Hayslett Renee L, Tizabi Yousef
Department of Pharmacology, Howard University College of Medicine, 520 W Street N.W., Washington, DC 20059, USA.
Pharmacol Biochem Behav. 2005 Aug;81(4):879-86. doi: 10.1016/j.pbb.2005.06.010.
We have previously reported that acute and chronic donepezil and nicotine administration significantly attenuate DOI-induced head twitch response (HTR) in mice. This behavior, primarily mediated by stimulation of 5-HT2A receptors, has been proposed to model tic symptoms seen in Tourette's syndrome (TS). Haloperidol, a drug widely used to treat symptoms of TS, has also been reported to reduce DOI-induced head shakes in rodents when administered acutely. These findings suggest an inhibitory interaction of these drugs with 5-HT2A receptors. To test this hypothesis, we evaluated the effects of chronic donepezil, nicotine and haloperidol on expression levels of 5-HT2A mRNA and 5-HT2A receptor density in select brain regions. Initially, we established a dose-response relationship for the acute and chronic haloperidol and DOI-induced HTR. Male ICR mice were treated twice daily with donepezil (0.1 mg/kg), nicotine (0.5 mg/kg), and once daily with haloperidol (0.4 mg/kg) for 14 days and were sacrificed 16-18 h after the last injection. These drug regimens were chosen because of their significant effects on DOI-induced HTR. Donepezil significantly increased 5-HT2A mRNA level, but not the receptor density in the striatum. In the midbrain, donepezil significantly decreased the receptor density without affecting the 5-HT2A mRNA level. In the frontal cortex, only haloperidol significantly reduced the 5-HT2A receptor density. The cortex was the only area where donepezil, nicotine and haloperidol significantly reduced the 5-HT2A receptor density. The results suggest that the anti-tic properties of donepezil, nicotine and haloperidol in this paradigm might be due to antagonism of cortical 5-HT2A receptors. Thus, further investigation of involvement of cortical 5-HT2A receptors in TS as well as evaluation of selective 5-HT2A receptor antagonists in this disorder is warranted.
我们之前报道过,急性和慢性给予多奈哌齐及尼古丁可显著减轻DOI诱导的小鼠头部抽搐反应(HTR)。这种行为主要由5-HT2A受体的刺激介导,已被用于模拟抽动秽语综合征(TS)中出现的抽动症状。氟哌啶醇是一种广泛用于治疗TS症状的药物,据报道,急性给药时它也能减少啮齿动物中DOI诱导的头部抖动。这些发现表明这些药物与5-HT2A受体存在抑制性相互作用。为了验证这一假设,我们评估了慢性给予多奈哌齐、尼古丁和氟哌啶醇对特定脑区中5-HT2A mRNA表达水平和5-HT2A受体密度的影响。最初,我们建立了急性和慢性氟哌啶醇及DOI诱导的HTR的剂量反应关系。雄性ICR小鼠每天接受两次多奈哌齐(0.1 mg/kg)、尼古丁(0.5 mg/kg)治疗,每天接受一次氟哌啶醇(0.4 mg/kg)治疗,持续14天,并在最后一次注射后16 - 18小时处死。选择这些药物方案是因为它们对DOI诱导的HTR有显著影响。多奈哌齐显著提高了纹状体中5-HT2A mRNA水平,但未影响受体密度。在中脑,多奈哌齐显著降低了受体密度,而不影响5-HT2A mRNA水平。在额叶皮质,只有氟哌啶醇显著降低了5-HT2A受体密度。皮质是多奈哌齐、尼古丁和氟哌啶醇显著降低5-HT2A受体密度的唯一区域。结果表明,在该模型中多奈哌齐、尼古丁和氟哌啶醇的抗抽动特性可能是由于对皮质5-HT2A受体的拮抗作用。因此,有必要进一步研究皮质5-HT2A受体在TS中的作用,以及评估该疾病中选择性5-HT2A受体拮抗剂的效果。