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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2017, Vol. 22 ›› Issue (4): 381-386.

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MiR-200a alleviates renal interstitial fibrosis by inhibiting Wnt/β-catenin signaling pathway

CHEN Hua, GONG Yi, ZHOU Baoshang, ZHANG Jing   

  1. Department of Nephrology, Xinqiao Hospital Affiliated to the Third Military Medical University, Chongqing 400037, China
  • Received:2016-08-24 Revised:2016-09-27 Online:2017-04-26 Published:2017-04-26

Abstract:

AIM: To investigate the inhibition of miR-200a on Wnt/β-catenin signaling pathway in unilateral ureteral obstruction mouse, and the effects of miR-200a on renal interstitial fibrosis.  METHODS: Models of renal interstitial fibrosis were established by unilateral ureteral obstruction (UUO). Twenty-four six-weeks C57BL/6 male mice were randomly divided into four groups (n=6), Sham group, UUO group, UUO + miR-200a group and UUO + NC group. From day 1, UUO + miR-200a group was given miR-200a (i.v. by tail vein, 40 mg/kg), while UUO + NC group was given Negative Control (i.v. by tail vein, 40 mg/kg). Both groups were administered for three consecutive days. On day 7, HE and Masson staining were used to detect pathological changes in kidneys; RT-PCR and Western blot were used to detect mRNA and protein expressions of Wnt4, β-catenin, Fibronectin and α-SMA. RESULTS: Compared with Sham group, UUO group exhibited obvious renal tubular damage and interstitial collagen deposition; expressions of Wnt4, β-catenin, Fibronectin and α-SMA mRNAs and proteins were also increased in UUO group(P<0.05). Compared with UUO group, UUO+miR-200a group presented minor renal tubular injury and interstitial collagen deposition; expressions of Wnt4, β-catenin, Fibronectin α-SMA mRNAs and proteins were also reduced in UUO+miR-200a group(P<0.05). CONCLUSION: miR-200a can alleviate renal interstitial fibrosis by inhibiting the Wnt/β-catenin signaling pathway.

Key words: miR-200a, Wnt/β-catenin signaling pathway, renal interstitial fibrosis

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