Epimedium polysaccharides attenuates hematotoxicity by reducing oxidative stress and enhancing immune function in mice model of benzene-induced bone marrow failure.
Animals
Antioxidants
/ pharmacology
Benzene
/ toxicity
Bone Marrow Failure Disorders
/ chemically induced
Dose-Response Relationship, Drug
Drugs, Chinese Herbal
/ pharmacology
Epimedium
Immunity, Cellular
/ drug effects
Male
Mice
Oxidative Stress
/ drug effects
Polysaccharides
/ pharmacology
Reactive Oxygen Species
/ antagonists & inhibitors
Benzene
Bone marrow failure
Epimedium polysaccharides
Immunotoxicity
Journal
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
ISSN: 1950-6007
Titre abrégé: Biomed Pharmacother
Pays: France
ID NLM: 8213295
Informations de publication
Date de publication:
May 2020
May 2020
Historique:
received:
07
10
2019
revised:
06
01
2020
accepted:
12
01
2020
pubmed:
6
2
2020
medline:
22
12
2020
entrez:
5
2
2020
Statut:
ppublish
Résumé
Chronic benzene (BZ) exposure is associated with multiple adverse health effects and leads to progressive bone marrow failure (BMF). BZ-induced BMF is an acquired aplastic anemia characterized by severe anemia, neutropenia and thrombocytopenia, which is likely caused by immunotoxicity and oxidative stress. Previous studies showed that Epimedium polysaccharides (EPS), a natural and major herbal compound derived from Epimedium, has immunomodulatory and antioxidant potential. The purpose of this study was to evaluate the potential efficacy of EPS against BZ-induced BMF. BMF mouse model was established by subcutaneous injection of 2 ml/kg BZ in CD1 mice. Mice received daily oral treatment with 100 mg/kg high-dose EPS and 20 mg/kg low-dose EPS for four weeks. Our data showed that EPS treatment alleviated BZ-associated weight loss and increased the number of whole blood cells in peripheral blood and nucleated cells in bone marrow. Furthermore, EPS treatment decreased apoptotic rate and reactive oxygen species production, S-phase arrest in bone marrow cells. Finally, EPS treatment improved T cell-mediated immune suppression by increasing CD3+, CD4 + T-cell counts, and CD4+/CD8+ ratio. and modulated hematopoietic cytokines including EPO, IL-11, and IL-2 in peripheral blood. Our study suggests that EPS is a potential therapeutic target to attenuate hematotoxicity induced by BZ.
Identifiants
pubmed: 32014688
pii: S0753-3322(20)30098-6
doi: 10.1016/j.biopha.2020.109908
pii:
doi:
Substances chimiques
Antioxidants
0
Drugs, Chinese Herbal
0
Polysaccharides
0
Reactive Oxygen Species
0
Benzene
J64922108F
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
109908Informations de copyright
Copyright © 2020. Published by Elsevier Masson SAS.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare that they have no potential competing interests.