TY  - JOUR
T1  - Complement-1 Inhibitor Attenuates Myocardial Ischemia Reperfusion Injury in a Guinea Pig Model
AU - , Yildirim Imren AU - , Timothy P. Martens AU - , Ariel A. Benson AU - , Gulbin Aygencel AU - , Eser Oz AU - , Mustafa Arslan AU - , Sedat Kalaycioglu 
JO  - Research Journal of Biological Sciences
VL  - 2
IS  - 5
SP  - 523
EP  - 528
PY  - 2007
DA  - 2001/08/19
SN  - 1815-8846
DO  - rjbsci.2007.523.528
UR  - https://makhillpublications.co/view-article.php?doi=rjbsci.2007.523.528
KW  - Complement inhibitor
KW  -ischemia
KW  -reperfusion injury pig model
KW  -MDA
AB  - 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.
ER  -