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Losartan Inhibits Vascular Smooth Muscle Cell Proliferation through Activation of AMP-Activated Protein Kinase
The Korean Journal of Physiology and Pharmacology ; : 299-304, 2010.
Article Dans Anglais | WPRIM | ID: wpr-728368
ABSTRACT
Losartan is a selective angiotensin II (Ang II) type 1 (AT1) receptor antagonist which inhibits vascular smooth muscle cells (VSMCs) contraction and proliferation. We hypothesized that losartan may prevent cell proliferation by activating AMP-activated protein kinase (AMPK) in VSMCs. VSMCs were treated with various concentrations of losartan. AMPK activation was measured by Western blot analysis and cell proliferation was measured by MTT assay and flowcytometry. Losartan dose- and time-dependently increased the phosphorylation of AMPK and its downstream target, acetyl-CoA carboxylase (ACC) in VSMCs. Losartan also significantly decreased the Ang II- or 15% FBS-induced VSMC proliferation by inhibiting the expression of cell cycle associated proteins, such as p-Rb, cyclin D, and cyclin E. Compound C, a specific inhibitor of AMPK, or AMPK siRNA blocked the losartan-induced inhibition of cell proliferation and the G0/G1 cell cycle arrest. These data suggest that losartan-induced AMPK activation might attenuate Ang II-induced VSMC proliferation through the inhibition of cell cycle progression.
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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Phosphorylation / Acetyl-coA carboxylase / Angiotensine-II / Protéines / Cycle cellulaire / Technique de Western / Cyclines / Losartan / Cycline E / Petit ARN interférent langue: Anglais Texte intégral: The Korean Journal of Physiology and Pharmacology Année: 2010 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Phosphorylation / Acetyl-coA carboxylase / Angiotensine-II / Protéines / Cycle cellulaire / Technique de Western / Cyclines / Losartan / Cycline E / Petit ARN interférent langue: Anglais Texte intégral: The Korean Journal of Physiology and Pharmacology Année: 2010 Type: Article