Natural aldose reductase inhibitors for treatment and prevention of diabetic cataract: A review

Q3 Medicine
N. Daoudi, Omar Bouziane, M. Bouhrim, M. Bnouham
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引用次数: 1

Abstract

Summary Introduction: Aldose reductase (AR) is an enzyme that catalyzes the reduction of glucose to sorbitol responsible for the development of diabetic complications like cataracts. Medicinal plants contain several phytocompounds that can inhibit this enzyme. Objective: The purpose of this review is to cite medicinal plants that have been tested for their ability to inhibit aldose reductase and consequently prevent cataracts and classify the major isolated compounds that have this activity. Methods: We reviewed 154 articles published between 1954 and 2020 in English via three databases: ScienceDirect, Web of Science, and PubMed. We have classified the plants that showed a significant anti-cataract effect, in the form of a list including the scientific and family names of each plant. Also, we have cited the IC50 values and the active constituents of each plant that showed inhibitory activity towards AR. Results: We have described 38 herbs belonging to 29 families. Besides, 47 isolated compounds obtained from the cited herbs have shown an AR inhibitory effect: luteolin, luteolin-7-O-β-D-glucopyranoside, apigenin, 3,5-di-O-caffeoyl-epi-quinic acid, delphinidin 3-O-β-galactopyranoside-3’-O-β-glucopyranoside, 3,5-di-O-caffeoylquinic acid methyl ester, andrographolide, 1,2,3,6-tetra-O-galloyl-β-D-glucose, 1,2,4,6-tetra-O-galloyl-β-D-glucose, 7-(3-hydroxypropyl)-3-methyl-8-β-O-D-glucoside-2H-chromen-2-one, E-4-(60-hydroxyhex-30-en-1-yl)phenyl propionate, delphinidin 3-O-β-galactopyranoside-3’,5’-di-O-β-glucopyranoside, 1,2,3-tri-O-galloyl-β-D-glucose, 1,2,3,4,6-penta-O-galloyl-β-D-glucose, 1,2,6-tri-O-galloyl-β-D-glucose, 2-(4-hydroxy-3-methoxyphenyl)ethanol, (4-hydroxy-3-methoxyphenyl)methanol, trans-anethole, gallic acid 4-O-β-D-(6’-O-galloyl)-glucoside, β-glucogallin, puerariafuran, quercetin, gallic acid 4-O-β-D-glucoside, 2,5-dihydroxybenzoic acid, 4-(4-hydroxy-3-methoxyphenyl)-2-butanone, protocatechuic acid, trans-cinnamic acid, gallic acid, p-coumaric acid and syringic acid. Conclusion: natural therapy becomes an interesting alternative in the treatment and prevention of cataract by using medicinal plants rich in active compounds considered as AR inhibitors.
天然醛糖还原酶抑制剂治疗和预防糖尿病性白内障的研究进展
简介:醛糖还原酶(AR)是一种催化葡萄糖还原为山梨醇的酶,负责糖尿病并发症(如白内障)的发展。药用植物含有几种可以抑制这种酶的植物化合物。目的:本综述的目的是引用已经测试过抑制醛糖还原酶从而预防白内障的药用植物,并对具有这种活性的主要分离化合物进行分类。方法:我们通过ScienceDirect、Web of Science和PubMed三个数据库,回顾了1954年至2020年间发表的154篇英文文章。我们对表现出显著抗白内障作用的植物进行了分类,并列出了每种植物的学名和科名。此外,我们还引用了每种植物对AR表现出抑制活性的IC50值和活性成分。结果:我们描述了属于29个科的38种草药。此外,从所引用的草药中获得的47个分离的化合物显示出AR抑制作用:木犀草素、木犀草蛋白-7-O-β-D-吡喃葡糖苷、芹菜素、3,5-二-O-咖啡酰基-表奎宁酸、飞燕草素3-O-β-吡喃半乳糖苷-3'-O-β-葡萄糖苷、3,5-二-O-咖啡酰奎宁酸甲酯、穿心莲内酯、1,2,3,6-四-O-没食子酰基-β-D-葡萄糖、1,2,4,6-四-没食子酰-β-D--葡萄糖,7-(3-羟丙基)-3-甲基-8-β-O-D-葡萄糖苷-2H-色烯-2-酮,E-4-(60-羟基己基-30-烯-1-基)丙酸苯酯,飞燕草素3-O-β-吡喃半乳糖苷-3',5'-二-O-β-吡吡喃葡糖苷,1,2,3-三-O-没食子酰基-β-D-葡萄糖,1,2,3,4,6-五-O-没食子酰基-β-D葡萄糖,1,2,6-三-O-没食子酰-,没食子酸4-O-β-D-(6'-O-没食子酰基)-葡萄糖苷、β-葡糖没食子酸、葛根呋喃、槲皮素、没食子酸4-0-β-D-葡萄糖苷、2,5-二羟基苯甲酸、4-(4-羟基-3-甲氧基苯基)-2-丁酮、原儿茶酸、反式肉桂酸、没食子酸、对香豆酸和丁香酸。结论:利用富含活性化合物的药用植物作为AR抑制剂,自然疗法成为治疗和预防白内障的一种有趣的替代方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Herba Polonica
Herba Polonica Medicine-Complementary and Alternative Medicine
CiteScore
1.70
自引率
0.00%
发文量
5
审稿时长
14 weeks
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