2006
DOI: 10.1016/j.acpain.2006.08.026
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CB2 cannabinoid receptor mediation of antinociception

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Cited by 25 publications
(37 citation statements)
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“…The anti-nociceptive action of CB2 agonists and inverse agonists has been previously demonstrated [2,36,81]. Our present molecular data highlight the role of CB2, as suggested by its overexpression following CCI, observed here.…”
Section: Discussionsupporting
confidence: 72%
“…The anti-nociceptive action of CB2 agonists and inverse agonists has been previously demonstrated [2,36,81]. Our present molecular data highlight the role of CB2, as suggested by its overexpression following CCI, observed here.…”
Section: Discussionsupporting
confidence: 72%
“…Malan et al [42] demonstrated that the CB 2 receptor selective agonist AM1241 increased hind-paw thermal withdrawal latency; an effect which was blocked by the CB 2 receptor selective antagonist AM630, but not by the CB 1 receptor selective antagonist AM251, indicating mediation by CB 2 receptors. This was further confirmed in a later study, which demonstrated that the anti-nociceptive effects of AM1241 were absent in CB 2 receptor-null mice [49]. Importantly, Malan and coworkers have demonstrated that AM1241-mediated anti-nociception was devoid of CNS side effects, as indicated by the lack of effects on immobility/catalepsy, locomotor activity and hypothermia [42].…”
Section: Antinociceptive Effects Of Cb 2 Receptor Agonists In Models mentioning
confidence: 87%
“…However, they show deficiency in some B-and T-cell subsets and lack immunomodulation by cannabinoids [7,8]. CB 2 R knockout mice are more susceptible to liver fibrosis, pain and neuroinflammation and they show more age-related bone loss [9][10][11][12].…”
Section: Introductionmentioning
confidence: 98%