Fatty acid amide hydrolase inhibition heightens anandamide signaling without producing reinforcing effects in primates.
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Hub and switches: endocannabinoid signalling in midbrain dopamine neuronsCannabinoid-based drugs targeting CB1 and TRPV1, the sympathetic nervous system, and arthritisChemical probes of endocannabinoid metabolismThe pharmacological landscape and therapeutic potential of serine hydrolasesMonoacylglycerol lipase - a target for drug development?Modulation of the endocannabinoid system: vulnerability factor and new treatment target for stimulant addictionFatty acid amide hydrolase inhibitors: a patent review (2009-2014)Inhibition of FAAH and activation of PPAR: new approaches to the treatment of cognitive dysfunction and drug addictionFatty acid amide hydrolase as a potential therapeutic target for the treatment of pain and CNS disordersElevating endocannabinoid levels: pharmacological strategies and potential therapeutic applicationsMethanandamide attenuates cocaine-induced hyperthermia in rats by a cannabinoid CB1-dopamine D2 receptor mechanismBlockade of nicotine reward and reinstatement by activation of alpha-type peroxisome proliferator-activated receptorsDopaminergic augmentation of delta-9-tetrahydrocannabinol (THC) discrimination: possible involvement of D2-induced formation of anandamideEndocannabinoid signalling in reward and addiction.In vivo pharmacology of endocannabinoids and their metabolic inhibitors: therapeutic implications in Parkinson's disease and abuse liabilityIntracranial self-stimulation to evaluate abuse potential of drugs.Cannabinoid Regulation of Brain Reward Processing with an Emphasis on the Role of CB1 Receptors: A Step Back into the FutureEnhancement of endocannabinoid signaling by fatty acid amide hydrolase inhibition: a neuroprotective therapeutic modalityAnimal models of cannabinoid reward.The role of fatty acid amide hydrolase inhibition in nicotine reward and dependence.Endocannabinoid 2-Arachidonoylglycerol Self-Administration by Sprague-Dawley Rats and Stimulation of in vivo Dopamine Transmission in the Nucleus Accumbens Shell.Inhibitor of fatty acid amide hydrolase normalizes cardiovascular function in hypertension without adverse metabolic effectsA second generation of carbamate-based fatty acid amide hydrolase inhibitors with improved activity in vivoDiscovery of potent and reversible monoacylglycerol lipase inhibitors.Drug addiction.Acetaminophen inhibits status epilepticus in cultured hippocampal neurons.Differential effects of endocannabinoid catabolic inhibitors on morphine withdrawal in mice.Inhibition of monoacylglycerol lipase reduces nicotine withdrawalReinforcing and neurochemical effects of cannabinoid CB1 receptor agonists, but not cocaine, are altered by an adenosine A2A receptor antagonist.The endogenous cannabinoid 2-arachidonoylglycerol is intravenously self-administered by squirrel monkeysFatty acid amide hydrolase blockade attenuates the development of collagen-induced arthritis and related thermal hyperalgesia in mice.Effects of fatty acid amide hydrolase inhibition on neuronal responses to nicotine, cocaine and morphine in the nucleus accumbens shell and ventral tegmental area: involvement of PPAR-alpha nuclear receptors.Chronic stimulation of the tone of endogenous anandamide reduces cue- and stress-induced relapse in rats.Blockade of endocannabinoid hydrolytic enzymes attenuates precipitated opioid withdrawal symptoms in mice.The fatty acid amide hydrolase inhibitor URB 597: interactions with anandamide in rhesus monkeysSimultaneous inhibition of fatty acid amide hydrolase and monoacylglycerol lipase shares discriminative stimulus effects with Δ9-tetrahydrocannabinol in mice.Endocannabinoid influence in drug reinforcement, dependence and addiction-related behaviors.Attenuation of persistent pain-related behavior by fatty acid amide hydrolase (FAAH) inhibitors in a rat model of HIV sensory neuropathy.Effects of Fatty Acid Amide Hydrolase (FAAH) Inhibitors in Non-Human Primate Models of Nicotine Reward and RelapseA polymorphism in the gene of the endocannabinoid-degrading enzyme FAAH (FAAH C385A) is associated with emotional-motivational reactivity.
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Fatty acid amide hydrolase inhibition heightens anandamide signaling without producing reinforcing effects in primates.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 23 September 2008
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Fatty acid amide hydrolase inh ...... inforcing effects in primates.
@en
Fatty acid amide hydrolase inh ...... inforcing effects in primates.
@nl
type
label
Fatty acid amide hydrolase inh ...... inforcing effects in primates.
@en
Fatty acid amide hydrolase inh ...... inforcing effects in primates.
@nl
prefLabel
Fatty acid amide hydrolase inh ...... inforcing effects in primates.
@en
Fatty acid amide hydrolase inh ...... inforcing effects in primates.
@nl
P2093
P2860
P50
P921
P1476
Fatty acid amide hydrolase inh ...... inforcing effects in primates.
@en
P2093
Alexey G Mukhin
Alvin R King
Daniele Piomelli
Godfrey H Redhi
Jason R Clapper
Sevil Yasar
Steven R Goldberg
Svetlana I Chefer
P2860
P304
P356
10.1016/J.BIOPSYCH.2008.08.008
P407
P577
2008-09-23T00:00:00Z