Su Zhonghao, Yu Ping, Sheng Lanyue, Ye Jin, Qin Zhenxia
School of Basic Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Institute of Interdisciplinary Integrative Medicine Research, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Cell Physiol Biochem. 2018;49(6):2124-2137. doi: 10.1159/000493816. Epub 2018 Sep 26.
BACKGROUND/AIMS: Acute kidney injury (AKI) is a frequent and serious complication of sepsis; however, there is no effective treatment for it. FangJiFuling (FF) decoction is widely used to treat acute glomerulonephritis and nephritic syndrome in the clinical setting.
On the basis of its anti-inflammatory properties, the renoprotective effect of FF on a mouse model of lipopolysaccharide (LPS)-induced AKI was investigated. Major compounds were identified in FF with high-performance liquid chromatography. A bioinformatics analysis tool was used to predict target genes. Quantitative real-time PCR and western blot analyses were performed to validate the targets. Furthermore, the expression of a target gene was silenced by small interfering RNA-mediated knockdown in vitro.
Bioinformatics analysis indicated that inflammation, apoptosis, and cell junction were closely related to the renoprotective effects of FF. Validation was confirmed by an in vivo test. A reduction of inflammatory cell infiltration and inflammatory cytokine mRNA expression (iNOS, NF-κB, MCP-1, and TNF-α) following the administration of FF (50 mg/kg) was observed in LPS-treated renal tissue. In addition, FF treatment suppressed mitochondrial-mediated apoptosis by regulating the Bax/Bcl-2 ratio in LPS-induced renal injury. Silencing Cx43, a cell-to-cell junction protein, was found to enhance the protective effect of FF against LPS-induced renal injury.
Our study suggests that FF exhibits a renoprotective effect against LPS-induced inflammatory and apoptotic responses. In addition, Cx43 might be involved in these processes. These findings indicate the potential role of FF as a natural renoprotective product.
背景/目的:急性肾损伤(AKI)是脓毒症常见且严重的并发症;然而,目前尚无有效的治疗方法。防己茯苓汤(FF)在临床中广泛用于治疗急性肾小球肾炎和肾病综合征。
基于其抗炎特性,研究了FF对脂多糖(LPS)诱导的AKI小鼠模型的肾脏保护作用。采用高效液相色谱法鉴定了FF中的主要化合物。使用生物信息学分析工具预测靶基因。进行定量实时PCR和蛋白质印迹分析以验证靶标。此外,通过体外小干扰RNA介导的敲低使靶基因的表达沉默。
生物信息学分析表明,炎症、凋亡和细胞连接与FF的肾脏保护作用密切相关。体内试验证实了这一验证。在LPS处理的肾组织中,观察到给予FF(50mg/kg)后炎症细胞浸润减少以及炎症细胞因子mRNA表达(诱导型一氧化氮合酶、核因子κB、单核细胞趋化蛋白-1和肿瘤坏死因子-α)降低。此外,FF治疗通过调节LPS诱导的肾损伤中的Bax/Bcl-2比值抑制线粒体介导的凋亡。发现沉默细胞间连接蛋白Cx43可增强FF对LPS诱导的肾损伤的保护作用。
我们的研究表明,FF对LPS诱导的炎症和凋亡反应具有肾脏保护作用。此外,Cx43可能参与这些过程。这些发现表明FF作为一种天然肾脏保护产品的潜在作用。