Effect of Sedum sarmentosum BUNGE Extract on Aristolochic Acid-Induced Renal Tubular Epithelial Cell Injury

被引:28
作者
Bai, Yongheng [1 ]
Lu, Hong [2 ]
Hu, Liping [2 ]
Hong, Dan [3 ]
Ding, Linchao [3 ]
Chen, Bicheng [1 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 1, Wenzhou Key Lab Surg, Wenzhou 325000, Peoples R China
[2] Wenzhou Med Univ, Affiliated Hosp 1, Dept Lab Med, Wenzhou 325000, Peoples R China
[3] Wenzhou Med Univ, Sch Lab Med & Life Sci, Wenzhou 325035, Peoples R China
关键词
aristolochic acid; epithelial-to-mesenchymal transition; renal fibrosis; Sedum sarmentosum BUNGE; inflammation; CHINESE NATURAL MEDICINES; NF-KAPPA-B; MEGASTIGMANE GLYCOSIDES; BIOACTIVE CONSTITUENTS; ABSOLUTE STRUCTURES; CANCER CELLS; DNA-ADDUCTS; NEPHROPATHY; APOPTOSIS; QUERCETIN;
D O I
10.1254/jphs.13216FP
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Aristolochic acid (AA) is known as a potent mutagen that induces significant cytotoxic and mutagenic effects on renal tubular epithelial cells. Clinically, the persistent injury of AA results in the infiltration of inflammatory cells, epithelial-to-mesenchymal transition (EMT), and renal tubulointerstitial fibrosis. There are no truly effective pharmaceuticals. In this study, we investigated the potential role of the extract of Sedum sarmentosum BUNGE (SSB), a traditional Chinese herbal medicine, on rat tubuloepithelial (NRK-52E) cells after AA injury in vitro. Evidence revealed that AA induced mitochondrial-pathway-mediated cellular apoptosis, accompanied by cell proliferation in a feedback mechanism. Treatment with SSB also induced cells to enter early apoptosis, but inhibited cell proliferation. In cultured NRK-52E cells, AA induced the imbalance of MMP-2/TIMP-2 and promoted EMT and ECM accumulation. SSB treatment significantly alleviated AA-induced NRK-52E cells fibrosis-like appearance, inhibited the induction of EMT, and deposition of ECM. SSB also decreased the activity of the NF-kappa B signaling pathway, resulting in down-regulated expression of NF-kappa B-controlled chemokines and pro-inflammatory cytokines, including MCP-1, MIF, and M-CSF, which may regulate the macrophage-mediated inflammatory reaction during renal fibrosis in vivo. Therefore, these findings suggest that SSB exerts protective effects against AA-induced tubular epithelial cells injury through suppressing the synthesis of inflammatory factors, EMT, and ECM production.
引用
收藏
页码:445 / 456
页数:12
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