The ameliorative impacts of Moringa oleifera leaf extract against oxidative stress and methotrexate-induced hepato-renal dysfunction.
Animals
Antioxidants
/ isolation & purification
Apoptosis
/ drug effects
Apoptosis Regulatory Proteins
/ genetics
Chemical and Drug Induced Liver Injury
/ etiology
Disease Models, Animal
Gene Expression Regulation
Inflammation Mediators
/ metabolism
Kidney
/ drug effects
Kidney Diseases
/ chemically induced
Liver
/ drug effects
Male
Methotrexate
Mice
Moringa oleifera
/ chemistry
Oxidative Stress
/ drug effects
Plant Extracts
/ isolation & purification
Plant Leaves
/ chemistry
Signal Transduction
Gene expression
Kidney
Liver
Methotrexate
Moringa oleifera
Oxidative stress
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
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
110259Informations de copyright
Copyright © 2020 The Author(s). Published by Elsevier Masson SAS.. All rights reserved.