Plane F, Garland C J
Department of Pharmacology, University of Bristol.
Br J Pharmacol. 1996 Sep;119(2):191-3. doi: 10.1111/j.1476-5381.1996.tb15970.x.
This study demonstrates directly that the relative contribution of nitric oxide (NO) and an NO synthase-independent repolarization to acetylcholine-evoked relaxation in rat isolated mesenteric resistance arteries is determined by the processes which mediate pre-contraction. Noradrenaline-induced contractions were reversed by acetylcholine via both NO and NO synthase-independent smooth muscle repolarization. In contrast, reversal of contractions to the thromboxane-mimetic, U46619, by acetylcholine was entirely mediated by the actions of NO, independently of a change in membrane potential.
本研究直接表明,在大鼠离体肠系膜阻力动脉中,一氧化氮(NO)和不依赖一氧化氮合酶的复极化对乙酰胆碱诱发的舒张的相对贡献,由介导预收缩的过程决定。去甲肾上腺素诱导的收缩可被乙酰胆碱通过NO和不依赖一氧化氮合酶的平滑肌复极化逆转。相比之下,乙酰胆碱对血栓素类似物U46619诱导的收缩的逆转完全由NO的作用介导,与膜电位变化无关。