Ukai M
Department of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, Meijo University, Nagoya, Japan.
Yakubutsu Seishin Kodo. 1993 Aug;13(4):257-61.
The effects of opioid peptides selective for opioid receptors on drinking, dopamine-related behavior, discriminative stimulus and memory processes were investigated in detail. Mu opioid receptors in the paraventricular nucleus of hypothalamus played an important role in drinking behavior. The stimulation of mu and kappa opioid receptors inhibited dopamine D2 receptor-related behavior. The discriminative stimulus effects of morphine and pentazocine were mediated through mu opioid receptors, while the stimulus effects of cocaine through delta opioid receptors. Mu opioid agonists elicited memory dysfunctions, whereas kappa opioid agonists such as dynorphin A-(1-13) improved amnesia induced by ischemia, basal forebrain-lesion or scopolamine. It appears that opioid receptors are fully involved in the neural basis of behavioral responses.
详细研究了对阿片受体具有选择性的阿片肽对饮水、多巴胺相关行为、辨别刺激和记忆过程的影响。下丘脑室旁核中的μ阿片受体在饮水行为中起重要作用。对μ和κ阿片受体的刺激抑制了多巴胺D2受体相关行为。吗啡和喷他佐辛的辨别刺激作用是通过μ阿片受体介导的,而可卡因的刺激作用是通过δ阿片受体介导的。μ阿片激动剂引起记忆功能障碍,而κ阿片激动剂如强啡肽A-(1-13)可改善由缺血、基底前脑损伤或东莨菪碱诱导的失忆。阿片受体似乎完全参与了行为反应的神经基础。