GHB: Difference between revisions

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[[File:GHB.jpg|right]]
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GHB (Gamma-Hydroxybutyric Acid) is a CNS depressant used as intoxicant. It is a naturally occurring substance found in the human central nervous system, as well as in wine, beef, small citrus fruits, and in small amounts in almost all animals. GHB has been used in a medical setting as a general anaesthetic, to treat conditions such as insomnia, clinical depression, narcolepsy, and alcohol withdrawal, and to improve athletic performance.
'''GHB''' (Gamma-Hydroxybutyric Acid) is a CNS depressant used as intoxicant. It is a naturally occurring substance found in the human central nervous system, as well as in wine, beef, small citrus fruits, and in small amounts in almost all animals. GHB has been used in a medical setting as a general anaesthetic, to treat conditions such as insomnia, clinical depression, narcolepsy, and alcohol withdrawal, and to improve athletic performance.


== History ==
== History ==
GHB was synthesized and introduced into medicine in 1960 and in 1963 discovered as a naturally occurring chemical in the human brain.
Synthesis of this chemical was first reported in 1874 by Alexander Zaytsev. But the first major research in humans was conducted in the early 1960's by Dr. Henri Laborit to use in studying the neurotransmitter GABA.  


= Dosage =
Throughout most of the 1960's it was a popular anesthetic, then was abandoned by doctors, following discoveries of its poor analgesic effects. In the 1970's was recommended for the treatment of narcolepsy, though the euphoric side of GHB made that unfavourable.


GBL dose: 1ml GBL is equal to 1.6g GHB
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 the medical use in recent times.
 
In the 1980's It was marketed for a short time as a fat burner and muscle developer. However, in 1990, based off many reports of GHB-linked illness, the FDA declared GHB unsafe, and ordered it to be removed from stores shelves. Following this, many users switched to GBL and 1 4-butanediol.
GHB (Xyrem) was approved by the FDA in 2002 for use in the treatment of narcolepsy/Cataplexy.
 
== Dosage ==
 
GBL dose: 1ml GBL is equal to 1.6ml GHB


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= Duration =
== Duration ==


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= Effects =
== Effects ==


== Positive ==
=== Positive ===
*Relaxation
*Relaxation
*Increased sociability
*Increased sociability
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*Enhanced sensuality
*Enhanced sensuality


== Neutral ==  
=== Neutral ===  
*Dizziness
*Dizziness


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*Amnesia
*Amnesia


== After effects ==
=== After effects ===


* Hangover (usually only occurs from high doses)
* Hangover (usually only occurs from high doses)
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= Harm Reduction =
== Harm Reduction ==
* The dosage curve of GHB is very steep, recreational doses being very close to doses which will cause a period of unrousable sleep, which are again relatively close to doses which may cause coma or death through respiratory depression.  
* The dosage curve of GHB is very steep, recreational doses being very close to doses which will cause a period of unrousable sleep, which are again relatively close to doses which may cause coma or death through respiratory depression.  
*The only way to know the concentration of liquid GHB is to know and trust information provided by the source. Users should be extremely careful about GHB dosages as even small overdoses can result in temporarily unrousable sleep.
*The only way to know the concentration of liquid GHB is to know and trust information provided by the source. Users should be extremely careful about GHB dosages as even small overdoses can result in temporarily unrousable sleep.
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* High addiction potential
* High addiction potential


= Chemistry and Pharmacology =  
== Chemistry and Pharmacology ==  
GHB has at least two distinct binding sites in the central nervous system. GHB is an agonist at the newly characterized GHB receptor, which is excitatory, and it is a weak agonist at the GABA-B receptor, which is inhibitory. GHB is a naturally occurring substance that acts in a similar fashion to some neurotransmitters in the mammalian brain. GHB is probably synthesized from GABA in GABAergic neurons, and released when the neurons fire.
GHB has at least two distinct binding sites in the central nervous system. GHB is an agonist at the newly characterized GHB receptor, which is excitatory, and it is a weak agonist at the GABA-B receptor, which is inhibitory. GHB is a naturally occurring substance that acts in a similar fashion to some neurotransmitters in the mammalian brain. GHB is probably synthesized from GABA in GABAergic neurons, and released when the neurons fire.


