA.
Brain Res. 2020 May 15;1735:146742. doi: 10.1016/j.brainres.2020.146742. Epub 2020 Feb 28.
The dynorphin / kappa opioid receptor (KOR) system has been implicated in many aspects that influence neuropsychiatric disorders. Namely, this system modulates neural circuits that primarily regulate reward seeking, motivation processing, stress responsivity, and pain sensitivity, thus affecting the development of substance and alcohol use disorder (AUD). The effects of this system are often bidirectional and depend on projection targets. To date, a majority of the studies focusing on this system have examined the KOR function using agonists and antagonists. Indeed, there are studies that have examined prodynorphin and dynorphin levels by measuring mRNA and tissue content levels; however, static levels of the neuropeptide and its precursor do not explain complete and online function of the peptide as would be explained by measuring dynorphin transmission in real time. New and exciting methods using optogenetics, chemogenetics, genetic sensors, fast scan cyclic voltammetry are now being developed to detect various neuropeptides with a focus on opioid peptides, including dynorphin. In this review we discuss studies that examine dynorphin projections in areas involved in AUD, its functional involvement in AUD and vulnerability to develop AUD at various ages. Moreover, we discuss dynorphin's role in promoting AUD by dysregulation motivation circuits and how advancements in opioid peptide detection will further our understanding.
内啡肽/κ 阿片受体(KOR)系统与影响神经精神疾病的许多方面有关。该系统调节主要调节奖励寻求、动机处理、应激反应性和疼痛敏感性的神经回路,从而影响物质和酒精使用障碍(AUD)的发展。该系统的影响通常是双向的,取决于投射目标。迄今为止,大多数关注该系统的研究都使用激动剂和拮抗剂来检查 KOR 功能。事实上,有一些研究通过测量 mRNA 和组织含量水平来检查前原啡肽和内啡肽的水平;然而,神经肽及其前体的静态水平并不能解释肽的完整在线功能,而通过实时测量内啡肽传递来解释。现在正在开发使用光遗传学、化学生物学、遗传传感器、快速扫描循环伏安法的新的和令人兴奋的方法来检测各种神经肽,重点是阿片肽,包括内啡肽。在这篇综述中,我们讨论了检查 AUD 相关区域内啡肽投射的研究,以及内啡肽在 AUD 中的功能参与以及在不同年龄阶段易患 AUD 的情况。此外,我们还讨论了内啡肽通过失调动机回路促进 AUD 的作用,以及阿片肽检测的进展将如何进一步加深我们的理解。