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a unit of magnetic field strength equal to one-hundred-thousandth of an oersted
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ガンマ(ギリシア語アルファベットの第3字Γ,γ;英語のG,gに相当)
(特に女性の)魅力的な脚,すんなりした脚

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/10/13 07:59:34」(JST)

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γ-Hydroxybutyric acid (GHB), also known as 4-hydroxybutanoic acid, is a naturally occurring neurotransmitter and a psychoactive drug. Chemically closely related to GABA, it acts on the GABA receptor and on the GHB receptor.

GHB has been used in a medical setting as a general anesthetic, for cataplexy, narcolepsy, and alcoholism.^[2]^[3] It is also used illegally as an intoxicant, to try to increase athletic performance, and as a date rape drug.^[4] It is commonly used in the form of a salt, such as sodium γ-hydroxybutyrate (Na.GHB, sodium oxybate, or Xyrem) or potassium γ-hydroxybutyrate (K.GHB, potassium oxybate).

GHB is also produced as a result of fermentation, and is found in small quantities in some beers and wines, beef and small citrus fruits.^[5]

Succinic semialdehyde dehydrogenase deficiency is a disease that causes GHB to accumulate in the blood.

1 Medical use
2 Recreational use
- 2.1 Party use
- 2.2 Sports and athletics
3 Date rape drug
- 3.1 United States
- 3.2 Other countries
4 Adverse effects
- 4.1 Combination with alcohol
- 4.2 Deaths
- 4.3 Neurotoxicity
- 4.4 Addiction
- 4.5 Withdrawal
5 Overdose
- 5.1 Detection of use
6 Endogenous production
7 Natural fermentation by-product
8 Pharmacology
9 History
10 Legal status
11 See also
12 References
13 External links

Medical use

The only common medical use for GHB today are in the treatment of narcolepsy and more rarely alcoholism.^[6]^[7]^[8] It is sometimes used off-label for the treatment of fibromyalgia.^[9]^[10]

GHB is the active ingredient in the prescription medication sodium oxybate (Xyrem). Sodium oxybate is approved by the U.S. Food and Drug Administration (FDA) for the treatment of cataplexy associated with narcolepsy^[11] and excessive daytime sleepiness (EDS) associated with narcolepsy.^[12]

GHB has been shown to reliably increase slow-wave sleep.^[13]

Recreational use

γ-Hydroxybutyrate powder

Addiction experts in psychiatry, chemistry, pharmacology, forensic science, epidemiology, and the police and legal services engaged in delphic analysis regarding 20 popular recreational drugs. GHB was ranked 15th in dependence, 19th in physical harm, and 14th in social harm.^[14]

GHB is a central nervous system depressant used as an intoxicant,^[15] although it produces a stimulant effect at lower doses due to its action on the GHB receptor.^{[citation needed]} It has many street names, including G, Liquid G, Liquid X, Liquid E,^[16] Georgia Home Boy, Juice, Mils, and Fantasy.^{[citation needed]} Its effects have been described anecdotally as comparable with ethanol (alcohol) and MDMA use, such as euphoria, disinhibition, enhanced libido and empathogenic states. At higher doses, GHB may induce nausea, dizziness, drowsiness, agitation, visual disturbances, depressed breathing, amnesia, unconsciousness, and death. When death is associated with GHB, it is sometimes in conjunction with other drugs, such as alcohol or benzodiazepine which influence the same neurotransmitter (GABA / gamma-Aminobutyric acid). The effects of GHB can last from 1.5 to 4 hours, or even longer if large doses have been consumed.^[17] Consuming GHB with alcohol is dangerous as it can lead to respiratory arrest and vomiting in combination with unrouseable sleep, a potentially lethal combination.^[18]^[19]

In general, the doses used recreationally are between 0.5 g and 3 g.^{[citation needed]} When used as a recreational drug, GHB may be found as the sodium or potassium salt, which is a white crystalline powder, or as GHB salt dissolved in water to form a clear solution. The sodium salt of GHB has a salty taste.^[17] Other salt forms such as calcium GHB and magnesium GHB have also been reported, but the sodium salt is by far the most common.

Some chemicals convert to GHB in the stomach and blood stream. γ-Butyrolactone (GBL) is one such prodrug. Other prodrugs include 1,4-butanediol (1,4-B). There may be additional toxicity concerns with these precursors. 1,4-B and GBL are normally found as pure liquids, though they may be mixed with other more harmful solvents when intended for industrial use, e.g., as paint stripper or varnish thinner.

