Monti Jaime M, Jantos Héctor
Department of Pharmacology and Therapeutics, School of Medicine Clinics Hospital, Montevideo, Uruguay.
Behav Pharmacol. 2015 Aug;26(5):418-26. doi: 10.1097/FBP.0000000000000142.
The effects of RO-600175, a selective 5-HT2C receptor agonist, were studied in adult rats implanted for chronic sleep recordings. Intraperitoneal administration of RO-600175 (4 mg/kg) during the light phase of the light-dark cycle significantly increased wakefulness and reduced slow wave sleep and rapid-eye-movement sleep during the first 2 h of the recording period. Direct infusion of RO-600175 into the dorsal raphe nucleus (4 mmol/l), laterodorsal tegmental nucleus (4 mmol/l), or horizontal limb of the diagonal band of Broca (4 mmol/l) also decreased rapid-eye-movement sleep. It is proposed that the activation of γ-aminobutyric acid-ergic cells located in the dorsal raphe nucleus, laterodorsal tegmental nucleus, and horizontal limb of the diagonal band of Broca is responsible, at least in part, for the effects of RO-600175 on rapid-eye-movement sleep. It is suggested that the increased wakefulness observed after systemic injection of the 5-HT2C receptor ligand could be partly related to the increased release of acetylcholine in the frontal cortex and hippocampus. However, additional studies are required to characterize the neurotransmitter systems responsible for the increase in wakefulness.
在植入用于慢性睡眠记录的成年大鼠中研究了选择性5-羟色胺2C(5-HT2C)受体激动剂RO-600175的作用。在明暗周期的光照阶段腹腔注射RO-600175(4毫克/千克),在记录期的前2小时内显著增加觉醒,并减少慢波睡眠和快速眼动睡眠。将RO-600175直接注入中缝背核(4毫摩尔/升)、外侧背盖核(4毫摩尔/升)或布罗卡斜角带水平支(4毫摩尔/升)也会减少快速眼动睡眠。有人提出,位于中缝背核、外侧背盖核和布罗卡斜角带水平支的γ-氨基丁酸能细胞的激活至少部分地导致了RO-600175对快速眼动睡眠的作用。有人认为,全身注射5-HT2C受体配体后观察到的觉醒增加可能部分与额叶皮质和海马中乙酰胆碱释放增加有关。然而,需要进一步的研究来确定导致觉醒增加的神经递质系统。