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N -Palmitoylethanolamide Exerts Antidepressant-Like Effects in Rats: Involvement of PPAR α Pathway in the Hippocampus.
- Source :
-
The Journal of pharmacology and experimental therapeutics [J Pharmacol Exp Ther] 2019 Apr; Vol. 369 (1), pp. 163-172. Date of Electronic Publication: 2019 Jan 11. - Publication Year :
- 2019
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Abstract
- N -Palmitoylethanolamide (PEA), an endocannabinoid-like molecule, participates in controlling behaviors associated with mental disorders as an endogenous neuroprotective factor. On the basis of accumulating evidence and our previous data, we tested the hypothesis that the antidepressant-like effects of PEA observed during chronic unpredictable mild stress (CUMS) are mediated by possible targets in the peroxisome proliferator-activated receptor alpha (PPAR α ) pathway. In this study, rats were subjected to 35 days of CUMS and treated with drugs such as PEA (2.5, 5.0, or 10 mg/kg, by mouth), fluoxetine (10 mg/kg, by mouth), or the combination of PEA and MK886 (1-[(4-chlorophenyl) methyl]-3-[(1,1-dimethylethyl) thio]- α , α -dimethyl-5-(1-methylethyl)-1 H -indole-2-propanoic acid). After behavioral tests, the animals were sacrificed and their hippocampi were dissected for subsequent studies. PEA normalized weight gain, sucrose preferences, locomotor activity in an open-field test, and levels of the PPAR α mRNA and protein in the hippocampus, and it reduced serum adrenocorticotropic hormone (ACTH) and corticosterone (CORT) levels in rats subjected to CUMS. PEA reversed the abnormal levels of several oxidative stress biomarkers and increased the concentrations of two neurotrophic factors in the hippocampus of CUMS-induced rats. In addition, PEA alleviated the decrease in hippocampal weight. However, the aforementioned effects of PEA were completely or partially abolished by MK886, a selective PPAR α antagonist. On the basis of these findings, the PPAR α pathway in the hippocampus is a possible target of the antidepressant effects of PEA, and the maintenance of a stable hypothalamic-pituitary-adrenal axis, the antioxidant defenses, and normalization of neurotrophic factor levels in the hippocampus are involved in this process.<br /> (Copyright © 2019 by The American Society for Pharmacology and Experimental Therapeutics.)
- Subjects :
- Adrenocorticotropic Hormone blood
Amides
Animals
Antidepressive Agents therapeutic use
Behavior, Animal drug effects
Body Weight drug effects
Brain-Derived Neurotrophic Factor metabolism
Corticosterone blood
Ethanolamines therapeutic use
Gene Expression Regulation drug effects
Glial Cell Line-Derived Neurotrophic Factor metabolism
Glutathione metabolism
Hippocampus pathology
Male
Malondialdehyde metabolism
Organ Size drug effects
Palmitic Acids therapeutic use
RNA, Messenger genetics
RNA, Messenger metabolism
Rats
Rats, Sprague-Dawley
Stress, Psychological blood
Stress, Psychological drug therapy
Stress, Psychological metabolism
Stress, Psychological pathology
Superoxide Dismutase metabolism
Antidepressive Agents pharmacology
Ethanolamines pharmacology
Hippocampus drug effects
Hippocampus metabolism
PPAR alpha metabolism
Palmitic Acids pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1521-0103
- Volume :
- 369
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- The Journal of pharmacology and experimental therapeutics
- Publication Type :
- Academic Journal
- Accession number :
- 30635472
- Full Text :
- https://doi.org/10.1124/jpet.118.254524