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γ-促黑素及相关肽的升压和心脏加速效应。

Pressor and cardioaccelerator effects of gamma MSH and related peptides.

作者信息

Klein M C, Hutchins P M, Lymangrover J R, Gruber K A

出版信息

Life Sci. 1985 Feb 25;36(8):769-75. doi: 10.1016/0024-3205(85)90197-3.

Abstract

We have recently demonstrated that the hypertensinogenic and natriuretic actions of ACTHI-39 can be found in a non-steroidogenic fragment of ACTH, ACTH4-10. These effects of ACTH or ACTH4-10 may be due to their ability to act as weak agonists of gamma MSH. gamma MSH is found in the 16K N-terminus of pro-opiocortin, and contains a sequence analogous to ACTH4-10, gamma MSH3-9. We investigated the cardiovascular effects of gamma 2MSH, gamma MSH3-9, and sterically restricted analogs of ACTH4-10. The results indicate that gamma MSH3-9, had essentially the same activities as ACTH4-10. The addition of five other amino acid residues to gamma MSH3-9 (gamma 2MSH) resulted in significant enhancement of pressor and cardioaccelerator activity. Steric restriction of the ACTH4-10 sequence by the substitution of a D-Phe in place of an L-Phe residue in position #7, or cyclization of the peptide by a half-Cys4, half Cys10 intramolecular disulfide-bridge derivatization, resulted in increased cardiovascular activities. Based on these data, the cardiovascular actions of ACTH4-10, gamma MSH3-9, and gamma 2MSH are predicted to be due to the assumption of a reverse-turn three-dimensional structure. The additional residues in gamma 2MSH appear to specifically enhance the cardiovascular activities of gamma MSH3-9. The results suggest the existence of a new class of hypophyseal peptides with cardiovascular activities, which require the assumption of a defined three-dimensional structure.

摘要

我们最近证实,促肾上腺皮质激素(ACTH)I-39的致高血压和利钠作用可在ACTH的一个非类固醇生成片段ACTH4-10中发现。ACTH或ACTH4-10的这些作用可能归因于它们作为γ-促黑激素(γ-MSH)弱激动剂的能力。γ-MSH存在于阿片促皮质素原的16K N端,并且包含与ACTH4-10类似的序列,即γ-MSH3-9。我们研究了γ2-MSH、γ-MSH3-9以及ACTH4-10的空间受限类似物对心血管的影响。结果表明,γ-MSH3-9具有与ACTH4-10基本相同的活性。在γ-MSH3-9上添加另外五个氨基酸残基(γ2-MSH)导致升压和心脏加速活性显著增强。通过将第7位的L-苯丙氨酸残基替换为D-苯丙氨酸对ACTH4-10序列进行空间限制,或通过半胱氨酸4、半胱氨酸10分子内二硫键衍生化使肽环化,均导致心血管活性增加。基于这些数据,预计ACTH4-10、γ-MSH3-9和γ2-MSH的心血管作用是由于呈现了一种反向转折的三维结构。γ2-MSH中的额外残基似乎特异性地增强了γ-MSH3-9的心血管活性。结果表明存在一类新的具有心血管活性的垂体肽,其需要呈现特定的三维结构。

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