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强啡肽相关肽对生长激素释放肽结合的抑制作用具有非阿片样模式。

A non-opioid pattern characterizes inhibition of growth hormone releasing peptide binding by dynorphin-related peptides.

作者信息

Codd E E, Aloyo V J, Walker R F

机构信息

R. W. Johnson Pharmaceutical Research Institute, Department of Biological Science, Springhouse, PA 19477-0776.

出版信息

Neuropeptides. 1990 Mar;15(3):133-7. doi: 10.1016/0143-4179(90)90144-n.

Abstract

GHRP-6 (His-D-Trp-Ala-Trp-D-Phe-LysNH2; SK&F 110679) is a hexapeptide that specifically releases growth hormone. Although derived from methionine enkephalin, 3H-SK&F 110679 binding profiles suggest that it retains little mu or delta opioid activity. In the present study, dynorphin A was a potent inhibitor of SK&F 110679 binding. However, detailed structure-activity studies using dynorphin-related compounds suggest that the interaction between SK&F 110679 and dynorphin was non-opioid in nature. The non-opioid peptide des-Tyr-dynorphin was virtually as potent an inhibitor of 3H-SK&F 110679 binding as the intact dynorphin peptide. Additionally, the non-peptide, kappa selective ligand U-50,488 was a very weak inhibitor of 3H-SK&F 110679 binding. Since dynorphin but not U-50,488 has been reported to release growth hormone, the present results suggest that a non-opioid dynorphin site participates in SK&F 110679's growth hormone releasing action.

摘要

生长激素释放肽-6(组氨酸-右旋色氨酸-丙氨酸-右旋色氨酸-右旋苯丙氨酸-赖氨酸氨基;SK&F 110679)是一种能特异性释放生长激素的六肽。尽管它由甲硫氨酸脑啡肽衍生而来,但3H-SK&F 110679的结合谱表明它几乎没有μ或δ阿片样活性。在本研究中,强啡肽A是SK&F 110679结合的有效抑制剂。然而,使用与强啡肽相关的化合物进行的详细构效关系研究表明,SK&F 110679与强啡肽之间的相互作用本质上是非阿片样的。非阿片样肽去酪氨酸强啡肽对3H-SK&F 110679结合的抑制作用几乎与完整的强啡肽肽一样有效。此外,非肽类κ选择性配体U-50488对3H-SK&F 110679结合的抑制作用非常弱。由于据报道强啡肽而非U-50488能释放生长激素,目前的结果表明一个非阿片样强啡肽位点参与了SK&F 110679的生长激素释放作用。

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