GHB can be easily manufactured with very little knowledge of chemistry, as it only involves the mixing of its two precursors, GBL and an alkali hydroxide, such as sodium hydroxide, to form the resulting GHB salt. Due to the ease of manufacture and the availability of its precursors, it is not mainly produced in illicit laboratories like most other synthetic drugs, but in private homes by low level producers instead. While available as a prescription for rare and severe forms of sleep disorders such as narcolepsy in some other countries, notably most of Europe, GHB was banned in the U.S. by the FDA in 1990. However, on 17 July 2002, GHB was approved for treatment of cataplexy, often associated with narcolepsy. GHB is "colourless and odorless".^[20]

Party use

GHB is often taken because users find that it enhances their experiences of being in a club, party, or rave; small doses of GHB can act as a stimulant and aphrodisiac. GHB is sometimes referred to as liquid ecstasy, lollipops, liquid X or liquid E due to its tendency to produce euphoria and sociability and its use in the dance party scene.^[21] Despite these nicknames, GHB and MDMA (ecstasy) have entirely separate chemical and pharmacological modes of action.

Sports and athletics

FDA warning against products containing GHB and its prodrugs.

Some athletes also use GHB, as GHB has been shown to elevate human growth hormone in vivo.^[22] One study found that it doubled growth hormone secretion in normal young males.^[13] The growth hormone elevating effects of GHB are mediated through muscarinic acetylcholine receptors and can be prevented by prior administration of pirenzepine, a muscarinic acetylcholine receptor blocking agent.^[23]

As certain succinate salts have been shown to elevate growth hormone in vitro,^[24] and because GHB is metabolized into succinate some people have suggested this plays a role in the growth hormone elevations from GHB. There is however currently no evidence to show that succinate plays any role in the growth hormone elevations from GHB.

Date rape drug

GHB is primarily known to the general public as a date rape drug. The drug is sometimes used to numb the other person, making it easier to then rape the person. When unobtrusively administered in a drink the victim will quickly feel groggy and sleepy, and will not be able to remember what happened after waking up. Consequently, the evidence and the identification of the perpetrator of rape is often difficult. Although unconfirmed sources say the above, it should be mentioned that the sodium form of GHB has a very strong salty taste and therefore will be tasted relatively easily. In addition, obtaining a correct dosage is difficult; at too high a dosage, the person will lose consciousness, which in a public place will probably lead to an emergency call.

Furthermore, a survey in the Netherlands shows that the proportion of GHB in rape cases is greatly overestimated by the media.^[25]

United States

Like alcohol and potent benzodiazepines such as flunitrazepam (Rohypnol), GHB has been labeled as a date rape drug.^[4] The sodium form of GHB has an extremely salty taste but, as it is colourless and odorless,^[20] it has been described as "very easy to add to drinks"^[20] that mask the flavor. GHB produced as a sodium salt (sodium oxybate) may provide a noticeable salty character to the drink, though individual sensitivity to the taste of salt varies.^[26] GHB can also be produced as different salts, some of which do not have a taste as distinctive as the sodium salt (e.g., magnesium oxybate), or much less commonly in the unstable free-acid form.^[27]

Allegedly, GHB has been used in cases of drug-related sexual assault, usually when the victim is vulnerable due to intoxication with a sedative, generally alcohol.^[28] It is difficult to establish how often GHB is used to facilitate rape as it is difficult to detect in a urine sample after a day, and many victims may only recall the rape some time after this,^[29]^[30] although GHB can be detected in hair.^[31] Hair testing can be a useful tool in court cases or for the victim's own information.^[32] Over-the-counter urine test kits only test for date rape drugs that are benzodiazepines, and GHB is not a benzodiazepine. To detect GHB in urine, the sample must be taken within four hours of GHB ingestion, and cannot be tested at home.^[33] GHB can be detected in hair for months after GHB ingestion. Other drugs, such as muscle relaxers (Carisoprodol for example), are sometimes mixed with GHB. Therefore, it can be beneficial to request that the hair sample be tested for multiple drugs.

There have been several high-profile cases of GHB as a date rape drug that received national attention in the United States. In early 1999 a 15-year-old girl, Samantha Reid of Rockwood, Michigan, died from GHB poisoning. Reid’s death inspired the legislation titled the "Hillory J. Farias and Samantha Reid Date-Rape Drug Prohibition Act of 2000." This is the law that made GHB a schedule 1 controlled substance.^[34]

In 2007 Germs drummer Don Bolles was arrested by Orange County, California police after his bottle of Dr. Bronner's Soap field tested positive for GHB; more sophisticated tests yielded negative results and he was released after five days.^[35]

Other countries

Since April 28, 1999 GHB is illegal in France under the Opium Act.

In the Netherlands GHB is illegal since January 1, 2002 under the Opium Act, previously under the Law on Medicines. Until May 7, 1996 the drug was available as a legal chemical. The Healthcare Inspectorate has sales prohibited by the Law on Medicines. In order to circumvent the ban on GHB, do it yourself packages were put on the market with which oneself could easily make GHB. These contained the basic raw materials to be mixed as well as instructions in order (in the proper proportions). The main ingredients for homemade GHB are still (separately) freely available commercially in the Netherlands (GBL (gamma-butyrolactone) or 1,4-butanediol, which is used as the alkaline industrial cleaning agent, sodium hydroxide, which can be found in drain cleaner, and distilled water or ethanol). Since 2005, GHB is medically used under the brand name Xyrem for the treatment of narcolepsy with cataplexy. In 2011 the party drug was placed on the list of hard drugs by the Dutch government, making it illegal other than for medical use prescribed by a doctor.^[36]^[37] Also it is in addiction clinics used during detoxification of GHB in a reduction schedule to prevent severe withdrawal symptoms.

