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积雪草酸对链脲佐菌素诱导的糖尿病大鼠视网膜氧化应激、炎症和生长因子的影响。

Effect of madecassic acid on retinal oxidative stress, inflammation and Growth Factors in streptozotocin-induced diabetic rats.

机构信息

Department of Ophthalmology, Shangrao Municipal Central Hospital, Shangrao, Jiangxi, 334000, China.

General Ophthalmology, GuangZhou Huangpu Ineye Hospital, Guangzhou, Guangdong,510700,China.

出版信息

Biochem Biophys Res Commun. 2024 Nov 26;735:150745. doi: 10.1016/j.bbrc.2024.150745. Epub 2024 Sep 25.

Abstract

Diabetic retinopathy (DR) is the leading cause of blindness and visual loss in people with diabetes. It has been suggested that the progression of DR is associated with chronic inflammation and oxidative stress. The aim of the present work was to evaluate the ability of the natural compound madecassic acid (MEA) to reverse the negative impact of streptozotocin (STZ) on retinal injury in rats. Diabetic rats induced by STZ were treated with MEA at the doses of 10 and 20 mg/kg bw for 8 weeks. The study compared the efficacy of the drug in controlling high blood sugar levels and its impact on therapeutic targets such as SOD, CAT, GPx, NF-κB, TNF-α, IL-6, IL-1β, VEGF, IGF, bFGF and Keap1/Nrf-2 pathway. The results showed that the treatment with MEA significantly restored the retinal SOD, CAT, and GPx levels in diabetic rats to the near-normal levels. Moreover, the level of inflammatory mediators (TNF-α, IL-1β, IL-6) and growth factors (VEGF, IGF, bFGF) was significantly lower in retinas of animals treated with MEA as compared to retinas of diabetic animals. The study also established that MEA administration reduced the NF-κB protein and altered the Nrf-2/Keap1 pathway thereby reducing oxidative stress and inflammation. Furthermore, the use of MEA prevented the progression of the retinal capillary basement membrane thickening. It has been found that MEA offers significant protection to the retina and therefore, the compound may be useful in the treatment of DR in humans.

摘要

糖尿病性视网膜病变(DR)是糖尿病患者失明和视力丧失的主要原因。有研究表明,DR 的进展与慢性炎症和氧化应激有关。本研究旨在评估天然化合物马卡因酸(MEA)逆转链脲佐菌素(STZ)对大鼠视网膜损伤的负面影响的能力。用 STZ 诱导糖尿病大鼠,用 MEA 以 10 和 20mg/kg bw 的剂量治疗 8 周。该研究比较了药物控制高血糖水平的疗效及其对 SOD、CAT、GPx、NF-κB、TNF-α、IL-6、IL-1β、VEGF、IGF、bFGF 和 Keap1/Nrf-2 途径等治疗靶点的影响。结果表明,MEA 治疗可显著恢复糖尿病大鼠视网膜中的 SOD、CAT 和 GPx 水平接近正常水平。此外,与糖尿病动物的视网膜相比,用 MEA 治疗的动物的视网膜中的炎症介质(TNF-α、IL-1β、IL-6)和生长因子(VEGF、IGF、bFGF)水平显著降低。该研究还表明,MEA 给药可降低 NF-κB 蛋白并改变 Nrf-2/Keap1 途径,从而减轻氧化应激和炎症。此外,MEA 的使用可阻止视网膜毛细血管基底膜增厚的进展。已经发现 MEA 对视网膜有显著的保护作用,因此,该化合物可能对人类 DR 的治疗有用。

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