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氯沙坦通过抑制肿瘤坏死因子信号通路改善肾纤维化。

Losartan ameliorates renal fibrosis by inhibiting tumor necrosis factor signal pathway.

作者信息

Wang Hongshuang, Liu Jiazhi, Fang Fang, Gao Lanjun, Zhao Chenchen, Wang Zheng, Zhong Yan, Wang Xiangting

机构信息

Graduate School, Hebei University of Chinese Medicine, Shijiazhuang 050091, China.

Hebei Key Laboratory of Integrative Medicine on Liver-Kidney Patterns, Shijiazhuang 050091, China; Institute of Integrative Medicine, College of Integrative Medicine, Hebei University of Chinese Medicine, Shijiazhuang 050200, China.

出版信息

Nefrologia (Engl Ed). 2024 Mar-Apr;44(2):139-149. doi: 10.1016/j.nefroe.2024.04.001.

Abstract

Losartan is widely used in the treatment of chronic kidney disease (CKD) and has achieved good clinical efficacy, but its exact mechanism is not clear. We performed high-throughput sequencing (HTS) technology to screen the potential target of losartan in treating CKD. According to the HTS results, we found that the tumor necrosis factor (TNF) signal pathway was enriched. Therefore, we conducted in vivo and in vitro experiments to verify it. We found that TNF signal pathway was activated in both unilateral ureteral obstruction (UUO) rats and human proximal renal tubular epithelial cells (HK-2) treated with transforming growth factor-β1 (TGF-β1), while losartan can significantly inhibit TNF signal pathway as well as the expression of fibrosis related genes (such as COL-1, α-SMA and Vimentin). These data suggest that losartan may ameliorate renal fibrosis through modulating the TNF pathway.

摘要

氯沙坦被广泛用于治疗慢性肾脏病(CKD),并取得了良好的临床疗效,但其确切机制尚不清楚。我们采用高通量测序(HTS)技术筛选氯沙坦治疗CKD的潜在靶点。根据HTS结果,我们发现肿瘤坏死因子(TNF)信号通路富集。因此,我们进行了体内和体外实验以进行验证。我们发现,在单侧输尿管梗阻(UUO)大鼠和用转化生长因子-β1(TGF-β1)处理的人近端肾小管上皮细胞(HK-2)中,TNF信号通路均被激活,而氯沙坦可显著抑制TNF信号通路以及纤维化相关基因(如COL-1、α-SMA和波形蛋白)的表达。这些数据表明,氯沙坦可能通过调节TNF通路改善肾纤维化。

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