Effect of Treatment with Cyanidin-3-O-β-D-Glucoside on Rat Ischemic/Reperfusion Brain Damage
Identifieur interne : 001350 ( Main/Curation ); précédent : 001349; suivant : 001351Effect of Treatment with Cyanidin-3-O-β-D-Glucoside on Rat Ischemic/Reperfusion Brain Damage
Auteurs : Claudia Di Giacomo [Italie] ; Rosaria Acquaviva [Italie] ; Rosa Santangelo [Italie] ; Valeria Sorrenti [Italie] ; Luca Vanella [Italie] ; Giovanni Li Volti [Italie] ; Nicolantonio D'Orazio [Italie] ; Angelo Vanella [Italie] ; Fabio Galvano [Italie]Source :
- Evidence-based Complementary and Alternative Medicine : eCAM [ 1741-427X ] ; 2012.
Abstract
This study investigated the effect of cyanidin-3-O-
Url:
DOI: 10.1155/2012/285750
PubMed: 23008739
PubMed Central: 3449154
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PMC:3449154Le document en format XML
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-D-Glucoside on Rat Ischemic/Reperfusion Brain Damage</title>
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<author><name sortKey="D Orazio, Nicolantonio" sort="D Orazio, Nicolantonio" uniqKey="D Orazio N" first="Nicolantonio" last="D'Orazio">Nicolantonio D'Orazio</name>
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<author><name sortKey="Galvano, Fabio" sort="Galvano, Fabio" uniqKey="Galvano F" first="Fabio" last="Galvano">Fabio Galvano</name>
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<series><title level="j">Evidence-based Complementary and Alternative Medicine : eCAM</title>
<idno type="ISSN">1741-427X</idno>
<idno type="eISSN">1741-4288</idno>
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<front><div type="abstract" xml:lang="en"><p>This study investigated the effect of cyanidin-3-O-<italic><italic>β</italic>
</italic>
-glucoside on an experimental model of partial/transient cerebral ischemia in the rats in order to verify the effectiveness of both pre- and posttreatments. Cyanidin-3-O-<italic><italic>β</italic>
</italic>
-glucoside-pretreated rats were injected with 10 mg/Kg i.p. 1 h before the induction of cerebral ischemia; in posttreated rats, the same dosage was injected during reperfusion (30 min after restoring blood flow). Cerebral ischemia was induced by bilateral clamping of common carotid arteries for 20 min. Ischemic rats were sacrificed immediately after 20 min ischemia; postischemic reperfused animals were sacrificed after 3 or 24 h of restoring blood flow. Results showed that treatment with cyanidin increased the levels of nonproteic thiol groups after 24 h of postischemic reperfusion, significantly reduced the lipid hydroperoxides, and increased the expression of heme oxygenase and <italic><italic>γ</italic>
</italic>
-glutamyl cysteine synthase; a significant reduction in the expression of neuronal and inducible nitric oxide synthases and the equally significant increase in the endothelial isoform were observed. Significant modifications were also detected in enzymes involved in metabolism of endogenous inhibitors of nitric oxide. Most of the effects were observed with both pre- and posttreatments with cyanidin-3-O-<italic><italic>β</italic>
</italic>
-glucoside suggesting a role of anthocyanin in both prevention and treatment of postischemic reperfusion brain damage.</p>
</div>
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