Branched chain amino Acids as in vitro and in vivo Anti-Oxidation Compounds

Author:

Alqaraleh Moath1,Kasabri Violet2,Al-Majali Ibrahim3,Al-Othman Nihad4,Al-Othman Nihad4,K. Khleifat5,Al‐Tawarah Nafe M3,Qaralleh Haitham3,Khwaldeh Alia S.6,Alalawi Sundus2,al majali Mohammad7

Affiliation:

1. Pharmacological and Diagnostic Research Center (PDRC), Faculty of Pharmacy, Al-Ahliyya Amman University, Amman 19328, Jordan.

2. Department of Pharmacy, Faculty of Pharmacy. The University of Jordan, Amman, Jordan.

3. Department of Medical Analysis, Mutah University, Mutah, Karak, 61710, Jordan.

4. Division of Anatomy, Biochemistry, and Genetics. Faculty of Medicine and Health Sciences, An-Najah National University, Nablus,

5. Department of Biology, Mutah University, Karak, Mutah, 61710 Jordan.

6. Department of Medical Laboratory Sciences, Faculty of Pharmacy, Jadara University, Irbid, Jordan.

7. Department of Biological Sciences, Faculty of Science. The University of Jordan, Amman, Jordan.

Abstract

Background and aims: Branched chain amino acids (BCAAs) can be tightly connected to metabolism syndrome (MetS) which can be counted as a metabolic indicator in the case of insulin resistance (IR). The aim of this study was to assess the potential role of these acids under oxidative stress. Material and Methods: the in vitro antioxidant activity of BCAAs was assessed using free radical 1, 1-diphenyl-2-picryl-hydrazyl (DPPH) scavenging assays. For further check, a qRT-PCR technique was madefor detection the extent of alterations in gene expression of antioxidative enzymes (catalase and glutathione peroxidase (Gpx)) in lipopolysaccharides (LPS(-induced macrophages RAW 264.7 cell line. Additionally, BCAAs antioxidant activity was evaluated based on plasma H2O2 levels and xanthine oxidase (XO) activity in prooxidative LPS-treated mice. Results: Different concentrations of BCAAs affected on DPPH radical scavenging activity but to lesser extent than the ascorbic acid. Besides, BCAAs obviously upregulated the gene expression levels of catalases and Gpx in LPS-modulated macrophage RAW 264.7 cell line. In vivo BCAAs significantly minimized the level of plasma H2O2 as well as the activity of XO activity under oxidative stress. Conclusion: our current findings suggest that BCAAs supplementation may potentially serve as a therapeutic target for treatment of oxidative stress occurs with atherosclerosis, IR-diabetes, MetS and tumorigenesis.

Publisher

A and V Publications

Subject

Pharmacology (medical),Pharmacology, Toxicology and Pharmaceutics (miscellaneous)

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