Wahl M
Department of Physiology, University of Munich, Federal Republic of Germany.
Pflugers Arch. 1989 Nov;415(2):250-2. doi: 10.1007/BF00370602.
The vasomotor effect of the K+ channel opener pinacidil was investigated in feline pial arteries of the parietal cortex. Perivascular microapplication (5 microliters in 40 sex) and an image splitting method for the measurement of vascular diameter were employed. Pinacidil (10(-11) - 10(-7) M) induced concentration-dependent dilatations at 10(-9) M and higher concentrations. A maximal dilatation of about 42% was achieved at 10(-8) M, the dilatation at 10(-7) M was reduced to 22%. The sulphonylurea tolbutamide exerted per se no effect in pial arteries but it blocked concentration-dependently the pinacidil induced dilatation. This is consistent with the presence of ATP-sensitive K+ channels in pial arteries which are closed under resting conditions.
在猫顶叶皮质的软脑膜动脉中研究了钾通道开放剂吡那地尔的血管运动效应。采用血管周围微量应用(40秒内5微升)和图像分割法测量血管直径。吡那地尔(10^(-11)-10^(-7)M)在10^(-9)M及更高浓度时引起浓度依赖性扩张。在10^(-8)M时达到约42%的最大扩张,在10^(-7)M时扩张降至22%。磺脲类药物甲苯磺丁脲本身对软脑膜动脉无作用,但它浓度依赖性地阻断吡那地尔诱导的扩张。这与软脑膜动脉中存在ATP敏感性钾通道一致,这些通道在静息条件下是关闭的。