Brayden J E, Nelson M T
Department of Pharmacology, University of Vermont, Colchester 05446.
Science. 1992 Apr 24;256(5056):532-5. doi: 10.1126/science.1373909.
Blood pressure and tissue perfusion are controlled in part by the level of intrinsic (myogenic) vascular tone. However, many of the molecular determinants of this response are unknown. Evidence is now presented that the degree of myogenic tone is regulated in part by the activation of large-conductance calcium-activated potassium channels in arterial smooth muscle. Tetraethylammonium ion (TEA+) and charybdotoxin (CTX), at concentrations that block calcium-activated potassium channels in smooth muscle cells isolated from cerebral arteries, depolarized and constricted pressurized cerebral arteries with myogenic tone. Both TEA+ and CTX had little effect on arteries when intracellular calcium was reduced by lowering intravascular pressure or by blocking calcium channels. Elevation of intravascular pressure through membrane depolarization and an increase in intracellular calcium may activate calcium-activated potassium channels. Thus, these channels may serve as a negative feedback pathway to control the degree of membrane depolarization and vasoconstriction.
血压和组织灌注部分受内在(肌源性)血管张力水平的控制。然而,这种反应的许多分子决定因素尚不清楚。现在有证据表明,肌源性张力的程度部分受动脉平滑肌中大电导钙激活钾通道激活的调节。四乙铵离子(TEA+)和蝎毒素(CTX),在阻断从脑动脉分离的平滑肌细胞中钙激活钾通道的浓度下,使具有肌源性张力的加压脑动脉去极化并收缩。当通过降低血管内压力或阻断钙通道来降低细胞内钙时,TEA+和CTX对动脉几乎没有影响。通过膜去极化升高血管内压力以及细胞内钙增加可能会激活钙激活钾通道。因此,这些通道可能作为负反馈途径来控制膜去极化程度和血管收缩。