Effects of GF-015535-00, a Novel α1 GABAA Receptor Ligand, on the Sleep-Wake Cycle in Mice, with Reference to Zolpidem

被引:9
作者
Anaclet, Christelle [1 ]
Zhang, Mei [1 ]
Zhao, Chunmei [1 ]
Buda, Colette [1 ]
Seugnet, Laurent [1 ]
Lin, Jian-Sheng [1 ]
机构
[1] Univ Lyon 1, Lyon Neurosci Res Ctr, INSERM, CNRS,Fac Med,U1028,UMR 5292, F-69373 Lyon 08, France
关键词
Zolpidem; insomnia; sleep fragmentation; alpha 1 GABA(A) receptor; mouse; COMPARATIVE TOLERABILITY; INSOMNIA; HISTAMINE; ZOPICLONE; SUBTYPES; DRUGS;
D O I
10.5665/sleep.1596
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study Objectives: Novel, safe, and efficient hypnotic compounds capable of enhancing physiological sleep are still in great demand in the therapy of insomnia. This study compares the sleep-wake effects of a new alpha 1 GABA(A) receptor subunit ligand, GF-015535-00, with those of zolpidem, the widely utilized hypnotic compound. Methods: Nine C57Bl6/J male mice were chronically implanted with electrodes for EEG and sleep-wake monitoring. Each mouse received 3 doses of GF-015535-00 and zolpidem. Time spent in sleep-wake states and cortical EEG power spectra were analyzed. Results: Both zolpidem and GF-015535-00 prominently enhanced slow wave sleep and paradoxical sleep in the mouse. However, as compared with zolpidem, GF-015535-00 showed several important differences: (1) a comparable sleep-enhancing effect was obtained with a 10 fold smaller dose; (2) the induced sleep was less fragmented; (3) the risk of subsequent wake rebound was less prominent; and (4) the cortical EEG power ratio between slow wave sleep and wake was similar to that of natural sleep and thus compatible with physiological sleep. Conclusion: The characteristics of the sleep-wake effects of GF-015535-00 in mice could be potentially beneficial for its use as a therapeutic compound in the treatment of insomnia. Further investigations are required to assess whether the same characteristics are conserved in other animal models and humans.
引用
收藏
页码:103 / 111
页数:9
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