The dopamine mesocorticolimbic pathway is affected by deficiency in n-3 polyunsaturated fatty acids

Autor: Denis Guilloteau, Sylvie Chalon, Luc Zimmer, Sylvie Vancassel, Sylvain Cantagrel, Patrick Breton, Séraphin Delamanche, Georges Durand
Přispěvatelé: Dynamique et pathologie du développement cérébral, Institut National de la Santé et de la Recherche Médicale (INSERM), Laboratoire de nutrition et sécurité alimentaire, Institut National de la Recherche Agronomique (INRA), Centre d'études du Bouchet
Rok vydání: 2002
Předmět:
Male
medicine.medical_specialty
030309 nutrition & dietetics
[SDV]Life Sciences [q-bio]
Dopamine
Microdialysis
Dopamine Agents
Medicine (miscellaneous)
Nucleus accumbens
Biology
Mesocortical pathway
03 medical and health sciences
0302 clinical medicine
Neurochemical
Internal medicine
Vesicular Biogenic Amine Transport Proteins
medicine
Animals
Rats
Wistar

Amphetamine
In Situ Hybridization
0303 health sciences
Analysis of Variance
Neurotransmitter Agents
Nutrition and Dietetics
Membrane Glycoproteins
Dopaminergic
Neuropeptides
Brain
Membrane Transport Proteins
Biological Transport
Diet
Rats
Ventral tegmental area
Vesicular monoamine transporter
medicine.anatomical_structure
Endocrinology
Vesicular Monoamine Transport Proteins
Fatty Acids
Unsaturated

Female
030217 neurology & neurosurgery
medicine.drug
Zdroj: Europe PubMed Central
American Journal of Clinical Nutrition
American Journal of Clinical Nutrition, American Society for Nutrition, 2002, 75 (4), pp.662-667. ⟨10.1093/ajcn/75.4.662⟩
ResearcherID
ISSN: 0002-9165
Popis: International audience; Background: Several findings in humans support the hypothesis of links between n-3 polyunsaturated fatty acid (PUFA) status and psychiatric diseases. Objective: The involvement of PUFAs in central nervous system function can be assessed with the use of dietary manipulation in animal models. We studied the effects of chronic dietary n-3 PUFA deficiency on mesocorticolimbic dopamine neurotransmission in rats. Design: Using dual-probe microdialysis, we analyzed dopamine release under amphetamine stimulation simultaneously in the frontal cortex and the nucleus accumbens. The messenger RNA (mRNA) expression of vesicular monoamine transporter, and dopamine D, receptor was studied with the use of in situ hybridization. The protein expression of the synthesis-limiting enzyme tyrosine 3-monooxygenase (tyrosine 3-hydroxylase) was studied with the use of immunocytochemistry. Results: Dopamine release was significantly lower in both cerebral areas in n-3 PUFA-deficient rats than in control rats, but this effect was abolished in the frontal cortex and reversed in the nucleus accumbens by reserpine pretreatment, which depletes the dopamine vesicular storage pool. The mRNA expression of vesicular monoamine transporter, was lower in both cerebral areas in n-3 PUFA-deficient rats than in control rats, whereas the mRNA expression of D, receptor was lower in the frontal cortex and higher in the nucleus accumbens in n-3 PUFA-deficient rats than in control rats. Finally, tyrosine 3-monooxygenase immunoreactivity was higher in the ventral tegmental area in n-3 PUFA-deficient rats than in control rats. Conclusions: Our results suggest that the mesolimbic dopamine pathway is more active whereas the mesocortical pathway is less active in n-3 PUFA-deficient rats than in control rats. This provides new neurochemical evidence supporting the effects of n-3 PUFA deficiency on behavior.
Databáze: OpenAIRE