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酸性多糖通过抑制炎症改善 2 型糖尿病大鼠的胰岛素抵抗。

Acidic Polysaccharide Improves the Insulin Resistance in Type 2 Diabetic Rats by Inhibiting Inflammation.

机构信息

Department of Pharmacology, College of Pharmacy, Beihua University, Jilin, China.

Department of Endocrinology, Affiliated Hospital, Beihua University, Jilin, China.

出版信息

J Med Food. 2020 Apr;23(4):358-366. doi: 10.1089/jmf.2019.4469. Epub 2020 Mar 16.

DOI:10.1089/jmf.2019.4469
PMID:32181695
Abstract

Polysaccharide from has the effect of lowering blood glucose and improving insulin resistance (IR). However, its underlying mechanism remains unclear. In this study, a rat model of type 2 diabetes (T2D) was created to explore whether acidic polysaccharide (SCAP) would improve the IR in T2D rats by inhibiting inflammation. A combination of a high-fat diet and low dose of streptozotocin (STZ, 30 mg/kg, intraperitoneally) were administered to rats for establishing the T2D model. Then, these T2D rats were orally administered with SCAP (25, 50, or 100 mg/kg) for 8 weeks. The results indicated that SCAP significantly lowered the fasting blood glucose, elevated the fasting insulin, and improved glucose tolerance. SCAP also decreased the serum interleukin-1 (IL-1), interleukin-6 (IL-6), tumor necrosis factor- (TNF-), C-reactive protein (CRP), and nuclear factor-B (NF-B) levels, as well as their mRNA expression in the liver tissue. Further, SCAP significantly inhibited the upregulation of phosphorylated c-Jun N-terminal kinase (p-JNK) and NF-B protein, and it increased phosphorylated insulin receptor substrate-1 (p-IRS-1), phosphorylated phosphatidylinositol 3-kinase (p-PI3K), and phosphorylated protein kinase B (p-AKT) protein expression levels significantly. These results suggest that SCAP improves the IR in T2D rats by inhibiting inflammation.

摘要

从 中提取的多糖具有降血糖和改善胰岛素抵抗(IR)的作用。然而,其潜在机制尚不清楚。在本研究中,建立了 2 型糖尿病(T2D)大鼠模型,以探讨 是否酸性多糖(SCAP)通过抑制炎症来改善 T2D 大鼠的 IR。采用高脂饮食联合小剂量链脲佐菌素(STZ,30mg/kg,腹腔注射)建立 T2D 大鼠模型。然后,这些 T2D 大鼠连续 8 周口服 SCAP(25、50 或 100mg/kg)。结果表明,SCAP 可显著降低空腹血糖,提高空腹胰岛素水平,改善葡萄糖耐量。SCAP 还降低了血清白细胞介素-1(IL-1)、白细胞介素-6(IL-6)、肿瘤坏死因子-(TNF-)、C 反应蛋白(CRP)和核因子-B(NF-B)水平,以及肝脏组织中这些因子的 mRNA 表达。此外,SCAP 还显著抑制磷酸化 c-Jun N 末端激酶(p-JNK)和 NF-B 蛋白的上调,并显著增加磷酸化胰岛素受体底物-1(p-IRS-1)、磷酸化磷脂酰肌醇 3-激酶(p-PI3K)和磷酸化蛋白激酶 B(p-AKT)蛋白表达水平。这些结果表明,SCAP 通过抑制炎症改善 T2D 大鼠的 IR。

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