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尿皮质素1对清醒绵羊的心脏交感神经活动具有强大的抑制作用。

Urocortin 1 exhibits potent inhibition of cardiac sympathetic nerve activity in conscious sheep.

作者信息

Charles Christopher J, Jardine David L, Nicholls M Gary, Rademaker Miriam T, Richards A Mark

机构信息

Christchurch Cardioendocrine Research Group, Christchurch School of Medicine and Health Sciences, Christchurch, New Zealand.

出版信息

J Hypertens. 2008 Jan;26(1):53-60. doi: 10.1097/HJH.0b013e3282f01428.

Abstract

OBJECTIVES

Urocortin 1 (Ucn1) and the sympathetic nervous system both participate in cardiac and circulatory regulation, but little is known about their possible interactions.

METHODS

We report the effects of Ucn1 on the cardiac sympathetic nerve activity (CSNA), haemodynamics and plasma catecholamines in normal sheep.

RESULTS

Bolus intravenous administration of Ucn1 at 2.5 and 10 microg in seven sheep had no significant effect on haemodynamic parameters, including heart rate, mean arterial pressure (MAP) and cardiac output. At these doses, however, Ucn1 administration reduced CSNA, with burst frequency (P = 0.011), burst incidence (P = 0.015) and burst area (P = 0.012) all significantly reduced in a dose-related manner compared with a time-matched control. At higher doses (25 and 100 microg; n = 5 sheep), Ucn1 induced significant rises in heart rate (P < 0.001) and cardiac output (P = 0.03) and reduced peripheral resistance (P = 0.03), but had no effect on MAP. Ucn1 administration at the higher doses reduced CSNA, with burst incidence (P < 0.001), burst area/min (P = 0.001) and burst area/100 beats (P < 0.001) all significantly reduced in a dose-related manner compared with a time-matched control. There was no change in plasma catecholamines at any dose.

CONCLUSION

The present study shows that Ucn1 induces potent inhibition of sympathetic traffic to the heart at doses both above and below the threshold for direct actions of Ucn1 on the myocardium. These findings suggest an important role for Ucn1 in cardiovascular homeostasis and warrant further investigation for potential therapeutic applications in acute myocardial injury and heart disease.

摘要

目的

尿皮质素1(Ucn1)和交感神经系统均参与心脏和循环调节,但它们之间可能的相互作用却鲜为人知。

方法

我们报告了Ucn1对正常绵羊心脏交感神经活动(CSNA)、血流动力学和血浆儿茶酚胺的影响。

结果

对7只绵羊静脉推注2.5微克和10微克的Ucn1,对包括心率、平均动脉压(MAP)和心输出量在内的血流动力学参数无显著影响。然而,在这些剂量下,Ucn1给药可降低CSNA,与时间匹配的对照组相比,爆发频率(P = 0.011)、爆发发生率(P = 0.015)和爆发面积(P = 0.012)均呈剂量依赖性显著降低。在更高剂量(25微克和100微克;n = 5只绵羊)时,Ucn1可使心率(P < 0.001)和心输出量显著升高(P = 0.03),并降低外周阻力(P = 0.03),但对MAP无影响。更高剂量的Ucn1给药可降低CSNA,与时间匹配的对照组相比,爆发发生率(P < 0.001)、每分钟爆发面积(P = 0.001)和每100次心跳爆发面积(P < 0.001)均呈剂量依赖性显著降低。任何剂量下血浆儿茶酚胺均无变化。

结论

本研究表明,Ucn1在高于和低于其对心肌直接作用阈值的剂量下,均可有效抑制心脏的交感神经活动。这些发现提示Ucn1在心血管稳态中起重要作用,值得进一步研究其在急性心肌损伤和心脏病潜在治疗应用中的价值。

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