Peng C F, Straub K D, Kane J J, Murphy M L, Wadkins C L
Biochim Biophys Acta. 1977 Nov 17;462(2):403-13. doi: 10.1016/0005-2728(77)90138-4.
Bongkrekic acid and atractyloside, inhibitors of adenine nucleotide translocase, do not inhibit Ca2+ uptake and H+ production by pig heart mitochondria. However, bongkrekic acid, but not atractyloside, inhibits dinitrophenol-induced Ca2+ efflux and H+ uptake. Conversely, ruthenium red blocks Ca2+ uptake and H+ production but does not prevent dinitrophenol-induced Ca2+ efflux and H+ uptake by mitochondria. These results suggest that mitochondrial Ca2+ uptake and release exist as two independent pathways. The efflux of Ca2+ from mitochondria is mediated by a bongkrekic acid sensitive component which is apparently not identical to the ruthenium red sensitive Ca2+ uptake carrier.
米酵菌酸和苍术苷是腺嘌呤核苷酸转位酶的抑制剂,它们并不抑制猪心脏线粒体对Ca2+的摄取和H+的产生。然而,米酵菌酸而非苍术苷,可抑制二硝基苯酚诱导的Ca2+外流和H+摄取。相反,钌红可阻断Ca2+摄取和H+产生,但不能阻止二硝基苯酚诱导的线粒体Ca2+外流和H+摄取。这些结果表明,线粒体Ca2+的摄取和释放是两条独立的途径。线粒体Ca2+外流由一个对米酵菌酸敏感的成分介导,该成分显然与对钌红敏感的Ca2+摄取载体不同。