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孤立肾动脉的加压会增加三磷酸肌醇和二酰基甘油。

Pressurization of isolated renal arteries increases inositol trisphosphate and diacylglycerol.

作者信息

Narayanan J, Imig M, Roman R J, Harder D R

机构信息

Department of Physiology, Medical College of Wisconsin, Milwaukee 53226.

出版信息

Am J Physiol. 1994 May;266(5 Pt 2):H1840-5. doi: 10.1152/ajpheart.1994.266.5.H1840.

Abstract

Inositol 1,4,5-trisphosphate (IP3) and 1,2-diacylglycerol (DAG) concentrations were measured in isolated, cannulated dog renal arteries under control conditions (0 mmHg) and in response to step elevations in transmural pressure. There was a pressure-dependent increase in IP3 at 60 and 120 mmHg, reaching significance at 120 mmHg (P < 0.05) and a significant increase in DAG at both 60 and 120 mmHg measured after maintaining pressure for 15 min. Similarly, IP3 measurements made 90 s after a step increase in transmural pressure also exhibited a pressure-dependent profile, again reaching significance at 120 mmHg. Calculation of active tension demonstrated these renal arteries developed pressure-dependent myogenic tone. To assess the role of the endothelium in this regard, IP3 was measured before and after endothelial removal at 0 and 60 mmHg. Pressure-dependent myogenic tone was still present upon endothelial removal. In the absence of the endothelium, we observed a significant increase in total IP3 at 60 compared with 0 mmHg; furthermore, the increase in IP3 in the absence of the endothelium was significantly greater than that observed when the endothelium was intact. Given that the primary source of IP3 is via the actions of phospholipase C (PLC) on phosphatidylinositol 4,5-bisphosphate, these biochemical data directly demonstrate that elevation of transmural pressure in dog renal arteries activates PLC.

摘要

在对照条件(0 mmHg)下以及对跨壁压逐步升高的反应中,测量了分离的、插管的犬肾动脉中肌醇1,4,5-三磷酸(IP3)和1,2-二酰甘油(DAG)的浓度。在60和120 mmHg时,IP3随压力依赖性增加,在120 mmHg时达到显著水平(P < 0.05),在维持压力15分钟后测量,60和120 mmHg时DAG均显著增加。同样,在跨壁压逐步升高90秒后进行的IP3测量也呈现出压力依赖性特征,同样在120 mmHg时达到显著水平。主动张力的计算表明,这些肾动脉产生了压力依赖性肌源性张力。为了评估内皮细胞在这方面的作用,在0和60 mmHg下,在内皮细胞去除前后测量了IP3。去除内皮细胞后,压力依赖性肌源性张力仍然存在。在内皮细胞缺失的情况下,我们观察到在60 mmHg时总IP3相较于0 mmHg有显著增加;此外,在内皮细胞缺失时IP3的增加显著大于内皮细胞完整时观察到的增加。鉴于IP3的主要来源是磷脂酶C(PLC)对磷脂酰肌醇4,5-二磷酸的作用,这些生化数据直接表明犬肾动脉中跨壁压的升高激活了PLC。

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