A 2006 study suggested that there was "no evidence to suggest widespread date rape drug use" in the UK and that less than 2% of cases involved GHB while 17% involved cocaine.^[38]^[39]

Adverse effects

Combination with alcohol

In humans, GHB has been shown to reduce the elimination rate of alcohol. This may explain the respiratory arrest that has been reported after ingestion of both drugs.^[40] A review of the details of 194 deaths attributed to or related to GHB over a ten-year period found that most were from respiratory depression caused by interaction with alcohol or other drugs.^[41]

Deaths

One publication has investigated 226 deaths attributed to GHB.^[42] Of 226 deaths included, 213 had a cardiorespiratory arrest and 13 had fatal accidents. Seventy-one deaths (34%) had no co-intoxicants. Postmortem blood GHB was 18–4400 mg/L (median=347) in deaths negative for co-intoxicants.

One report has suggested that sodium oxybate overdose might be fatal, based on deaths of three patients who had been prescribed the drug.^[43] However, for two of the three cases, post-mortem GHB concentrations were 141 and 110 mg/L, which is within the expected range of concentrations for GHB after death, and the third case was a patient with a history of intentional drug overdose.^[44] The toxicity of GHB has been an issue in criminal trials, as in the death of Felicia Tang, where the defense argued that death was due to GHB, not murder.

GHB is produced in the body in very small amounts, and blood levels may climb after death to levels in the range of 30–50 mg/L.^[45] Levels higher than this are found in GHB deaths. Levels lower than this may be due to GHB or to postmortem endogenous elevations.

A UK parliamentary committee commissioned report found the use of GHB to be less dangerous than tobacco and alcohol in social harms, physical harm and addiction.^[46]

Neurotoxicity

In multiple studies, GHB has been found to impair spatial memory, working memory, learning and memory in rats with chronic administration.^[47]^[48]^[49]^[50] These effects are associated with decreased NMDA receptor expression in the cerebral cortex and possibly other areas as well.^[47]

Pedraza et al. (2009) found that repeated administration of GHB to rats for 15 days drastically reduced the number of neurons and non-neuronal cells in the CA1 region of the hippocampus and in the prefrontal cortex. With doses of 10 mg/kg of GHB, they were decreased by 61% in the CA1 region and 32% in the prefrontal cortex, and with 100 mg/kg, they were decreased by 38% and 9%, respectively. It is interesting to note that GHB has biphasic effects on neuronal loss, with lower doses (10 mg/kg) producing the most neurotoxicity, and higher doses (100 mg/kg) producing less.

Pretreatment with NCS-382, a GHB receptor antagonist, prevents both learning/memory deficits and neuronal loss in GHB-treated animals, suggesting that GHB's neurotoxic actions are mediated via activation of the GHB receptor.^[50] In addition, the neurotoxicity appears to be caused by oxidative stress.^[50]^[51]^[52]

Addiction

Although there have been reported fatalities due to GHB withdrawal, reports are inconclusive and further research is needed.^[53] Addiction occurs when repeated drug use disrupts the normal balance of brain circuits that control rewards, memory and cognition, ultimately leading to compulsive drug taking.^[54]^[55]

Rats forced to consume massive doses of GHB will intermittently prefer GHB solution to water but, after experiments on rats, it was noted that "no rat showed any sign of withdrawal when GHB was finally removed at the end of the 20-week period" or during periods of voluntary abstinence.^[56]^[57]

Withdrawal

GHB has also been associated with a withdrawal syndrome of insomnia, anxiety, and tremor that usually resolves within three to twenty-one days.^[15]^[53]^[58] The withdrawal syndrome can be severe producing acute delirium and may require hospitalization in an intensive care unit for management.^[15] The mainstay of treatment for severe withdrawal is supportive care and benzodiazepines for control of acute delirium, but larger doses are often required compared to acute delirium of other causes (e.g. > 100 mg/d of diazepam). Baclofen has been suggested as an alternative or adjunct to benzodiazepines based on anecdotal evidence and some animal data.^[59] However, there is less experience with the use of baclofen for GHB withdrawal, and additional research in humans is needed. Baclofen was first suggested as an adjunct because benzodiazepines do not affect GABA_B receptors and thus have no cross-tolerance with GHB while baclofen, which works via GABA_B receptors, is cross-tolerant with GHB and may be more effective in alleviating withdrawal effects of GHB.^[60]

GHB withdrawal is not widely discussed in textbooks and some psychiatrists, general practitioners, and even hospital emergency physicians may not be familiar with this withdrawal syndrome.^[61]

