Hwang Jiyi, Jung Ji Seung, Kim Donghee, Kwon Myeongjee, Yong Jungyeon, Yoon Haerin, Park Kyung-Mee
Laboratory of Veterinary Ophthalmology, College of Veterinary Medicine, Chungbuk National University, Cheongju, Republic for Korea.
Laboratory of Veterinary Ophthalmology, College of Veterinary Medicine, Chungbuk National University, Cheongju, Republic for Korea
In Vivo. 2025 Jan-Feb;39(1):132-145. doi: 10.21873/invivo.13811.
BACKGROUND/AIM: Diabetic retinopathy (DR), a complication of diabetes, causes damage to retinal blood vessels and can lead to vision impairment. Persistent high blood glucose levels contribute to this damage, and despite ongoing research, effective treatment options for DR remain limited. Dimethyl sulfoxide (DMSO) has shown anti-inflammatory and antioxidant properties in both in vivo and in vitro studies; however, its potential as an anti-inflammatory agent in the context of DR has not yet been explored. This study aimed to assess the effects of subconjunctival injection of DMSO on the progression of DR.
DR was induced in rats using intraperitoneal injections of streptozotocin (55 mg/kg), confirmed by measuring blood glucose levels and electroretinography (ERG). The rats were divided into five groups: a normal control group (CON), a DR control group receiving PBS injections (DMSO 0), and three DR groups receiving different concentrations of DMSO (98%, 50%, and 10%). Retinal function was evaluated using ERG at weeks 10 and 14, and histological analysis at week 16.
The DMSO 50 group had significantly higher B-wave amplitude in ERG compared to the DMSO 0 group (p<0.05). Flicker response amplitudes were also significantly greater in the DMSO 50 and DMSO 10 groups compared to DMSO 0 (p<0.05). Histological examination revealed thinner retinal layers in the DMSO 0 group compared to the CON group, while the DMSO-treated groups showed improved retinal thickness.
Subconjunctival injection of 50% DMSO appears to improve retinal function in a rat model of DR.
背景/目的:糖尿病视网膜病变(DR)是糖尿病的一种并发症,会损害视网膜血管并可能导致视力障碍。持续的高血糖水平会导致这种损害,尽管研究不断,但DR的有效治疗选择仍然有限。二甲基亚砜(DMSO)在体内和体外研究中均显示出抗炎和抗氧化特性;然而,其在DR背景下作为抗炎剂的潜力尚未得到探索。本研究旨在评估结膜下注射DMSO对DR进展的影响。
通过腹腔注射链脲佐菌素(55mg/kg)诱导大鼠患DR,并通过测量血糖水平和视网膜电图(ERG)进行确认。将大鼠分为五组:正常对照组(CON)、接受PBS注射的DR对照组(DMSO 0)以及接受不同浓度DMSO(98%、50%和10%)的三个DR组。在第10周和第14周使用ERG评估视网膜功能,并在第16周进行组织学分析。
与DMSO 0组相比,DMSO 50组的ERG中B波振幅显著更高(p<0.05)。与DMSO 0组相比,DMSO 50组和DMSO 10组的闪烁反应振幅也显著更大(p<0.05)。组织学检查显示,与CON组相比,DMSO 0组的视网膜层更薄,而DMSO治疗组的视网膜厚度有所改善。
结膜下注射50%DMSO似乎可改善DR大鼠模型的视网膜功能。