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Improvement in Diabetic Retinopathy through Protection against Retinal Apoptosis in Spontaneously Diabetic Torii Rats Mediated by Ethanol Extract of Osteomeles schwerinae CK Schneid

Authors
Kim, Chan-SikKim, JunghyunKim, Young SookJo, KyuhyungLee, Yun MiJung, Dong HoLee, Ik SooKim, Joo-HwanKim, Jin Sook
Issue Date
4-Mar-2019
Publisher
MDPI
Keywords
Osteomeles schwerinae; diabetic retinopathy (DR); spontaneously diabetic Torii (SDT) rat; human retinal microvascular endothelial cells (HRMECs); advanced glycation end products (AGEs); retinal apoptosis; oxidative stress; mitochondrial function; adjunctive effect; combination therapy
Citation
NUTRIENTS, v.11, no.3
Journal Title
NUTRIENTS
Volume
11
Number
3
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/1696
DOI
10.3390/nu11030546
ISSN
2072-6643
Abstract
Retinal apoptosis plays a critical role in the progression of diabetic retinopathy (DR), a common diabetic complication. Currently, the tight control of blood glucose levels is the standard approach to prevent or delay the progression of DR. However, prevalence of DR among diabetic patients remains high. Focusing on natural nutrients or herbal medicines that can prevent or delay the onset of diabetic complications, we administered an ethanol extract of the aerial portion of Osteomeles schwerinae (OSSCE), a Chinese herbal medicine, over a period of 17 weeks to spontaneously diabetic Torii (SDT) rats. OSSCE was found to ameliorate retinal apoptosis through the regulation of advanced glycation end product (AGE) accumulation, oxidative stress, and mitochondrial function via the inhibition of NF-kappa B activity, in turn, through the downregulation of PKC delta, P47phox, and ERK1/2. We further demonstrated in 25 mM glucose-treated human retinal microvascular endothelial cells (HRMECs) that hyperoside (3-O-galactoside-quercetin), quercitrin (3-O-rhamnoside-quercetin), and 2 ''-O-acetylvitexin (8-C-(2 ''-O-acetyl-glucoside)-apigenin) were the active components of OSSCE that mediated its pharmacological action. Our results provide evidence that OSSCE is a powerful agent that may directly mediate a delay in the development or disease improvement in patients of DR.
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