4.2 Article

Tanshinone IIA Inhibits High Glucose-Induced Collagen Synthesis via Nuclear Factor Erythroid 2-Related Factor 2 in Cardiac Fibroblasts

期刊

CELLULAR PHYSIOLOGY AND BIOCHEMISTRY
卷 51, 期 5, 页码 2250-2261

出版社

KARGER
DOI: 10.1159/000495870

关键词

Tanshinone IIA; High Glucose; Cardiac Fibroblast; Collagen Synthesis; Nuclear Factor Erythroid 2-related Factor 2

资金

  1. Ministry of Science and Technology [MOST 106-2314-B-016 -037 -MY3, MOST 106-2320-B-016-003-MY2]
  2. National Defense Medical Center [MAB-106-033]
  3. Teh-Tzer Study Group for Human Medical Research Foundation [A1061037, A1061054]
  4. Tri-Service General Hospital Grants, Taipei, Taiwan, R.O.C [TSGH-C105-028, C106-021, C108-008-S04]

向作者/读者索取更多资源

Background/Aims: Diabetes is associated with increased incidence of myocardial dysfunction, which is partly characterized by interstitial and perivascular fibrosis. Cardiac fibroblasts have been identified as an important participant in the development of cardiac fibrosis. Exposure of cultured cardiac fibroblasts to high glucose resulted in increased collagen synthesis. Tanshinone IIA can alleviate the ventricular fibrosis that develops in a number of different experimental conditions. However, whether tanshinone IIA can prevent high glucose-induced collagen synthesis in cardiac fibroblasts remains unknown. The aim of this study was to evaluate the effects of tanshinone IIA on high glucose-induced collagen synthesis in cardiac fibroblasts. Methods: Rat cardiac fibroblasts were cultured in high glucose (25 mM) media in the absence or presence of tanshinone IIA and the changes in collagen synthesis, transforming growth factor-beta 1 (TGF-beta 1) production and related signaling molecules were assessed by H-3-proline incorporation, quantitative polymerase chain reaction, enzyme linked immunosorbent assay, and Western blotting. Results: The results indicate cardiac fibroblasts exposed to high glucose condition show increased cell proliferation and collagen synthesis and these effects were abolished by tanshinone IIA treatment. Furthermore, the inhibitory effect of tanshinone IIA on high glucose induced cell proliferation and collagen synthesis may be associated with its activation of the nuclear factor erythroid 2-related factor 2 (Nrf2) and the inhibition of TGF-beta 1 production and Smad2/3 phosphorylation. Conclusion: In summary, our results highlights the critical role tanshinone IIA plays as an antioxidant in attenuating high glucose-mediated collagen synthesis through inhibiting TGF-beta 1/Smad signaling in cardiac fibroblasts which provide a mechanistic basis for the clinical application of tanshinone IIA in the treating diabetic-related cardiac fibrosis. (C) 2018 The Author(s) Published by S. Karger AG, Basel

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