Nolan Christopher J, Prentki Marc
Department of Endocrinology, The Canberra Hospital, Medical School, The Australian National University, Garran, ACT 2605, Australia.
Trends Endocrinol Metab. 2008 Oct;19(8):285-91. doi: 10.1016/j.tem.2008.07.006. Epub 2008 Sep 6.
The pancreatic beta-cell senses blood nutrient levels and is modulated by neurohormonal signals so that it secretes insulin according to the need of the organism. Nutrient sensing involves marked metabolic activation, resulting in the production of coupling signals that promote insulin biosynthesis and secretion. The beta-cell's high capacity for nutrient sensing, however, necessitates reduced protection to nutrient toxicity. This potentially explains why in susceptible individuals, chronic fuel surfeit results in beta-cell failure and type 2 diabetes. Here we discuss recent insights into first, the biochemical basis of beta-cell signaling in response to glucose, amino acids and fatty acids, and second, beta-cell nutrient detoxification. We emphasize the emerging role of glycerolipid/fatty acid cycling in these processes.
胰腺β细胞感知血液中的营养水平,并受到神经激素信号的调节,从而根据机体的需要分泌胰岛素。营养感知涉及显著的代谢激活,导致产生促进胰岛素生物合成和分泌的偶联信号。然而,β细胞对营养感知的高能力需要降低对营养毒性的保护。这可能解释了为什么在易感个体中,长期的营养过剩会导致β细胞功能衰竭和2型糖尿病。在这里,我们首先讨论关于β细胞对葡萄糖、氨基酸和脂肪酸作出反应的信号传导的生化基础,其次讨论β细胞的营养解毒方面的最新见解。我们强调甘油olipid/脂肪酸循环在这些过程中日益重要的作用。 (注:原文中“glycerolipid”可能有误,推测可能是“glycerolipid”,暂按此翻译)