Institute of Physiology and Center for Applied Genomics, Academy of Sciences of the Czech Republic, Vídenská 1083, 142 20 Prague, Czech Republic.
Biochem Biophys Res Commun. 2010 Jan 15;391(3):1348-51. doi: 10.1016/j.bbrc.2009.12.050. Epub 2009 Dec 16.
The functional role of CD36 protein detected in mitochondrial fractions in long chain fatty acid (LCFA) oxidation is unclear due to conflicting results obtained in Cd36 knockout mice and experiments using sulfo-N-succinimidyl oleate (SSO) for inhibition of CD36 mediated LCFA transport. We investigated effect of SSO on mitochondrial respiration and found that SSO substantially inhibits not only LCFA oxidation, but also oxidation of flavoprotein- and NADH-dependent substrates and generation of mitochondrial membrane potential. Experiments in rat liver, heart and kidney mitochondria demonstrated a direct effect on mitochondrial respiratory chain with the most pronounced inhibition of the complex III (IC(50) 4microM SSO). The results presented here show that SSO is a potent and irreversible inhibitor of mitochondrial respiratory chain.
由于在 Cd36 基因敲除小鼠和使用磺基琥珀酰亚胺辛酯(SSO)抑制 CD36 介导的长链脂肪酸(LCFA)转运的实验中得到了相互矛盾的结果,因此在线粒体部分检测到的 CD36 蛋白在长链脂肪酸(LCFA)氧化中的功能作用尚不清楚。我们研究了 SSO 对线粒体呼吸的影响,发现 SSO 不仅显著抑制 LCFA 的氧化,还抑制黄素蛋白和 NADH 依赖性底物的氧化以及线粒体膜电位的产生。在大鼠肝、心和肾线粒体中的实验表明,SSO 对线粒体呼吸链具有直接的作用,其中对复合物 III 的抑制作用最为明显(IC(50)为 4μM SSO)。这里呈现的结果表明,SSO 是线粒体呼吸链的一种有效和不可逆的抑制剂。