Karler R, Calder L D, Sangdee P, Turkanis S A
Neuropharmacology. 1984 Nov;23(11):1315-20. doi: 10.1016/0028-3908(84)90052-2.
Mice were kindled to produce minimal convulsions by repeated application of either electrical or chemical stimuli. Electrical kindling involved the use of corneal electrodes; chemical kindling involved the use of pentylenetetrazol or picrotoxin. Delta-9-tetrahydrocannabinol (delta-9-THC) appeared to be capable of enhancing kindling to all three stimuli. In the studies with electroshock and pentylenetetrazol, in contrast to those with picrotoxin, a single exposure to delta-9-THC sufficed to facilitate the subsequent kindling, and the enhancement of kindling persisted after withdrawal of the cannabinoid. In the case of electrical kindling, the cannabinoid may promote the phenomenon by decreasing the convulsion threshold. Because the threshold was not lowered to all kindling stimuli, however, other mechanisms must be involved. In general, the data indicate that even a single dose of delta-9-THC can promote the development of long-lasting elevations of CNS excitability.
通过反复施加电刺激或化学刺激,使小鼠产生轻微惊厥以实现点燃效应。电刺激点燃使用角膜电极;化学刺激点燃使用戊四氮或印防己毒素。Δ-9-四氢大麻酚(Δ-9-THC)似乎能够增强对所有这三种刺激的点燃效应。在电休克和戊四氮的研究中,与印防己毒素的研究不同,单次接触Δ-9-THC就足以促进随后的点燃效应,并且在停用大麻素后,点燃增强效应仍然存在。在电刺激点燃的情况下,大麻素可能通过降低惊厥阈值来促进这一现象。然而,由于并非所有点燃刺激的阈值都降低,所以必然涉及其他机制。总体而言,数据表明,即使是单剂量的Δ-9-THC也能促进中枢神经系统兴奋性的长期升高。