The protective effect of zeranol in cerebral ischemia reperfusion via p-CREB overexpression.
Animals
Brain
/ drug effects
Brain Ischemia
/ drug therapy
Cyclic AMP Response Element-Binding Protein
/ analysis
Female
Inflammation Mediators
/ analysis
Matrix Metalloproteinase 9
/ analysis
Neurogenesis
/ drug effects
Neuronal Plasticity
/ drug effects
Nitric Oxide Synthase Type II
/ analysis
Oxidative Stress
/ drug effects
Phytoestrogens
/ therapeutic use
Rats, Wistar
Reperfusion Injury
/ drug therapy
Zeranol
/ therapeutic use
Cerebral ischemia reperfusion
GLUT-3 and BDNF
Inflammatory markers
Oxidative stress
p-CREB
Journal
Life sciences
ISSN: 1879-0631
Titre abrégé: Life Sci
Pays: Netherlands
ID NLM: 0375521
Informations de publication
Date de publication:
15 Jan 2019
15 Jan 2019
Historique:
received:
04
11
2018
revised:
09
12
2018
accepted:
10
12
2018
pubmed:
15
12
2018
medline:
12
1
2019
entrez:
15
12
2018
Statut:
ppublish
Résumé
Cerebral ischemia reperfusion (I/R) is a neurovascular disease leading to cerebral damage. It was found that postmenopausal women are liable to more dangerous effects than men at same age in stroke. The objective of this study is to investigate the neuroprotective effect of zeranol against cerebral ischemia reperfusion in ovariectomized rats. 36 female wistar rats divided in to 3 groups: sham group, I/R group (where I/R was induced 7 weeks after ovariectomy), zeranol group (0.5 mg/kg every 3 days for 5 weeks before I/R). Cerebral ischemia reperfusion (I/R) was performed by bilateral common carotid artery occlusion then de-ligated to restore blood flow. After 24 h of reperfusion, rats performed cylinder test to evaluate behavioral dysfunction followed by decapitation. Brain tissues were collected for biochemical measures such as oxidative stress marker malondialdehyde, antioxidant markers reduced glutathione, inflammatory markers (interleukin-1 beta, tumor necrosis factor alpha, and inducible nitric oxide synthase), matrix metalloproteinase-9, adenosine triphosphate, brain derived neurotrophic factor, glucose transporter-3, phosphorylated c-AMP response element binding protein and finally nissl staining for histopathological examination. The zeranol administered group showed a reversal of neuronal damage caused by ischemia evidenced by the decrease in MDA, IL-1β, TNF-α, and MMP-9 levels, increase GSH, and ATP levels, decrease expression of iNOS in both regions cortex and hippocampus, increase protein level of p-CREB, GLUT-3 and BDNF, increase number of intact neuron cells in both regions and attenuated histological changes in both cortex and hippocampus regions. Zeranol has neuroprotective potential against cerebral ischemia reperfusion in ovariectomized rats.
Identifiants
pubmed: 30550883
pii: S0024-3205(18)30800-2
doi: 10.1016/j.lfs.2018.12.017
pii:
doi:
Substances chimiques
Creb1 protein, rat
0
Cyclic AMP Response Element-Binding Protein
0
Inflammation Mediators
0
Phytoestrogens
0
Zeranol
76LO2L2V39
Nitric Oxide Synthase Type II
EC 1.14.13.39
Nos2 protein, rat
EC 1.14.13.39
Matrix Metalloproteinase 9
EC 3.4.24.35
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
212-221Informations de copyright
Copyright © 2018 Elsevier Inc. All rights reserved.