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首页> 外文期刊>Acta Pharmacologica Sinica >Expression of apoptosis-related factors in chronic cyclosporine nephrotoxicity after cyclosporine withdrawal
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Expression of apoptosis-related factors in chronic cyclosporine nephrotoxicity after cyclosporine withdrawal

机译:环孢素戒断后慢性环孢素肾毒性中细胞凋亡相关因子的表达

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AIM: To examine whether the reversibility of chronic cyclosporine A (CsA) nephrotoxicity is associated with apoptotic cell death and its regulatory factors. METHODS: Chronic CsA nephrotoxicity was induced in Sprague-Dawley rats by administering CsA (15 mg/kg, sc) for 5 weeks, and then withdrawing it for 5 or 10 weeks. The effect of CsA withdrawal on apoptotic cell death was evaluated by an in situ TdT-mediated deoxyuridine triphos-phate-biotin nick end-labeling (TUNEL) assay and the expression of pro-apoptotic [(transforming growth factor-betal (TGF-β1) and Fas] and anti-apoptotic [epidermal growth factors (EGF) and Bcl-2] factors. RESULTS: Discontinuation of CsA induced significant decreases in TUNEL-positive cells in a time-dependent manner and the reduction in TUNEL-positive cells was correlated with the tubulointerstitial fibrosis score (r=0.919, P<0.01). Upregulation of TGF-β1 and Fas expression in CsA-treated rat kidneys was decreased significantly after withdrawal of CsA. In contrast, downregulated EGF and Bcl-2 expression returned to normal or supernormal levels. CONCLUSION: CsA withdrawal is associated with a decrease in apoptotic cell death and with changes in the expression of pro-apoptotic and anti-apoptotic molecules involved in renal wound repair. This may constitute one of the mechanisms underlying the reversibility of chronic CsA nephrotoxicity.
机译:目的:研究慢性环孢素A(CsA)肾毒性的可逆性是否与凋亡细胞死亡及其调节因子有关。方法:Sprague-Dawley大鼠慢性CsA肾毒性是通过给予CsA(15 mg / kg,皮下注射)5周,然后停用5周或10周来诱导的。通过原位TdT介导的脱氧尿苷三磷酸-生物素缺口末端标记(TUNEL)分析和促凋亡[(转化生长因子-壁(TGF-β1)的表达,评估CsA撤回对凋亡细胞死亡的影响)和Fas]和抗凋亡的[表皮生长因子(EGF)和Bcl-2]因子。结果:停止CsA诱导TUNEL阳性细胞显着减少,呈时间依赖性,而TUNEL阳性细胞减少。与肾小管间质纤维化评分相关(r = 0.919,P <0.01),撤除CsA后,CsA处理的大鼠肾脏中TGF-β1和Fas表达的上调明显减少;相反,EGF和Bcl-2表达下调恢复至结论:CsA戒断与凋亡细胞死亡的减少以及参与肾脏创面修复的促凋亡和抗凋亡分子表达的改变有关,这可能是其中一种机制提示慢性CsA肾毒性具有可逆性的短信。

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