Abstract | BACKGROUND: METHODS AND RESULTS: Rats underwent 2 h of middle cerebral artery occlusion (MCAo). DHA, neuroprotectin D1 (NPD1) or vehicle (saline) was administered 3 h after onset of stroke. Neurological function was evaluated on days 1, 2, 3, and 7. DHA treatment improved functional recovery and reduced cortical, subcortical and total infarct volumes 7 days after stroke. DHA also reduced microglia infiltration and increased the number of astrocytes and neurons when compared to vehicle on days 1 and 7. Increases in p473 AKT and p308 AKT phosphorylation/activation were observed in animals treated with DHA 4 h after MCAo. Activation of other members of the AKT signaling pathway were also observed in DHA treated animals including increases in pS6 at 4 h and pGSK at 24 h. DHA or NPD1 remarkably reduced total and cortical infarct in aged rats. Moreover, we show that in young and aged rats DHA treatment after MCAo potentiates NPD1 biosynthesis. The phosphorylation of p308 AKT or pGSK was not different between groups in aged rats. However, pS6 expression was increased with DHA or NPD1 treatment when compared to vehicle. CONCLUSIONS: We suggest that DHA induces cell survival, modulates the neuroinflammatory response and triggers long term restoration of synaptic circuits. Both DHA and NPD1 elicited remarkable protection in aged animals. Accordingly, activation of DHA signaling might provide benefits in the management of ischemic stroke both acutely as well as long term to limit ensuing disabilities.
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Authors | Tiffany N Eady, Ludmila Belayev, Larissa Khoutorova, Kristal D Atkins, Changde Zhang, Nicolas G Bazan |
Journal | PloS one
(PLoS One)
Vol. 7
Issue 10
Pg. e46151
( 2012)
ISSN: 1932-6203 [Electronic] United States |
PMID | 23118851
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- protectin D1
- Docosahexaenoic Acids
- Proto-Oncogene Proteins c-akt
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Topics |
- Animals
- Behavior
(drug effects)
- Brain Ischemia
(metabolism, pathology, therapy)
- Cell Survival
(drug effects)
- Disease Models, Animal
- Docosahexaenoic Acids
(administration & dosage, biosynthesis)
- Gene Expression Regulation
(drug effects)
- Humans
- Infarction, Middle Cerebral Artery
- Male
- Phosphorylation
- Proto-Oncogene Proteins c-akt
(metabolism)
- Rats
- Recovery of Function
(drug effects)
- Signal Transduction
- Stroke
(metabolism, pathology, therapy)
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