Meeting details menu

Meeting Authors
Meeting Abstracts
Keynote lectures
Oral communications
Poster presentations
Special symposia
Other

Acta Physiologica Congress

Back

Acta Physiologica 2011; Volume 201, Supplement 682
The 90th Annual Meeting of The German Physiological Society
3/26/2011-3/29/2011
Regensburg, Germany


EFFECTS OF MESENCHYMAL STEM CELL THERAPY ON CARDIAC REMODELING IN A RAT MODEL OF CARDIAC ISCHEMIA/REPERFUSION
Abstract number: P079

*Werner1 F., Frohlich1 W., Nitzsche1 B., Deten1 A.

Question: 

In this study the effects of bone marrow mesenchymal stem cells (BM-MSCs) on cardiac remodeling in a rat model of ischemia/reperfusion (I/R) were investigated.

Methods: 

BM-MSCs were delivered by i.v. (each 1 Mill. cells on day 1, 2 and 3 after MI) or direct intramyocardial injections (each 1Mill. cells on day 1 and 3 [early] or day 7 [late] after MI). After 6 weeks, heart function was measured by LV catheterization. The mRNA expression of IL-1b, IL-6, and TGF-b1-3 isoforms was analyzed by real-time PCR and histological sections were stained with picrosirius red for analysis of collagen content.

Results: 

In all I/R groups, the content of collagen I and collagen III was significantly higher in the infarct area compared to the non-infarcted septum and the free LV wall of sham-operated animals. All MSC-treated groups showed significantly higher collagen type III content in the infarct scar compared with untreated I/R, but not the respective medium treated control. Of note, both BM-MSC and medium early IM treated groups showed significantly higher collagen type I content in the infarct scar than control and late IM, but there were no further statistical significant differences compared with untreated I/R or medium treated controls. Also of note, both early IM groups had significantly higher IL1-b expression in the infarct area than I/R control and the worst cardiac function of all I/R groups.

Conclusion: 

Despite increased collagen III, there was, however, no functional improvement in the BM-MCS treated groups.

To cite this abstract, please use the following information:
Acta Physiologica 2011; Volume 201, Supplement 682 :P079

Our site uses cookies to improve your experience.You can find out more about our use of cookies in our standard cookie policy, including instructions on how to reject and delete cookies if you wish to do so.

By continuing to browse this site you agree to us using cookies as described in our standard cookie policy .

CLOSE