Planta Med 2007; 73(11): 1163-1168
DOI: 10.1055/s-2007-981584
Pharmacology
Original Paper
© Georg Thieme Verlag KG Stuttgart · New York

Cudraflavanone A, a Flavonoid Isolated from the Root Bark of Cudrania tricuspidata, Inhibits Vascular Smooth Muscle Cell Growth via an Akt-Dependent Pathway

Hyeong-Jun Han1 [*] , Tack-Joong Kim1 [*] , Yong-Ri Jin2 , Seong-Su Hong1 , Ji-Hye Hwang1 , Bang-Yeon Hwang1 , Kwang-Ho Lee3 , Tae-Kyu Park3 , Yeo-Pyo Yun1
  • 1College of Pharmacy, Research Center for Bioresource and Health, Chungbuk National University, Cheongju, Korea
  • 2Research Institute of Veterinary Medicine, Chungbuk National University, Cheongju, Korea
  • 3Department of Biotechnology, Division of Life Science, Konkuk University, Chungju, Korea
Further Information

Publication History

Received: March 24, 2007 Revised: July 3, 2007

Accepted: July 6, 2007

Publication Date:
23 August 2007 (online)

Abstract

In previous studies of the root bark of Cudrania tricuspidata, various isoprenylated xanthones and flavonoids were isolated, some of which have anticancer, hepatoprotective, and antiperoxidative activities. Cytokines and growth factors are involved in the regulation of vascular smooth muscle cells (VSMCs) in atherosclerotic plaques. To assess whether cudraflavanone A isolated from the root bark of C. tricuspidata may be useful in the prevention of atherosclerosis or restenosis after angioplasty, we investigated the ability of cudraflavanone A to inhibit VSMCs growth under 25 ng/mL platelet-derived growth factor BB (PDGF-BB)-stimulated conditions. Cudraflavanone A (0.1 - 1 μM) significantly inhibited PDGF-BB-induced cell numbers in a concentration-dependent manner. The antigrowth effects of cudraflavanone A on VSMCs were also examined in [3H]-thymidine incorporation and cell cycle assays. Consistent with the inhibitory effect on cell number, PDGF-BB-stimulated [3H]-thymidine incorporation and cell cycle progression in VSMCs was also concentration-dependently reduced by cudraflavanone A. Furthermore, PDGF-BB markedly activated PDGF-beta receptor (PDGF-Rβ) tyrosine kinase activity, leading to activation of intracellular signals required for VSMC growth. However, PDGF-BB-induced this kinase activity was not affected by cudraflavanone A. PDGF-BB also increased the activation of extracellular signal-regulated kinases 1 and 2 (ERK1/2), Akt, and phospholipase C gamma (PLCγ)1, which are important signaling molecules in cell growth. Cudraflavanone A (0.1 - 1 μM) suppressed PDGF-BB-stimulated Akt activation, which is involved in cell survival, but had no effect on the activation of ERK1/2 and PLCγ1. Selective modification of Akt activation by cudraflavanone A in VSMCs may suppress intimal thickening after angioplasty and plaque formation in atherosclerosis. These results suggest that cudraflavanone A from C. tricuspidata inhibits PDGF-BB-induced rat aortic VSMC growth via an Akt-dependent pathway.

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1 Both authors contributed equally to this work

Prof. Dr. Yeo-Pyo Yun

College of Pharmacy

Chungbuk National University

12 Gaesin-Dong

Heungduk-Gu

Cheongju

Chungbuk 361-763

Korea

Phone: +82-43-261-2821

Fax: +82-43-268-2732

Email: ypyun@chungbuk.ac.kr