Department of Gastroenterology, Nagoya University Graduate School of Medicine, Tsurumai-cho, Showa-ku, Japan.
Biochem Biophys Res Commun. 2010 Mar 5;393(2):303-7. doi: 10.1016/j.bbrc.2010.02.004. Epub 2010 Feb 6.
Branched-chain alpha-keto acid dehydrogenase (BCKDH) kinase (BDK) is responsible for the regulation of BCKDH complex, which is the rate-limiting enzyme in the catabolism of branched-chain amino acids (BCAAs). In the present study, we investigated the expression and activity of hepatic BDK in spontaneous type 2 diabetes using hyperinsulinemic Zucker diabetic fatty rats aged 9weeks and hyperglycemic, but not hyperinsulinemic rats aged 18weeks. The abundance of hepatic BDK mRNA and total BDK protein did not correlate with changes in serum insulin concentrations. On the other hand, the amount of BDK bound to the complex and its kinase activity were correlated with alterations in serum insulin levels, suggesting that hyperinsulinemia upregulates hepatic BDK. The activity of BDK inversely corresponded with the BCKDH complex activity, which was suppressed in hyperinsulinemic rats. These results suggest that insulin regulates BCAA catabolism in type 2 diabetic rats by modulating the hepatic BDK activity.
支链α-酮酸脱氢酶(BCKDH)激酶(BDK)负责调节 BCKDH 复合物,该复合物是支链氨基酸(BCAA)分解代谢的限速酶。在本研究中,我们使用 9 周龄的自发性 2 型糖尿病高脂胰岛素 Zucker 肥胖大鼠和 18 周龄的高血糖但非高胰岛素血症大鼠研究了肝 BDK 的表达和活性。肝 BDK mRNA 的丰度和总 BDK 蛋白与血清胰岛素浓度的变化没有相关性。另一方面,与复合物结合的 BDK 量及其激酶活性与血清胰岛素水平的变化相关,提示高胰岛素血症上调肝 BDK。BDK 的活性与 BCKDH 复合物活性呈负相关,而在高胰岛素血症大鼠中该复合物活性受到抑制。这些结果表明,胰岛素通过调节肝 BDK 活性来调节 2 型糖尿病大鼠的支链氨基酸分解代谢。