نتایج جستجو برای: cannabinoid receptors

تعداد نتایج: 229376  

Journal: :Life sciences 2010
Jeannie Hwang Crista Adamson David Butler David R Janero Alexandros Makriyannis Ben A Bahr

AIMS This review posits that fatty acid amide hydrolase (FAAH) inhibition has therapeutic potential against neuropathological states including traumatic brain injury; Alzheimer's, Huntington's, and Parkinson's diseases; and stroke. MAIN METHODS This proposition is supported by data from numerous in vitro and in vivo experiments establishing metabolic and pharmacological contexts for the neuro...

2014
James J. Burston Stephen G. Woodhams

The endocannabinoid (EC) system consists of two main receptors: cannabinoid type 1 receptor cannabinoid receptors are found in both the central nervous system (CNS) and periphery, whereas the cannabinoid type 2 receptor cannabinoid receptor is found principally in the immune system and to a lesser extent in the CNS. The EC family consists of two classes of well characterised ligands; the N-acyl...

Journal: :Alcohol and alcoholism 2005
Jorge Manzanares Sergio Ortiz José M Oliva Sandra Pérez-Rial Tomás Palomo

Over the past few years, advances in the investigation of the neurochemical circuits involved in the development and treatment of alcohol dependence have identified peptides and receptors as potential key targets in the treatment of problems related to alcohol consumption. The endogenous opioid system is modified by alcohol intake in areas of the brain related to reward systems, and differentia...

2017
V. Maida P. J. Daeninck

“Cannabinoid” is the collective term for a group of chemical compounds that either are derived from the Cannabis plant, are synthetic analogues, or occur endogenously. Although cannabinoids interact mostly at the level of the currently recognized cannabinoid receptors, they might have cross reactivity, such as at opioid receptors. Patients with malignant disease represent a cohort within health...

2016
Sara L. Dunn Jeremy Mark Wilkinson Aileen Crawford Rowena A.D. Bunning Christine L. Le Maitre

Introduction: Cannabinoids have shown to reduce joint damage in animal models of arthritis and reduce matrix metalloproteinase expression in primary human osteoarthritic (OA) chondrocytes. The actions of cannabinoids are mediated by a number of receptors, including cannabinoid receptors 1 and 2 (CB1 and CB2), G-protein-coupled receptors 55 and 18 (GPR55 and GPR18), transient receptor potential ...

Journal: :British journal of pharmacology 2008
B N Dittel

The cannabinoid system is now recognized as a regulator of both the nervous and immune systems. Although marijuana has been used for centuries for the treatment of a variety of disorders, its therapeutic mechanisms are only now being understood. The best-studied plant cannabinoid, delta9-tetrahydrocannabinol (THC), produced by Cannabis sativa and found in marijuana, has shown evidence of being ...

2016
Jaesuk Yun Tac-hyung Lee Yun Jeong Song Seonhwa Seong Young-Hoon Kim Hye Jin Cha Kyoung moon Han Jisoon Shin Oh Hokyung Kikyung Jung Chiyoung Ahn Choon-gon Jang Ji-Young Hwang Hye-Kyung Park Hyung Soo Kim

The problem of new psychoactive substances is emerging globally. Cannabinoid receptors mediate the action of synthetic cannabinoids, which are one of most abused drugs. Recently, cannabinoid receptors 1 (CB1R) have been reported to silence glutamatergic nerve terminals in cerebellar granule cells via synaptic vesicle redistribution. This study aimed to determine whether synthetic cannabinoid ad...

Journal: :Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 2006
Keizo Waku

Marijuana has been used as a traditional medicine and a pleasure-inducing drug for thousands of years around the world, especially in Asia. Delta(9)-tetrahydrocannabinol, major psychoactive component of marijuana, has been shown to interact with specific cannabinoid receptors, thereby eliciting a variety of pharmacological responses in experimental animals and human. In 1990, the gene encoding ...

Journal: :Molecular pharmacology 2000
P L Prather N A Martin C S Breivogel S R Childers

Previous studies had shown that the amplification factors for cannabinoid receptors, defined as the number of total G proteins activated per occupied receptor, differs between several rat brain regions. In this study, we sought to determine which specific Gi/Go(alpha) subunits were activated by CB1 receptors in several rat brain regions and if this coupling might explain the regional difference...

Journal: :Endocrinology 2000
D Melck L De Petrocellis P Orlando T Bisogno C Laezza M Bifulco V Di Marzo

Anandamide and 2-arachidonoylglycerol (2-AG), two endogenous ligands of the CB1 and CB2 cannabinoid receptor subtypes, inhibit the proliferation of PRL-responsive human breast cancer cells (HBCCs) through down-regulation of the long form of the PRL receptor (PRLr). Here we report that 1) anandamide and 2-AG inhibit the nerve growth factor (NGF)-induced proliferation of HBCCs through suppression...

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