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机构地区:[1]陕西中医学院药理教研室,陕西咸阳712046
出 处:《中成药》2013年第10期2067-2072,共6页Chinese Traditional Patent Medicine
摘 要:目的探讨山茱萸环烯醚萜总苷对晚期糖基化终末产物(AGEs)诱导的大鼠肾系膜HBZY-1细胞炎症反应的影响以及可能的作用机制。方法采用巨噬细胞和肾系膜细胞共培养体系,评估巨噬细胞的迁移能力;采用ELISA试剂盒评估炎症因子的分泌水平;采用Western blot分析法评估炎症相关蛋白的表达。结果与AGEs诱导的模型组相比,山茱萸环烯醚萜总苷显著抑制AGEs诱导的巨噬细胞迁移能力,不同剂量山茱萸环烯醚萜总苷(1.0、0.5、0.25mg/mL),对巨噬细胞迁移抑制率分别为42.09%±7.25%、26.44%±10.23%、20.84%±6.84%;山茱萸环烯醚萜总苷显著抑制AGEs诱导的炎症因子IL-6,IL-10,MCP-1和TNF-α的分泌水平;Western blot分析显示山茱萸环烯醚萜总苷及AGEs受体特异性抗体显著下调AGEs诱导的ICAM-1和TGF-β1的蛋白表达。结论山茱萸环烯醚萜总苷可剂量依赖性地减轻AGEs诱导的大鼠肾系膜细胞HBZY-1炎症反应,对糖尿病肾病的发生发展具有一定的保护作用。AIM To investigate the regulation of iridoid glycoside from Corni officinalis Fructus on advanced glycation end-products (AGEs) -induced inflammatory response in rat renal mesangial HBZY-1 cell. METHODS The macrophage and renal mesangial cells co-culture system was established to assess the migration of macropha- ges to mesangial cells. ELISA kits were used to evaluate the secretion level of inflammatory cytokines. Western blot analysis was developed to assess the inflammation-related protein expression. RESULTS Compared with AGEs- induced model group, iridoid glycoside from Corni officinalis Fructus significantly inhibited AGEs-induced the mi- gration ability of macrophage to mesangial cells. The migration inhibitory rates of different doses of iridoid glycoside from Corni officinalis Fructus ( 1.0 , 0. 5 and 0. 25 mg/mL) were 42.09% ± 7.25% , 26. 44% ± 10. 23% and 20. 84% ± 6.84% , respectively. The pretreatment with iridoid glycoside from Corni officinalis Fructus significantly inhibited the levels of inflammatory cytokines induced by AGEs, including IL-6, IL-10, MCP-1 and TNF-α secre- tion levels. Furthermore, western blot analysis showed that iridoid glycoside from Corni officinalis Fructus and re- ceptor for AGEs antibody ( RAGE-Ab, 5 μg/mL) significantly attenuated AGEs-induced ICAM-1 and TGF-β1 pro- tein expression. CONCLUSION Iridoid glycoside from Corni officinalis Fructus could attenuate AGEs-induced inflammatory response in rat mesangial cells HBZY-1 in a dose-dependent manner via blocking AGEs-RAGE path- way, and has a protective effect on the development of diabetic nephropathy.
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