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利用α-酮异戊酸和丙酸作为前体对肝脏糖异生的调节。

The regulation of hepatic gluconeogenesis using alpha-ketoisovalerate and propionate as precursors.

作者信息

Patel T B, Lapointe D S, Olson M S

出版信息

Arch Biochem Biophys. 1984 Sep;233(2):362-9. doi: 10.1016/0003-9861(84)90457-0.

Abstract

The regulation of gluconeogenesis from alpha-ketoisovalerate and propionate was investigated in perfused livers from fasted rats. With alpha-ketoisovalerate as the gluconeogenic precursor, infusion of beta-hydroxybutyrate and acetate stimulated the rate of alpha-ketoisovalerate decarboxylation, but inhibited the rate of glucose production. Oleate, on the other hand, inhibited both alpha-ketoisovalerate decarboxylation and glucose production. When propionate was the primary gluconeogenic substrate, oleate, beta-hydroxybutyrate, and acetate infusion did not significantly alter hepatic glucose production. The present studies suggest that gluconeogenesis from alpha-ketoisovalerate is regulated at the level of various dehydrogenases prior to formation of propionyl-CoA, but subsequent to the branched-chain alpha-keto acid dehydrogenase reaction.

摘要

在禁食大鼠的灌注肝脏中研究了由α-酮异戊酸和丙酸生成葡萄糖的调节机制。以α-酮异戊酸作为糖异生的前体,输注β-羟基丁酸和乙酸可刺激α-酮异戊酸脱羧速率,但抑制葡萄糖生成速率。另一方面,油酸既抑制α-酮异戊酸脱羧又抑制葡萄糖生成。当丙酸是主要的糖异生底物时,输注油酸、β-羟基丁酸和乙酸不会显著改变肝脏葡萄糖生成。目前的研究表明,由α-酮异戊酸生成葡萄糖在形成丙酰辅酶A之前的各种脱氢酶水平受到调节,但在支链α-酮酸脱氢酶反应之后。

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