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Metabolic surgery improves insulin resistance through the reduction of gut-secreted heat shock proteins

机译:代谢外科手术通过减少肠道分泌的热休克蛋白改善胰岛素抵抗

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摘要

Metabolic surgery improves insulin resistance and is associated with the remission of type 2 diabetes, but the mechanisms involved remain unknown. We find that human jejunal mucosa secretes heat shock proteins (HSPs) in vitro, in particular HSP70 and GRP78. Circulating levels of HSP70 are higher in people resistant to insulin, compared to the healthy and normalize after duodenal–jejunal bypass. Insulin sensitivity negatively correlates with the plasma level of HSP70, while body mass index does not. A high-energy diet increases the circulating levels of HSP70 and insulin resistance. HSP70 stimulates the accumulation of lipid droplets and inhibits Ser473 phosphorylation of Akt and glucose uptake in immortalized liver cells and peripheral blood cells. Serum depleted of HSPs, as well as the serum from the insulin-resistant people subjected to a duodenal–jejunal bypass, reverse these features, identifying gut-secreted HSPs as possible causes of insulin resistance. Duodenal–jejunal bypass might reduce the secretion of HSPs either by shortening the food transit or by decreasing the fat stimulation of endocrine cells.
机译:代谢外科手术可改善胰岛素抵抗,并与2型糖尿病的缓解相关,但涉及的机制尚不清楚。我们发现人空肠黏膜在体外分泌热休克蛋白(HSPs),尤其是HSP70和GRP78。与健康人相比,十二指肠-空肠旁路术后正常人的胰岛素抵抗中HSP70的循环水平更高。胰岛素敏感性与HSP70的血浆水平呈负相关,而体重指数则与之无关。高能量饮食会增加HSP70的循环水平和胰岛素抵抗。 HSP70刺激脂质滴的积累,并抑制永生化肝细胞和外周血细胞中Akt的Ser473磷酸化和葡萄糖摄取。缺乏HSP的血清,以及接受十二指肠-空肠搭桥的胰岛素抵抗人群的血清,可逆转这些特征,从而确定肠道分泌的HSPs可能是胰岛素抵抗的原因。十二指肠-空肠旁路可以通过缩短食物运输或减少脂肪对内分泌细胞的刺激来减少HSP的分泌。

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