Nozaki K
Department of Neurosurgery, Faculty of Medicine, Kyoto University.
Nihon Geka Hokan. 1990 Jan 1;59(1):55-67.
Changes in the density of cerebroarterial nerve fibers containing calcitonin gene-related peptide (CGRP) and vasoactive intestinal polypeptide (VIP)-like substance, as well as changes in dilatory responses of isolated cerebral arteries to these neuropeptides, after subarachnoid hemorrhage (SAH) were examined in dogs. Moreover, the effects of these neuropeptides to the experimentally produced cerebral arterial spasm were also examined in dogs. SAH was produced by a single injection of fresh autologous arterial blood (1 ml/kg body weight) or double injection of arterial blood (0.5 ml/kg body weight, 48 hours apart) into the cisterna magna. Constriction of basilar artery was most prominent on Day 3 in the single injection model, and on Day 7 in the double injection model. The density of nerve fibers with CGRP-or VIP-like immunoreactivity (LI) was markedly decreased during 7-14 days or 3-7 days after SAH. Vasodilatory actions of CGRP and VIP to isolated basilar artery in vitro were markedly impaired during acute stage of post-SAH period and significantly enhanced during chronic stage of post-SAH period. Intracisternal bolus injection of 10(-10) mol/kg CGRP completely reversed cerebral arterial constriction on Day 3 of single injection SAH model, and intracisternal injection of 10(-11) to 2 x 10(-10) mol/kg CGRP reversed cerebral vasospasm dose-dependently. Intraarterial injection of CGRP could not reversed cerebral arterial constriction. The effects of VIP was much weaker than CGRP.
在犬类中研究蛛网膜下腔出血(SAH)后,含降钙素基因相关肽(CGRP)和血管活性肠肽(VIP)样物质的脑动脉神经纤维密度变化,以及离体脑动脉对这些神经肽舒张反应的变化。此外,还在犬类中研究了这些神经肽对实验性产生的脑动脉痉挛的影响。通过向枕大池单次注射新鲜自体动脉血(1 ml/kg体重)或两次注射动脉血(0.5 ml/kg体重,间隔48小时)来制造SAH。在单次注射模型中,基底动脉收缩在第3天最为明显,在两次注射模型中在第7天最为明显。SAH后7 - 14天或3 - 7天,具有CGRP或VIP样免疫反应性(LI)的神经纤维密度显著降低。SAH急性期,CGRP和VIP对离体基底动脉的舒张作用明显受损,而在SAH慢性期则显著增强。在单次注射SAH模型的第3天,向枕大池推注10^(-10) mol/kg CGRP可完全逆转脑动脉收缩,向枕大池注射10^(-11)至2×10^(-10) mol/kg CGRP可剂量依赖性地逆转脑血管痉挛。动脉内注射CGRP不能逆转脑动脉收缩。VIP的作用比CGRP弱得多。