Premium
In vivo brain levels of acetylcholine and 5‐hydroxytryptamine after oleoylethanolamide or palmitoylethanolamide administrations are mediated by PPARα engagement
Author(s) -
MurilloRodríguez Eric,
ArankowskySandoval Gloria,
Budde Henning,
Imperatori Claudio,
Machado Sérgio,
Yamamoto Tetsuya,
Yadollahpour Ali,
Torterolo Pablo
Publication year - 2021
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1111/ejn.15409
Subject(s) - palmitoylethanolamide , microdialysis , basal forebrain , medicine , chemistry , acetylcholine , endocrinology , peroxisome proliferator activated receptor , receptor , pharmacology , neurotransmitter , receptor antagonist , antagonist , cholinergic , biology , biochemistry , extracellular , cannabinoid receptor
The peroxisome proliferator‐activated receptor alpha (PPARα) is a nuclear receptor that has been linked to the modulation of several physiological functions, including the sleep–wake cycle. The PPARα recognizes as endogenous ligands the lipids oleoylethanolamide (OEA) and palmitoylethanolamide (PEA), which in turn, if systemically injected, they exert wake‐promoting effects. Moreover, the activation of PPARα by the administration of OEA or PEA increases the extracellular contents of neurotransmitters linked to the control of wakefulness; however, the role of PPARα activated by OEA or PEA on additional biochemicals related to waking regulation, such as acetylcholine (ACh) and 5‐hydroxytryptamine (5‐HT), has not been fully studied. Here, we have investigated the effects of treatments of OEA or PEA on the contents of ACh and 5‐HT by using in vivo microdialysis techniques coupled to HPLC means. For this purpose, OEA or PEA were systemically injected (5, 10 or 30 mg/kg; i.p.), and the levels of ACh and 5‐HT were collected from the basal forebrain, a wake‐related brain area. These pharmacological treatments significantly increased the contents of ACh and 5‐HT as determined by HPLC procedures. Interestingly, PPARα antagonist MK‐886 (30 mg/kg; i.p.) injected before the treatments of OEA or PEA blocked these outcomes. Our data suggest that the activation of PPARα by OEA or PEA produces significant changes on ACh and 5‐HT levels measured from the basal forebrain and support the conclusion that PPARα is a suitable molecular element involved in the regulation of wake‐related neurotransmitters.