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Hydrogen sulfide treatment promotes glucose uptake by increasing insulin receptor sensitivity and ameliorates kidney lesions in type 2 diabetes

机译:硫化氢治疗通过增加胰岛素受体的敏感性促进葡萄糖的摄取,并改善2型糖尿病的肾脏损害

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Aims: To examine if hydrogen sulfide (H2S) can promote glucose uptake and provide amelioration in type 2 diabetes. Results: Treatment with sodium hydrosulfide (NaHS, an H2S donor) increased glucose uptake in both myotubes and adipocytes. The H2S gas solution showed similar effects. The NaHS effects were blocked by an siRNA-mediated knockdown of the insulin receptor (IR). NaHS also increased phosphorylation of the IR, PI3K, and Akt. In Goto-Kakizaki (GK) diabetic rats, chronic NaHS treatment (30 μmol·kg-1·day-1) decreased fasting blood glucose, increased insulin sensitivity, and increased glucose tolerance with increased phosphorylation of PI3K and Akt in muscles. Similar insulin-sensitizing effects of NaHS treatment were also observed in Wistar rats. Moreover, glucose uptake was reduced in the cells with siRNA-mediated knockdown of the H2S-generating enzyme cystathionine γ-lyase in the presence or absence of exogenous H2S. Moreover, chronic NaHS treatment reduced oxygen species and the number of crescentic glomeruli in the kidney of GK rats. Innovation and Conclusion: This study provides the first piece of evidence for the insulin-sensitizing effect of NaHS/H2S in the both in vitro and in vivo models of insulin resistance. Rebound Track: This work was rejected during a standard peer review and rescued by the Rebound Peer Review (Antoxid Redox Signal 16: 293-296, 2012) with the following serving as open reviewers: Jin-Song Bian, Samuel Dudley, Hideo Kimura, and Xian Wang. Antioxid. Redox Signal. 19, 5-23.
机译:目的:检查硫化氢(H2S)是否可以促进葡萄糖摄取并改善2型糖尿病。结果:用硫化氢钠(NaHS,H2S供体)治疗可增加肌管和脂肪细胞的葡萄糖摄取。 H2S气体溶液显示出相似的效果。 NaHS的作用被siRNA介导的胰岛素受体(IR)的敲低所阻断。 NaHS还增加了IR,PI3K和Akt的磷酸化。在五岛崎崎(GK)糖尿病大鼠中,慢性NaHS治疗(30μmol·kg-1·day-1)降低了空腹血糖,增加了胰岛素敏感性并增加了糖耐量,同时增加了肌肉中PI3K和Akt的磷酸化。在Wistar大鼠中也观察到了类似的NaHS治疗胰岛素致敏作用。此外,在存在或不存在外源H2S的情况下,通过siRNA介导的H2S生成酶胱硫醚γ-裂合酶的敲低可以降低细胞中的葡萄糖摄取。此外,慢性NaHS治疗可降低GK大鼠肾脏中的氧种类和新月肾小球数量。创新与结论:这项研究为NaHS / H2S在体外和体内胰岛素抵抗模型中的胰岛素增敏作用提供了第一条证据。反弹轨迹:这项工作在标准同行评审中被拒绝,并被反弹同行评审(Antoxid Redox Signal 16:293-296,2012)挽救,以下人员担任公开评审:Jin-Song Bian,Samuel Dudley,Hideo Kimura,和西安王。抗氧化。氧化还原信号。 19,5-23。

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