Cannabinoid receptor CB (CBR) is upregulated on activated microglia and astrocytes in the brain under inflammatory conditions and plays important roles in many neurological diseases, such as Alzheimer's disease, amyotrophic lateral sclerosis, and ischemic stroke. The advent of positron emission tomography (PET) using CBR radiotracers has enabled the visualization of CBR distribution in vivo in animal models of central nervous system inflammation, however translation to humans has been less successful. Several novel CBR radiotracers have been developed and evaluated to quantify microglial activation. In this review, we summarize the recent preclinical and clinical imaging results of CBR PET tracers and discuss the prospects of CBR imaging us...
Delta(9)-Tetrahydrocannabinol, the main psychoactive component of cannabis, exerts its central effec...
The development of the radioligands for PET imaging of the cerebral cannabinoid receptor (CB1) is of...
[(18)F]MK-9470 is a selective, high-affinity, inverse agonist (human IC(50), 0.7 nM) for the cannabi...
Cannabinoid receptor CB (CBR) is upregulated on activated microglia and astrocytes in the brain unde...
Cannabinoid type 2 receptors (CB2R) have emerged as promising targets for the diagnosis and therapy ...
The cannabinoid type 2 (CB2) receptor is an immunomodulatory receptor mainly expressed in peripheral...
Neuroinflammation, which involves microglial activation, is thought to play a key role in the develo...
Abstract Neuroinflammation, which involves microglial activation, is thought to play a key role in ...
Neuroinflammation, which involves microglial activation, is thought to play a key role in the develo...
The actions of marijuana (cannabis) are mediated by receptors (primarily the cannabinoid CB1 recept...
BACKGROUND AND PURPOSE: Non-invasive in vivo imaging of cannabinoid CB2 receptors using PET is pursu...
Studies using radiolabeled psychoactive drugs in conjunction with positron emission tomography (PET)...
In this study, we assessed the feasibility of using positron emission tomography (PET) and the trace...
The endocannabinoid system (ECS) is involved in a wide range of biological functions and comprises c...
INTRODUCTION: Up-regulation of the type 2 cannabinoid receptor (CB(2)R) has been reported in (neuro)...
Delta(9)-Tetrahydrocannabinol, the main psychoactive component of cannabis, exerts its central effec...
The development of the radioligands for PET imaging of the cerebral cannabinoid receptor (CB1) is of...
[(18)F]MK-9470 is a selective, high-affinity, inverse agonist (human IC(50), 0.7 nM) for the cannabi...
Cannabinoid receptor CB (CBR) is upregulated on activated microglia and astrocytes in the brain unde...
Cannabinoid type 2 receptors (CB2R) have emerged as promising targets for the diagnosis and therapy ...
The cannabinoid type 2 (CB2) receptor is an immunomodulatory receptor mainly expressed in peripheral...
Neuroinflammation, which involves microglial activation, is thought to play a key role in the develo...
Abstract Neuroinflammation, which involves microglial activation, is thought to play a key role in ...
Neuroinflammation, which involves microglial activation, is thought to play a key role in the develo...
The actions of marijuana (cannabis) are mediated by receptors (primarily the cannabinoid CB1 recept...
BACKGROUND AND PURPOSE: Non-invasive in vivo imaging of cannabinoid CB2 receptors using PET is pursu...
Studies using radiolabeled psychoactive drugs in conjunction with positron emission tomography (PET)...
In this study, we assessed the feasibility of using positron emission tomography (PET) and the trace...
The endocannabinoid system (ECS) is involved in a wide range of biological functions and comprises c...
INTRODUCTION: Up-regulation of the type 2 cannabinoid receptor (CB(2)R) has been reported in (neuro)...
Delta(9)-Tetrahydrocannabinol, the main psychoactive component of cannabis, exerts its central effec...
The development of the radioligands for PET imaging of the cerebral cannabinoid receptor (CB1) is of...
[(18)F]MK-9470 is a selective, high-affinity, inverse agonist (human IC(50), 0.7 nM) for the cannabi...