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Featured Article Inhibition of diabetic cataract by glucose tolerance factor extracted from yeast

机译:酵母提取的葡萄糖耐量因子对糖尿病性白内障的抑制作用

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Diabetes leads to many complications; among them is the development of cataract. Hyperglycemia brings to increased polyol concentration in the lens, to glycation of lens proteins, and to elevated level of ROS (Reactive Oxygen Species) causing oxidative stress. The glucose tolerance factor (GTF) was found by several groups to decrease hyperglycemia and oxidative stress both in diabetic animals and humans. The aim of our study was to explore the damages induced by high glucose to the eye lens and to assess the protective effects of GTF both in vivo and in vitro. The in vivo study included control healthy rats, streptozotocin (STZ) diabetic untreated rats, and STZ diabetic rats orally treated with 15 doses of GTF. The diabetic untreated rats developed cataracts, whereas the development of cataract was totally or partially prevented in GTF treated animals. In vitro studies were done on bovine lenses incubated for 14 days. Half of the lenses were incubated in normal glucose conditions, and half in high glucose conditions (450mg%). To one group of the normal or high glucose condition GTF was added. The optical quality of all the lenses was measured daily by an automated scanning laser system. The control lenses, whether with or without GTF addition, did not show any reduction in their quality. High glucose conditions induced optical damage to the lenses. Addition of GTF to high glucose conditions prevented this damage. High glucose conditions affected the activity of aldose reductase and sodium potassium ATPase in lens epithelial cell. Addition of GTF decreased the destructive changes induced by high glucose conditions. The amount of soluble cortical lens proteins was decreased and structural changes were detected in lenses incubated in high glucose medium. These changes could be prevented when GTF was added to high glucose medium. Our findings demonstrate the anticataractogenic potential of GTF.
机译:糖尿病导致许多并发症。其中包括白内障的发展。高血糖症会导致晶状体中多元醇浓度升高,晶状体蛋白糖基化,以及引起氧化应激的ROS(活性氧)水平升高。葡萄糖耐量因子(GTF)被几组人发现,可降低糖尿病动物和人类的高血糖症和氧化应激。我们研究的目的是探讨高糖诱导的对晶状体的损害,并评估GTF在体内和体外的保护作用。体内研究包括对照组健康大鼠,未经治疗的链脲佐菌素(STZ)糖尿病大鼠和经15剂量GTF口服治疗的STZ糖尿病大鼠。未治疗的糖尿病大鼠发展为白内障,而在GTF治疗的动物中,白内障的发展被完全或部分阻止。在温育14天的牛晶状体上进行了体外研究。一半的镜片在正常葡萄糖条件下孵育,一半在高葡萄糖条件下(450mg%)孵育。向正常或高血糖状态的一组中添加GTF。每天通过自动扫描激光系统测量所有镜片的光学质量。不论是否添加GTF,对照镜片的质量均未降低。高葡萄糖条件会引起镜片的光学损伤。在高葡萄糖条件下添加GTF可以防止这种损害。高葡萄糖条件影响晶状体上皮细胞中醛糖还原酶和钠钾ATP酶的活性。 GTF的添加减少了由高葡萄糖条件引起的破坏性变化。在高葡萄糖培养基中孵育的晶状体中可溶性皮质晶状体蛋白的量减少,并且检测到结构变化。当将GTF添加到高葡萄糖培养基中时,可以防止这些变化。我们的发现证明了GTF的抗白内障潜力。

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