作者: S Lemaire , V K Shukla
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摘要: Dynorphin A (Dyn A) and related opioid peptides derived from prodynorphin possess a high affinity for kappa receptors, but they also bind to other receptors (mu delta) as well some non-opioid receptor sites. Although the physiological role of these is not established, recent experimental data pinpoint their particular involvement in pathophysiological conditions that relate algesia, spinal cord injury epilepsy. In this paper, we review which support concept behavioral effects Dyn endogenous are observed under physiologically pathophysiologically relevant.