The ameliorative impacts of Moringa oleifera leaf extract against oxidative stress and methotrexate-induced hepato-renal dysfunction.


Journal

Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
ISSN: 1950-6007
Titre abrégé: Biomed Pharmacother
Pays: France
ID NLM: 8213295

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 22 03 2020
revised: 03 05 2020
accepted: 10 05 2020
pubmed: 3 6 2020
medline: 27 2 2021
entrez: 3 6 2020
Statut: ppublish

Résumé

Moringa Oleifera (MO) is a herbal plant native to South Asia known for its anti-oxidative and anti-inflammatory properties. This study explored the protective effects of MO leaf extract (MOLE) against oxidative stress and hepatic and renal injuries caused by methotrexate (MTX) therapy. Mice received a single intraperitoneal injection of 20 mg/kg body weight MTX to induce hepatic and kidney injuries. They then received 300 mg/kg body weight of MOLE orally for seven days, followed by MTX on day 7 then five more days of MOLE (12 days total). Blood, liver and kidney samples were collected from all groups and the following biochemical parameters were tested: serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), catalase, superoxide dismutase (SOD), malondialdehyde (MDA) and total proteins. Quantitative real time PCR (qRT-PCR) was used to examine Nrf2, HO-1, BAX, TIMP, XIAP, and NFkB, which are associated with apoptosis, anti-apoptosis and oxidative stress. Capase-9 and Bcl2 genes underwent immunohistochemical analysis. Pretreatment with MOLE reduced the effect of MTX on ALT, AST and total proteins, and reversed its effect on serum and tissue antioxidants. Nrf2/HO-1, apoptotic and anti-apoptotic gene expression was regulated, and Bax and TIMP were reduced; XIAP expression was increased in both the liver and kidney samples, and immunoreactivity of caspase-9 and Bcl2 was restored in the MOLE-administered experimental group. Overall, the study concluded that MOLE can inhibit the effects of hepato-renal injuries caused by MTX by regulating oxidative stress, apoptosis and anti-apoptotic genes at biochemical, molecular and cellular levels.

Identifiants

pubmed: 32485567
pii: S0753-3322(20)30451-0
doi: 10.1016/j.biopha.2020.110259
pii:
doi:

Substances chimiques

Antioxidants 0
Apoptosis Regulatory Proteins 0
Inflammation Mediators 0
Plant Extracts 0
Methotrexate YL5FZ2Y5U1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

110259

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier Masson SAS.. All rights reserved.

Auteurs

Mohamed Mohamed Soliman (MM)

Clinical Laboratory Sciences Department, Turabah University College, Taif University, 21995, Saudi Arabia; Biochemistry Department, Faculty of Veterinary Medicine, Benha University, Benha 13736, Egypt. Electronic address: mohamed.soliman@fvtm.bu.edu.eg.

Adil Aldhahrani (A)

Clinical Laboratory Sciences Department, Turabah University College, Taif University, 21995, Saudi Arabia.

Adel Alkhedaide (A)

Clinical Laboratory Sciences Department, Turabah University College, Taif University, 21995, Saudi Arabia.

Mohamed Abdo Nassan (MA)

Department of Pathology, Faculty of Veterinary Medicine, Zagazig University, Zagazig 44519, Egypt.

Fayez Althobaiti (F)

Biotechnology Department, College of Science, Taif University, 21995, Saudi Arabia.

Wafaa Abdou Mohamed (WA)

Department of Clinical Pathology, Faculty of Veterinary Medicine, Zagazig University, Zagazig 44519, Egypt.

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Classifications MeSH