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    Zolpidem is a prescription short-acting nonbenzodiazepine hypnotic that potentiates gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter, by binding to benzodiazepine type 1 (BZ1) receptors.
    Zolpidem is used for the short-term treatment of insomnia. It works quickly (usually within 15 minutes) and has a short half-life (2-3 hours). Some trade names of zolpidem are Ambien®, Stilnox®, Stilnoct®, Hypnogen® or Myslee®. Its hypnotic effects are similar to those of the benzodiazepine class of drugs, but it is actually classified as an imidazopyridine. Flumazenil, which is used for benzodiazepine overdose, can also reverse zolpidem's sedative/hypnotic effects. As an anticonvulsant and muscle relaxant, the beneficial effects start to emerge at 10 and 20 times the dose required for sedation, respectively. For that reason, it has never been approved for either muscle relaxation or seizure prevention. Such drastically increased doses are more inclined to induce one or more negative side effects, including hallucinations and/or amnesia. (See below.)

    Recently, zolpidem has been cited in various medical reports mainly in the United Kingdom as waking persistent vegetative state (PVS) patients, and dramatically improving the conditions of people with brain injuries. More information is available on the BBC world news site under zolpidem.*, and The Guardian*. Widespread reproduction of these results would be a medical revolution.

    The patent in the United States on zolpidem is held by the French pharmaceutical corporation Sanofi-Aventis. The patent 4382938, as listed on the FDA Electronic Orange Book site is due to expire in October 21, 2006. As of September 16, 2006, no six-month extension is listed in the Orange Book as having been granted. *. *. Zolpidem is available from several generic manufacturers in the UK, as generic from Sandoz in South Africa, as well as from other manufacturers such as Ratiopharm.


        Zolpidem
            Uses
            Mechanism of action
            Recreational use and abuse
            Side-effects
            See also
            Notes

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    Uses

    Zolpidem is approved for the short-term (usually two to six weeks) treatment of insomnia, and it has been studied for nightly use up to six months in a single-blind, open-label trial published in 1991, an open-label study lasting 180 days published in 1992 (with continued efficacy in patients who had kept taking it as of 180 days after the end of the trial), and in an open-label trial lasting 179 days published in 1993.

    The United States Air Force uses zolpidem, under trade name Ambien®, as "no-go pills" to help pilots sleep after a mission; another drug used for the same purpose is temazepam (Restoril®). (Cf. the "go-pills" amphetamine served under the name Dexedrine® act as a stimulant for the same pilots, ostensibly to reverse the effects of the "no-go pills," or its recent modafinil (Provigil®) replacement).

    It is also used off-label to treat restless leg syndrome.

    As is the case with many prescription sedative/hypnotic drugs, zolpidem is sometimes used by stimulant users to "come down" after the use of stimulants such as methamphetamine, cocaine, MDMA (ecstasy), or amphetamine.

    Recently, the drug has been found to have positive effects for sufferers of persistent vegetative state. The drug reacts with the presumed-dead brain cells, in essence waking them up from a deep cellular hibernation. This unintended effect seems to preempt the sedentary reaction normally caused by the drug.

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    Mechanism of action

    In 1990, Pritchett and Seeburg noted that zolpidem binds with high affinity to the α1, with medium affinity to the α2, α3-GABAA receptor subunits, and found that it had no affinity for the α5 subunit. Two years later, zolpidem was noted to have a high affinity for ω1; benzodiazepine receptors, a low affinity for ω2 and a very low affintity for ω3, respectively by Ruano et al in 1992. In other words, it has the highest affinity for ω1 binding sites on α-1GABAA receptor subunits, and it is this that s its sedative and weak anticonvulsant properties.

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    Recreational use and abuse
    When Ambien abuse occurs, people may take it orally, crush and snort it, or cook it for an intravenous injection. Ambien abuse can occur when used longer than recommended (no longer than a few weeks), at high doses (more than the usual 10mg), and in people who have been dependent on other drugs or alcohol in the past. Ambien effects can increase in intensify if mixed with other substances like alcohol.

    Recreational use of this drug (specifically the Ambien® brand) is becoming more common in young people. Recreational users claim that "fighting" the effects of the drug by forcing themselves to stay awake will sometimes cause vivid visuals and a body high (see side-effects below.) Some recreational users report decreased anxiety, and even mild to moderate euphoria, as well as moderate perceptual changes and slight visual distortions, but lacking hallucinogenic entities. The likelihood of experiencing any of these effects seems to be completely arbitrary regardless of the size of the dose. Audiotory disortions have been reported in some users. The drug can make them belive that the room they are in is fully crowded, while in reality it is empty.

    Recreational zolpidem use is speculated to lead to tolerance and dependence much more quickly than prescribed use. Recreational use is rising, as demonstrated by the use of street names for the pill, such as: "A-" (which is most likely due to the imprint on the Ambien CR® brand of zolpidem, which consists of a capital A along with a tilde, which looks roughly like A~, as well as for sedative and calming effects, "A+" is a street name for Adderall, named so because of its stimulant effects) and "zombie pills" (because of the waking sleep/sensory deprivation effect some users have reported experiencing). Another buzz term for Ambien is "tic-tacs", referring to the shape and color of commonly abused 10mg tablets.