Overdose

Overdose of GHB can sometimes be difficult to treat because of its multiple effects on the body.^[3]^[62]^[63] GHB tends to cause rapid unconsciousness at doses above 3500 mg, with single doses over 7000 mg often causing life-threatening respiratory depression, and higher doses still inducing bradycardia and cardiac arrest. Other side-effects include convulsions (especially when combined with stimulants), and nausea/vomiting (especially when combined with alcohol).^[15]

The greatest life threat due to GHB overdose (with or without other substances) is respiratory arrest.^[15]^[64] Other relatively common causes of death due to GHB ingestion include aspiration of vomitus, positional asphyxia, and trauma sustained while intoxicated (e.g., motor vehicle accidents while driving under the influence of GHB).^{[citation needed]} The risk of aspiration pneumonia and positional asphyxia risk can be reduced by laying the patient down in the recovery position. People are most likely to vomit as they become unconscious, and as they wake up. It is important to keep the victim awake and moving, who must not be left alone due to the risk of death through vomiting. Frequently they will be in a good mood but this does not mean they are not in danger. GHB overdose is a medical emergency and immediate assessment in an emergency department is needed.

Convulsions from GHB can be treated with the benzodiazepines diazepam or lorazepam.^[15] Even though these benzodiazepines are also CNS depressants, they are GABA_A agonists whereas GHB is primarily a GABA_B agonist, and so do not worsen CNS depression as much as might be expected.^{[citation needed]}

Because of the faster and more complete absorption of GBL relative to GHB, its dose-response curve is steeper, and overdoses of GBL tend to be more dangerous and problematic than overdoses involving only GHB or 1,4-B. Any GHB/GBL overdose is a medical emergency and should be cared for by appropriately trained personnel.

A newer synthetic drug SCH-50911, which acts as a selective GABA_B antagonist, quickly reverses GHB overdose in mice.^[65] However, this treatment has yet to be tried in humans, and it is unlikely that it will be researched for this purpose in humans due to the illegal nature of clinical trials of GHB, and the lack of medical indemnity coverage inherent in using an untested treatment for a life-threatening overdose.^{[original research?]}

Detection of use

GHB may be quantitated in blood or plasma to confirm a diagnosis of poisoning in hospitalized patients,^[15] provide evidence in an impaired driving arrest or to assist in a medicolegal death investigation. Blood or plasma GHB concentrations are usually in a range of 50–250 mg/L in persons receiving the drug therapeutically (during general anesthesia), 30–100 mg/L in those arrested for impaired driving, 50–500 mg/L in acutely intoxicated patients and 100–1000 mg/L in victims of fatal overdosage. Urine is often the preferred specimen for routine drug abuse monitoring purposes. Both γ-butyrolactone (GBL) and 1,4-butanediol are converted to GHB in the body.^[66]^[67]^[68]

In January 2016, it was announced scientists had developed a way to detect GHB, among other things, in saliva.^[69]

Endogenous production

Cells produce GHB by reduction of succinic semialdehyde via succinic semialdehyde reductase (SSR). This enzyme appears to be induced by cAMP levels,^[70] meaning substances that elevate cAMP, such as forskolin and vinpocetine, may increase GHB synthesis and release. People with the disorder known as succinic semialdehyde dehydrogenase deficiency, also known as γ-hydroxybutyric aciduria, have elevated levels of GHB in their urine, blood plasma and cerebrospinal fluid.^[71]

The precise function of GHB in the body is not clear. It is known, however, that the brain expresses a large amount of receptors that are activated by GHB.^[72] These receptors are excitatory and not responsible for the sedative effects of GHB – they have been shown to elevate the principal excitatory neurotransmitter—glutamate.^[73] The benzamide antipsychotics—amisulpride, sulpiride—have been shown to bind to this receptor in vivo.^[74] Other antipsychotics were tested and were not found to have an affinity for this receptor.

It is a precursor to GABA, glutamate, and glycine in certain brain areas.^[75]

GHB has neuroprotective properties and has been found to protect cells from hypoxia.^[76]

Natural fermentation by-product

GHB is also produced as a result of fermentation and so is found in small quantities in some beers and wines, in particular fruit wines. The amount found in wine is pharmacologically insignificant and not sufficient to produce psychoactive effects.^[77]

Pharmacology

GHB has at least two distinct binding sites^[78] in the central nervous system. GHB is an agonist at the newly characterized GHB receptor, which is excitatory,^[79]^[80] and it is a weak agonist at the GABA_B receptor, which is inhibitory.^[80] GHB is a naturally occurring substance that acts in a similar fashion to some neurotransmitters in the mammalian brain.^[81] GHB is probably synthesized from GABA in GABAergic neurons, and released when the neurons fire.^[80]

If taken orally, GABA itself does not effectively cross the blood-brain-barrier.^[82]

GHB induces the accumulation of either a derivative of tryptophan or tryptophan itself in the extracellular space, possibly by increasing tryptophan transport across the blood–brain barrier. The blood content of certain neutral amino-acids, including tryptophan, is also increased by peripheral GHB administration. GHB-induced stimulation of tissue serotonin turnover may be due to an increase in tryptophan transport to the brain and in its uptake by serotonergic cells. As the serotonergic system may be involved in the regulation of sleep, mood, and anxiety, the stimulation of this system by high doses of GHB may be involved in certain neuropharmacological events induced by GHB administration.

