首页|地榆皂苷Ⅱ通过PI3K/Akt/mTOR通路在体内外减轻糖尿病视网膜病变的作用机制研究

地榆皂苷Ⅱ通过PI3K/Akt/mTOR通路在体内外减轻糖尿病视网膜病变的作用机制研究

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目的 探讨地榆皂苷Ⅱ通过PI3K/Akt/mTOR通路对链脲佐菌素诱导的大鼠视网膜病变的影响。方法 通过ip链脲佐菌素 35 mg/kg建立糖尿病大鼠模型,通过高糖诱导的Müller细胞建立糖尿病细胞模型。采用ELISA法检测血清、视网膜和细胞上清液中细胞因子水平。采用试剂盒检测血清胰岛素和口服葡萄糖耐量(OGTT)、血清超氧化物歧化酶(SOD)活性和丙二醛(MDA)含量。通过苏木精-伊红(HE)染色评估视网膜组织的病理变化。采用Western blotting检测糖尿病小鼠视网膜组织和高糖诱导的Müller细胞中的磷脂酰肌醇 3-激酶(PI3K)/蛋白激酶B(Akt)/哺乳动物雷帕霉素靶蛋白(mTOR)信号通路蛋白表达水平。结果 与模型组相比,地榆皂苷Ⅱ显著降低血清胰岛素水平并改善OGTT;显著增加血清、视网膜和Müller细胞中的SOD并降低MDA水平。地榆皂苷Ⅱ还显著降低糖尿病大鼠和高糖诱导的Müller细胞中的血清和视网膜细胞因子。结论 地榆皂苷Ⅱ可抑制视网膜组织和高糖诱导的Müller细胞中的PI3K/Akt/mTOR信号通路,从而改善糖尿病视网膜病变。
Ziyuglycoside Ⅱ alleviates diabetic retinopathy in diabetes in vitro and in vivo based on PI3K/Akt/mTOR pathway
Objective To explore the effect of ziyuglycoside Ⅱ on diabetic retinopathy in streptozotocin-induced rats based on PI3K/Akt/mTOR pathway.Methods Rat model of diabetic retinopathy was established by intraperitoneal injection of streptozotocin 35mg/kg.Cell model of diabetic retinopathy was established by glucose-induced Müller cell.The levels of cytokines in serum,retina and cell supernatant were detected by ELISA.Serum insulin and OGTT,serum SOD activity and MDA content were measured by the kit.The pathological changes of retinal tissue were evaluated by HE staining.Western blotting was used to detect the PI3K/Akt/mTOR signaling pathway in retinal tissues of diabetic mice and Müller cells induced by high glucose.Results Compared with model group,ziyuglycoside Ⅱ significantly decreased serum insulin level and improved OGTT.SOD levels in serum,retina and Müller cells were significantly increased and MDA levels were decreased.ziyuglycoside Ⅱ also significantly reduced serum and retinal cytokines in diabetic rats and high-sugar-induced Müller cells.Conclusions Ziyuglycoside Ⅱ could inhibited PI3K/Akt/mTOR signal pathway in retina tissue and glucose-induced Müller cell.ziyuglycoside Ⅱ may improve retinopathy in diabetic retinopathy,oxidative stress and inflammation in the retina tissue of rats and glucose-induced Müller cell.

ziyuglycoside Ⅱdiabetic retinopathyPI3KAktmTORSODMDA

李光云、周霖、李鹏、叶柳、胡柱晴

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新乡医学院第一附属医院 临床药学学部,新乡 河南 453100

郑州大学第一附属医院 药学部,郑州 河南 450052

郑州大学第一附属医院 康复医学科,郑州 河南 450052

地榆皂苷Ⅱ 视网膜病变 磷脂酰肌醇3-激酶(PI3K) 蛋白激酶B(Akt) 哺乳动物雷帕霉素靶蛋白 超氧化物歧化酶 丙二醛

河南省科技攻关计划项目河南省高等学校重点科研项目

24210231126123A360018

2024

现代药物与临床
天津药物研究院,中国药学会

现代药物与临床

CSTPCD
影响因子:1.179
ISSN:1674-5515
年,卷(期):2024.39(10)
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