Borrebaek B, Dolva K, Singh B
Int J Biochem. 1984;16(5):477-81. doi: 10.1016/0020-711x(84)90163-0.
Isolated mitochondria from rat liver were incubated in the presence of [U-14C]palmitate, ATP, CoA, carnitine, EGTA (ethylene glycol bis (beta-aminoethyl ether) N,N'-tetraacetic acid) and varying amounts of calcium. When a KC1-based incubation medium was used, the oxidation of palmitate was inhibited when the concentration of free calcium was increased from about 0.1-10 microM. When a sucrose-based incubation medium was used, the basal rate of palmitate oxidation was about half of that observed with the KC1-medium and calcium had a stimulatory effect. With the KC1-medium the rate of oxygen consumption was inhibited by calcium with alpha-ketoglutarate as well as palmitate as the respiratory substrate. No inhibitory effect of calcium was observed with succinate or beta-hydroxybutyrate. With the KC1-medium and with alpha-ketoglutarate as the respiratory substrate, state 3 respiration but not state 4 respiration was inhibited by calcium. When the sucrose-medium was used, state 3 respiration was first inhibited by calcium, but this inhibition was gradually relieved and the respiratory rate finally became higher than it was before calcium addition.
将从大鼠肝脏分离得到的线粒体与[U-14C]棕榈酸、ATP、辅酶A、肉碱、乙二醇双(β-氨基乙醚)N,N'-四乙酸(EGTA)以及不同量的钙一起孵育。当使用基于KCl的孵育培养基时,当游离钙浓度从约0.1微摩尔增加到10微摩尔时,棕榈酸的氧化受到抑制。当使用基于蔗糖的孵育培养基时,棕榈酸氧化的基础速率约为在KCl培养基中观察到的速率的一半,并且钙具有刺激作用。使用KCl培养基时,以α-酮戊二酸以及棕榈酸作为呼吸底物时,钙会抑制氧气消耗速率。使用琥珀酸或β-羟基丁酸时未观察到钙的抑制作用。使用KCl培养基且以α-酮戊二酸作为呼吸底物时,钙会抑制状态3呼吸,但不抑制状态4呼吸。当使用蔗糖培养基时,状态3呼吸首先受到钙的抑制,但这种抑制会逐渐解除,最终呼吸速率变得高于添加钙之前的速率。