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Hepcidin inhibits autophagy in intracerebral hemorrhage models in vitro and in vivo.
- Source :
-
Molecular and cellular neurosciences [Mol Cell Neurosci] 2021 Mar; Vol. 111, pp. 103589. Date of Electronic Publication: 2021 Jan 08. - Publication Year :
- 2021
-
Abstract
- Iron has a key role in the activation of the autophagic pathway in rats with intracerebral hemorrhage (ICH), and hepcidin has the ability to reduce brain iron in ICH-rats. We therefore hypothesized that hepcidin might be able to inhibit autophagy by reducing iron in an ICH brain. Here, we investigated the effects of Ad-hepcidin and/or hepcidin peptide on autophagic activities in ICH models in vitro and in vivo. We demonstrated that ad-hepcidin and hepcidin peptide both inhibited hemin-induced increase in LC3-II/LC3-I conversion ratio and reversed the reduction in p62 content in cortical neurons in vitro. We also showed that ad-hepcidin inhibited ICH-induced increase in LC3-II/LC3-I conversion ratio and reversed ICH-induced reduction in p62 content in the brain cortex of rats in vivo. Based on these findings plus previous data on the effects of ad-hepcidin and/or hepcidin peptide on iron contents in ICH models, we suggested that hepcidin-induced inhibition of autophagy might be mediated via reducing iron in hemin-treated neurons in vitro and ICH-rat brain in vivo.<br /> (Copyright © 2021 Elsevier Inc. All rights reserved.)
- Subjects :
- Adenoviridae genetics
Animals
Cells, Cultured
Cerebral Cortex cytology
Cerebral Cortex metabolism
Genetic Vectors genetics
Hepcidins genetics
Male
Microtubule-Associated Proteins metabolism
Neurons metabolism
Rats
Rats, Sprague-Dawley
Recombinant Proteins genetics
Recombinant Proteins metabolism
Sequestosome-1 Protein metabolism
Autophagy
Cerebral Hemorrhage metabolism
Hepcidins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1095-9327
- Volume :
- 111
- Database :
- MEDLINE
- Journal :
- Molecular and cellular neurosciences
- Publication Type :
- Academic Journal
- Accession number :
- 33422672
- Full Text :
- https://doi.org/10.1016/j.mcn.2021.103589