Kravchenko A N, Shkhvatsabaia I K, Nekrasova A A, Men'shikov M Iu, Avdonin P V
Biull Vsesoiuznogo Kardiol Nauchn Tsentra AMN SSSR. 1988;11(1):33-7.
The effect of antihypertensive drugs on receptor-dependent increase in Ca2+ basal level and its changes under stimulators action (thrombocytes activating factor, ADP and vasopressin) were studied by means of a fluorescent calcium probe "quin-2". Nifedipine blocked receptor-dependent increase of Ca2+ in thrombocytes in vitro as well as by oral administration, which was accompanied by decrease in vascular tone and BP. The degree of BP decrease correlated with that of depression of receptor-dependent increase of Ca2+ in thrombocytes. Combined therapy including nifedipine, propranolol and a diuretic resulted in more manifest inhibition of receptor-dependent calcium channels than monotherapy with nifedipine. Effect of antihypertensive drugs evidently depends on their influence on receptor-dependent Ca2+ cellular entrance.
采用荧光钙探针“喹啉-2”研究了抗高血压药物对血小板Ca2+基础水平受体依赖性升高及其在刺激剂(血小板激活因子、ADP和血管加压素)作用下变化的影响。硝苯地平在体外以及口服给药时均能阻断血小板中受体依赖性Ca2+的升高,同时伴有血管张力和血压降低。血压降低程度与血小板中受体依赖性Ca2+升高的抑制程度相关。包括硝苯地平、普萘洛尔和利尿剂的联合治疗比单用硝苯地平更能明显抑制受体依赖性钙通道。抗高血压药物的作用显然取决于它们对受体依赖性Ca2+细胞内流的影响。