Shobhaben Pratapbhai Patel School of Pharmacy & Technology Management, SVKM's NMIMS, V.L. Mehta Road, Vile Parle (West), Mumbai 400056, India.
Shobhaben Pratapbhai Patel School of Pharmacy & Technology Management, SVKM's NMIMS, V.L. Mehta Road, Vile Parle (West), Mumbai 400056, India.
Life Sci. 2021 Jan 15;265:118779. doi: 10.1016/j.lfs.2020.118779. Epub 2020 Nov 17.
The present study was designed to check the effect of daidzein in the management of diabetic retinopathy.
Streptozotocin at dose 55 mg/kg was used for inducing diabetes in rats. After 28 days of diabetic induction, animals were treated with daidzein at dose 25, 50, and 100 mg/kg for the next 28 days. Electroretinography, estimation of plasma glucose, lactate dehydrogenase, aldose reductase, sorbitol dehydrogenase and oxidative stress parameters were performed at the end of the study. Histopathology of retina was carried out at the end of the study.
Diabetic control animals showed a significant increase in levels of plasma glucose and plasma lactate dehydrogenase (p < 0.001). Treatment with daidzein at a dose of 50 and 100 mg/kg significantly reduced the elevated level of blood glucose (p < 0.01 and p < 0.01). Whereas, treatment with daidzein at a dose 100 mg/kg significantly reduced the elevated level of lactate dehydrogenase in plasma after 28 days of treatment (p < 0.01). Treatment with daidzein at a dose of 100 mg/kg significantly reduced the level of aldose reductase and sorbitol dehydrogenase (p < 0.01 and p < 0.001 respectively). Electroretinography revealed that daidzein treatment at a dose of 100 mg/kg significantly prevented the change in 'a' and 'b' wave amplitude and latency. Oxidative stress was also found to be significantly reduced after 28 days of daidzein treatment. Histopathological findings showed a reduction in retinal thickness after daidzein treatment.
Daidzein treatment protected retina from damage in hyperglycaemic conditions. Thus, Daidzein can be considered as an effective treatment option for diabetic retinopathy.
本研究旨在考察大豆苷元在糖尿病性视网膜病变治疗中的作用。
用 55mg/kg 的链脲佐菌素诱导大鼠糖尿病。糖尿病诱导 28 天后,动物用 25、50 和 100mg/kg 的大豆苷元治疗 28 天。研究结束时进行视网膜电图、血浆葡萄糖、乳酸脱氢酶、醛糖还原酶、山梨醇脱氢酶和氧化应激参数的测定。研究结束时进行视网膜组织病理学检查。
糖尿病对照组动物的血浆葡萄糖和血浆乳酸脱氢酶水平显著升高(p<0.001)。大豆苷元 50 和 100mg/kg 剂量治疗可显著降低血糖升高水平(p<0.01 和 p<0.01)。而大豆苷元 100mg/kg 剂量治疗可显著降低治疗 28 天后血浆中乳酸脱氢酶的升高水平(p<0.01)。大豆苷元 100mg/kg 剂量治疗可显著降低醛糖还原酶和山梨醇脱氢酶的水平(p<0.01 和 p<0.001)。视网膜电图显示,大豆苷元 100mg/kg 剂量治疗可显著防止“a”和“b”波幅度和潜伏期的变化。28 天大豆苷元治疗后,氧化应激也明显降低。组织病理学检查发现,大豆苷元治疗后视网膜厚度减少。
大豆苷元治疗可保护视网膜免受高血糖损伤。因此,大豆苷元可作为糖尿病性视网膜病变的有效治疗选择。