Abstract

Objective To investigate the efficacy of Niao Du Kang (NDK) mixture in renal fibrosis of rats and to explore the mechanism underlying the effect of NDK on renal fibrosis. Methods Unilateral ureteral obstruction (UUO) was used to replicate a rat renal interstitial fibrosis model. The drug-administered groups were given 20 ml/kg (NDK-H), 10 ml/kg (NDK-M), and 5 ml/kg (NDK-L) NDK mixture once a day for 21 days beginning 48 hours after surgery. The 24-hour urine protein and serum creatinine (CR) levels in the sham group rats, UUO rats, and NDK mixture-treated rats were measured after the last administration. The pathological changes of rat kidney tissue were observed by HE staining. The degree of fibrosis was observed by Masson's staining and scored. The expression levels of TGF-β, α-SMA mRNA, and mir-129-5p in kidney were detected by qRT-PCR. HK-2 cells were treated with 5 ng/ml TGF-β to induce HK-2 cell fibrosis. The expression levels of TGF-β, α-SMA mRNA, and mir-129-5p in HK-2 cells were detected by qRT-PCR. TargetScan predicted the target gene of mir-129-5p, HK-2 cells were transfected with mir-129-5p mimic, and an overexpressed mir-129-5p HK-2 cell model was constructed. qRT-PCR was used to detect the expression of PDPK1 mRNA. Western blot was used to detect the expression of PDPK1, AKT, and p-AKT in HK-2 cells induced by TGF-β and in UUO rats. Results NDK mixture significantly reduced the 24-hour urine protein and CR levels of UUO rats. HE staining showed that the NDK mixture group exhibited a significantly reduced degree of renal interstitial fibrosis. NDK mixture also reduced the expression of TGF-β and α-SMA, and the middle-dose group showed a better therapeutic effect. In vitro studies showed that NDK mixture-containing serum increased the expression of mir-129-5p to reduce renal fibrosis. In addition, NDK mixture increased the expression of mir-129-5p in vivo. Further studies indicated that mir-129-5p could target PDPKl to reduce its expression. The NDK-containing serum group also exhibited reduced expression of PDPK1. Conclusion NDK mixture can significantly improve renal function and improve renal fibrosis in UUO model rats. Furthermore, NDK mixture can inhibit the expression of PDPK1 by upregulating the expression of mir-129-5p and then inhibiting the PI3K/AKT pathway to improve renal fibrosis.

Highlights

  • Renal fibrosis is one of the main pathological features of chronic kidney disease and is the main pathological change and common pathway for renal failure caused by various chronic kidney diseases

  • Semiquantitative analysis showed that the degree of renal interstitial fibrosis in the ureteral obstruction (UUO) group was significantly higher than that in the sham group, while the Niao Du Kang (NDK) mixture groups exhibited a significantly reduced degree of renal interstitial fibrosis (Figure 1(e))

  • According to our previous study, it is hypothesized that increases in mir129-5p may be related to the amelioration of renal fibrosis caused by NDK mixture. us, we examined differences in the expression of mir-129-5p among the control, Transforming growth factor-β (TGF-β), and NDK mixture groups by qRT-PCR. e results showed that compared with that in the control group, the expression of Application TGF-β α-SMA phosphoinositide-dependent protein kinase 1 (PDPK1) GAPDH mir-129-5p U6

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Summary

Introduction

Renal fibrosis is one of the main pathological features of chronic kidney disease and is the main pathological change and common pathway for renal failure caused by various chronic kidney diseases. Transforming growth factor-β (TGF-β) is the strongest known fibrogenic factor and plays an important role in the pathogenesis of renal interstitial fibrosis [3]. MiRNA research represents a new horizon for the study of the mechanism of renal fibrosis. In-depth research on the roles of miRNAs in renal fibrosis will contribute to the discovery of new drug targets and prognostic biomarkers for this condition [5,6,7]. Research on the role of mir-129-5p in renal fibrosis will be very valuable. Our previous research profiled changes in microRNA levels in the HK-2 human kidney proximal tubular cell line with TGF-β treatment and identified significantly altered miRNAs, and miR-129-5p is one of the significantly downregulated miRNAs in experimental models. Further research indicated that miR-129-5p suppressed PDPK1 mRNA and protein levels in HK-2 cells. MiR-129-5p inhibited epithelial-to-mesenchymal transition (EMT) via PDPK1 in HK-2 cells [15]

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