    To counteract recreational use of zolpidem in the United States, Sanofi-Aventis coats their pills with a flexible plastic-like coating, which sticks to unpulverized "bumps" or "chunks" and can be difficult to remove, thus hindering the process of insufflation; although this a relatively minor obstacle to a serious drug abuser.

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    Side-effects

    Side effects at any dose may include:

      Hallucinations, through all physical senses, of varying intensity
      Increased appetite
      Increased libido
      Impaired judgment and reasoning
      Uninhibited extroversion in social or interpersonal settings
      Increased impulsivity

    Some users take zolpidem recreationally for these side effects. However, it may be less common than benzodiazepine abuse. In the United States, recreational use may be less common than in countries where the drug is available as a less expensive generic. Zolpidem can become addictive if taken for extended periods of time, due to dependence on its ability to put one to sleep or to the euphoria it can sometimes produce. Like most addictive drugs, a tolerance in the zolpidem user develops and increases all the more quickly the longer she or he has been regularly taking it. Under the influence of the drug it is common to take more zolpidem than is necessary due to either forgetting that one has already taken a pill (elderly users are particularly at risk here), or knowingly taking more than the prescribed dosage. Users with a predilection for abuse are advised to keep additional zolpidem in a safe place that is unlikely to be remembered or accessed while intoxicated to avoid this risk. A trustworthy friend or relative is the best defense if such people are available; otherwise, a box or cupboard locked with a combination padlock is a good defense against this tendency, as the abovementioned side-effects can easily prevent a user from operating such a lock while under the drug's influence.

    The recent release of Ambien CR® (zolpidem tartrate extended release) in the United States renewed interest in the drug among recreational drug users.

    Before a user becomes fully acclimated to these effects (or if the user does not become acclimated), these symptoms can be severe enough to be deemed as drug-induced psychosis. Incidentally, antipsychotics like ziprasidone (Geodon®) or quetiapine (Seroquel®) may be prescribed alongside zolpidem to both combat these side effects and to aid in sleep-induction, as both of them contain mild hypnotic properties. However, because some antidepressants are known for being mildly sedating (i.e., paroxetine), it may be inadvisable to use zolpidem and an antidepressant simultaneously.

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    See also


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    Notes
      Depoortere H, Zivkovic B, Lloyd KG, Sanger DJ, Perrault G, Langer SZ, Bartholini G. "Zolpidem, a novel nonbenzodiazepine hypnotic. I. Neuropharmacological and behavioral effects." Journal of Pharmacology and Experimental Therapeutics. 1986 May;237(2):649-58. PMID 2871178
      Schlich D, L'Heritier C, Coquelin JP, Attali P, Kryrein HJ. "Long-term treatment of insomnia with zolpidem: a multicentre general practitioner study of 107 patients." J Int Med Res. 1991 May-Jun;19(3):271-9. PMID 1670039
      Maarek L, Cramer P, Attali P, Coquelin JP, Morselli PL. "The safety and efficacy of zolpidem in insomniac patients: a long-term open study in general practice." J Int Med Res. 1992 Apr;20(2):162-70. PMID 1521672
      Kummer J, Guendel L, Linden J, Eich FX, Attali P, Coquelin JP, Kyrein HJ. "Long-term polysomnographic study of the efficacy and safety of zolpidem in elderly psychiatric in-patients with insomnia." J Int Med Res. 1993 Jul-Aug;21(4):171-84. PMID 8112475
      Caldwell JA, Caldwell JL. "Fatigue in military aviation: an overview of US military-approved pharmacological countermeasures." Aviation, Space, and Environmental Medicine. 2005 Jul;76(7 Suppl):C39-51. PMID 16018329
      Evidente, Virgilio Gerald H., Caviness, John N., and Adler, Charles H. "Case Studies in Movement Disorders." Seminars in Neurology. 23(3):277-284, 2003. Thieme Medical Publishers. 26 Jan 2004. Medscape Fulltext Thieme Fulltext PMID 14722823
      Pritchett DB, Seeburg PH. "Gamma-aminobutyric acidA receptor alpha 5-subunit creates novel type II benzodiazepine receptor pharmacology." Journal of Neurochemistry. 1990 May;54(5):1802-4. PMID 2157817
      Ruano D, Vizuete M, Cano J, Machado A, Vitorica J. "Heterogeneity in the allosteric interaction between the gamma-aminobutyric acid (GABA) binding site and three different benzodiazepine binding sites of the GABAA/benzodiazepine receptor complex in the rat nervous system." Journal of Neurochemistry. 1992 Feb;58(2):485-93. PMID 1309562
      Pidd, Helen. "Reborn." Guardian Unlimited. 2006 Sep 12. Fulltext
      Crestani F, Martin JR, Mohler H, Rudolph U. "Mechanism of action of the hypnotic zolpidem in vivo." British Journal of Pharmacology. 2000 Dec;131(7):1251-4. PMID 11090095 Fulltext
      Angelettie M.S.W., Lisa. "Ambien Abuse" Fulltext
     
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