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首页> 外文期刊>Chemico-biological interactions >Renoprotective effect of calycosin in high fat diet-fed/STZ injected rats: Effect on IL-33/ST2 signaling, oxidative stress and fibrosis suppression
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Renoprotective effect of calycosin in high fat diet-fed/STZ injected rats: Effect on IL-33/ST2 signaling, oxidative stress and fibrosis suppression

机译:钙霉素在高脂肪饮食喂养/ STZ注射大鼠中的重新调试作用:对IL-33 / ST2信号传导,氧化应激和纤维化抑制的影响

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摘要

Type 2 diabetes mellitus (T2DM) is a disease with a drastically growing worldwide prevalence. It is usually associated with numerous complications of which; diabetic nephropathy (DN); is a main complication of microvasculature and more seriously, a common cause of end-stage renal disease (ESRD). Unfortunately, both the lack of a definitive remedy alongside the economic and the social burden on DN patients enforces considerable impetus for developing alternative therapies. IL-33 is a newly discovered member of the IL-1 cytokine family. IL33/ST2 signaling plays a crucial role in acute and chronic kidney diseases. Calycosin is an isoflavone with reported IL33 signaling inhibitory activity. The present study aimed to investigate if calycosin possess renal protective effect in high-fat diet/STZ-induced T2DM model and to clarify the potential underlying mechanisms. HFD-STZ control rats showed functional and structural renal damage confirmed by increased serum creatinine, blood urea nitrogen and albuminuria associated with marked renal glomerulosclerosis and interstitial fibrosis. Initiation of inflammation, oxidative stress, and fibrosis was evident as depicted by elevated renal levels of IL33/ST2 mRNA as well as increased renal NF-kappa Bp65, TNF-alpha, IL-1 beta, MDA, and TGF-beta contents with suppressed Nrf2 and TAC. Calycosin treatment markedly improved the aforementioned makers of renal injury and dysfunction, modulated IL33/ST2 signaling, inflammatory cytokines, oxidative stress and fibrotic processes. This was accompanied by improvement of T2DM-induced renal ultramicroscopic and histopathological alterations.
机译:2型糖尿病(T2DM)是一种疾病,全世界普遍性地增长。它通常与许多并发症有关;糖尿病肾病(DN);是微血管系统的主要复杂性,更严重,常见原因是末期肾病(ESRD)。不幸的是,与DN患者的经济和社会负担以及DN患者的社会负担缺乏明确的补救措施都是为了开发替代疗法的相当大的推动力。 IL-33是IL-1细胞因子家族的新发现成员。 IL33 / ST2信号传导在急性和慢性肾疾病中起着至关重要的作用。 Calycosin是一种异黄酮,具有报告的IL33信号传导抑制活性。目前的研究旨在调查Calycosin在高脂饮食/ STZ诱导的T2DM模型中具有肾脏保护作用,并阐明潜在的潜在机制。 HFD-STZ对照大鼠表现出血清肌酐,血尿尿素氮和白蛋白尿具有明显肾肾小球粥样硬化和间质纤维化的血清肌酐和血红蛋白尿的功能性和结构肾损伤。如IL33 / ST2 mRNA的肾脏水平升高,肾NF-Kappa BP65,TNF-α,IL-1β,MDA和TGF-β含量增加,发出炎症,氧化应激和纤维化,如肾脏水平的肾脏水平升高。 NRF2和TAC。钙霉素治疗明显改善了上述肾损伤和功能障碍的制造商,调制IL33 / ST2信号传导,炎症细胞因子,氧化应激和纤维化过程。这伴随着改善T2DM诱导的肾超微镜和组织病理学改变。

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