Rigel D F
Department of Pharmacology and Cell Biophysics, University of Cincinnati College of Medicine, Ohio 45267.
Am J Physiol. 1988 Aug;255(2 Pt 2):H311-7. doi: 10.1152/ajpheart.1988.255.2.H311.
This study was designed to evaluate the potential chronotropic actions of several cardiac neuropeptides in pentobarbital-anesthetized dogs. After bilateral vagotomy and stellectomy and muscarinic receptor blockade, I injected vasoactive intestinal polypeptide, peptide histidine isoleucine, neuropeptide Y, neurotensin, and calcitonin gene-related peptide into the intact sinus node artery. Neurotensin, calcitonin gene-related peptide, and neuropeptide Y exhibited no physiologically significant changes in heart rate. However, the structural homologues vasoactive intestinal polypeptide and peptide histidine isoleucine each augmented heart rate with maximal increases (approximately 120 beats/min) similar to those of norepinephrine. Vasoactive intestinal polypeptide and peptide histidine isoleucine were twice and 1/18, respectively, as potent as norepinephrine. The cardioacceleratory responses to vasoactive intestinal polypeptide and peptide histidine isoleucine were more slowly developing and longer lasting than those of norepinephrine. The responses to these two peptides were unchanged after beta-adrenergic blockade with propranolol in a dose sufficient to eliminate or greatly attenuate the norepinephrine tachycardia. These results indicate a potential role of endogenous vasoactive intestinal polypeptide and peptide histidine isoleucine in nonadrenergic, noncholinergic heart rate control in the dog.
本研究旨在评估几种心脏神经肽对戊巴比妥麻醉犬的潜在变时作用。在双侧迷走神经切断术、星状神经节切除术及毒蕈碱受体阻断后,我将血管活性肠肽、组异肽、神经肽Y、神经降压素和降钙素基因相关肽注入完整的窦房结动脉。神经降压素、降钙素基因相关肽和神经肽Y在心率方面未表现出具有生理意义的变化。然而,结构同源物血管活性肠肽和组异肽均使心率增加,最大增加幅度(约120次/分钟)与去甲肾上腺素相似。血管活性肠肽和组异肽的效力分别是去甲肾上腺素的两倍和1/18。血管活性肠肽和组异肽引起的心脏加速反应比去甲肾上腺素的反应发展更慢且持续时间更长。在用足以消除或大大减弱去甲肾上腺素所致心动过速的剂量的普萘洛尔进行β肾上腺素能阻断后,对这两种肽的反应未改变。这些结果表明内源性血管活性肠肽和组异肽在犬的非肾上腺素能、非胆碱能心率控制中具有潜在作用。