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γ-黑素细胞刺激素对大鼠压力反射敏感性和脑血流自动调节的影响。

Effect of gamma-melanocyte-stimulating hormones on baroreflex sensitivity and cerebral blood flow autoregulation in rats.

作者信息

Nijsen M J, de Ruiter G J, Kasbergen C M, de Wildt D J

机构信息

Department of Medical Pharmacology, Rudolf Magnus Institute for Neurosciences, Utrecht University, Universiteitsweg 100, 3584 CG, Utrecht, The Netherlands.

出版信息

Cardiovasc Res. 2001 Jan;49(1):226-33. doi: 10.1016/s0008-6363(00)00204-2.

Abstract

OBJECTIVE

In the present paper, we are interested in the effects of gamma-melanocyte-stimulating hormones (gamma-MSHs) on cardiovascular regulatory systems.

METHODS

Mean arterial pressure (MAP), cerebral blood flow (CBF) and heart rate (HR) were measured in urethane-anaesthetised rats after intravenous administration of lysgamma(2)-MSH, gamma(2)-MSH, gamma(2)-MSH(6-12) or phenylephrine.

RESULTS

The gamma-MSHs caused an increase in MAP, CBF and HR, whereas phenylephrine caused an increase in MAP and CBF and baroreceptor reflex-mediated bradycardia. All tested gamma-MSHs showed a significant impairment of the baroreceptor reflex sensitivity and CBF autoregulation as compared to the phenylephrine group. gamma(2)-MSH shows identical effects on the baroreceptor reflex and CBF as the endogenous occurring lysgamma(2)-MSH. In addition, the C-terminal fragment of gamma(2)-MSH, gamma(2)-MSH(6-12), induced similar effects as gamma(2)-MSH. The level of increase in MAP was comparable between the gamma-MSHs and the phenylephrine group.

CONCLUSIONS

The present study suggests that gamma(2)-MSH and the shorter fragment gamma(2)-MSH(6-12) impair baroreceptor reflex sensitivity, due to a strong increase in sympathetic tone and/or change in baroreceptor reflex setpoint, and induce cerebrovasodilatation, which can counteract an autoregulation-mediated cerebrovasoconstriction due to systemic pressor effects. Furthermore, the results indicate that the C-terminal site of gamma(2)-MSH is relevant for its central-mediated inhibitory effects on the baroreceptor reflex and CBF.

摘要

目的

在本文中,我们关注γ-黑素细胞刺激激素(γ-MSHs)对心血管调节系统的影响。

方法

在静脉注射赖氨酸γ(2)-MSH、γ(2)-MSH、γ(2)-MSH(6 - 12)或去氧肾上腺素后,测量乌拉坦麻醉大鼠的平均动脉压(MAP)、脑血流量(CBF)和心率(HR)。

结果

γ-MSHs导致MAP、CBF和HR升高,而去氧肾上腺素导致MAP和CBF升高以及压力感受器反射介导的心动过缓。与去氧肾上腺素组相比,所有测试的γ-MSHs均显示出压力感受器反射敏感性和CBF自动调节的显著受损。γ(2)-MSH对压力感受器反射和CBF的影响与内源性的赖氨酸γ(2)-MSH相同。此外,γ(2)-MSH的C末端片段γ(2)-MSH(6 - 12)诱导出与γ(2)-MSH相似的效应。γ-MSHs组和去氧肾上腺素组之间MAP的升高水平相当。

结论

本研究表明,γ(2)-MSH和较短片段γ(2)-MSH(6 - 12)会损害压力感受器反射敏感性,这是由于交感神经张力的强烈增加和/或压力感受器反射调定点的改变,并诱导脑血管舒张,这可以抵消由于全身升压效应导致的自动调节介导的脑血管收缩。此外,结果表明γ(2)-MSH的C末端位点与其对压力感受器反射和CBF的中枢介导的抑制作用相关。

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