However, at therapeutic doses, GHB reaches much higher concentrations in the brain and activates GABA_B receptors, which are primarily responsible for its sedative effects.^[83] GHB's sedative effects are blocked by GABA_B antagonists.

The role of the GHB receptor in the behavioural effects induced by GHB is more complex. GHB receptors are densely expressed in many areas of the brain, including the cortex and hippocampus, and these are the receptors that GHB displays the highest affinity for. There has been somewhat limited research into the GHB receptor; however, there is evidence that activation of the GHB receptor in some brain areas results in the release of glutamate, the principal excitatory neurotransmitter.^[73] Drugs that selectively activate the GHB receptor cause absence seizures in high doses, as do GHB and GABA(B) agonists.^[84]

Activation of both the GHB receptor and GABA(B) is responsible for the addictive profile of GHB. GHB's effect on dopamine release is biphasic.^[85] Low concentrations stimulate dopamine release via the GHB receptor.^[86] Higher concentrations inhibit dopamine release via GABA(B) receptors as do other GABA(B) agonists such as baclofen and phenibut.^[87] After an initial phase of inhibition, dopamine release is then increased via the GHB receptor. Both the inhibition and increase of dopamine release by GHB are inhibited by opioid antagonists such as naloxone and naltrexone. Dynorphin may play a role in the inhibition of dopamine release via kappa opioid receptors.^[88]

This explains the paradoxical mix of sedative and stimulatory properties of GHB, as well as the so-called "rebound" effect, experienced by individuals using GHB as a sleeping agent, wherein they awake suddenly after several hours of GHB-induced deep sleep. That is to say that, over time, the concentration of GHB in the system decreases below the threshold for significant GABA_B receptor activation and activates predominantly the GHB receptor, leading to wakefulness.

Recently, analogs of GHB, such as 4-hydroxy-4-methylpentanoic acid (UMB68) have been synthesised and tested on animals, in order to gain a better understanding of GHB's mode of action.^[89] Analogues of GHB such as 3-methyl-GHB, 4-methyl-GHB, and 4-phenyl-GHB have been shown to produce similar effects to GHB in some animal studies, but these compounds are even less well researched than GHB itself. Of these analogues, only 4-methyl-GHB (γ-hydroxyvaleric acid, GHV) and a prodrug form γ-valerolactone (GVL) have been reported as drugs of abuse in humans, and on the available evidence seem to be less potent but more toxic than GHB, with a particular tendency to cause nausea and vomiting.

Other prodrug ester forms of GHB have also rarely been encountered by law enforcement, including 1,4-butanediol diacetate (BDDA/DABD), methyl-4-acetoxybutanoate (MAB), and ethyl-4-acetoxybutanoate (EAB),^{[citation needed]} but these are, in general, covered by analogue laws in jurisdictions where GHB is illegal, and little is known about them beyond their delayed onset and longer duration of action. The intermediate compound γ-hydroxybutyraldehyde (GHBAL) is also a prodrug for GHB; however, as with all aliphatic aldehydes this compound is caustic and is strong-smelling and foul-tasting; actual use of this compound as an intoxicant is likely to be unpleasant and result in severe nausea and vomiting.

Metabolic pathway of GHB.

Both of the metabolic breakdown pathways shown for GHB can run in either direction, depending on the concentrations of the substances involved, so the body can make its own GHB either from GABA or from succinic semialdehyde. Under normal physiological conditions, the concentration of GHB in the body is rather low, and the pathways would run in the reverse direction to what is shown here to produce endogenous GHB. However, when GHB is consumed for recreational or health promotion purposes, its concentration in the body is much higher than normal, which changes the enzyme kinetics so that these pathways operate to metabolise GHB rather than producing it.

History

Synthesis of the chemical GHB was first reported in 1874 by Alexander Zaytsev,^[90] but the first major research into its use in humans was conducted in the early 1960s by Dr. Henri Laborit to use in studying the neurotransmitter GABA.^[91] It quickly found a wide range of uses due to its minimal side-effects and short duration of action, the only difficulties being the narrow therapeutic dosage range and the dangers presented by its combination with alcohol and other nervous system depressants.

GHB was widely used in France, Italy, and other European countries for several decades as a sleeping agent and an anesthetic in childbirth but problems with its abuse potential and development of newer drugs have led to a decrease in legitimate medical use of GHB in recent times. In the Netherlands, GHB could be bought as aphrodisiac and euphoriant in a smartshop for several years, until several incidents caused it to become regulated. The only common medical applications for GHB today are in the treatment of narcolepsy and more rarely alcoholism. In the typical scenario, GHB has been synthesized from γ-butyrolactone (GBL) by adding sodium hydroxide (lye) in ethanol or water.

