Ghosh S K, Chakraborti T, Michael J R, Chakraborti S
Department of Biochemistry and Biophysics, University of Kalyani, India.
FEBS Lett. 1996 Jun 3;387(2-3):171-4. doi: 10.1016/0014-5793(96)00471-1.
Treatment of bovine pulmonary artery smooth muscle tissue microsomes with H2O2 (1 mM) markedly stimulated protease activity tested with a synthetic substrate N-benzoyl-DL-arginine p-nitroanilide (BAPNA), and also enhanced Ca(2+)-ATPase activity. ATP-dependent Ca(2+) uptake was found to be stimulated upon treatment of the microsomes with H2O2. Pretreatment of the microsomes with vitamin E and aprotinin prevented the H2O2-induced stimulation of Ca(2+)-ATPase activity and also ATP-dependent Ca(2+) uptake. In contrast, H2O2-induced inhibition of Na(+)-dependent Ca(2+) uptake was reversed by vitamin E and aprotinin.
用H2O2(1 mM)处理牛肺动脉平滑肌组织微粒体,可显著刺激用合成底物N-苯甲酰-DL-精氨酸对硝基苯胺(BAPNA)检测的蛋白酶活性,同时也增强Ca(2+)-ATP酶活性。发现用H2O2处理微粒体后,ATP依赖的Ca(2+)摄取受到刺激。用维生素E和抑肽酶预处理微粒体可防止H2O2诱导的Ca(2+)-ATP酶活性刺激以及ATP依赖的Ca(2+)摄取。相反,维生素E和抑肽酶可逆转H2O2诱导的Na(+)-依赖的Ca(2+)摄取抑制。