Ishophloroglucin A Isolated from Ishige okamurae Protects Glomerular Cells from Methylglyoxal-Induced Diacarbonyl Stress and Inhibits the Pathogenesis of Diabetic Nephropathy.

IF 5.4 2区 医学 Q1 CHEMISTRY, MEDICINAL Marine Drugs Pub Date : 2025-01-20 DOI:10.3390/md23010048
Chi-Heung Cho, Min-Gyeong Kim, Bomi Ryu, Sang-Hoon Lee
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Abstract

Ishige okamurae (I. okamuare), an edible brown alga, is rich in isophloroglucin A (IPA) phlorotannin compounds and is effective in preventing diseases, including diabetes. We evaluated its anti-glycation ability, intracellular reactive oxygen species scavenging activity, inhibitory effect on the accumulation of intracellular MGO/MGO-derived advanced glycation end products (AGE), and regulation of downstream signaling pathways related to the AGE-receptor for AGEs (RAGE) interaction. IPA (0.2, 1, and 5 μM) demonstrated anti-glycation ability by inhibiting the formation of glucose-fructose-BSA-derived AGEs by up to 54.63% compared to the untreated control, reducing the formation of irreversible cross-links between MGO-derived AGEs and collagen by 67.68% and the breaking down of existing cross-links by approximately 91% (p < 0.001). IPA protected cells from MGO-induced oxidative stress by inhibiting intracellular MGO accumulation (untreated cells: 1.62 μg/mL, MGO treated cells: 25.27 μg/mL, and IPA 5 μM: 11.23 μg/mL) (p < 0.001) and AGE generation and inhibited MGO-induced renal cell damage via the downregulation of MGO-induced RAGE protein expression (relative protein expression levels of MGO treated cells: 9.37 and IPA 5 μM:1.74) (p < 0.001). Overall, these results suggest that IPA has the potential to be utilized as a useful natural agent for the prevention and management of AGE-related diabetic nephropathy, owing to its strong anti-glycation activity.

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Ishige okamurae中分离的isophloroglucin A保护肾小球细胞免受甲基乙二醛诱导的二羰基应激并抑制糖尿病肾病的发病机制。
石重okamurae (I. okamuare)是一种可食用的褐藻,含有丰富的异光葡聚糖A (IPA)绿单素化合物,对预防包括糖尿病在内的疾病有效。我们评估了其抗糖基化能力、细胞内活性氧清除活性、对细胞内MGO/MGO衍生的晚期糖基化终产物(AGE)积累的抑制作用,以及与AGE受体(RAGE)相互作用相关的下游信号通路的调节作用。与未处理的对照组相比,IPA(0.2、1和5 μM)通过抑制葡萄糖-果糖- bsa衍生的AGEs形成高达54.63%,减少mgo衍生的AGEs与胶原之间不可逆交联的形成67.68%,并减少现有交联的破坏约91% (p < 0.001),显示出抗糖基化能力。IPA通过抑制MGO在细胞内的积累(未处理细胞:1.62 μg/mL, MGO处理细胞:25.27 μg/mL, IPA 5 μM: 11.23 μg/mL) (p < 0.001)和AGE的产生来保护MGO诱导的氧化应激细胞,并通过下调MGO诱导的RAGE蛋白表达(MGO处理细胞的相对蛋白表达水平:9.37,IPA 5 μM:1.74)来抑制MGO诱导的肾细胞损伤(p < 0.001)。总之,这些结果表明IPA由于其强大的抗糖基化活性,有可能被用作一种有用的天然药物来预防和治疗age相关的糖尿病肾病。
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来源期刊
Marine Drugs
Marine Drugs 医学-医药化学
CiteScore
9.60
自引率
14.80%
发文量
671
审稿时长
1 months
期刊介绍: Marine Drugs (ISSN 1660-3397) publishes reviews, regular research papers and short notes on the research, development and production of drugs from the sea. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible, particularly synthetic procedures and characterization information for bioactive compounds. There is no restriction on the length of the experimental section.
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