4.3 Article

MicroRNA-29a increased the intestinal membrane permeability of colonic epithelial cells in irritable bowel syndrome rats

期刊

ONCOTARGET
卷 8, 期 49, 页码 85828-85837

出版社

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.20687

关键词

diarrhea-predominant irritable bowel syndrome (IBS-D); microRNA-29a; intestinal membrane permeability; aquaporins (AQPs)

资金

  1. national science foundation [81573760]
  2. zhejiang provincial natural science foundation [LY16H030010]
  3. Traditional Chinese medicine science and technology plan projects of zhejiang province [2014ZA030]
  4. Medical health general research plan of zhejiang province [2014KYB175]
  5. Medicine and health science and technology plan projects in Zhejiang province [2017179719]
  6. Traditional Chinese medicine science and technology plan of Zhejiang province [2017ZA089, 2016ZB071]

向作者/读者索取更多资源

Background: The whole pathogenesis of diarrhea-predominant irritable bowel syndrome(IBS-D) is poorly understood. Our goal was to evaluate the expression change of microRNA-29a(miR-29a) in colonic epithelial cells in IBS rats and clarify the mechanism of miR-29a increasing the intestinal membrane permeability through aquaporins(AQPs). Methods: The IBS-D rats models were induced by rectal distention pressure combining with extremities constraint. The colonic epithelial cells were divided into four groups. A: normal group. B: IBS-D control group. C: IBS-D + miR-29a NC. D: IBS-D + miR-29a antagomir. The expression of miR-29a, the concentration of the K+ and Lactate Dehydrogenase(LDH) and the expression of AQPs were detected. Results: The miR-29a expression increased in IBS-D control group(2.090 +/- 0.022) compared with the control group(1.00 +/- 0.031) (P<0.001) while it decreased in IBS-D+ miR-29a antagomir group(1.403 +/- 0.042) compared with IBS-D control group(P< 0.001). The K+ decreased in IBS-D control group(1.305 +/- 0.289) compared with the control group(2.171 +/- 0.204)(P<0.05) while it increased in IBS-D+ miR-29a antagomir group(1.813 +/- 0.102)(P<0.05) compared with IBS-D control group. The LDH increased in IBS-D control group(4153.440 +/- 177.365) compared with the control group(1434.573 +/- 96.111)(P<0.001) while it decreased in IBS-D+ miR-29a antagomir group(2700.473 +/- 275.414) compared with IBS-D control group (P<0.01). The expression of AQP1, AQP3 and AQP8 decreased in IBS-D control group(0.132 +/- 0.010,0.110 +/- 0.005,0.108 +/- 0.007) compared with the control group (P< 0.001) while it increased in IBS-D+ miR-29a antagomir group( 0.197 +/- 0.005,0.182 +/- 0.011,0.194 +/- 0.003) compared with IBS-D control group(P<0.001). The IBS-D+ miR-29a negative control(NC) group, a comparison with IBS-D+ miR-29a antagomir group, each date showed the similar trend to the IBS-D control group. Conclusions: MiR-29a increased the intestinal membrane permeability of colonic epithelial cells by reducing the AQPs expression in IBS-D rats.

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