Monti Jaime M, Jantos Héctor, Monti Daniel
Department of Pharmacology and Therapeutics, Clinics Hospital, 11300, Montevideo, Uruguay.
Eur Neuropsychopharmacol. 2002 Feb;12(1):47-55. doi: 10.1016/s0924-977x(01)00133-x.
The effects of 8-OHDPAT and flesinoxan, two selective 5-HT(1A) receptor agonists, and of WAY 100635, a selective 5-HT(1A) receptor antagonist, on spontaneous sleep were studied in adult rats implanted for chronic sleep recordings. The serotonergic ligands were microinjected directly into the dorsal raphe nucleus (DRN). Direct administration of flesinoxan (25.0-50.0 ng) into the DRN induced a significant increment of REM sleep (REMS) during the second and third 2 h of recording. Microinjection of 8-OHDPAT (50.0 ng) induced similar effects on REMS during the second 2 h of recording. On the other hand, intra-DRN injection of WAY 100635 (12.5-50.0 ng) significantly reduced REMS during the second 2 h recording period. REM sleep values had also decreased significantly during the first 2 h of recording after the 50 ng dose. Pretreatment with WAY 100635 (25.0 or 50.0 ng) prevented the increase of REMS induced by flesinoxan (25.0 ng) during the second two recording hours. Our findings support the proposal that activation of somatodendritic 5-HT(1A) receptors in the DRN increases REMS, whereas their blockade induces the opposite effect.
在植入用于慢性睡眠记录的成年大鼠中,研究了两种选择性5-羟色胺(5-HT)1A受体激动剂8-羟基二丙胺三嗪(8-OHDPAT)和氟司必林以及一种选择性5-HT1A受体拮抗剂WAY 100635对自发睡眠的影响。将血清素能配体直接微量注射到中缝背核(DRN)中。向DRN直接注射氟司必林(25.0 - 50.0纳克)可在记录的第二个和第三个2小时期间使快速眼动睡眠(REMS)显著增加。在记录的第二个2小时期间,微量注射8-OHDPAT(50.0纳克)对REMS产生类似影响。另一方面,在DRN内注射WAY 100635(12.5 - 50.0纳克)在第二个2小时记录期内显著减少了REMS。在注射50纳克剂量后,记录的第一个2小时期间REMS值也显著下降。用WAY 100635(25.0或50.0纳克)预处理可防止氟司必林(25.0纳克)在记录的后两个小时内诱导的REMS增加。我们的研究结果支持以下观点,即DRN中躯体树突状5-HT1A受体的激活会增加REMS,而对其进行阻断则会产生相反的效果。