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碲化合物AS101可提高SIRT1水平和活性,并预防2型糖尿病。

The Tellurium compound, AS101, increases SIRT1 level and activity and prevents type 2 diabetes.

作者信息

Halperin-Sheinfeld Meital, Gertler Asaf, Okun Eitan, Sredni Benjamin, Cohen Haim Y

机构信息

The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan 52900, Israel.

出版信息

Aging (Albany NY). 2012 Jun;4(6):436-47. doi: 10.18632/aging.100468.

Abstract

The histone deacetylase, SIRT1, plays a major role in glucose regulation and lipid metabolism. Ammonium Trichloro (dioxoethylene-o,o') Tellurate, AS101, is a potent in vitro and in vivo immunomodulator, with several potential therapeutic applications. AS101 administration resulted in upregulation of SIRT1 protein expression and activity. These effects were associated with decreased levels of serum insulin like growth factor-1 (IGF-1) and of insulin. The properties of AS101 prompted us to investigate its potential therapeutic role in rats with type 2 diabetes (T2D). T2D was induced by a high fat diet combined with a low dose of Streptozotocin (STZ). Treatment with AS101 before manifestation of hyperglycemia, resulted in increased insulin sensitivity, and decreased blood glucose levels, and prevented symptoms of diabetes including defective glucose clearance, fatty liver, and abnormal distribution of insulin-producing beta cells in the pancreas. Treatment after disease emergence resulted in partial restoration of normal glucose homeostasis. Diabetic rats showed a reduction in liver SIRT1 levels. In both treatment regimens the reduction in SIRT1 levels in the liver were blocked by AS101 consumption. Together, these findings demonstrate the therapeutic potential of AS101 for treating T2D, and for reversing impaired fat and glucose metabolism.

摘要

组蛋白脱乙酰酶SIRT1在葡萄糖调节和脂质代谢中起主要作用。三氯(二氧乙烯 - o,o')碲酸铵AS101是一种有效的体内外免疫调节剂,具有多种潜在的治疗应用。给予AS101导致SIRT1蛋白表达和活性上调。这些作用与血清胰岛素样生长因子-1(IGF-1)和胰岛素水平降低有关。AS101的特性促使我们研究其在2型糖尿病(T2D)大鼠中的潜在治疗作用。通过高脂肪饮食联合低剂量链脲佐菌素(STZ)诱导T2D。在高血糖症出现之前用AS101治疗,导致胰岛素敏感性增加,血糖水平降低,并预防糖尿病症状,包括葡萄糖清除缺陷、脂肪肝和胰腺中产生胰岛素的β细胞分布异常。疾病出现后进行治疗导致正常葡萄糖稳态部分恢复。糖尿病大鼠肝脏SIRT1水平降低。在两种治疗方案中,肝脏中SIRT1水平的降低都被AS101的消耗所阻断。总之,这些发现证明了AS101治疗T2D以及逆转脂肪和葡萄糖代谢受损的治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8825/3409680/47d7a55938f5/aging-04-436-g001.jpg

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