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清醒大鼠体内三种促黑素细胞激素的不同心血管特征;γ2-促黑素与促肾上腺皮质激素-(1-24)之间拮抗作用的证据

Different cardiovascular profiles of three melanocortins in conscious rats; evidence for antagonism between gamma 2-MSH and ACTH-(1-24).

作者信息

Van Bergen P, Kleijne J A, De Wildt D J, Versteeg D H

机构信息

Department of Medical Pharmacology, Rudolf Magnus Institute for Neurosciences, Utrecht University, The Netherlands.

出版信息

Br J Pharmacol. 1997 Apr;120(8):1561-7. doi: 10.1038/sj.bjp.0701065.

Abstract
  1. We investigated the effects of [Nle4,D-Phe7]alpha-melanocyte-stimulating hormone (NDP-MSH), adrenocorticotropin-(1-24) (ACTH-(1-24)) and gamma 2-MSH, three melanocortins with different agonist selectivity for the five cloned melanocortin receptors, on blood pressure and heart rate in conscious, freely moving rats following intravenous administration. 2. As was previously found by other investigators as well as by us gamma 2-MSH, a peptide suggested to be an agonist with selectivity for the melanocortin MC3 receptor, caused a dose-dependent, short lasting pressor response in combination with a tachycardia. Despite the fact that NDP-MSH is a potent agonist of various melanocortin receptor subtypes, among which the melanocortin MC1 receptor, it did not affect blood pressure or heart rate, when administered i.v. in doses of up to 1000 nmol kg-1. 3. ACTH-(1-24) caused a dose-dependent decrease in blood pressure in combination with a dose-dependent increase in heart rate in a dose-range from 15 to 500 nmol kg-1. The cardiovascular effects of ACTH-(1-24) were independent of the presence of the adrenals. 4. Pretreatment with ACTH-(1-24) caused a pronounced, dose-dependent parallel shift to the right of the dose-response curve for the pressor and tachycardiac effects of gamma 2-MSH. The antagonistic effect of ACTH-(1-24) was already apparent following a dose of this peptide as low as 10 nmol kg-1, which when given alone had no intrinsic hypotensive activity. 5. These results form further support for the notion that it is not via activation of one of the as yet cloned melanocortin receptors that gamma-MSH-like peptides increase blood pressure and heart rate. The cardiovascular effects of ACTH-(1-24) seem not to be mediated by the adrenal melanocortin MC3 receptors, for which ACTH-(1-24) is a selective agonist, or by adrenal catecholamines. 6. There appears to be a functional antagonism between ACTH-(1-24) and gamma 2-MSH, two melanocortins derived from a common precursor, with respect to their effect on blood pressure and heart rate. Whether this antagonism plays a (patho)physiological role remains to be shown.
摘要
  1. 我们研究了[Nle4,D - Phe7]α - 黑素细胞刺激素(NDP - MSH)、促肾上腺皮质激素 - (1 - 24)(ACTH - (1 - 24))和γ2 - MSH这三种对五种克隆的黑素皮质素受体具有不同激动剂选择性的黑素皮质素,静脉注射后对清醒、自由活动大鼠血压和心率的影响。2. 正如其他研究者以及我们之前所发现的,γ2 - MSH是一种被认为对黑素皮质素MC3受体具有选择性的激动剂,它会引起剂量依赖性的、短暂的升压反应并伴有心动过速。尽管NDP - MSH是多种黑素皮质素受体亚型的强效激动剂,其中包括黑素皮质素MC1受体,但静脉注射高达1000 nmol·kg⁻¹的剂量时,它对血压或心率没有影响。3. 在15至500 nmol·kg⁻¹的剂量范围内,ACTH - (1 - 24)引起剂量依赖性的血压降低并伴有剂量依赖性的心率增加。ACTH - (1 - 24)的心血管效应与肾上腺的存在无关。4. 用ACTH - (1 - 24)预处理会导致γ2 - MSH的升压和心动过速效应的剂量 - 反应曲线明显的、剂量依赖性的平行右移。ACTH - (1 - 24)的拮抗作用在低至10 nmol·kg⁻¹的该肽剂量后就已明显,而该剂量单独使用时没有内在的降压活性。5. 这些结果进一步支持了这样一种观点,即γ - MSH样肽并非通过激活目前已克隆的黑素皮质素受体之一来升高血压和心率。ACTH - (1 - 24)的心血管效应似乎不是由肾上腺黑素皮质素MC3受体介导的,ACTH - (1 - 24)是该受体的选择性激动剂,也不是由肾上腺儿茶酚胺介导的。6. 在对血压和心率的影响方面,ACTH - (1 - 24)和γ2 - MSH这两种源自共同前体的黑素皮质素之间似乎存在功能拮抗作用。这种拮抗作用是否发挥(病理)生理作用仍有待证实。

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