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氟尼辛酮可预防急性肾损伤。

Fluorofenidone protects against acute kidney injury.

机构信息

Department of Nephrology, School of Pharmaceutical Sciences, Central South University, Changsha, China.

Department of Nutriology, School of Pharmaceutical Sciences, Central South University, Changsha, China.

出版信息

FASEB J. 2019 Dec;33(12):14325-14336. doi: 10.1096/fj.201901468RR. Epub 2019 Oct 26.

Abstract

Cisplatin (CP) is one of the most effective chemotherapeutics in the treatment of human cancers. However, the beneficial effects of CP are limited by the toxic effects, especially nephrotoxicity. Fluorofenidone (AKFPD) is a promising multifunctional antifibrosis pyridinone drug discovered by our group. But there is no evidence of its protective effects against acute kidney injury (AKI). Therefore, we investigated the protective effects of AKFPD on CP-induced AKI and . Compared with the model group, treatment with AKFPD effectively ameliorated kidney damages. In order to elucidate the mechanisms, we discovered that AKFPD treatment notably alleviated generation of reactive oxygen species, reduced the phosphorylation levels of MAPKs (ERK1 and 2, JNKs, and p38), suppressed inflammatory response, inhibited apoptosis, and abated the expression of CP transporters (organic cation transporter 2 and copper transport protein 1) compared with the model group. Moreover, because renal ischemia reperfusion injury (IRI)-induced AKI and LPS-induced AKI are the major models representative of renal transplantation-correlated AKI and sepsis-related AKI, which are also the main causes of AKI, we have also proved the effectiveness of AKFPD on these models. In conclusion, these findings suggest that AKFPD is a potent drug for CP-, IRI-, and LPS-caused AKI and elucidate the underlying mechanism.-Jiang, Y., Quan, J., Chen, Y., Liao, X., Dai, Q., Lu, R., Yu, Y., Hu, G., Li, Q., Meng, J., Xie, Y., Peng, Z., Tao, L. Fluorofenidone protects against acute kidney injury.

摘要

顺铂(CP)是治疗人类癌症最有效的化疗药物之一。然而,CP 的有益作用受到毒性作用的限制,尤其是肾毒性。氟苯尼酮(AKFPD)是我们小组发现的一种有前途的多功能抗纤维化吡啶酮药物。但是,没有证据表明它对急性肾损伤(AKI)有保护作用。因此,我们研究了 AKFPD 对 CP 诱导的 AKI 的保护作用。与模型组相比,AKFPD 治疗有效改善了肾脏损伤。为了阐明机制,我们发现 AKFPD 治疗明显减轻了活性氧的产生,降低了 MAPKs(ERK1 和 2、JNKs 和 p38)的磷酸化水平,抑制了炎症反应,抑制了细胞凋亡,并减轻了 CP 转运体(有机阳离子转运体 2 和铜转运蛋白 1)的表达与模型组相比。此外,由于肾缺血再灌注损伤(IRI)诱导的 AKI 和 LPS 诱导的 AKI 是肾移植相关 AKI 和脓毒症相关 AKI 的主要模型代表,也是 AKI 的主要原因,我们还证明了 AKFPD 对这些模型的有效性。总之,这些发现表明 AKFPD 是 CP、IRI 和 LPS 引起的 AKI 的有效药物,并阐明了其潜在机制。

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