脂肪酸代谢中的肝细胞异质性:乙酰辅酶a羧化酶的分区差异。

Enzyme Pub Date : 1992-01-01 DOI:10.1159/000468778
B Quistorff, N Katz, L A Witters
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引用次数: 27

摘要

脂质代谢似乎比碳水化合物和蛋白质代谢更不具有分区性。脂质代谢的分带性研究主要集中在脂肪酸的合成上,根据代谢分带的概念,脂肪酸的合成应该是一个主要的静脉周围过程,而脂肪酸的氧化应该是门静脉周围过程。然而,关于脂肪生成酶的活性梯度以及脂肪酸和极低密度脂蛋白的实际合成测量数据存在矛盾。通过显微解剖获得的数据显示,在静脉周围区乙酰辅酶a羧化酶和柠檬酸裂解酶的活性高出1.5至2倍,这与肝细胞制剂中脂肪酸合成的实际速率相一致,富集于门静脉周围细胞或静脉周围细胞。另一方面,双地黄苷脉冲灌注技术的结果显示相反的梯度,基于乙酰辅酶a羧化酶蛋白本身的测量,在门静脉周围区乙酰辅酶a羧化酶的比活性提高了2至3倍。这种特定的活动梯度,适用于雄性而不是雌性大鼠,在脂肪生成被强烈诱导的快速喂食动物中几乎完全消失。在这篇综述中,我们试图将结果中的这些差异合理化为方法上的差异,特别是适用于以下参数:(1)结果的表达(参考物质);(2)区域取样的选择性;(3)乙酰辅酶a羧化酶测定方法的差异。由此得出结论,这些因素可以解释差异,但需要进一步研究,特别是对乙酰辅酶a羧化酶mRNA的分区,以进一步了解脂质代谢的分区及其在肝脏代谢调节中的可能作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hepatocyte heterogeneity in the metabolism of fatty acids: discrepancies on zonation of acetyl-CoA carboxylase.

Lipid metabolism appears to be less zonated than carbohydrate and protein metabolism. Studies on the zonation of lipid metabolism have been centered in particular on fatty acid synthesis which, according to the concept of metabolic zonation, should be a predominantly perivenous process while fatty acid oxidation should be periportal. There are, however, conflicting data on the activity gradients of lipogenic enzymes as well as measurements of actual synthesis of fatty acid and very low density lipoprotein. Data obtained by microdissection show a 1.5- to 2-fold higher activity of acetyl-CoA carboxylase and citrate lyase in the perivenous zone in agreement with measurements of the actual rate of fatty acid synthesis in preparations of hepatocyte, enriched in periportal or perivenous cells. On the other hand, results obtained with the dual-digitonin-pulse perfusion technique demonstrate the opposite gradient in the form of a 2- to 3-fold higher specific activity of acetyl-CoA carboxylase in the periportal zone based on measurements of the acetyl-CoA carboxylase protein proper. This specific activity gradient, which applies to male and not female rats, disappears almost completely in the fasted-refed animal, were lipogenesis is strongly induced. In this review we attempt to rationalize these discrepancies in the results as methodological differences which in particular apply to the following parameters: (1) expression of results (reference substance); (2) selectivity of zonal sampling, and (3) differences in methodology of acetyl-CoA carboxylase measurements. It is concluded that these factors could account for the discrepancies, but further studies, in particular on the zonation acetyl-CoA carboxylase mRNA, are required in order to further understand the zonation of lipid metabolism and its possible role in the metabolic regulation of the liver.

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