2014
DOI: 10.1016/j.ejphar.2014.10.016
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Involvement of central and peripheral cannabinoid receptors on antinociceptive effect of tetrahydrocannabinol in muscle pain

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Cited by 22 publications
(9 citation statements)
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“…in a rat model of acute muscle pain produced antinociceptive effects, which was blocked by the CB 1 R antagonist AM281 and to a lesser extent by the CB 2 R antagonist AM630 (0.5 mg/kg i.p.). 40 Furthermore, in a model of inflammatory and neuropathic pain, mice lacking CB 1 R in peripheral nociceptive neurons showed a reduced analgesic effect to local and systemic administration of the cannabinoid WIN55,212-2. With intrathecal application, the analgesic effect of WIN55,212-2 was absent, suggesting that peripheral CB 1 R in nociceptive neurons plays an important role in producing the analgesic effects of cannabinoids.…”
Section: Discussionmentioning
confidence: 99%
“…in a rat model of acute muscle pain produced antinociceptive effects, which was blocked by the CB 1 R antagonist AM281 and to a lesser extent by the CB 2 R antagonist AM630 (0.5 mg/kg i.p.). 40 Furthermore, in a model of inflammatory and neuropathic pain, mice lacking CB 1 R in peripheral nociceptive neurons showed a reduced analgesic effect to local and systemic administration of the cannabinoid WIN55,212-2. With intrathecal application, the analgesic effect of WIN55,212-2 was absent, suggesting that peripheral CB 1 R in nociceptive neurons plays an important role in producing the analgesic effects of cannabinoids.…”
Section: Discussionmentioning
confidence: 99%
“…In addition, the role of the CB2 receptors (which are mostly peripherally distributed) in muscle and tendon pain relief in fibromyalgia following cannabis treatment is not clear. There are nearly no reports about the existence of CB2 receptors in the muscles or tendons [ 20 ]. One of the theories behind the pathogenesis of fibromyalgia, however, is endocannabinoid deficiency.…”
Section: Discussionmentioning
confidence: 99%
“…Cannabinoid agonists and endocannabinoids exhibited strong antinociceptive activity via activation of CB1 in spinal cord level in different animal models of pain (31)(32)(33).…”
Section: Discussionmentioning
confidence: 99%