Endogenous Opioids: Their Physiological Role and Receptors

Endogenous Opioids: Their Physiological Role and Receptors
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内源性阿片类药物:其生理作用和受体

DOI:
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发表时间:
2009
期刊:
影响因子:
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通讯作者:
Shaik Rizwan
Shaik Rizwan
中科院分区:
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文献类型:
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作者:
Anupama Koneru;S. Satyanarayana;Shaik Rizwan

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2 摘要:内源性阿片系统包含大量阿片肽,它们是多种阿片受体的配体。内源性阿片肽的三个不同家族已得到充分表征:内啡肽、脑啡肽和强啡肽。最近,另外两种短肽 Endomorphin-1 和 Endomorphin-2 已被发现,它们对 µ 阿片受体具有高亲和力和选择性。内源性阿片肽与介导镇痛的三种主要阿片受体类型结合,分别称为 µ 和 。优选地,脑啡肽与受体相互作用,强啡肽与受体相互作用,内啡肽以相当的亲和力与μ和受体结合。
2 Abstract: The Endogenous Opioid system includes a large number of opioid peptides that are ligands for numerous types of opioid receptors. Three distinct families of endogenous opioid peptides have been well characterized-Endorphins, Enkephalins and Dynorphins. More recently, two additional short peptides, Endomorphin-1 and Endomorphin-2 that display a high affinity and selectivity for µ opioid receptors have been identified. The Endogenous opioid peptides bind to three primary opioid receptor types that mediate analgesia, designated µ, and . Preferentially, Enkephalins interact with the receptor, Dynorphins interact with the receptor and Endorphins bind to both µ and receptors with comparable affinity.