Shukla V K, Lemaire S
Department of Pharmacology, Faculty of Medicine, University of Ottawa, Ontario, Canada.
J Psychiatry Neurosci. 1992 Sep;17(3):106-19.
Dynorphin A (Dyn A) and related opioid peptides derived from prodynorphin possess a high affinity for kappa opioid receptors, but they also bind to other opioid receptors (mu and delta) as well as to some non-opioid receptor sites. Although the physiological role of these peptides is not well established, recent experimental data pinpoint their particular involvement in physiological and pathophysiological conditions that relate to algesia, spinal cord injury and epilepsy. In this paper, we review data which support the concept that the non-opioid behavioral effects of Dyn A and related endogenous peptides which are observed under these conditions are physiologically and pathophysiologically relevant.
强啡肽A(Dyn A)以及源自前强啡肽的相关阿片肽对κ阿片受体具有高亲和力,但它们也能与其他阿片受体(μ和δ)以及一些非阿片受体位点结合。尽管这些肽的生理作用尚未完全明确,但最近的实验数据表明它们特别参与了与痛觉过敏、脊髓损伤和癫痫相关的生理和病理生理状况。在本文中,我们回顾了相关数据,这些数据支持了在这些条件下观察到的Dyn A和相关内源性肽的非阿片行为效应在生理和病理生理方面具有相关性这一概念。