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非诺贝特对肾缺血再灌注损伤的保护作用:参与抑制激酶2(JAK2)/转录因子3(STAT3)/p53信号通路激活。

Protective effect of Fenofibrate in renal ischemia reperfusion injury: Involved in suppressing kinase 2 (JAK2)/transcription 3 (STAT3)/p53 signaling activation.

作者信息

Lv J, Wang X, Liu S Y, Liang P F, Feng M, Zhang L L, Xu A P

机构信息

Sun Yat-Sen University, Sun Yat-Sen Memorial Hospital, Department of Nephrology, Guangzhou, People's Republic of China.

Sun Yat-Sen University, Sun Yat-Sen Memorial Hospital, Department of Nephrology, Guangzhou, People's Republic of China.

出版信息

Pathol Biol (Paris). 2015 Dec;63(6):236-42. doi: 10.1016/j.patbio.2015.07.010. Epub 2015 Sep 2.

Abstract

OBJECTIVE

Renal ischemia reperfusion (I/R) injury is a common reason of acute kidney injury. Apoptosis play an important role in the IRI. Fenofibrate, one of agonist Peroxisome proliferator-activated receptor-alpha (PPARα) has the effect of anti-apoptosis. This study was to explore the effect of Fenofibrate on renal ischemia reperfusion injury and its mechanism.

MATERIALS AND METHODS

IRI was induced by bilateral renal ischemia for 45 min followed by reperfusion for 24h. Eighteen male C57BL/6 mice were randomly divided into three groups: Sham group (Sham), IRI group (IRI), I/R-Fenofibrate group (FEN). Fenofibrate was injected at 45 min before renal ischemia. Renal histology, function, and the expression of Bax, Bcl-2, Bcl-xl p21, p53, Caspase3, CytC, p-JAK2, p-STAT3 and p-PPAR-α were assessed.

RESULTS

Fenofibrate precondition can significantly alleviate the renal dysfunction, the pathological change, up-regulate the expression of p-PPAR-α, Bcl-2, Bcl-xl, Caspase3 and down-regulate the expression of p-JAK2, p-STAT3, p53, p21, CytC and Bax induced by renal IR injury.

CONCLUSION

Fenofibrate precondition can protect mice against IRI by suppressing p53-mediating apoptosis which was associated with inhibiting JAK2/STAT3 signaling activation though further activating PPAR-α. Our findings suggest that Fenofibrate could be useful for preventing IR-induced renal injury.

摘要

目的

肾缺血再灌注(I/R)损伤是急性肾损伤的常见原因。细胞凋亡在缺血再灌注损伤中起重要作用。非诺贝特是过氧化物酶体增殖物激活受体α(PPARα)激动剂之一,具有抗凋亡作用。本研究旨在探讨非诺贝特对肾缺血再灌注损伤的影响及其机制。

材料与方法

通过双侧肾缺血45分钟,随后再灌注24小时诱导缺血再灌注损伤。18只雄性C57BL/6小鼠随机分为三组:假手术组(Sham)、缺血再灌注组(IRI)、缺血再灌注-非诺贝特组(FEN)。在肾缺血前45分钟注射非诺贝特。评估肾组织学、功能以及Bax、Bcl-2、Bcl-xl、p21、p53、Caspase3、CytC、p-JAK2、p-STAT3和p-PPAR-α的表达。

结果

非诺贝特预处理可显著减轻肾功能障碍、病理变化,上调p-PPAR-α、Bcl-2、Bcl-xl、Caspase3的表达,下调肾缺血再灌注损伤诱导的p-JAK2、p-STAT3、p53、p21、CytC和Bax的表达。

结论

非诺贝特预处理可通过抑制p53介导的细胞凋亡保护小鼠免受缺血再灌注损伤,这与通过进一步激活PPAR-α抑制JAK2/STAT3信号激活有关。我们的研究结果表明非诺贝特可能对预防缺血再灌注诱导的肾损伤有用。

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