(Hypertension. 2004;43:1214.)
© 2004 American Heart Association, Inc.
Scientific Contributions |
From the Departments of Cardiovascular Medicine (M.S., K.T., N.I.,Y.H, R.N.), Urology (H.N.), Metabolic Diseases (J.O., S.I.), University of Tokyo Graduate School of Medicine, Japan; Division of Endocrinology and Metabolism (S.I.), Department of Medicine, Jichi Medical School, Tochigi, Japan; and PRESTO (M.S.), Japan Science and Technology Agency, Kawaguchi, Saitama, Japan.
Correspondence to Dr Masataka Sata, Department of Cardiovascular Medicine, University of Tokyo Graduate School of Medicine, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan. E-mail msata-circ{at}umin.ac.jp
3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors, or statins, are widely prescribed to lower cholesterol. Recent reports suggest that statins may promote angiogenesis in ischemic tissues. It remains to be elucidated whether statins potentially enhance unfavorable angiogenesis associated with tumor and atherosclerosis. Here, we induced hind limb ischemia in wild-type mice by resecting the right femoral artery and subsequently inoculated cancer cells in the same animal. Cerivastatin enhanced blood flow recovery in the ischemic hind limb as determined by laser Doppler imaging, whereas tumor growth was significantly retarded. Cerivastatin did not affect capillary density in tumors. Cerivastatin, pitavastatin, and fluvastatin inhibited atherosclerotic lesion progression in apolipoprotein E-deficient mice, whereas they augmented blood flow recovery and capillary formation in ischemic hind limb. Low-dose statins were more effective than high-dose statins in both augmentation of collateral flow recovery and inhibition of atherosclerosis. These results suggest that statins may not promote the development of cancer and atherosclerosis at the doses that augment collateral flow growth in ischemic tissues.
Key Words: cholesterol atherosclerosis nitric oxide circulation
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