Simpson K J, Venkatesan S, Martin A, Brindley D N, Peters T J
Division of Clinical Cell Biology, MRC Clinical Research Centre, Harrow, Middlesex, UK.
Alcohol Alcohol. 1995 Jan;30(1):31-6.
A micromethod was developed to assay the hepatic activity and subcellular distribution of phosphatidate phosphohydrolase (PAH, EC 3.1.3.4), an important regulatory enzyme in triacylglycerol synthesis, in human needle biopsy specimens. In normal liver PAH is predominantly cytosolic in distribution, but on treatment with oleic acid it shifts to the membranous compartments of the cell, its physiologically active site. The hepatic specific activity of PAH was similar in controls and patients with fatty liver but significantly more of the enzyme was associated with the membranous compartments in patients with severe alcoholic fatty liver. These observations may explain the enhanced rates of triacylglycerol synthesis observed in these patients and may be implicated in the pathogenesis of alcoholic fatty liver.
已开发出一种微量方法,用于测定人体针吸活检标本中磷脂酸磷酸水解酶(PAH,EC 3.1.3.4)的肝脏活性和亚细胞分布。PAH是三酰甘油合成中的一种重要调节酶。在正常肝脏中,PAH主要分布于胞质溶胶中,但用油酸处理后,它会转移至细胞的膜性区室,即其生理活性位点。对照组和脂肪肝患者肝脏中PAH的比活性相似,但在重度酒精性脂肪肝患者中,与膜性区室相关的该酶显著增多。这些观察结果可能解释了在这些患者中观察到的三酰甘油合成速率增加的现象,并且可能与酒精性脂肪肝的发病机制有关。