Gupta M P, Dixon I M, Zhao D, Dhalla N S
Division of Cardiovascular Sciences, St Boniface General Hospital Research Centre, Winnipeg, Manitoba.
Can J Cardiol. 1989 Jan-Feb;5(1):55-63.
Ruthenium red inhibited Ca2+-ATPase and ATP-independent Ca2+ binding with rat heart sarcolemma in a concentration dependent manner; significant effects were evident at 0.25 microM and higher concentrations. The apparent Ka for Ca2+-ATPase was 1.02 +/- 0.02 mM Ca2+ and 1.47 +/- 0.12 mM Ca2+ in the absence and presence of 2.5 microM ruthenium red, respectively; however, no change in the Vmax (41.2 +/- 1.6 mumol Pi/mg/h) was observed. Likewise, the affinity of Ca2+ for both low and high affinity Ca2+ binding sites in sarcolemma was decreased by ruthenium red. Sarcolemmal Na+-dependent Ca2+ uptake, ATP-dependent Ca2+ accumulation, Mg2+-ATPase and Na+,K+-ATPase activities were not affected by ruthenium red. In sarcoplasmic reticulum preparations, ruthenium red (0.25 to 25 microM) enhanced Ca2+ uptake without altering the Ca2+-stimulated ATPase activity. The observed increase in Ca2+ uptake appears to be due to the depressant effect of the dye on Ca2+ release from the sarcoplasmic reticulum. In mitochondrial preparations, ruthenium red (0.025 to 25 microM) showed a marked inhibitory effect on Ca2+ uptake activity whereas the Mg2+-ATPase activity was unaltered. In isolated rat hearts, 0.025 microM ruthenium red produced a slight negative inotropic effect, whereas 0.25 to 2.5 microM ruthenium red elicited a biphasic response both in terms of developed tension and resting tension. High concentrations of ruthenium red (12.5 to 25 microM) resulted in the development of contracture. Electron microscopic studies revealed the presence of ruthenium red in the myoplasm of hearts perfused for 15 to 30 mins with 2.5 to 5 microM dye.(ABSTRACT TRUNCATED AT 250 WORDS)
钌红以浓度依赖性方式抑制大鼠心肌肌膜的Ca2 + -ATP酶和非ATP依赖性Ca2 +结合;在0.25 microM及更高浓度时,显著作用明显。在不存在和存在2.5 microM钌红的情况下,Ca2 + -ATP酶的表观Ka分别为1.02±0.02 mM Ca2 +和1.47±0.12 mM Ca2 +;然而,未观察到Vmax(41.2±1.6 μmol Pi/mg/h)有变化。同样,钌红降低了肌膜中Ca2 +对低亲和力和高亲和力Ca2 +结合位点的亲和力。肌膜依赖Na +的Ca2 +摄取、依赖ATP的Ca2 +积累、Mg2 + -ATP酶和Na +,K + -ATP酶活性不受钌红影响。在肌浆网制剂中,钌红(0.25至25 microM)增强了Ca2 +摄取,而不改变Ca2 +刺激的ATP酶活性。观察到的Ca2 +摄取增加似乎是由于该染料对肌浆网Ca2 +释放的抑制作用。在线粒体制剂中,钌红(0.025至25 microM)对Ca2 +摄取活性有显著抑制作用,而Mg2 + -ATP酶活性未改变。在离体大鼠心脏中,0.025 microM钌红产生轻微的负性肌力作用,而0.25至2.5 microM钌红在舒张期张力和静息张力方面均引起双相反应。高浓度的钌红(12.5至25 microM)导致挛缩的发生。电子显微镜研究显示,在用2.5至5 microM染料灌注15至30分钟的心脏肌浆中存在钌红。(摘要截断于250字)