Inhibitory effects of Cnidium officinale Makino and Tabanus fulvus Meigan on the high glucose-induced proliferation of glomerular mesangial cells

This study describes a potent activity of Cnidium officinale Makino (Cnidii rhizoma) and Tabanus fulvus Meigan (Tabanus) as an inhibitor of high glucose-induced proliferation of glomerular mesangial cells (GMCs). Raising the ambient glucose concentration from 5.6 to 25 mM for 24 h caused a dramatic...

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Veröffentlicht in:Phytomedicine (Stuttgart) 2005-09, Vol.12 (9), p.648-655
Hauptverfasser: Jeong, S.I., Kwak, D.H., Lee, S., Choo, Y.K., Woo, W.H., Keum, K.S., Choi, B.K., Jung, K.Y.
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Sprache:eng
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Zusammenfassung:This study describes a potent activity of Cnidium officinale Makino (Cnidii rhizoma) and Tabanus fulvus Meigan (Tabanus) as an inhibitor of high glucose-induced proliferation of glomerular mesangial cells (GMCs). Raising the ambient glucose concentration from 5.6 to 25 mM for 24 h caused a dramatic increase in [ 3H]thymidine incorporation, and these increases were attenuated by treatment of GMCs with the extracts of Cnidii rhizoma and Tabanus (2.5–20 μg/ml) in a dose-dependent manner. In contrast, extracts of Cnidii rhizoma or Tabanus (20 μg/ml) did not change the growth of GMCs cultured under normal glucose condition. To clarify the mechanism involved in anti-proliferative activity of these medicines, this study examined the effects of Cnidii rhizoma and Tabanus on high glucose-stimulated extracellular matrix (ECM) protein accumulation and transforming growth factor- β 1 (TGF- β 1 ) production. Exposure of GMCs to high glucose significantly stimulated the ECM protein, collagen and fibronectin, accumulation and TGF- β 1 secretion, and these changes were dramatically diminished by treatment of GMCs with extracts of Cnidii rhizoma or Tabanus (10 μg/ml). Taken together, these results indicate that Cnidii rhizoma and Tabanus inhibit the high glucose-induced GMC proliferation partially through suppressing the ECM accumulation and TGF- β 1 production, suggesting that these medicines may be a promising agent for treating the development and progression of diabetic glomerulopathy.
ISSN:0944-7113
1618-095X
DOI:10.1016/j.phymed.2004.01.014