Zhang Y, Agarwal K C, Beylot M, Soloviev M V, David F, Reider M W, Anderson V E, Tserng K Y, Brunengraber H
Department of Nutrition, Case Western Reserve University, Cleveland, Ohio 44106.
J Biol Chem. 1994 Apr 15;269(15):11025-9.
The labeling of liver extra-mitochondrial acetyl-CoA was investigated in isolated rat livers perfused with [2-(13)C]acetate, [1-(13)C]octanoate, or [1,2,3,4-(13)C4]docosanoate and with drugs that undergo acetylation (phenylaminobutyrate, paraaminobenzoate, and sulfamethoxazole; singly or in combination). The 13C enrichment of mitochondrial acetyl-CoA was probed by the enrichment of R-beta-hydroxybutyrate. The latter was not enriched from [1,2,3,4-(13)C4]docosanoate, thus excluding mitochondrial beta-oxidation of docosanoate. The 13C enrichment of extra-mitochondrial acetyl-CoA was probed by the enrichments of acetylated drugs and of free acetate. In most cases, the four probes yielded different enrichments. Thus, extra-mitochondrial acetyl-CoA appears nonhomogeneous. Competition between drugs alters the labeling of individual acetyl-CoA sub-pools. The labeling pattern of acetylated drugs suggests the existence of more than the two N-acetyltransferases identified so far by others. Our data question the possibility of probing the pool of lipogenic acetyl-CoA via drug acetylation.
在灌注了[2-(13)C]乙酸盐、[1-(13)C]辛酸酯或[1,2,3,4-(13)C4]二十二烷酸酯以及可进行乙酰化的药物(苯氨基丁酸盐、对氨基苯甲酸盐和磺胺甲恶唑;单独或联合使用)的离体大鼠肝脏中,对肝脏线粒体外乙酰辅酶A的标记情况进行了研究。通过R-β-羟基丁酸酯的富集来探测线粒体乙酰辅酶A的13C丰度。后者并非由[1,2,3,4-(13)C4]二十二烷酸酯富集而来,因此排除了二十二烷酸酯的线粒体β-氧化。通过乙酰化药物和游离乙酸盐的富集来探测线粒体外乙酰辅酶A的13C丰度。在大多数情况下,这四种探针产生了不同的丰度。因此,线粒体外乙酰辅酶A似乎是不均一的。药物之间的竞争改变了各个乙酰辅酶A亚池的标记情况。乙酰化药物的标记模式表明,存在的N-乙酰转移酶不止目前其他人所鉴定出的两种。我们的数据对通过药物乙酰化探测生脂乙酰辅酶A池的可能性提出了质疑。