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酪氨酰-甲酰甲硫氨酰-异亮氨酰-苯丙氨酰-缬氨酰胺(Tyr-MIF-1)和血啡肽在豚鼠回肠中既可以作为阿片激动剂也可以作为拮抗剂发挥作用。

Tyr-MIF-1 and hemorphin can act as opiate agonists as well as antagonists in the guinea pig ileum.

作者信息

Zadina J E, Kastin A J, Kersh D, Wyatt A

机构信息

Veterans Affairs Medical Center, Research Service, New Orleans, LA 70146.

出版信息

Life Sci. 1992;51(11):869-85. doi: 10.1016/0024-3205(92)90615-v.

Abstract

The brain peptide Tyr-MIF-1 (Tyr-Pro-Leu-Gly-NH2) was tested for its effects on electrically stimulated contractions in the guinea pig ileum assay. Tyr-MIF-1 acted as an opiate agonist in reducing these contractions. Its IC50 was about 9 microM, and its effects were reversed by naloxone and CTOP. The ability of Tyr-MIF-1 also to antagonize the inhibitory effects of opiates on electrically stimulated contractions was more evident in the ileum removed from a guinea pig tolerant to morphine or after partial inactivation of opiate receptors with beta-CNA. Similar results were observed with hemorphin. The endogenous peptide Tyr-MIF-1 and the blood-derived peptide hemorphin, therefore, can act as agonists as well as antagonists in the guinea pig ileum. The effects as antagonists are best observed in preparations of ileum with reduced receptor reserve (tolerant or beta-CNA treated) and are consistent with the idea that properties of endogenous peptides as opiate antagonists are enhanced in the tolerant state.

摘要

在豚鼠回肠实验中,对脑肽酪氨酰-促黑素细胞抑制因子-1(Tyr-Pro-Leu-Gly-NH2)对电刺激收缩的影响进行了测试。酪氨酰-促黑素细胞抑制因子-1在减少这些收缩方面表现为阿片类激动剂。其半数抑制浓度(IC50)约为9微摩尔,其作用可被纳洛酮和CTOP逆转。酪氨酰-促黑素细胞抑制因子-1拮抗阿片类对电刺激收缩的抑制作用的能力,在取自对吗啡耐受的豚鼠的回肠中或在用β-氰化钠使阿片受体部分失活后更为明显。血啡肽也观察到类似结果。因此,内源性肽酪氨酰-促黑素细胞抑制因子-1和源自血液的肽血啡肽在豚鼠回肠中既可以作为激动剂,也可以作为拮抗剂起作用。作为拮抗剂的作用在受体储备减少(耐受或经β-氰化钠处理)的回肠制剂中最易观察到,这与内源性肽作为阿片类拮抗剂的特性在耐受状态下增强的观点一致。

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