AJP - Heart Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Heart Circ Physiol 295: H2046-H2053, 2008. First published September 12, 2008; doi:10.1152/ajpheart.00133.2008
0363-6135/08 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
295/5/H2046    most recent
00133.2008v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Google Scholar
Right arrow Articles by Grönros, J.
Right arrow Articles by Gan, L. M.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Grönros, J.
Right arrow Articles by Gan, L. M.

Effects of rosuvastatin on cardiovascular morphology and function in an ApoE-knockout mouse model of atherosclerosis

J. Grönros,1 J. Wikström,3 U. Brandt-Eliasson,3 G. B. Forsberg,3 M. Behrendt,3 G. I. Hansson,3 and L. M. Gan2,3

1Department of Physiology, Institute of Neuroscience and Physiology, The Sahlgrenska Academy, Göteborg University, Göteborg; 2Department of Clinical Physiology, Sahlgrenska University Hospital, Sahlgrenska Academy of Göteborg University, Göteborg; 3Bioscience, AstraZeneca Research and Development, Mölndal, Sweden

Submitted 7 February 2008 ; accepted in final form 10 September 2008

This study investigated the effects of rosuvastatin on plaque progression and in vivo coronary artery function in apolipoprotein E-knockout (ApoE-KO) mice, using noninvasive high-resolution ultrasound techniques. Eight-week-old male ApoE-KO mice (n = 20) were fed a high-fat diet with or without rosuvastatin (10 µmol·kg–1·day–1) for 16 wk. When compared with control, rosuvastatin reduced total cholesterol levels (P < 0.05) and caused significant retardation of lesion progression in the brachiocephalic artery, as visualized in vivo using an ultrasound biomicroscope (P < 0.05). Histological analysis confirmed the reduction of brachiocephalic atherosclerosis and also revealed an increase in collagen content in the statin-treated group (P < 0.05). Coronary volumetric flow was measured by simultaneous recording of Doppler velocity signals and left coronary artery morphology before and during adenosine infusion. The hyperemic flow in response to adenosine was significantly greater in left coronary artery following 16 wk of rosuvastatin treatment (P < 0.001), whereas the baseline flow was similar in both groups. In conclusion, rosuvastatin reduced brachiocephalic artery atherosclerotic plaques in ApoE-KO mice. Coronary artery function assessed using recently developed in vivo ultrasound-based protocols, also improved.

apolipoprotein E-knockout mouse; ultrasound imaging; atherosclerosis; rosuvastatin



Address for reprint requests and other correspondence: L.-M. Gan, Dept. of Clinical Physiology, Inst. of Medicine, Sahlgrenska Univ. Hospital, SE-413 45 Göteborg, Sweden (e-mail: li-ming.gan{at}hjl.gu.se)







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2008 by the American Physiological Society.