A popular children's toy, Bindeez (also known as Aqua Dots, in the United States), produced by Melbourne company Moose, was banned in Australia in early November 2007 when it was discovered that 1,4-butanediol (1,4-B), which is metabolized into GHB, had been substituted for the non-toxic plasticiser 1,5-pentanediol in the bead manufacturing process. Three young children were hospitalized as a result of ingesting a large number of the beads, and the toy was recalled.^[92]

Legal status

GHB sold in Italy for therapeutic use.

In the United States, it was placed on Schedule I of the Controlled Substances Act in March 2000. However, when sold as sodium oxybate, it is considered a Schedule III substance but with Schedule I trafficking penalties, one of several drugs that are listed in multiple schedules.^[64]^[93] On 20 March 2001, the Commission on Narcotic Drugs placed GHB in Schedule IV of the 1971 Convention on Psychotropic Substances.^[94]

In the UK GHB was made a class C drug in June 2003. In October 2013 the ACMD recommended upgrading it from schedule IV to schedule II in line with UN recommendations. Their report concluded that the minimal use of Xyrem in the UK meant that prescribers would be minimally inconvenienced by the rescheduling.^[95]

In Hong Kong, GHB is regulated under Schedule 1 of Hong Kong's Chapter 134 Dangerous Drugs Ordinance. It can only be used legally by health professionals and for university research purposes. The substance can be given by pharmacists under a prescription. Anyone who supplies the substance without prescription can be fined HK$10,000. The penalty for trafficking or manufacturing the substance is a HK$150,000 fine and life imprisonment. Possession of the substance for consumption without license from the Department of Health is illegal with a HK$100,000 fine or 5 years of jail time.

In New Zealand and Australia, GHB, 1,4-B and GBL are all Class B illegal drugs, along with any possible esters, ethers and aldehydes. GABA itself is also listed as an illegal drug in these jurisdictions, which seems unusual given its failure to cross the blood–brain barrier, but there was a perception among legislators that all known analogues should be covered as far as this was possible. Attempts to circumvent the illegal status of GHB have led to the sale of derivatives such as 4-methyl-GHB (γ-hydroxyvaleric acid, GHV) and its prodrug form γ-valerolactone (GVL), but these are also covered under the law by virtue of their being "substantially similar" to GHB or GBL and; so importation, sale, possession and use of these compounds is also considered to be illegal.

In Chile, GHB is a controlled drug under the law "Ley de substancias psicotropicas y estupefacientes" (psychotropic substances and narcotics).

In Norway^[96] and in Switzerland,^[97] GHB is considered a narcotic and is only available by prescription under the trade name Xyrem (Union Chimique Belge S.A.).

Sodium oxybate is also used therapeutically in Italy under the brand name Alcover for treatment of alcohol withdrawal and dependence.^[98]

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External links

Gamma-hydroxybutyrate MS Spectrum
The Cognitive Enhancement Research Institute – Research findings on GHB and other substances
EMCDDA Report on the risk assessment of GHB in the framework of the joint action on new synthetic drugs
Erowid GHB Vault (also contains information about addiction and dangers)
InfoFacts – Rohypnol and GHB (National Institute on Drug Abuse)

UpToDate Contents

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

1. 成人におけるナルコレプシーの治療treatment of narcolepsy in adults [show details]
…States licensing information . Gamma hydroxybutyrate gained notoriety as a "date rape" drug and has potential for abuse . Thus, access to sodium oxybate and oxybate salts is restricted in the United States …
2. ガンマヒドロキシブチレート（GHB）中毒gamma hydroxybutyrate ghb intoxication [show details]
…therapeutic agent in the United States and in Europe. In Europe, GHB is available as Xyrem (sodium oxybate) for the treatment of cataplexy and excessive daytime sleepiness in narcolepsy. Somsanit (an anesthetic) …
3. γ-ヒドロキシ酪酸（GHB）の離脱症状と依存gamma hydroxybutyrate ghb withdrawal and dependence [show details]
…Organization provides a listing of international poison centers at its website: Illicit use of gamma hydroxybutyrate (GHB) occurs for recreation and for a number of alleged health benefits, including bodybuilding…
4. 睡眠医学の最新情報whats new in sleep medicine [show details]
…sodium oxybate in patients who require a second-line therapy. A mixed-salt formulation of gamma hydroxybutyrate (GHB) comprised of calcium, magnesium, potassium, and sodium oxybate has been …
5. デートレイプ：危険因子および予防date rape risk factors and prevention [show details]
…flunitrazepam [Rohypnol]), 3,4-methylendioxymethamphetamine (MDMA or ecstasy), ketamine, gamma hydroxybutyrate (GHB), and over-the-counter antihistamines, among others . The combination of alcohol with…

English Journal

Increases in Serum Growth Hormone Concentrations Associated with GHB Administration.

