Behavioral Neuroscience and Drug Development, Maj Institute of Pharmacology, Polish Academy of Sciences, Kraków, Poland.
Department of Medicinal Chemistry, Maj Institute of Pharmacology, Polish Academy of Sciences, Kraków, Poland.
J Psychopharmacol. 2019 Nov;33(11):1447-1455. doi: 10.1177/0269881119867603. Epub 2019 Aug 27.
Like other psychedelics, D-lysergic acid diethylamide (LSD) affects numerous serotonin receptors, and according to the current dogma, the 5-HT receptors are considered the main target for its hallucinogenic effects. LSD, however, also displays agonistic activity at the 5-HT receptors, which mediate some of LSD-induced behavioural effects.
Using male Sprague Dawley rats, we examined the effects of 5-HT and 5-HT receptor antagonists on LSD-induced stimulus control in the two-lever drug discrimination test using a FR10 schedule of reinforcement.
In animals trained to discriminate 0.08 mg/kg LSD from vehicle 15 minutes after injection, LSD produced dose-related increases in response, with an ED50 (±95% confidence limits) of 0.0384 (± 0.025-0.051) mg/kg). LSD-like responses were observed when the training dose of LSD was given 5-30 but not 90 minutes before the test. Confirming earlier reports, the 5-HT antagonist ketanserin (2 mg/kg) attenuated the LSD response in 50% of rats, and due to pretreatment with 0.2 and 2 mg/kg MDL 100907, 63% and 67% of animals, respectively, failed to select the LSD lever. We then investigated the effects of two 5-HT receptor antagonists, and we found that 56% and 60% of rats pretreated with 3 and 10 mg/kg SB 699551, respectively, failed to select the LSD lever. Due to pretreatment with 0.01 mg/kg ASP 5736, 58% of rats did not select the LSD lever. This dose also reduced the response rate but not the number of rats failing to complete the test.
The present results suggest that antagonists of the 5-HT receptor may inhibit subjective effects of LSD in rats.
与其他迷幻剂一样,D-麦角酸二乙酰胺(LSD)作用于众多血清素受体,根据当前的理论,5-HT 受体被认为是 LSD 致幻作用的主要靶点。然而,LSD 也对 5-HT 受体表现出激动活性,这种激动活性介导了 LSD 引起的一些行为效应。
使用雄性 Sprague Dawley 大鼠,我们在 FR10 强化方案下,使用双杠药物辨别测试,检查 5-HT 和 5-HT 受体拮抗剂对 LSD 诱导的刺激控制的影响。
在训练大鼠辨别注射后 15 分钟时 0.08mg/kg LSD 与载体的情况下,LSD 产生了剂量依赖性的反应增加,ED50(±95%置信区间)为 0.0384(±0.025-0.051)mg/kg)。当 LSD 的训练剂量在测试前 5-30 分钟而不是 90 分钟给予时,观察到 LSD 样反应。证实了早期的报告,5-HT 拮抗剂酮色林(2mg/kg)在 50%的大鼠中减弱了 LSD 的反应,并且由于分别用 0.2 和 2mg/kg MDL 100907 预处理,63%和 67%的动物未能选择 LSD 杠杆。然后,我们研究了两种 5-HT 受体拮抗剂的作用,我们发现,分别用 3 和 10mg/kg SB 699551 预处理的大鼠中,有 56%和 60%未能选择 LSD 杠杆。由于用 0.01mg/kg ASP 5736 预处理,58%的大鼠没有选择 LSD 杠杆。该剂量还降低了反应率,但没有减少未能完成测试的大鼠数量。
本研究结果表明,5-HT 受体拮抗剂可能抑制大鼠 LSD 的主观效应。