Kobayashi S, Somlyo A V, Somlyo A P
Pennsylvania Muscle Institute, University of Pennsylvania School of Medicine, Philadelphia 19104-6083.
Biochem Biophys Res Commun. 1988 Jun 16;153(2):625-31. doi: 10.1016/s0006-291x(88)81141-0.
The effects of heparin on the release of intracellular Ca2+, assessed by tension development in saponin-permeabilized rabbit main pulmonary artery, were determined. Heparin inhibited (IC50 = 5 micrograms/ml) inositol 1,4,5-trisphosphate (InsP3)-induced, but not caffeine-induced, Ca2+ release. The initial (InsP3-dependent) component of GTP gamma S-induced Ca2+-release was also inhibited by heparin, but the InsP3-independent component was resistant to both heparin and procaine. These results support the existence of a G protein activated mechanism of Ca2+ release that is not mediated by InsP3 or by Ca2+-induced Ca2+ release.
通过皂角苷通透的兔主肺动脉中的张力发展来评估肝素对细胞内Ca2+释放的影响。肝素抑制(IC50 = 5微克/毫升)肌醇1,4,5-三磷酸(InsP3)诱导的Ca2+释放,但不抑制咖啡因诱导的Ca2+释放。GTPγS诱导的Ca2+释放的初始(InsP3依赖性)成分也受到肝素的抑制,但InsP3非依赖性成分对肝素和普鲁卡因均有抗性。这些结果支持存在一种不通过InsP3或Ca2+诱导的Ca2+释放介导的G蛋白激活的Ca2+释放机制。