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D2-like receptor activation does not initiate a brain docosahexaenoic acid signal in unanesthetized rats

BACKGROUND: The polyunsaturated fatty acid, docosahexaenoic acid (DHA), participates in neurotransmission involving activation of calcium-independent phospholipase A(2) (iPLA(2)), which is coupled to muscarinic, cholinergic and serotonergic neuroreceptors. Drug induced activation of iPLA(2) can be m...

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Detalles Bibliográficos
Autores principales: Taha, Ameer Y, Chang, Lisa, Chen, Mei, Rapoport, Stanley I, Ramadan, Epolia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4295280/
https://www.ncbi.nlm.nih.gov/pubmed/25359512
http://dx.doi.org/10.1186/1471-2202-15-113
Descripción
Sumario:BACKGROUND: The polyunsaturated fatty acid, docosahexaenoic acid (DHA), participates in neurotransmission involving activation of calcium-independent phospholipase A(2) (iPLA(2)), which is coupled to muscarinic, cholinergic and serotonergic neuroreceptors. Drug induced activation of iPLA(2) can be measured in vivo with quantitative autoradiography using (14)C-DHA as a probe. The present study used this approach to address whether a DHA signal is produced following dompaminergic (D)2-like receptor activation with quinpirole in rat brain. Unanesthetized rats were infused intravenously with (14)C-DHA one minute after saline or quinpirole infusion, and serial blood samples were collected over a 20-minute period to obtain plasma. The animals were euthanized with sodium pentobarbital and their brains excised, coronally dissected and subjected to quantitative autoradiography to derive the regional incorporation coefficient, k*, a marker of DHA signaling. Plasma labeled and unlabeled unesterified DHA concentrations were measured. RESULTS: The incorporation coefficient (k*) for DHA did not differ significantly between quinpirole-treated and control rats in any of 81 identified brain regions. Plasma labeled DHA concentration over the 20-minute collection period (input function) and unlabeled unesterified DHA concentration did not differ significantly between the two groups. CONCLUSION: These findings demonstrate that D2-like receptor initiated signaling does not involve DHA as a second messenger, and likely does not involve iPLA(2) activation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2202-15-113) contains supplementary material, which is available to authorized users.