نتایج جستجو برای: cb1 cannabinoid receptors

تعداد نتایج: 229945  

Journal: :Anesthesiology 2003
Aline Quartilho Heriberto P Mata Mohab M Ibrahim Todd W Vanderah Frank Porreca Alexandros Makriyannis T Philip Malan

BACKGROUND Cannabinoid receptor agonists inhibit inflammatory hyperalgesia in animal models. Nonselective cannabinoid receptor agonists also produce central nervous system (CNS) side effects. Agonists selective for CB2 cannabinoid receptors, which are not found in the CNS, do not produce the CNS effects typical of nonselective cannabinoid receptor agonists but do inhibit acute nociception. The ...

Journal: :Bioorganic & medicinal chemistry 2008
Angel Gonzalez Leonardo Sepulveda Duran Raul Araya-Secchi Jose A Garate C David Pessoa-Mahana Carlos F Lagos Tomas Perez-Acle

The seven transmembrane helices (TMH) G-protein-coupled receptors (GPCRs) constitute one of the largest superfamily of signaling proteins found in mammals. Some of its members, in which the cannabinoid (CB) receptors are included, stand out because their functional states can be modulated by a broad spectrum of effector molecules. The relative ligand promiscuity exhibited by these receptors cou...

Journal: :European journal of endocrinology 2002
Anna Porcella Giorgio Marchese Maria Antonietta Casu Antonio Rocchitta Maria Letizia Lai Gian Luigi Gessa Luca Pani

OBJECTIVE Previous reports have shown that the Delta(9)-tetrahydrocannabinol (Delta(9)TCH), the major psychoactive cannabinoid components of marijuana, is able [corrected] to inhibit thyroid hormonal activity. The aim of this study was to characterize the CB1 functional expression in the rat thyroid by a multi-methods approach. METHODS AND RESULTS RT-PCR was used to detect the mRNA expression...

Journal: :Molecular pharmacology 2006
Laura J Sim-Selley Nicole S Schechter W Kirk Rorrer George D Dalton Jerry Hernandez Billy R Martin Dana E Selley

Long-term cannabinoid administration produces region-dependent CB1 receptor desensitization and down-regulation. This study examined the time course for normalization of CB1 receptors and G-protein activation using 3H-labeled N-(piperidin-1-yl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboximide hydrochloride (SR141716A) and guanosine 5'-O-(3-[35S]thio)triphosphate ([35...

Journal: :Rheumatology 2009
Estrella Garcia-Gonzalez Enrico Selvi Epifania Balistreri Sauro Lorenzini Roberta Maggio Maria-Rita Natale Pier-Leopoldo Capecchi Pietro-Enea Lazzerini Marco Bardelli Franco Laghi-Pasini Mauro Galeazzi

OBJECTIVE It has been demonstrated that the endocannabinoid system is up-regulated in pathologic fibrosis and that modulation of the cannabinoid receptors might limit the progression of uncontrolled fibrogenesis. The aim of this study was to investigate whether the synthetic cannabinoid receptor agonist WIN55,212-2 could modulate fibrogenesis in an in vitro model of dcSSc. METHODS The express...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1996
S D Skaper A Buriani R Dal Toso L Petrelli S Romanello L Facci A Leon

The amino acid L-glutamate is a neurotransmitter that mediates fast neuronal excitation in a majority of synapses in the central nervous system. Glutamate stimulates both N-methyl-D-aspartate (NMDA) and non-NMDA receptors. While activation of NMDA receptors has been implicated in a variety of neurophysiologic processes, excessive NMDA receptor stimulation (excitotoxicity) is thought to be prima...

Journal: :Neuron 2007
Vivien Chevaleyre Boris D. Heifets Pascal S. Kaeser Thomas C. Südhof Pablo E. Castillo

Endocannabinoids (eCBs) have emerged as key activity-dependent signals that, by activating presynaptic cannabinoid receptors (i.e., CB1) coupled to G(i/o) protein, can mediate short-term and long-term synaptic depression (LTD). While the presynaptic mechanisms underlying eCB-dependent short-term depression have been identified, the molecular events linking CB1 receptors to LTD are unknown. Here...

Journal: :The Journal of pharmacology and experimental therapeutics 1996
V M Showalter D R Compton B R Martin M E Abood

Two cannabinoid receptors have been identified to date; one is located predominantly in the central nervous system (CB1), whereas the other is located exclusively in the periphery (CB2). The purposes of this study were to explore further the binding requirements of the CB2 receptor and to search for compounds displaying distinct affinities for either cannabinoid receptor. The binding affinities...

Journal: :Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 2011
V Di Marzo F Piscitelli

Stemming from the centuries-old and well known effects of Cannabis on intestinal motility and secretion, research on the role of the endocannabinoid system in gut function and dysfunction has received ever increasing attention since the discovery of the cannabinoid receptors and their endogenous ligands, the endocannabinoids. In this article, some of the most recent developments in this field a...

Journal: :Biochemical Society transactions 1997
A A Makda M A Elmore M E Hill A Stamps S Tejura M J Finnen

In addition to their well known psychotrophic effects, the cannabinoids also display immunosuppressive and anti inflammatory properties including inhibition of T and B lymphocyte proliferation and inhibition of macrophage microbiocidal acitivity. Two subtypes of cannabinoid receptors, CB1 and CB2 have been described [1,2]. While CB1, the central cannabinoid receptor, is predominantly found in t...

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