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降钙素基因相关肽的全身和局部血流动力学效应。

Systemic and regional hemodynamic effects of calcitonin gene-related peptide.

作者信息

DiPette D J, Schwarzenberger K, Kerr N, Holland O B

出版信息

Hypertension. 1987 Jun;9(6 Pt 2):III142-6. doi: 10.1161/01.hyp.9.6_pt_2.iii142.

DOI:10.1161/01.hyp.9.6_pt_2.iii142
PMID:3496276
Abstract

Calcitonin gene-related peptide, a 37-amino-acid neuropeptide, has been shown to be widely distributed in periadventitial nerves throughout the cardiovascular system, particularly in association with coronary arteries. In vivo and in vitro studies have demonstrated that calcitonin gene-related peptide possesses potent vasodilator properties. Circulating calcitonin gene-related peptide is derived primarily from periadventitial nerves, though its systemic and regional hemodynamic effects are unknown. In this study, systemic and regional hemodynamics were determined by the radioactive microsphere technique prior to and following the intravenous administration of 65-pmol and 2.2-nmol doses of calcitonin gene-related peptide and vehicle to three groups of conscious, unrestrained rats. Vehicle administration did not change any systemic or regional organ hemodynamic parameter determined. In contrast, 65 pmol and 2.2 nmol of calcitonin gene-related peptide significantly decreased mean blood pressure and total peripheral resistance and increased heart rate in a dose-dependent manner, while only slightly increasing cardiac output. Both 65-pmol and 2.2-nmol doses of calcitonin gene-related peptide significantly increased blood flow (percentage of cardiac output) to the heart. There was no difference in blood flow to the heart between the two doses. In addition, the 2.2-nmol dose of calcitonin gene-related peptide significantly increased blood flow to the stomach, liver, and skin and decreased it to the brain, kidneys, and spleen. In conclusion, calcitonin gene-related peptide infusion decreases blood pressure in a dose-dependent manner primarily by peripheral vasodilation. In addition, calcitonin gene-related peptide selectively changes regional organ blood flow, particularly to cause coronary vasodilation.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

降钙素基因相关肽是一种由37个氨基酸组成的神经肽,已被证明广泛分布于整个心血管系统的外膜周围神经中,尤其是与冠状动脉相关的神经。体内和体外研究表明,降钙素基因相关肽具有强大的血管舒张特性。循环中的降钙素基因相关肽主要来源于外膜周围神经,但其对全身和局部血流动力学的影响尚不清楚。在本研究中,对三组清醒、不受限制的大鼠静脉注射65 pmol和2.2 nmol剂量的降钙素基因相关肽及赋形剂前后,采用放射性微球技术测定全身和局部血流动力学。注射赋形剂未改变所测定的任何全身或局部器官血流动力学参数。相比之下,65 pmol和2.2 nmol的降钙素基因相关肽显著降低平均血压和总外周阻力,并以剂量依赖的方式增加心率,而仅轻微增加心输出量。65 pmol和2.2 nmol剂量的降钙素基因相关肽均显著增加心脏的血流量(心输出量的百分比)。两种剂量之间心脏血流量无差异。此外,2.2 nmol剂量的降钙素基因相关肽显著增加胃、肝脏和皮肤的血流量,并减少大脑、肾脏和脾脏的血流量。总之,输注降钙素基因相关肽主要通过外周血管舒张以剂量依赖的方式降低血压。此外,降钙素基因相关肽选择性地改变局部器官血流量,尤其是引起冠状动脉舒张。(摘要截短至250字)

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