McCormack J G, Osbaldeston N J
Department of Biochemistry, University of Leeds, England.
Eur J Biochem. 1990 Aug 28;192(1):239-44. doi: 10.1111/j.1432-1033.1990.tb19221.x.
In extracts of rat heart mitochondria, Sr2+ mimicked the activatory effects of Ca2+ on the Ca2(+)-sensitive intramitochondrial enzymes, pyruvate dehydrogenase phosphate phosphatase, isocitrate dehydrogenase (NAD+), and 2-oxoglutarate dehydrogenase, but at about tenfold higher concentrations (effective range approximately 1-100 muM) in each case. Ba2+ had no effect on extracted phosphatase, but did mimic the effect of Ca2+ on the other two enzymes with effective concentration ranges similar to those of Sr2+; as with Ca2+ and Sr2+, effective Ba2+ ranges were slightly (2-3-fold) raised by increases in ATP/ADP. In intact uncoupled rat heart mitochondria, the effects of Sr2+ and Ba2+ on the pyruvate and 2-oxoglutarate dehydrogenases were essentially similar to their effects in extracts. In fully coupled rat heart or liver mitochondria, the effective concentration ranges of extramitochondrial Sr2+, leading to activation of the matrix enzymes, were always approximately tenfold higher than those for Ca2+ under all conditions. Ba2+ did not affect pyruvate dehydrogenase in coupled mitochondria, but was shown to activate 2-oxoglutarate dehydrogenase in heart or liver mitochondria, and also isocitrate dehydrogenase (NAD+) in the latter; effective concentration ranges for extramitochondrial Ba2+ were approximately 100-fold greater than those for Ca2+, and like those for Ca2+ and Sr2+, were affected markedly by Mg2+ and spermine (which inhibit and promote mitochondrial Ca2+ uptake, respectively) but, in contrast to Ca2+ and Sr2+, they were hardly affected at all by Na+ (which promotes mitochondrial Ca2+ egress). Ba2+ effects were also blocked by ruthenium red (an inhibitor of mitochondrial Ca2+ uptake), but not so effectively as its blockage of the effects of Sr2+ and Ca2+. Ba2+ and Sr2+ both mimicked the inhibitory effects of extramitochondrial Ca2+ on the Na+/Ca2+ exchanger, but only Sr2+ could mimic Ca2+ in exchanging for internal Ca2+ by this mechanism. Both Sr2+ and Ba2+ changed the fluorescent properties of fura-2 or indo-1 in a similar manner to Ca2+, but with higher kd values. In fura-2-loaded rat heart mitochondria, increases in matrix Sr2+ and Ba2+ and the effects of the transport effectors could be readily demonstrated.
在大鼠心脏线粒体提取物中,Sr2+模拟了Ca2+对Ca2+敏感的线粒体内酶、丙酮酸脱氢酶磷酸酶、异柠檬酸脱氢酶(NAD+)和2-氧代戊二酸脱氢酶的激活作用,但在每种情况下其浓度约高10倍(有效范围约为1-100μM)。Ba2+对提取的磷酸酶无作用,但确实模拟了Ca2+对其他两种酶的作用,其有效浓度范围与Sr2+相似;与Ca2+和Sr2+一样,ATP/ADP增加会使Ba2+的有效范围略有升高(2-3倍)。在完整的解偶联大鼠心脏线粒体中,Sr2+和Ba2+对丙酮酸和2-氧代戊二酸脱氢酶的作用与其在提取物中的作用基本相似。在完全偶联的大鼠心脏或肝脏线粒体中,导致基质酶激活的线粒体外Sr2+的有效浓度范围在所有条件下总是比Ca2+高约10倍。Ba2+对偶联线粒体中的丙酮酸脱氢酶无影响,但已证明其可激活心脏或肝脏线粒体中的2-氧代戊二酸脱氢酶,以及后者中的异柠檬酸脱氢酶(NAD+);线粒体外Ba2+的有效浓度范围比Ca2+大约100倍,并且与Ca2+和Sr2+一样,受到Mg2+和精胺的显著影响(分别抑制和促进线粒体Ca2+摄取),但与Ca2+和Sr2+不同的是,它们几乎不受Na+(促进线粒体Ca2+外流)的影响。Ba2+的作用也被钌红(线粒体Ca2+摄取抑制剂)阻断,但不如其对Sr2+和Ca2+作用的阻断有效。Ba2+和Sr2+都模拟了线粒体外Ca2+对Na+/Ca2+交换体的抑制作用,但只有Sr2+能通过这种机制模拟Ca2+与内部Ca2+进行交换。Sr2+和Ba2+改变fura-2或indo-1荧光特性的方式与Ca2+相似,但解离常数(kd)值更高。在装载fura-2的大鼠心脏线粒体中,基质Sr2+和Ba2+的增加以及转运效应物的作用很容易得到证明。