Abstract | AIMS: RESULTS: Global ischemia was induced in 3- and 18-month-old male Sprague-Dawley rats and CA1 and CA3 hippocampal areas, dentate gyrus and cerebral cortex of sham-operated and I/R animals were removed 48 h after insult. Real-time PCR analysis revealed that I/R challenge resulted in a significant decrease of the VGLUT mRNA levels in young animals. Western blot assays showed a lessened age-dependent response to the ischemic damage in VGLUT1 and VGLUT3, while VGLUT2 presented an age and structure-dependent response to challenge. The use of the anti-inflammatory agent meloxicam following challenge showed that COX2 inhibition promotes the expression of VGLUTs in both sham and injured animals, which results in a lessened response to I/R injury. CONCLUSIONS: VGLUT1 and VGLUT3 presented an age-dependent response to ischemic damage, while this VGLUT response was age both and structure-dependent. In addition, COX-2 inhibition resulted in an increase of VGLUT1 and VGLUT2 protein amounts both in sham and injured animals together with a lessening of the transporters' response to ischemia.
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Authors | Irene L Llorente, Diego Pérez-Rodríguez, Taiana C Burgin, José M Gonzalo-Orden, Beatriz Martínez-Villayandre, Arsenio Fernández-López |
Journal | Brain research bulletin
(Brain Res Bull)
Vol. 94
Pg. 90-7
(May 2013)
ISSN: 1873-2747 [Electronic] United States |
PMID | 23458738
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2013 Elsevier Inc. All rights reserved. |
Chemical References |
- Anti-Inflammatory Agents, Non-Steroidal
- Thiazines
- Thiazoles
- Vesicular Glutamate Transport Proteins
- Meloxicam
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Topics |
- Age Factors
- Animals
- Anti-Inflammatory Agents, Non-Steroidal
(pharmacology)
- Blotting, Western
- Brain
(drug effects, metabolism)
- Brain Ischemia
(metabolism)
- Disease Models, Animal
- Male
- Meloxicam
- Rats
- Rats, Sprague-Dawley
- Real-Time Polymerase Chain Reaction
- Thiazines
(pharmacology)
- Thiazoles
(pharmacology)
- Vesicular Glutamate Transport Proteins
(biosynthesis)
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