Pancreatic insulin release in vitamin C-deficient senescence marker protein-30/gluconolactonase knockout mice.

Pancreatic insulin release in vitamin C-deficient senescence marker protein-30/gluconolactonase knockout mice.
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DOI:
10.3164/jcbn.11-52
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发表时间:
2012-03
影响因子:
2.4
通讯作者:
Hasegawa G
Hasegawa G
中科院分区:
医学4区
文献类型:
--
作者:
Senmaru T;Yamazaki M;Okada H;Asano M;Fukui M;Nakamura N;Obayashi H;Kondo Y;Maruyama N;Ishigami A;Hasegawa G

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我们最近确定衰老标记蛋白-30为内酯水解酶β-内酯酶,其参与维生素C的生物合成。在这项研究中,我们研究了维生素C对胰岛β细胞分泌胰岛素的影响,使用衰老标记蛋白-30/β-内酯酶基因敲除小鼠。在腹膜内葡萄糖耐量试验中,维生素C缺乏的衰老标记蛋白-30/β-内酯酶敲除小鼠表现出葡萄糖耐量受损,在攻击后30和120分钟血液胰岛素水平显著低于野生型小鼠(p<0.01-0.05)。相比之下,维生素C充足的衰老标志物蛋白-30/β-内酯酶敲除小鼠仅在攻击后30分钟时间点表现出显著更高的血糖和更低的胰岛素(p<0.05)。无论维生素C状况如何,衰老标志物蛋白-30/葡萄糖酸内酯酶敲除小鼠均表现出胰岛素敏感性增强。胰岛的静态孵育显示,相对于野生型小鼠,仅在维生素C缺陷型SMP 30/GNL敲除小鼠中,20 mM葡萄糖刺激的胰岛素分泌和胰岛ATP产生在60分钟时显著降低(p<0.05)。这些结果表明,维生素C的作用位点位于糖酵解和线粒体氧化磷酸化之间,而SMP 30缺陷本身损害了胰岛素分泌途径的远端部分。
We recently identified senescence marker protein-30 as the lactone-hydrolyzing enzyme gluconolactonase, which is involved in vitamin C biosynthesis. In this study, we investigated the effects of vitamin C on insulin secretion from pancreatic β-cells using senescence marker protein-30/gluconolactonase knockout mice. In intraperitoneal glucose tolerance tests, vitamin C-deficient senescence marker protein-30/gluconolactonase knockout mice demonstrated impaired glucose tolerance with significantly lower blood insulin levels at 30 and 120 min post-challenge than in wild type mice (p<0.01–0.05). In contrast, vitamin C-sufficient senescence marker protein-30/gluconolactonase knockout mice demonstrated significantly higher blood glucose and lower insulin only at the 30 min post-challenge time point (p<0.05). Senescence marker protein-30/gluconolactonase knockout mice showed enhanced insulin sensitivity regardless of vitamin C status. Static incubation of islets revealed that 20 mM glucose-stimulated insulin secretion and islet ATP production were significantly decreased at 60 min only in vitamin C-deficient SMP30/GNL knockout mice relative to wild type mice (p<0.05). These results indicate that the site of vitamin C action lies between glycolysis and mitochondrial oxidative phosphorylation, while SMP30 deficiency itself impairs the distal portion of insulin secretion pathway.
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