Crocin induces anti-ischemia in middle cerebral artery occlusion rats and inhibits autophagy by regulating the mammalian target of rapamycin.
Autophagy
Crocin
Mammalian target of rapamycin
Middle cerebral artery occlusion/reperfusion
Journal
European journal of pharmacology
ISSN: 1879-0712
Titre abrégé: Eur J Pharmacol
Pays: Netherlands
ID NLM: 1254354
Informations de publication
Date de publication:
15 Aug 2019
15 Aug 2019
Historique:
received:
15
03
2019
revised:
24
05
2019
accepted:
27
05
2019
pubmed:
1
6
2019
medline:
15
1
2020
entrez:
1
6
2019
Statut:
ppublish
Résumé
Crocin, an active compound found in Gardenia jasminoides Ellis, has been shown to possess neuron-protective properties, but its potential mechanisms of action still remain poorly understood. In this study, the anti-ischemic effect and underlying mechanism of action of crocin were investigated in male rats with right middle cerebral artery occlusion/reperfusion. Computed tomography and magnetic resonance imaging were used to evaluate the area of infarction 24 h after reperfusion. Neurological scores were employed to evaluate nerve injury. Direct 2,3,5-triphenyltetrazolium chloride staining was used to calculate the infarct ratio 120 h after reperfusion. Finally, HT22 cells and Western blot were used to study the underlying mechanisms. Crocin showed a decreased infarct volume and neurological score in vivo, while the expression of LC3-II/I and AMP-activated protein kinase was remarkably down-regulated with increased levels of p62 and mammalian target of rapamycin (mTOR) expression. However, rapamycin significantly inhibited mTOR, which can impact the anti-ischemic effect of crocin in vitro. These results suggest that crocin may elicit an anti-ischemic effect probably through the mTOR pathway.
Identifiants
pubmed: 31150648
pii: S0014-2999(19)30375-9
doi: 10.1016/j.ejphar.2019.172424
pii:
doi:
Substances chimiques
Carotenoids
36-88-4
crocin
877GWI46C2
TOR Serine-Threonine Kinases
EC 2.7.11.1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
172424Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.