Hillard C J, Bloom A S
Eur J Pharmacol. 1983 Jul 15;91(1):21-7. doi: 10.1016/0014-2999(83)90357-6.
In vitro, the cannabinoids delta 9-tetrahydrocannabinol (delta 9-THC), 11-OH-delta 9-THC, cannabidiol and cannabinol all increased adenylate cyclase activity in mouse cerebral cortical homogenates. Levonantradol, a synthetic cannabinoid analog, also increased adenylate cyclase activity while its optical isomer dextronantradol did not. The increases in enzyme activity produced by the active compounds were biphasic with significant increases at 10 microM and/or 30 microM concentrations with return to control levels at 100 microM. The increases did not occur in the absence of added GTP nor did delta 9-THC have any effect on fluoride-stimulation of adenylate cyclase activity. The prostaglandin synthetase inhibitors acetyl salicylic acid and indomethacin and the phospholipase A2 inhibitor quinacrine all abolished the increase in adenylate cyclase activity produced by delta 9-THC, suggesting the involvement of prostaglandins in this cannabinoid action.
在体外,大麻素Δ9-四氢大麻酚(Δ9-THC)、11-羟基-Δ9-THC、大麻二酚和大麻酚均能增加小鼠大脑皮质匀浆中的腺苷酸环化酶活性。合成大麻素类似物左南曲朵也能增加腺苷酸环化酶活性,而其光学异构体右南曲朵则无此作用。活性化合物引起的酶活性增加呈双相性,在10微摩尔和/或30微摩尔浓度时显著增加,在100微摩尔时恢复到对照水平。在不添加鸟苷三磷酸(GTP)的情况下不会出现活性增加,并且Δ9-THC对氟化物刺激的腺苷酸环化酶活性没有任何影响。前列腺素合成酶抑制剂乙酰水杨酸和吲哚美辛以及磷脂酶A2抑制剂奎纳克林均消除了Δ9-THC引起的腺苷酸环化酶活性增加,这表明前列腺素参与了这种大麻素作用。