Nalwalk Julia W, Svokos Konstantina, Hough Lindsay B
Center for Neuropharmacology and Neuroscience, Albany Medical College MC-136, Albany, NY 12208, USA.
Eur J Pharmacol. 2006 Nov 7;549(1-3):79-83. doi: 10.1016/j.ejphar.2006.08.035. Epub 2006 Aug 26.
Improgan is a non-opioid analgesic which does not act at known histamine or cannabinoid receptors. Because improgan antinociception is blocked by low doses of a cannabinoid CB1 antagonist, the present experiments determined if development of cannabinoid tolerance in mice would alter improgan antinociception. Twice-daily injections of Delta9-tetrahydrocannabinol (THC, 10 mg/kg, s.c.) for 3.5 days induced 47-54% and 42-56% reductions in cannabinoid (WIN 55,212-2, 20 microg, i.c.v.) and improgan (30 microg, i.c.v.) antinociception, respectively, as compared with responses from vehicle-treated groups. Because improgan lacks cannabinoid-like side effects in rats, and does not act directly on cannabinoid CB1 receptors, the finding that development of cannabinoid tolerance reduces improgan antinociception suggests that this drug may release endocannabinoids, or activate novel cannabinoid sites. Either possibility offers the potential for developing new types of analgesics.
英普罗根是一种非阿片类镇痛药,它不作用于已知的组胺或大麻素受体。由于低剂量的大麻素CB1拮抗剂可阻断英普罗根的镇痛作用,因此本实验确定了小鼠体内大麻素耐受性的形成是否会改变英普罗根的镇痛作用。每天两次皮下注射Δ9-四氢大麻酚(THC,10 mg/kg),持续3.5天,与溶剂处理组相比,大麻素(WIN 55,212-2,20 μg,脑室内注射)和英普罗根(30 μg,脑室内注射)的镇痛作用分别降低了47%-54%和42%-56%。由于英普罗根在大鼠中没有类似大麻素的副作用,且不直接作用于大麻素CB1受体,大麻素耐受性的形成会降低英普罗根的镇痛作用这一发现表明,这种药物可能会释放内源性大麻素,或激活新的大麻素位点。这两种可能性都为开发新型镇痛药提供了潜力。