Asimakis G K, DiPette D J, Conti V R, Holland O B, Zwischenberger J B
Life Sci. 1987 Aug 3;41(5):597-603. doi: 10.1016/0024-3205(87)90413-9.
The effects of calcitonin gene-related peptide (CGRP) on heart rate, coronary flow, pressure development, and time to ischemic contracture were studied in the isolated, perfused rat heart. A bolus of CGRP (2640 pmols) caused significant increases in heart rate and coronary flow; these effects were sustained for at least five minutes after injection. The increase in coronary flow was independent of heart rate, since CGRP caused an increase in coronary flow in non-beating (potassium-arrested) hearts. The dose-response of CGRP was studied using five doses (65, 218, 658, 1320 and 2640 pmols) given as bolus injections. Although the increase in heart rate was apparently dose-dependent, significant increases above baseline were observed only with the two highest doses. In contrast, coronary flow increased significantly above baseline with the injection of all but the lowest dose of CGRP. Ten minutes after injection of CGRP, all hearts were made ischemic. The time to onset of ischemic contracture was approximately 11 minutes for those hearts that received 65 pmols of CGRP; however, for those hearts receiving all other doses of CGRP, the time to onset of contracture was approximately 8 minutes. We conclude that CGRP significantly decreases the resistance of the coronary vascular bed, and that it may be an important regulator of regional blood flow in the heart.
在离体灌注大鼠心脏中研究了降钙素基因相关肽(CGRP)对心率、冠脉血流量、压力变化及缺血性挛缩时间的影响。静脉注射一剂CGRP(2640皮摩尔)可使心率和冠脉血流量显著增加;注射后这些效应至少持续5分钟。冠脉血流量的增加与心率无关,因为CGRP可使非搏动性(钾停搏)心脏的冠脉血流量增加。采用静脉注射5种剂量(65、218、658、1320和2640皮摩尔)研究CGRP的剂量反应。虽然心率增加显然呈剂量依赖性,但仅在两种最高剂量时观察到显著高于基线的增加。相反,除最低剂量外,注射所有剂量的CGRP后冠脉血流量均显著高于基线水平。注射CGRP 10分钟后,所有心脏均进入缺血状态。接受65皮摩尔CGRP的心脏缺血性挛缩开始时间约为11分钟;然而,接受所有其他剂量CGRP的心脏,挛缩开始时间约为8分钟。我们得出结论,CGRP可显著降低冠脉血管床阻力,且可能是心脏局部血流的重要调节因子。