作者: William I. Rosenblum , Enoch P. Wei , Hermes A. Kontos
DOI: 10.1016/J.BRAINRES.2004.01.035
关键词: Nitric oxide synthase 、 Pharmacology 、 Nitric oxide 、 Potassium channel 、 Biochemistry 、 Vasodilation 、 Vascular smooth muscle 、 Potassium channel blocker 、 Amiloride 、 Benzamil 、 Chemistry 、 Developmental biology 、 General Neuroscience 、 Molecular biology 、 Clinical neurology
摘要: Pial artrioles of rats were monitored in vivo and found to dilate dose-dependent fashion upon application either benzamil or ethyl isopropyl amiloride, both which are inhibitors the sodium-hydrogen antiport. Antiport blockade is known decrease internal pH vascular smooth muscle (VSM). The dilation was blocked by 1 microm glibenclamide, that dose a selective inhibitor ATP sensitive potassium channels (K(ATP)). nitric oxide synthase nitro-l arginine (l-NNA) also response. Previous studies this preparation under same experimental conditions showed l-NNA inhibited K(ATP) openers had no permissive action setting. Moreover, one study others has demonstrated site on surface while another sodium propionate, direct acidifier cell, dilates rat basilar artery K(ATP)-dependent fashion. Therefore, present data support following conclusions: brain arterioles; response dependent; some situations, can inhibit dilations including those produced pH.