<i>Castanea sativa</i> Mill. Bark Extract Protects U‐373 MG Cells and Rat Brain Slices Against Ischemia and Reperfusion Injury
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- Chiara Santulli
- Dipartimento di Scienze della Vita Università di Siena Via Aldo Moro 2‐53100 Siena Italy
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- Claudia Brizi
- Dipartimento di Scienze della Vita Università di Siena Via Aldo Moro 2‐53100 Siena Italy
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- Matteo Micucci
- Dipartimento di Farmacia e Biotecnologie Università di Bologna Via Belmeloro 6‐40126 Bologna Italy
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- Ambra Del Genio
- Dipartimento di Scienze della Vita Università di Siena Via Aldo Moro 2‐53100 Siena Italy
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- Assunta De Cristofaro
- Dipartimento di Scienze della Vita Università di Siena Via Aldo Moro 2‐53100 Siena Italy
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- Federica Bracco
- Dipartimento di Scienze della Vita Università di Siena Via Aldo Moro 2‐53100 Siena Italy
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- Giuseppina Lucia Pepe
- Dipartimento di Scienze della Vita Università di Siena Via Aldo Moro 2‐53100 Siena Italy
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- Ilaria di Perna
- Dipartimento di Scienze della Vita Università di Siena Via Aldo Moro 2‐53100 Siena Italy
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- Roberta Budriesi
- Dipartimento di Farmacia e Biotecnologie Università di Bologna Via Belmeloro 6‐40126 Bologna Italy
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- Alberto Chiarini
- Dipartimento di Farmacia e Biotecnologie Università di Bologna Via Belmeloro 6‐40126 Bologna Italy
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- Maria Frosini
- Dipartimento di Scienze della Vita Università di Siena Via Aldo Moro 2‐53100 Siena Italy
抄録
<jats:title>ABSTRACT</jats:title><jats:sec><jats:label /><jats:p>Ischemic brain injury is one of the most important causes of death worldwide. The use of one‐drug‐multi‐target agents based on natural compounds is a promising therapeutic option for cerebral ischemia due to their pleiotropic properties. This study assessed the neuroprotective properties of <jats:italic>Castanea sativa Mill</jats:italic>. bark extract (ENC) in human astrocytoma U‐373 MG cells subjected to oxygen‐glucose deprivation and reperfusion and rat cortical slices subjected to ischemia‐like conditions or treated with glutamate or hydrogen peroxide. Neuroprotective effects were determined by assessing cells or slices viability (MTT assay), ROS formation (DCFH‐DA assay), apoptosis (sub G0/G1 peak), nuclear fragmentation and chromatin condensation (DAPI staining) as well as changes in lysosomes and mitochondria morphology (Acridine Orange and Rhodamine123 staining, respectively). ENC treatment before injury on U‐373 MG cells (5–50 μg/ml) and cortical slices (50–100 μg/ml) provided neuroprotection, while lower or higher concentrations (100 μg/ml U‐373 MG cells, 200 μg/ml brain slices) were ineffective. ENC addition during reperfusion or after the injury was not found to be effective. The results suggest that ENC might hold potential as preventive neuroprotective agent, and indicate the importance of further studies exploring its mechanism of action. J. Cell. Biochem. 118: 839–850, 2017. © 2016 Wiley Periodicals, Inc.</jats:p></jats:sec>
収録刊行物
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- Journal of Cellular Biochemistry
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Journal of Cellular Biochemistry 118 (4), 839-850, 2016-11-28
Wiley