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颅内压升高对局部脑血流的影响:纳洛酮和促甲状腺激素释放激素对局部脑缺血微循环影响的比较

Effects of raised intracranial pressure on regional cerebral blood flow: a comparison of effects of naloxone and TRH on the microcirculation in partial cerebral ischaemia.

作者信息

Koskinen L O

出版信息

Br J Pharmacol. 1985 Jun;85(2):489-97. doi: 10.1111/j.1476-5381.1985.tb08886.x.

Abstract

The effects on regional cerebral blood flow (rCBF) of raised intracranial pressure (ICP) and of naloxone and thyrotropin releasing hormone (TRH) during this condition were studied in anaesthetized rabbits. The ICP was elevated until a central ischaemic response was observed. The regional blood flow was determined with the microsphere technique before and during elevation of the ICP (ICPe) and after drug treatment. Total CBF was reduced by about 70% during ICPe while the uveal blood flow increased slightly and some other peripheral tissue blood flows remained unaffected. The administration of TRH caused an increase in mean arterial blood pressure (MAP) from 11.9 +/- 0.6 to 14.6 +/- 0.7 kPa and a normalization of the rCBF. In some peripheral tissues, e.g. gastric mucosa and spleen, TRH reduced the blood flow by 53% and 76%, respectively. In blood pressure stabilized animals no effect on rCBF was seen after TRH. Naloxone had no consistent effect on MAP or local blood flow. It was concluded that in the range of cerebral perfusion pressure studied there was a passive relationship between cerebral blood flow and perfusion pressure. The lack of effect of naloxone and the marked effect of TRH during cerebral ischaemia are consistent with a mechanism of action of TRH not related to a 'physiological' antagonism of opioids.

摘要

在麻醉兔身上研究了颅内压升高(ICP)以及在此情况下纳洛酮和促甲状腺激素释放激素(TRH)对局部脑血流量(rCBF)的影响。将ICP升高直至观察到中枢缺血反应。在ICP升高(ICPe)之前、期间以及药物治疗后,采用微球技术测定局部血流量。ICP升高期间,脑血流量总量减少约70%,而葡萄膜血流量略有增加,其他一些外周组织血流量未受影响。给予TRH后,平均动脉血压(MAP)从11.9±0.6kPa升高至14.6±0.7kPa,rCBF恢复正常。在一些外周组织,如胃黏膜和脾脏,TRH分别使血流量减少53%和76%。在血压稳定的动物中,给予TRH后未观察到对rCBF有影响。纳洛酮对MAP或局部血流量没有一致的影响。得出的结论是,在所研究的脑灌注压范围内,脑血流量与灌注压之间存在被动关系。纳洛酮无作用以及TRH在脑缺血期间有显著作用,这与TRH的作用机制与阿片类药物的“生理性”拮抗无关是一致的。

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