| publication name | The effect of carvedilol on post-ischemic splanchnic tissue injury. Benha Medical Journal, 18(3):1153-1166 |
|---|---|
| Authors | AM El Abd, M Abdel-Aziz,, A Hussein, and A Tawfik, |
| year | 2001 |
| keywords | |
| journal | |
| volume | Not Available |
| issue | Not Available |
| pages | Not Available |
| publisher | Not Available |
| Local/International | Local |
| Paper Link | - |
| Full paper | download |
| Supplementary materials | Not Available |
Abstract
The objective of the current work aimed to investigate whether carvedilol is an effective antishock agent in the well established in vivo ischemia/reperfusion model of splanchnic artery occlusion shock. Also, to investigate the mechanism of this protection, such as antioxidant properties, preservation of endothelial function, and inhibition of neutrophil accumulation and adhesion. For this study, 36 rats weighing 120-200gm were selected. They were classified into 4 groups; control, splanchnic ischemia-reperfusion (SI/R), SI/R rats injected by 0.5mg/kg carvedilol and SI/R rats injected by 1.0 mg/kg carvedilol. Each group was formed of 9 rats. The results obtained showed that; hematocrite, tissue malondialdehyde (MDA), and tissue myeloperoxidase (MPO) were significantly increased (p<0.001) while plasma MDA and anti MPO were non-significantly increased in ischemic-reperfusion group compared with the control group. Comparative study of injected groups versus noninjected SI/R group, the result showed that; significant decrease of hematocrite (p<0.01), tissue MDA (p<0.001) and MPO (p<0.001) while plasma MDA and anti MPO were non-significantly changed in SI/R rats injected with 1.0 mg/Kg carvedilol. Mean while, SI/R rats injected with 0.5mg/Kg carvedilol showed non significant changes of all studied biochemical parameters when compared with the non-injected SI/R rats. We could conclude that; carvedilol pretreatment leads to amelioration of the adverse effects of SI/R shock by scavenging oxygen free radicals, counteracting the increased microvascular permeability and inhibiting the adhesion and activation of neutrophils in this model of splanchnic ischemia/reperfusion.