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新生羔羊低温体外循环期间脑微循环中的内皮功能障碍。

Endothelial dysfunction in cerebral microcirculation during hypothermic cardiopulmonary bypass in newborn lambs.

作者信息

Wagerle L C, Russo P, Dahdah N S, Kapadia N, Davis D A

机构信息

Department of Cardiothoracic Surgery, Allegheny University of the Health Sciences, St. Christopher's Hospital for Children, Philadelphia, PA 19102, USA.

出版信息

J Thorac Cardiovasc Surg. 1998 May;115(5):1047-54. doi: 10.1016/S0022-5223(98)70404-0.

Abstract

OBJECTIVES

Inflammatory stimuli or mechanical stresses associated with hypothermic cardiopulmonary bypass could potentially impair cerebrovascular function, resulting in inadequate cerebral perfusion. We hypothesize that hypothermic cardiopulmonary bypass is associated with endothelial or vascular smooth muscle dysfunction and associated cerebral hypoperfusion. Therefore we studied the cerebrovascular response to endothelium-dependent vasodilator, acetylcholine, endothelium-independent nitric oxide donor, sodium nitroprusside, and vasoactive amine, serotonin, in newborn lambs undergoing hypothermic cardiopulmonary bypass (nasopharygeal temperature = 18 degrees C).

METHODS

Studies were performed on 13 newborn lambs equipped with a closed cranial window, allowing for direct visualization of surface pial arterioles. Six animals were studied while undergoing hypothermic cardiopulmonary bypass, whereas seven served as nonbypass, warm (37 degrees C) controls. Pial arteriolar caliber (range = 111 to 316 microm diameter) was monitored using video microscopy.

RESULTS

Topical application of acetylcholine caused a dose-dependent increase in arteriolar diameter in the control group that was absent in animals undergoing hypothermic cardiopulmonary bypass. Hypothermic cardiopulmonary bypass did not alter the vasodilation in response to sodium nitroprusside. Furthermore, the contractile response to serotonin was fully expressed during hypothermic cardiopulmonary bypass.

CONCLUSIONS

The specific loss of acetylcholine-induced vasodilation suggests endothelial cell dysfunction rather than impaired ability of vascular smooth muscle to respond to nitric oxide. It is speculated that loss of endothelium-dependent regulatory factors in the cerebral microcirculation during hypothermic cardiopulmonary bypass may enhance vasoconstriction, and impaired cerebrovascular function may be a basis for associated neurologic injury during or after hypothermic cardiopulmonary bypass.

摘要

目的

与低温体外循环相关的炎症刺激或机械应力可能会损害脑血管功能,导致脑灌注不足。我们假设低温体外循环与内皮或血管平滑肌功能障碍及相关的脑灌注不足有关。因此,我们研究了在接受低温体外循环(鼻咽温度 = 18摄氏度)的新生羔羊中,脑血管对内皮依赖性血管舒张剂乙酰胆碱、内皮非依赖性一氧化氮供体硝普钠以及血管活性胺5-羟色胺的反应。

方法

对13只配备封闭颅窗的新生羔羊进行研究,以便直接观察软脑膜小动脉表面。6只动物在接受低温体外循环时进行研究,而7只作为非体外循环、体温正常(37摄氏度)的对照组。使用视频显微镜监测软脑膜小动脉内径(范围 = 111至316微米)。

结果

在对照组中,局部应用乙酰胆碱会导致小动脉直径呈剂量依赖性增加,而在接受低温体外循环的动物中则未出现这种情况。低温体外循环并未改变对硝普钠的血管舒张反应。此外,在低温体外循环期间,对5-羟色胺的收缩反应充分表现出来。

结论

乙酰胆碱诱导的血管舒张反应的特异性丧失表明是内皮细胞功能障碍,而非血管平滑肌对一氧化氮反应能力受损。据推测,低温体外循环期间脑微循环中内皮依赖性调节因子的丧失可能会增强血管收缩,而脑血管功能受损可能是低温体外循环期间或之后相关神经损伤的一个基础。

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