The Effects of Benzodiazepine and Nonbenzodiazepine Agents, Ramelteon, Low-dose Doxepin, Suvorexant, and Selective Serotonin 5-HT2A Receptor Antagonists and Inverse Agonists on Sleep and Wakefulness

被引:2
作者
Monti, Jaime M. [1 ]
Torterolo, Pablo [2 ]
Pandi-Perumal, Seithikurippu R. [3 ]
机构
[1] Univ Republica, Sch Med Clin Hosp, Dept Pharmacol & Therapeut, Montevideo, Uruguay
[2] Univ Republica, Sch Med, Dept Physiol, Montevideo, Uruguay
[3] Somnogen Canada Inc, Toronto, ON, Canada
来源
CLINICAL MEDICINE INSIGHTS-THERAPEUTICS | 2016年 / 8卷
关键词
sleep; slow wave sleep; N3; serotonin; 5-HT2A receptor antagonist; 5-HT2A receptor inverse agonist;
D O I
10.4137/CMT.S38232
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Several agents are known to improve sleep induction and/or maintenance in patients with insomnia disorder. These include the benzodiazepine (BZD) and non-BZD receptor allosteric modulators, the melatonin receptor agonist ramelteon, low-dose doxepin, and suvorexant. One of the drawbacks of the BZDs is their known reduction in both N3 sleep [also known as slow wave sleep or delta sleep and characterized by the occurrence of slow high amplitude delta (0.5-2 Hz) waves] and rapid eye movement (REM) sleep. Low-dose doxepin has shown similar association with decrease in REM sleep. By contrast, suvorexant increases REM sleep. The available evidence tends to indicate that irrespective of their mechanisms of action, the selective serotonin 5-HT2A receptor antagonists and inverse agonists, including volinanserin, pruvanserin, and nelotanserin, when given in isolated administration, increases slow wave sleep in laboratory animals. Wakefulness and REM sleep were decreased in some studies. Moreover, subjects with normal sleep showed significant increase in N3 sleep following the administration of eplivanserin, nelotanerin, and pimavanserin. Nelotanserin has also been shown to augment N3 sleep in patients with chronic insomnia disorder. N2 sleep tended to decrease in most of these studies, while REM sleep showed no significant changes. Taken together, these evidences suggest that the coadministration of a selective 5-HT2A receptor antagonist or inverse agonist with a hypnotic drug could be a valid clinical strategy for normalizing sleep induction and maintenance and for promoting N3 sleep in patients with insomnia disorder. Additionally, the 5-HT2A receptor agents may have a potential value for improving the cognition and memory deficits in patients with a chronic insomnia disorder as well as elderly patients who show reductions in N3 sleep.
引用
收藏
页码:29 / 36
页数:8
相关论文
共 47 条
  • [11] 2-P
  • [12] Sleep and the sleep electroencephalogram across the menstrual cycle in young healthy women
    Driver, HS
    Dijk, DJ
    Werth, E
    Biedermann, K
    Borbely, AA
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (02) : 728 - 735
  • [13] Serotonin 2A receptor antagonists for treatment of schizophrenia
    Ebdrup, Bjorn H.
    Rasmussen, Hans
    Arnt, Jorn
    Glenthoj, Birte
    [J]. EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2011, 20 (09) : 1211 - 1223
  • [14] Further evidence for the sleep-promoting effects of 5-HT2A receptor antagonists and demonstration of synergistic effects with the hypnotic, zolpidem in rats
    Griebel, Guy
    Beeske, Sandra
    Jacquet, Agnes
    Laufrais, Christian
    Alonso, Richard
    Decobert, Michel
    Avenet, Patrick
    Francon, Dominique
    [J]. NEUROPHARMACOLOGY, 2013, 70 : 19 - 26
  • [15] Susceptibility to Declarative Memory Interference Is Pronounced in Primary Insomnia
    Griessenberger, Hermann
    Heib, Dominik P. J.
    Lechinger, Julia
    Luketina, Nikolina
    Petzka, Marit
    Moeckel, Tina
    Hoedlmoser, Kerstin
    Schabus, Manuel
    [J]. PLOS ONE, 2013, 8 (02):
  • [16] Hannon Jason, 2008, P155, DOI 10.1007/978-3-7643-8561-3_6
  • [17] Orexin receptor antagonism for treatment of insomnia A randomized clinical trial of suvorexant
    Herring, W. Joseph
    Snyder, Ellen
    Budd, Kerry
    Hutzelmann, Jill
    Snavely, Duane
    Liu, Kenneth
    Lines, Christopher
    Roth, Thomas
    Michelson, David
    [J]. NEUROLOGY, 2012, 79 (23) : 2265 - 2274
  • [18] Iber C., 2007, AASM MANUAL SCORING
  • [19] Kales A., 1984, EVALUATION TREATMENT
  • [20] Kehne JH, 1996, J PHARMACOL EXP THER, V277, P968