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Featured Article: Inhibition of diabetic cataract by glucose tolerance factor extracted from yeast
Nitsa Mirsky1, Revital Cohen2, Anat Eliaz2
1Department of Biology, Faculty of Natural Sciences, University of Haifa at Oranim, Tivon 3600600, Israel nmirsky@bezeqint.net.
Abstract:
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 (450 mg%). 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.
Insights
Glucose tolerance factor (GTF) prevents cataracts in diabetic rats and bovine lenses. GTF protects the eye lens from high glucose damage, reducing oxidative stress and preserving optical quality.
Area of Science:
- Ophthalmology
- Endocrinology
- Biochemistry
Background:
- Diabetes mellitus is a leading cause of various complications, including cataracts.
- Hyperglycemia in diabetes increases polyol concentration and protein glycation in the lens, leading to oxidative stress.
- Reactive Oxygen Species (ROS) contribute to lens protein damage and cataract formation.
Purpose of the Study:
- To investigate the damaging effects of high glucose on the eye lens.
- To evaluate the protective potential of glucose tolerance factor (GTF) against high glucose-induced lens damage.
- To assess GTF's effects both in vivo and in vitro.
Main Methods:
- In vivo: Streptozotocin (STZ)-induced diabetic rats were treated with GTF and compared to untreated diabetic and healthy control rats.
- In vitro: Bovine lenses were incubated in normal or high glucose conditions, with and without GTF, and optical quality was measured daily.
- Biochemical analysis assessed aldose reductase activity, Na+/K+-ATPase activity, and soluble cortical lens proteins.
Main Results:
- Diabetic rats treated with GTF showed prevention or reduction in cataract development compared to untreated diabetic rats.
- In vitro, high glucose induced optical damage to lenses, which was prevented by GTF addition.
- GTF mitigated the destructive effects of high glucose on lens epithelial cell enzymes and prevented the decrease in soluble lens proteins.
Conclusions:
- GTF exhibits significant anticataractogenic properties.
- GTF protects the eye lens from hyperglycemia-induced damage by reducing oxidative stress and preserving lens structure and function.
- GTF holds potential for preventing or treating diabetic cataracts.
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