Acetyl-11-Keto-β-Boswellic Acid and Incensole Acetate Attenuate Lipopolysaccharide-Induced Acute Kidney Injury by Inhibiting Inflammation and Oxidative Stress

Author:

Sharifi Mohammad Rahim1,Hakimi Zhara1,Ghalibaf Mohammad Hosein Eshaghi2,Fazeli Elham3,Behshti Farimah45,Marefati Narges6,Hosseini Mahmoud7

Affiliation:

1. Department of Physiology, Faculty of Medicine, Ghalib University, Herat, Afghanistan

2. Applied Biomedical Research Center, Mashhad University of Medical Sciences, Mashhad, Iran

3. Department of Biology, Islamic Azad University Mashhad Branch, Mashhad, Iran

4. Neuroscience Research Center, Torbat Heydariyeh University of Medical Sciences, Torbat Heydariyeh, Iran

5. Department of Physiology, School of Medicine, Torbat Heydariyeh University of Medical Sciences, Torbat Heydariyeh, Iran

6. Department of Physiology and Medical Physics, Faculty of Medicine, Baqiyatallah University of Medical Sciences, Tehran, Iran

7. Department of Physiology, Psychiatry and Behavioral Sciences Research Center, School of Medicine, Azadi Square, Mashhad, Iran

Abstract

Boswellia serrata has been used in traditional medicine to treat various inflammatory diseases. Acetyl-11-keto-β-boswellic acid (AKBA) and incensole acetate (IA) are two active ingredients of B. serrata that possess anti-inflammatory and antioxidant activities. The present study aimed to investigate the protective effects of AKBA and IA against lipopolysaccharide (LPS)- induced acute kidney injury (AKI) in rats. Wistar rats were intraperitoneally pretreated with AKBA or IA for 2 weeks. After 30 min, an LPS injection was applied to induce AKI. Blood samples and kidney tissues were collected and used for biochemical assays. AKBA and IA not only significantly decreased interleukin-6 as a marker of renal inflammation but also attenuated the oxidative stress markers in kidney tissues. AKBA and IA also remarkably decreased serum creatinine and blood urea nitrogen. These results suggest that AKBA and IA have protective effects against AKI in rats through regulating inflammation and oxidative stress.

Publisher

Medknow

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