Brailsford AD1, Bartlett C2, Kicman AT2, Cowan DA2.
Journal of analytical toxicology.J Anal Toxicol.2016 Oct 15. [Epub ahead of print]
The administration of gamma-hydroxybutyrate (GHB) has been reported to augment the increase in growth hormone (GH) secretion associated with the onset of sleep. The ability of GHB to stimulate GH production in the absence of sleep in both male and female volunteers was investigated as part of a GHB
PMID 27744373

Impact of concomitant medications on obstructive sleep apnea.

Jullian-Desayes I1,2, Revol B1,2,3, Chareyre E1,2, Camus P4, Villier C3, Borel JC1,2, Pepin JL1,2, Joyeux-Faure M5,6.
British journal of clinical pharmacology.Br J Clin Pharmacol.2016 Oct 13. doi: 10.1111/bcp.13153. [Epub ahead of print]
Obstructive sleep apnea (OSA) is characterized by repeated episodes of apnea and hypopnea during sleep. Little is known about the potential impact of therapy drugs on the underlying respiratory disorder. Any influence should be taken into account and appropriate action taken, including drug withdraw
PMID 27735059

Footprint area analysis of binary imaged Cupriavidus necator cells to study PHB production at balanced, transient, and limited growth conditions in a cascade process.

Vadlja D1, Koller M2,3, Novak M1, Braunegg G4, Horvat P1.
Applied microbiology and biotechnology.Appl Microbiol Biotechnol.2016 Oct 3. [Epub ahead of print]
Statistical distribution of cell and poly[3-(R)-hydroxybutyrate] (PHB) granule size and number of granules per cell are investigated for PHB production in a five-stage cascade (5CSTR). Electron microscopic pictures of cells from individual cascade stages (R1-R5) were converted to binary pictures to
PMID 27695913

Japanese Journal

人脳脊髄液中のgamma-Hydroxybutyrateの定性及び定量方法の訂正版

荒井光治
藍野学院紀要 21, 1-8, 2007
荒井らのガンマヒドロキシ酪酸の先のレポートは,タイトル,データその他の数ケ所で間違っていた。今回の報告は前回の訂正版である。ガンマヒドロキシ酪酸は薬理学的に重要で興味ある物質である。人脳脊髄液中のガンマヒドロキシ酪酸の存在は始めて荒井らが証明した。前回のレポートでは血清中のガンマヒドロキシ酪酸の存在について否定した。そして人脳脊髄液中のガンマヒドロキシ酪酸の濃度を間違って報告した。人血清中のガンマ …
NAID 110007126690

The impact of donor chemical overdose on the outcome of liver transplantation

Komokata Teruo
日本外科学会雑誌 103(臨時増刊), 606, 2002-03-10
NAID 110003951464

Evidence for a gamma-hydroxybutyrate (GHB) up-take by rat brain synaptic vesicles

MULLER C
J Neurochem 80, 899-904, 2002
NAID 30014568469

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★リンクテーブル★

リンク元	「γ-ヒドロキシ酪酸」
関連記事	「gamma」

「γ-ヒドロキシ酪酸」

γ-Hydroxybutyric acid
Systematic (IUPAC) name
	4-Hydroxybutanoic acid
Clinical data
Pregnancy; category	B;
Routes of; administration	Usually oral; intravenous
Legal status
Legal status	AU: S8 (Controlled); CA: Schedule I; DE: Anlage III (Prescription only); NZ: Class B; UK: Class C; US: Schedule I and Schedule III;
Pharmacokinetic data
Bioavailability	25% (oral)
Metabolism	95%, mainly Hepatic, also in blood and tissues
Onset of action	Within 5-15 min
Biological half-life	30–60 minutes
Excretion	5%, renal
Identifiers
CAS Number	591-81-1
ATC code	N01AX11 (WHO) N07XX04 (WHO)
PubChem	CID 3037032
IUPHAR/BPS	4711
DrugBank	DB01440
ChemSpider	9984
UNII	30IW36W5B2
KEGG	C00989
ChEBI	CHEBI:30830
ChEMBL	CHEMBL1342
Synonyms	γ-Hydroxybutyric acid; γ-Hydroxybutyrate; GHB
Chemical data
Formula	C4H8O3
Molar mass	104.10 g/mol (GHB); 126.09 g/mol (sodium salt); 142.19 g/mol (potassium salt)
	SMILES O=C(O)CCCO ;
	InChI InChI=1S/C4H8O3/c5-3-1-2-4(6)7/h5H,1-3H2,(H,6,7) ; Key:SJZRECIVHVDYJC-UHFFFAOYSA-N ;
(verify)

　　[★]

英: γ-hydroxybutyric acid gamma hydroxybutyric acid gamma-hydroxybutyrate gamma hydroxybutyrate GHBA GHB
同: 4-ヒドロキシ酪酸 4-hydroxybutyric acid
関: γ-アミノ酪酸 GABA

