SAGE Journals Online
Advertisement
Sign In to gain access to subscriptions and/or personal tools.

 

Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Advertisement

Sign In to gain access to subscriptions and/or personal tools.
Angiology
This Article
Right arrow Full Text (PDF)
Right arrow References
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 Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Rogers, S. J.
Right arrow Articles by Ikram, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rogers, S. J.
Right arrow Articles by Ikram, H.
Right arrowPubmed/NCBI databases
*Compound via MeSH
*Substance via MeSH
Medline Plus Health Information
*Heart Attack
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

An Ovine Model of Acute Myocardial Infarction and Chronic Left Ventricular Dysfunction

Sandra Jane Rogers, MSc

Christopher John Charles, PhD

Jennifer Sands, DCR

Arthur Mark Richards, MD, PhD, FRACP

Paul Gavin Bridgman, MB, ChB

Ravi Gooneratne, PhD

H. Ikram, MD

Department of Cardiology Christchurch Hospital Private Bag 4710 Christchurch, New Zealand

In order to develop and validate an ovine model of myocardial infarction with subse quent impairment of left ventricular function, 15 instrumented sheep underwent selective microembolization of the left coronary arteries with 0.5 mL 90 micron polystyrene beads. Hemodynamics and plasma hormones were measured preembolization (baseline) and then at hours 2, 4, 6, and 12 and days 1, 2, 3, 5 and 7 postembolization. Of the 15 sheep studied, 2 (13%) died on the day of embolization from arrhythmias. In the remaining sheep, left ventricular systolic pressure and stroke work (both P<0.001 ) were reduced promptly and remained below basal levels. Mean arterial pressure (P<0.001) increased initially, then decreased to below basal levels by hour 6. Heart rate (P<0.001) and left atrial pressure (P<0.05) were increased while cardiac output was decreased (P<0.05). Left ventricular ejection fraction at day 7 was reduced (38.8 ±3.5 vs 46.0 ±3.9% preem bolization ; P<0.05). The cardiac enzymes creatine kinase (P<0.001) and troponin-T (P< 0.001) were increased following microembolization and returned to basal levels by days 2 and 5 respectively. Plasma atrial and brain natriuretic peptides (both P< 0.001) and plasma renin activity (P<0.005) were all increased following embolization. This ovine model mimics the hemodynamic and neurohumoral features of acute myocardial infarction, resulting in left ventricular dysfunction, and should prove suitable for the study of interventions in a number of these conditions.

Angiology, Vol. 48, No. 8, 679-688 (1997)
DOI: 10.1177/000331979704800803


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?




Advertisement