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首页> 外文期刊>Biochemical and Biophysical Research Communications >ER stress attenuation by Aloe-derived polysaccharides in the protection of pancreatic beta-cells from free fatty acid-induced lipotoxicity
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ER stress attenuation by Aloe-derived polysaccharides in the protection of pancreatic beta-cells from free fatty acid-induced lipotoxicity

机译:通过芦荟衍生的多糖在免受游离脂肪酸诱导的脂毒性保护胰腺β细胞中的ER应力衰减

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摘要

Insulin resistance, a pathophysiology of type 2 diabetes, is associated with obesity. Lipotoxicity in obesity leads to the dysfunction and death of pancreatic beta-cells and inadequate insulin production, thereby aggravating type 2 diabetes. The present study was conducted to determine the effect of Aloe vera polysaccharides (APs) as an anti-hyperglycemic agent and their mechanisms of action. Gel polysaccharides from Aloe extracts were separated using ultrafiltration devices with molecular weight-cutoff membranes, and the protective effect of APs on pancreatic beta-cells in response to free fatty acids (FFAs) was determined. Hamster pancreatic beta-cell line HIT-T15 was treated with palmitate and APs to analyze cellular responses. We observed a large number of apoptotic beta-cell death after treatment with high levels of palmitate, but this was efficiently prevented by the addition of APs in a dose-dependent manner. It was found that the anti-apoptotic properties of APs were largely due to the relief of endoplasmic reticulum (ER) stress signaling. APs were effective in interfering with the FFA-induced activation of the PERK and IRE1 pathways as well as ROS generation, thereby protecting pancreatic beta-cells from lipotoxicity. Although variation in the chain length of APs can influence the activity of FFA-mediated ER stress signaling in different ways, polysaccharide mixtures with molecular weights higher than 50 kDa showed greater antiapoptotic and antioxidant activity in beta-cells. After oral administration of APs, markedly lowering fasting blood glucose levels were observed in db/db mice, providing evidence of the potential of APs as an alternative insulin sensitizer. Therefore, it was concluded that APs have a protective effect against type 2 diabetes by modulating obesity-induced ER stress in pancreatic beta-cells. (C) 2018 Elsevier Inc. All rights reserved.
机译:胰岛素抵抗,2型糖尿病的病理生理学与肥胖有关。肥胖症的脂毒性导致胰腺β细胞的功能障碍和死亡,胰岛素产生不足,因此加重2型糖尿病。进行本研究以确定芦荟多糖(APS)作为抗高血糖剂的影响及其作用机制。使用具有分子量截止膜的超滤装置分离来自芦荟提取物的凝胶多糖,并测定APS对胰腺β细胞对游离脂肪酸(FFAs)的保护作用。 Hamster胰腺β-细胞系HIT-T15用棕榈酸盐和AP处理,分析细胞反应。在用高水平的棕榈酸盐处理后,我们观察到大量凋亡β细胞死亡,但通过以剂量依赖性方式加入APS有效地防止了这一点。发现AP的抗凋亡性质主要是由于内质网(ER)应激信号传导的浮雕。 APS有效地干扰FFA诱导的PERK和IS1途径的活化以及ROS产生,从而保护胰腺β细胞免受脂毒性。尽管AP的链长的变化可以以不同方式影响FFA介导的ER应激信号传导的活性,但分子量高于50kDa的多糖混合物在β细胞中显示出更大的抗曝光和抗氧化活性。口服施用APS后,在DB / DB小鼠中观察到显着降低空腹血糖水平,提供APS作为替代胰岛素敏化剂的潜力的证据。因此,得出结论,APS通过调节肥胖诱导的胰腺β细胞中的肥胖诱导的ER应力对2型糖尿病具有保护作用。 (c)2018年Elsevier Inc.保留所有权利。

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