Prazosin Protects the Liver Against Renal Ischemia/Reperfusion Injury in Rats

Author:

Khajepour Fatemeh1,Mahmoodpoor Fariba23,Jafari Elmira1,Kakaei Farzad4,Bahraminia Farina1,Aghajani Shadi1,Vahed Sepideh Zununi2,Bagheri Yasin2

Affiliation:

1. Faculty of Veterinary Medicine, Tabriz Branch, Islamic Azad University, Tabriz, Iran

2. Kidney Research Center, Tabriz University of Medical Sciences, Tabriz, Iran

3. Department of Persian Medicine, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran

4. Department of General and Vascular Surgery, Tabriz University of Medical Sciences, Tabriz, Iran

Abstract

AbstractAcute kidney injury (AKI) is a common subsequent problem after many medical conditions. AKI is associated with distant organ dysfunction where systemic inflammation and oxidative stress play major roles. In this study, the effect of Prazosin, an α1-Adrenergic receptor antagonist, was investigated on the liver injury induced by kidney ischemia-reperfusion (I/R) in rats. Male adult Wistar rats (n=21) were divided into three groups: sham, kidney I/R, and kidney I/R pre-treated with Prazosin (1 mg/kg). Kidney I/R was induced by vascular clamping of the left kidney for 45 min to reduce the blood flow. Oxidative and antioxidant factors along with apoptotic (Bax, Bcl-2, caspase3), and inflammatory (NF-κβ, IL-1β, and IL-6) factors were measured in the liver at protein levels. Prazosin could reserve liver function (p<0.01) and increase glutathione level (p<0.05) after kidney I/R significantly. Malonil dialdehyde (MDA), a lipid peroxidation marker, was diminished more significantly in Prazosin-treated rats compared to the kidney I/R group (p<0.001). Inflammatory and apoptotic factors were diminished by Prazosin pre-treatment in the liver tissue (p<0.05). Pre-administration of Prazosin could preserve liver function and decrease its inflammatory and apoptotic factors under kidney I/R conditions.

Funder

Kidney Research Center of Tabriz University of Medical Sciences

Publisher

Georg Thieme Verlag KG

Subject

Drug Discovery,General Medicine

Reference32 articles.

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