Academic Journals Database
Disseminating quality controlled scientific knowledge

Complement-1 Inhibitor Attenuates Myocardial Ischemia Reperfusion Injury in a Guinea Pig Model

ADD TO MY LIST
 
Author(s): Yildirim Imren | Timothy P. Martens | Ariel A. Benson | Gulbin Aygencel | Eser Oz | Mustafa Arslan | Sedat Kalaycioglu

Journal: Research Journal of Biological Sciences
ISSN 1815-8846

Volume: 2;
Issue: 5;
Start page: 523;
Date: 2007;
VIEW PDF   PDF DOWNLOAD PDF   Download PDF Original page

Keywords: Complement inhibitor | ischemia | reperfusion injury pig model | MDA

ABSTRACT
Complement-1 esterase inhibitor (C1-INH), an endogenously derived compound, is a key mediator providing regulation of the complement system. In this study, the protective role of C1-INH was investigated in the setting of myocardial ischemia reperfusion injury. Guinea pig hearts (n = 20) were studied in control (n = 10) and experimental (n = 10) groups, using a modified Langendorff perfusion apparatus. Control hearts were perfused with Krebs Henseleit solution during pre-ischemia and reperfusion periods while C1-INH was added to the perfusates of experimental hearts during the reperfusion period. Heart rate (pulse/minute), contractility (mm) and aortic pressure (mmHg) values were recorded at the end of pre-ischemia, post-ischemia and reperfusion periods. Perfusate and tissue analysis for glutathione and malondialdehyde levels and perfusate analysis for nitric oxide levels were obtained at the end of each experimental period. Both increased aortic pressure and cardiac contractility as well as elevated levels of tissue glutathione and MDA were observed in the experimental group during reperfusion. Perfusate levels of glutathione and MDA remained unchanged. As a result, it was concluded that C1 esterase inhibitor preserved cardiac contractility and protected against ischemia reperfusion injury.
Why do you need a reservation system?      Affiliate Program