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JOURNAL

Clinical Medicine Insights: Therapeutics

Pharmacotherapy of Insomnia: Focus on Zolpidem Extended Release

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Clinical Medicine Insights: Therapeutics 2009:1 123-140

Published on 01 Apr 2009


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J.M. Monti1, D. Warren Spence2, S.R. Pandi-Perumal3, Salomon Z. Langer4 and R. Hardeland5

1Dept. of Pharmacology and Therapeutics, School of Medicine, Clinics Hospital, Montevideo 11300, Uruguay. 2Sleep and Alertness Clinic, 750 Dundas Street West, Toronto, ON M6J-3S3, Canada. 3Somnogen Inc, 8790 112th Street, New York, NY 11418, U.S.A. 4Euthymia Ltd, 8 H. Rosenblum St., apt. 4650, Tel Aviv 69379, Israel. 5Johann Friedrich Blumenbach Institute of Zoology and Anthropology, University of Göttingen, Göttingen, Germany.

Abstract

The imidazopyridine drug zolpidem (N,N,6-trimethyl-2[4-methyl-phenyl]imidazo[1,2-a]pyridine-3-acetamide) is a sedative/hypnotic with relative selectivity for α1 subunits of the GABAA receptor/chloride channel complex. Because of this selectivity and regional receptor distribution, zolpidem is less generalized in its CNS depressive actions than benzo- diazepines and largely devoid of their major, undesired side- and after-effects, at recommended doses. Zolpidem is rapidly taken up and distributed, binds extensively to plasma proteins, and is readily inactivated by hepatic cytochrome P450 mono-oxygenases, especially CYP3A4. Zolpidem is thus a rapidly acting agent which provides effective facilitation of sleep onset. However, plasma levels of the immediate release (IR) formulation frequently decline too quickly for effective sleep maintenance. To address this problem zolpidem extended release (ER) has been developed. At age-specific dosages, it increases, in middle-aged and elderly patients, total sleep time and reduces the number of nocturnal awakenings. Both zolpidem IR and ER have favorable toxicological profiles. Adverse effects are moderate, frequently in the incidence range of placebos, and certainly less frequent and severe than those of benzodiazepines. Zolpidem IR and ER are practically devoid of next-day hangover effects and only infrequently cause rebound insomnia of usually short duration. Both variants of zolpidem have a limited potential for dependence and abuse.



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