「gamma」

　　[★] γ ガンマ　　　

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[Kompendium_Xyrem-97] Xyrem untersteht dem Bundesgesetz über die Betäubungsmittel und die psychotropen Stoffe

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v t e Neurotransmitters

Amino acid-derived	Major excitatory/inhibitory systems: Glutamate system: Agmatine Aspartic acid (aspartate) Cycloserine Glutamic acid (glutamate) Glutathione Glycine GSNO GSSG Kynurenic acid NAA NAAG Proline Serine; GABA system: GABA GABOB GHB; Glycine system: α-Alanine β-Alanine Glycine Hypotaurine Proline Sarcosine Serine Taurine; GHB system: GHB T-HCA (GHC) Biogenic amines: Monoamines: 6-OHM Dopamine Epinephrine (adrenaline) Melatonin NAS (normelatonin) Norepinephrine (noradrenaline) Serotonin (5-HT); Trace amines: 3-Iodothyronamine N-Methylphenethylamine N-Methyltryptamine m-Octopamine p-Octopamine Phenylethanolamine Phenethylamine Synephrine Tryptamine m-Tyramine p-Tyramine; Others: Histamine Neuropeptides: See here instead.

Lipid-derived	Endocannabinoids: 2-AG 2-AGE (noladin ether) 2-ALPI 2-OG AA-5-HT Anandamide (AEA) DEA LPI NADA NAGly OEA Oleamide PEA RVD-Hpα SEA Virodhamine (O-AEA) Neurosteroids: See here instead.

Nucleobase-derived	Nucleosides: Adenosine system: Adenosine ADP AMP ATP

Vitamin-derived	Cholinergic system: Acetylcholine

Miscellaneous	Gasotransmitters: Carbon monoxide (CO) Hydrogen sulfide (H₂S) Nitric oxide (NO); Candidates: Acetaldehyde Ammonia (NH₃) Carbonyl sulfide (COS) Nitrous oxide (N₂O) Sulfur dioxide (SO₂)

Systematic (IUPAC) name


4-Hydroxybutanoic acid
Clinical data
Pregnancy category	B
Routes of administration	Usually oral; intravenous
Legal status
Legal status	AU: S8 (Controlled) CA: Schedule I DE: Anlage III (Prescription only) NZ: Class B UK: Class C US: Schedule I and Schedule III
Pharmacokinetic data
Bioavailability	25% (oral)
Metabolism	95%, mainly Hepatic, also in blood and tissues
Onset of action	Within 5-15 min^[1]
Biological half-life	30–60 minutes
Excretion	5%, renal
Identifiers
CAS Number	591-81-1^Y
ATC code	N01AX11 (WHO) N07XX04 (WHO)
PubChem	CID 3037032
IUPHAR/BPS	4711
DrugBank	DB01440^Y
ChemSpider	9984^Y
UNII	30IW36W5B2^Y
KEGG	C00989^Y
ChEBI	CHEBI:30830^Y
ChEMBL	CHEMBL1342^Y
Synonyms	γ-Hydroxybutyric acid γ-Hydroxybutyrate GHB
Chemical data
Formula	C₄H₈O₃
Molar mass	104.10 g/mol (GHB) 126.09 g/mol (sodium salt) 142.19 g/mol (potassium salt)
SMILES O=C(O)CCCO
InChI InChI=1S/C4H8O3/c5-3-1-2-4(6)7/h5H,1-3H2,(H,6,7)^Y Key:SJZRECIVHVDYJC-UHFFFAOYSA-N^Y
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v t e Euphoriants

μ-Opioid receptor agonists (opioids) (e.g., morphine, heroin, hydrocodone, oxycodone, opium, kratom) α₂δ subunit-containing voltage-dependent calcium channels blockers (gabapentinoids) (e.g., gabapentin, pregabalin, phenibut) AMPA receptor antagonists (e.g., perampanel) CB₁ receptor agonists (cannabinoids) (e.g., THC, cannabis) Dopamine receptor agonists (e.g., levodopa) Dopamine releasing agents (e.g., amphetamine, methamphetamine, MDMA, mephedrone) Dopamine reuptake inhibitors (e.g., cocaine, methylphenidate) GABA_A receptor positive allosteric modulators (e.g., barbiturates, benzodiazepines, carbamates, ethanol (drinking alcohol), inhalants, nonbenzodiazepines, quinazolinones) GHB (sodium oxybate) and analogues Glucocorticoids (corticosteroids) (e.g., dexamethasone, prednisone) nACh receptor agonists (e.g., nicotine, tobacco, arecoline, areca nut) Nitric oxide prodrugs (e.g., alkyl nitrites (poppers)) NMDA receptor antagonists (e.g., DXM, ketamine, methoxetamine, nitrous oxide, phencyclidine, inhalants) Orexin receptor antagonists (e.g., suvorexant)

See also: Recreational drug use

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gamma-hydroxybutyrate