JAC Advance Access published online on April 21, 2005
Journal of Antimicrobial Chemotherapy, doi:10.1093/jac/dki128
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1 Department of Pathobiology, University of Washington, Seattle, WA 98195, USA, USA
* To whom correspondence should be addressed. Objectives: To evaluate whether antimicrobial chemotherapy prevents acceleration of atherosclerotic lesion development induced by infection with Chlamydia pneumoniae. Methods: ApoE-deficient mice which develop hyperlipidaemia and atherosclerosis spontaneously were inoculated intranasally with C. pneumoniae. Animals were treated with azithromycin for 6 weeks after the third inoculation and the atherosclerotic lesion areas in the aortic sinus were measured by computer-assisted morphometry. Results: At 12 weeks post-infection, infected untreated animals developed significantly larger lesion areas compared with sham-inoculated controls (8.7 x 104±2.3 x 104 µm2 versus 5.6 x 104±2.4 x 104 µm2). However, there were no differences in lesion size of infected mice treated with azithromycin in comparison with untreated infected controls (11.0 x 104±3.0 x 104 µm2 versus 8.7 x 104±2.3 x 104 µm2). Conclusions: Antibiotic treatment against C. pneumoniae has no beneficial effects on hyperlipidaemia-induced atherosclerosis accelerated by C. pneumoniae in a mouse model.
Received October 1, 2004
Revised February 9, 2005
Accepted March 17, 2005
Brief report
A 6 week course of azithromycin treatment has no beneficial effect on atherosclerotic lesion development in apolipoprotein E-deficient mice chronically infected with Chlamydia pneumoniae
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2 Department of Pathobiology, University of Washington, Seattle, WA 98195, USA, USA
C.-C. Kuo, E-mail: cckuo{at}u.washington.edu
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Abstract
Present address. Innere Medizin III, Ruprecht-Karl-Universitat Heidelberg, Heidelberg, Germany.
Present address. Department of Anesthesia, University of California at San Francisco, San Francisco, CA, USA.![]()
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