We hypothesized that the cannabinoid (CB) system may mediate the brain orexin- or ghrelin-induced visceral antinociception. Intraperitoneal injection of either CB1/2 agonist, WIN 55212 or O-Arachidonoyl ethanolamine increased the threshold volume of colonic distension-induced abdominal withdrawal reflex in rats, suggesting CB could induce visceral antinociception. Pretreatment with either the CB1 or CB2 antagonist potently blocked the centrally injected orexin-A-induced antinociceptive action against colonic distension while CB2 but not CB1 antagonist blocked the brain ghrelin-induced visceral antinociception. These results suggest that the cannabinoid signaling may be involved in the central orexin- or ghrelin-induced antinociceptive actio...
While most of the studies concerning the role of cannabinoids on gastric motility have focused the a...
The cannabinoid agonist, HU210 has been evaluated in vivo in nociceptive and inflammatory pain model...
Cannabinoid receptors of type 1 and 2 (CB(1) and CB(2)), endogenous ligands that activate them (endo...
This is an open access article under the CC BY-NC-ND license(http://creativecommons.org/ licenses/by...
Increasing evidence has suggested that brain orexins are implicated in a wide variety of physiologic...
Endocannabinoids acting through cannabinoid receptor type 1 (CB1) are major modulators of peripheral...
INTRODUCTION: Ghrelin and cannabinoids stimulate appetite, this effect possibly being mediated by th...
The digestive tract contains endogenous cannabinoids (anandamide and 2-arachidonylglycerol), enzymes...
INTRODUCTION: Ghrelin and cannabinoids stimulate appetite, this effect possibly being mediated b...
Preparations of the Cannabis sativa plant have been used to analgesic effect for millenia, but only ...
The analgesic potential of cannabinoids may be hampered by their ability to produce aversive emotion...
The management of visceral pain in patients with disorders of gut-brain interaction, notably irritab...
The endocannabinoid system, consisting of the cannabinoid(1) receptor (CB1R) and cannabinoid(2) rece...
This study was designed to investigate the possibility that the enhanced nociceptive responsiveness ...
Central antinociceptive effects of cannabinoids have been well documented. However, relatively littl...
While most of the studies concerning the role of cannabinoids on gastric motility have focused the a...
The cannabinoid agonist, HU210 has been evaluated in vivo in nociceptive and inflammatory pain model...
Cannabinoid receptors of type 1 and 2 (CB(1) and CB(2)), endogenous ligands that activate them (endo...
This is an open access article under the CC BY-NC-ND license(http://creativecommons.org/ licenses/by...
Increasing evidence has suggested that brain orexins are implicated in a wide variety of physiologic...
Endocannabinoids acting through cannabinoid receptor type 1 (CB1) are major modulators of peripheral...
INTRODUCTION: Ghrelin and cannabinoids stimulate appetite, this effect possibly being mediated by th...
The digestive tract contains endogenous cannabinoids (anandamide and 2-arachidonylglycerol), enzymes...
INTRODUCTION: Ghrelin and cannabinoids stimulate appetite, this effect possibly being mediated b...
Preparations of the Cannabis sativa plant have been used to analgesic effect for millenia, but only ...
The analgesic potential of cannabinoids may be hampered by their ability to produce aversive emotion...
The management of visceral pain in patients with disorders of gut-brain interaction, notably irritab...
The endocannabinoid system, consisting of the cannabinoid(1) receptor (CB1R) and cannabinoid(2) rece...
This study was designed to investigate the possibility that the enhanced nociceptive responsiveness ...
Central antinociceptive effects of cannabinoids have been well documented. However, relatively littl...
While most of the studies concerning the role of cannabinoids on gastric motility have focused the a...
The cannabinoid agonist, HU210 has been evaluated in vivo in nociceptive and inflammatory pain model...
Cannabinoid receptors of type 1 and 2 (CB(1) and CB(2)), endogenous ligands that activate them (endo...