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膜电位在豚鼠冠状动脉平滑肌内皮依赖性舒张中的作用。

Role of membrane potential in endothelium-dependent relaxation of guinea-pig coronary arterial smooth muscle.

作者信息

Parkington H C, Tonta M A, Coleman H A, Tare M

机构信息

Department of Physiology, Monash University, Clayton, Victoria, Australia.

出版信息

J Physiol. 1995 Apr 15;484 ( Pt 2)(Pt 2):469-80. doi: 10.1113/jphysiol.1995.sp020679.

Abstract
  1. Membrane potential and tension were measured simultaneously in ring segments of main coronary artery of guinea-pigs. The synthetic thromboxane A2 analogue U46619 depolarized the tissues from -58 +/- 2 to -40 +/- 1 mV and increased tension by 12 +/- 1 mN mm-1. Nitric oxide (NO) and Iloprost, the stable analogue of prostacyclin, evoked hyperpolarization and relaxation. 2. The concentration of NO required to evoke half-maximal hyperpolarization (EC50 of 2 x 10(-5) M) was 40-fold higher than that which was required to induce relaxation (EC50 of 5 x 10(-7) M). The EC50 for Iloprost-induced hyperpolarization (3 x 10(-8) M) was similar to that for relaxation (4 x 10(-8) M). 3. Glibenclamide (10(-6) M) abolished the hyperpolarization in response to both NO and Iloprost but was without effect on the amplitudes of the relaxations over the complete concentration-response curves. 4. Acetylcholine evoked concentration-dependent hyperpolarization and relaxation in the presence of N omega-nitro-L-arginine methyl ester (NAME; 10(-5) M) and indomethacin (10(-6) M), and these responses were attributed to endothelium-derived hyperpolarizing factor (EDHF). The hyperpolarization produced by EDHF always preceded relaxation, and relaxation never occurred at concentrations of acetylcholine that were insufficient to evoke hyperpolarization. 5. The concentration-hyperpolarization and concentration-relaxation curves in response to acetylcholine were not affected by glibenclamide or barium (1-3 mM) but were shifted to the right 4- and 5-fold, respectively, by 1 mM tetraethylammonium. The hyperpolarization and relaxation evoked by acetylcholine were also reduced in a parallel manner when the potassium concentration in the superfusate was increased. 6. Hyperpolarizing current steps, applied to spiral strips of coronary artery denuded of endothelium and depolarized and constricted with U46619, caused relaxation. The relationship between hyperpolarization and relaxation evoked electronically was similar to that which was due to EDHF in intact tissues stimulated with acetylcholine. 7. It is concluded that the ability of NO or Iloprost to relax guinea-pig coronary artery does not depend upon hyperpolarization of the smooth muscle. In contrast, hyperpolarization is likely to play a major, if not the only, role in the relaxation in response to EDHF in this tissue.
摘要
  1. 同时测量豚鼠主冠状动脉环段的膜电位和张力。合成血栓素A2类似物U46619使组织去极化,从-58±2 mV降至-40±1 mV,并使张力增加12±1 mN/mm-1。一氧化氮(NO)和前列环素的稳定类似物伊洛前列素可引起超极化和舒张。2. 引起半数最大超极化所需的NO浓度(EC50为2×10-5 M)比诱导舒张所需的浓度(EC50为5×10-7 M)高40倍。伊洛前列素诱导超极化的EC50(3×10-8 M)与舒张的EC50(4×10-8 M)相似。3. 格列本脲(10-6 M)消除了对NO和伊洛前列素的超极化反应,但对整个浓度-反应曲线的舒张幅度没有影响。4. 在Nω-硝基-L-精氨酸甲酯(NAME;10-5 M)和吲哚美辛(10-6 M)存在的情况下,乙酰胆碱引起浓度依赖性的超极化和舒张,这些反应归因于内皮衍生的超极化因子(EDHF)。EDHF产生的超极化总是先于舒张,并且在不足以引起超极化的乙酰胆碱浓度下从不发生舒张。5. 对乙酰胆碱的浓度-超极化和浓度-舒张曲线不受格列本脲或钡(1-3 mM)的影响,但分别被1 mM四乙铵向右移动4倍和5倍。当 superfusate中的钾浓度增加时,乙酰胆碱引起的超极化和舒张也以平行的方式降低。6. 对用U46619去极化和收缩的内皮剥脱的冠状动脉螺旋条施加超极化电流阶跃,可引起舒张。电诱发的超极化和舒张之间的关系类似于完整组织中用乙酰胆碱刺激时EDHF引起的关系。7. 得出结论,NO或伊洛前列素舒张豚鼠冠状动脉的能力不依赖于平滑肌的超极化。相反,超极化可能在该组织中对EDHF的反应性舒张中起主要作用,如果不是唯一作用的话。

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