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内皮舒张因子协调血管阻力血管的活动。

EDRF coordinates the behaviour of vascular resistance vessels.

作者信息

Griffith T M, Edwards D H, Davies R L, Harrison T J, Evans K T

机构信息

Department of Diagnostic Radiology & Cardiology, University of Wales College of Medicine, Heath Park, Cardiff, UK.

出版信息

Nature. 1987;329(6138):442-5. doi: 10.1038/329442a0.

Abstract

Constriction of vascular smooth muscle in response to the stimulus of raised intravascular pressure--the myogenic response--represents a positive feedback mechanism which, if unopposed, could theoretically lead to instability in the intact circulation. Dilation in response to increased intraluminal flow would provide an opposing feedback mechanism which could confer overall stability. Flow-dependent dilation in conduit vessels is mediated by endothelium-derived relaxing factor (EDRF), but the relationship between flow and EDRF activity has not been studied in resistance vessels in situ. We here demonstrate that EDRF can coordinate the aggregate hydrodynamic properties of an intact network. Under control conditions, EDRF maintains a fourth-power relationship between diameter and flow so that the pressure gradient in each vessel asymptotically approaches a constant value at high flow rates. Basal EDRF release may also maintain a similar spatial distribution of flow at different flow rates, even under conditions of moderate pharmacological constriction.

摘要

血管平滑肌对血管内压力升高刺激的收缩——肌源性反应——代表一种正反馈机制,理论上如果不受抑制,可能导致完整循环系统的不稳定。对管腔内流量增加的舒张反应将提供一种相反的反馈机制,从而赋予整体稳定性。传导血管中流量依赖性舒张由内皮衍生舒张因子(EDRF)介导,但流量与EDRF活性之间的关系尚未在原位阻力血管中进行研究。我们在此证明,EDRF可协调完整网络的总体流体动力学特性。在对照条件下,EDRF维持直径与流量之间的四次方关系,以便在高流量时每个血管中的压力梯度渐近地接近一个恒定值。即使在适度药物收缩的条件下,基础EDRF释放也可能在不同流量下维持相似的流量空间分布。

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