Schubert Rudolf, Kalentchuk Vjatscheslav U, Krien Ulrike
University of Rostock, Institute of Physiology, Germany.
Am J Physiol Heart Circ Physiol. 2002 Dec;283(6):H2288-95. doi: 10.1152/ajpheart.00549.2002. Epub 2002 Aug 29.
The hypothesis that Rho kinase is involved in myogenic reactivity was investigated in pressurized rat tail small arteries using videomicroscopic diameter determination and calcium fluorimetry. The potent Rho kinase inhibitor Y-27632 reversibly increased vessel diameter at 80 mmHg without changing the intracellular calcium concentration (Ca) shifting the relationship between diameter change and Ca to higher calcium levels. Neither endothelium removal nor inhibition of neural transmission affected the Y-27632-induced effect. Y-27632 at 3 x 10(-6) mol/l attenuated the myogenic response in the pressure range from 10 to 120 mmHg, shifting the relationship between vessel tone and Ca to higher calcium levels. In addition, the Y-27632-induced shift of the relationship between vessel tone and Ca was larger at 80 than at 10 mmHg. These results suggest that smooth muscle cell Rho kinase in rat tail small arteries 1) is in an active state partly determining the level of the myogenic tone, and 2) alters the strength of the myogenic response by changing calcium sensitivity, probably caused by the pressure-induced activation of the kinase.
运用视频显微镜直径测定法和钙荧光测定法,在压力作用下的大鼠尾部小动脉中研究了Rho激酶参与肌源性反应的假说。强效Rho激酶抑制剂Y-27632在80 mmHg时可逆地增加血管直径,而不改变细胞内钙浓度([Ca]i),使直径变化与[Ca]i之间的关系向更高钙水平偏移。去除内皮和抑制神经传递均不影响Y-27632诱导的效应。3×10⁻⁶ mol/l的Y-27632减弱了10至120 mmHg压力范围内的肌源性反应,使血管张力与[Ca]i之间的关系向更高钙水平偏移。此外,Y-27632诱导的血管张力与[Ca]i之间关系的偏移在80 mmHg时比在10 mmHg时更大。这些结果表明,大鼠尾部小动脉中的平滑肌细胞Rho激酶:1)处于活跃状态,部分决定肌源性张力水平;2)通过改变钙敏感性改变肌源性反应的强度,这可能是由压力诱导的激酶激活所致。