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作 者:柴青春 杨丽霞[2,3] 薛建军[2,3] 程涛[2,3] 张定华[2,3] 刘铜华[4]
机构地区:[1]瓜州县人民医院,甘肃酒泉736100 [2]甘肃省中医药研究院 [3]甘肃省中医院,甘肃兰州730050 [4]北京中医药大学,北京100029
出 处:《中国中医药信息杂志》2014年第10期58-60,共3页Chinese Journal of Information on Traditional Chinese Medicine
基 金:国家自然科学基金面上项目(30973909);甘肃省中医药科学技术研究课题(GZK-2011-13);北京中医药大学创新团队项目(2011-CXTD-19)
摘 要:目的探讨糖肾康防治糖尿病肾病的作用机制。方法将体外培养的人肾小管上皮细胞(HK-2)分为空白组、高糖诱导组(30 mmol/L D-葡萄糖)、对照组(30 mmol/L D-葡萄糖+10%空白血清)和糖肾康低(30 mmol/L D-葡萄糖+5%糖肾康药物血清)、中(30 mmol/L D-葡萄糖+10%糖肾康药物血清)、高剂量组(30 mmol/L D-葡萄糖+20%糖肾康药物血清)。药物干预24、48 h后,ELISA检测细胞培养上清液中基质金属蛋白酶-9(MMP-9)及其抑制剂-1(TIMP-1)的含量。结果 HK-2经高糖诱导后,MMP-9分泌显著减少,TIMP-1分泌显著增加,与空白组比较,差异有统计学意义(P<0.05);经糖肾康干预后,MMP-9含量显著上升,TIMP-1含量显著下降,与高糖诱导组比较,差异有统计学意义(P<0.05)。结论糖肾康通过调控高糖诱导人肾HK-2纤维化因子的分泌,达到防治糖尿病肾病的目的。Objective To explore the mechanism of Tangshenkang in the prevention and treatment of diabetic nephropathy. Methods HK-2 cells were cultured in vitro and divided into control group, high glucose group (30 mmol/L D-glucose), control group (30 mmol/L D-glucose+10% animal serum), and Tangshenkang drug-containing serum therapy groups (30 mmol/L D-glucose+5%low concentration Tangshenkang, 30 mmol/L D-glucose+10%middle concentration Tangshenkang, 30 mmol/L D-glucose+20% high concentration Tangshenkang). After 24 h and 48 h treatment, MMP-9 and TIMP-1 in cell cultural supernatant were observed by ELISA. Results MMP-9 of HK-2 cultured with high glucose was much decreased and TIMP-1 increased significantly than the control group, with statistical significance (P〈0.05). TIMP-1 significantly decreased and MMP-9 increased in HK-2 cultured with high glucose plus Tangshenkang compared with those only induced by high glucose, with statistical significance (P〈0.05). Conclusion Tangshenkang could regulate the secretion of fibrosis cell factor of HK-2 cell induced by high glucose, which may be one of the mechanisms in its treatment of diabetic nephropathy.
关 键 词:糖肾康 高糖 人肾小管上皮细胞 基质金属蛋白酶-9 基质金属蛋白酶抑制剂-1
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