首页> 美国卫生研究院文献>The Journal of Physiology >Endothelium-derived relaxing factor inhibits the formation of inositol trisphosphate by rabbit aorta.
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Endothelium-derived relaxing factor inhibits the formation of inositol trisphosphate by rabbit aorta.

机译:内皮源性舒张因子抑制兔主动脉肌醇三磷酸的形成。

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摘要

1. The effects of endothelium-derived relaxing factor (EDRF), sodium nitroprusside, 8-bromo-cyclic GMP and atrial natriuretic factor (ANF) on inositol trisphosphate (IP3) levels were studied in isolated rabbit aortic preparations stimulated with noradrenaline. 2. In endothelium-containing preparations, acetylcholine, which stimulated EDRF release, inhibited noradrenaline-stimulated IP3 formation. The EDRF inhibitor haemoglobin reversed this effect. 3. In endothelium-denuded preparations, sodium nitroprusside, 8-bromo-cyclic GMP and ANF each similarly inhibited the rise in IP3 levels stimulated by noradrenaline. 4. These findings show that in rabbit aorta, agents which increase cyclic GMP inhibit the noradrenaline-induced rise in IP3 levels and may provide an explanation for the previously reported observations that cyclic GMP inhibits the noradrenaline-stimulated increase in calcium influx and release of intracellular calcium in vascular smooth muscle.
机译:1.在去甲肾上腺素刺激的离体兔主动脉制剂中研究了内皮源性舒张因子(EDRF),硝普钠,8-溴环GMP和心钠素对三磷酸肌醇(IP3)水平的影响。 2.在含内皮的制剂中,乙酰胆碱刺激EDRF的释放,抑制去甲肾上腺素刺激的IP3的形成。 EDRF抑制剂血红蛋白逆转了这种作用。 3.在具有内皮剥蚀作用的制剂中,硝普钠,8溴环GMP和ANF分别抑制去甲肾上腺素刺激的IP3水平升高。 4.这些发现表明,在兔主动脉中,增加环状GMP的药物可抑制去甲肾上腺素诱导的IP3水平升高,并且可以为以前报道的观察结果提供解释,即环状GMP抑制去甲肾上腺素刺激的钙内流和细胞内释放血管平滑肌中的钙。

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