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


== Dopamine Rebound ==
=== Dopamine Rebound ===


GHB will reduce dopamine levels in high amounts, but increase dopamine levels in the brain in low amounts<ref>https://www.ncbi.nlm.nih.gov/pubmed/1847191</ref>. This leads to what is known as dopamine rebound among users. Users can experience strong wakefullness about 4 hours after the last dose was consumed. This is often strong enough to wake the user up from sleep, and may be accompanied by a strong redose compulsion. The longer and higher the dose of GHB used, the more pronounced the effect may become.  
GHB will reduce dopamine levels in high amounts, but increase dopamine levels in the brain in low amounts<ref>https://www.ncbi.nlm.nih.gov/pubmed/1847191</ref>. This leads to what is known as dopamine rebound among users. Users can experience strong wakefullness about 4 hours after the last dose was consumed. This is often strong enough to wake the user up from sleep, and may be accompanied by a strong redose compulsion. The longer and higher the dose of GHB used, the more pronounced the effect may become.  


== Production ==
=== Production ===
Production of GHB consists simply of mixing "lactone" (short for gamma butyrlactone) and lye (sodium hydroxide) in the proper amounts. It can also be converted from GBL.
Production of GHB consists simply of mixing "lactone" (short for gamma butyrlactone) and lye (sodium hydroxide) in the proper amounts. It can also be converted from GBL.


= Legal status =
== Legal status ==


GHB is illegal in most parts of the world, GBL is legal in parts of Europe.
GHB is illegal in most parts of the world, GBL is legal in parts of Europe.


= Links =
== Links ==


[http://en.wikipedia.org/wiki/Gamma-Hydroxybutyric_acid Wikipedia]
[http://en.wikipedia.org/wiki/Gamma-Hydroxybutyric_acid Wikipedia]
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[https://www.erowid.org/chemicals/ghb/ghb.shtml Erowid]
[https://www.erowid.org/chemicals/ghb/ghb.shtml Erowid]


= References =
== References ==


<references />
<references />

Latest revision as of 16:09, 9 October 2018

GHB (Gamma-Hydroxybutyric Acid) is a CNS depressant used as intoxicant. It is a naturally occurring substance found in the human central nervous system, as well as in wine, beef, small citrus fruits, and in small amounts in almost all animals. GHB has been used in a medical setting as a general anaesthetic, to treat conditions such as insomnia, clinical depression, narcolepsy, and alcohol withdrawal, and to improve athletic performance.

History

Synthesis of this chemical was first reported in 1874 by Alexander Zaytsev. But the first major research in humans was conducted in the early 1960's by Dr. Henri Laborit to use in studying the neurotransmitter GABA.

Throughout most of the 1960's it was a popular anesthetic, then was abandoned by doctors, following discoveries of its poor analgesic effects. In the 1970's was recommended for the treatment of narcolepsy, though the euphoric side of GHB made that unfavourable.

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 the medical use in recent times.

In the 1980's It was marketed for a short time as a fat burner and muscle developer. However, in 1990, based off many reports of GHB-linked illness, the FDA declared GHB unsafe, and ordered it to be removed from stores shelves. Following this, many users switched to GBL and 1 4-butanediol.

GHB (Xyrem) was approved by the FDA in 2002 for use in the treatment of narcolepsy/Cataplexy.

Dosage

GBL dose: 1ml GBL is equal to 1.6ml GHB

Oral
Light 0.5-1.5g
Common 1-2.5g
Strong 2-4g

Duration

Oral
Onset 10-40 minutes
Total 1-3 hours

Effects

Positive

  • Relaxation
  • Increased sociability
  • Positive mood changes
  • Euphoria
  • Empathogenic
  • Enhanced sensuality

Neutral

  • Dizziness

Negative

  • Nausea
  • Restlessness
  • Unconsciousness
  • Amnesia

After effects


Harm Reduction

  • The dosage curve of GHB is very steep, recreational doses being very close to doses which will cause a period of unrousable sleep, which are again relatively close to doses which may cause coma or death through respiratory depression.
  • The only way to know the concentration of liquid GHB is to know and trust information provided by the source. Users should be extremely careful about GHB dosages as even small overdoses can result in temporarily unrousable sleep.
  • Avoid driving and operating heavy machinery
  • Don't mix it with alcohol, or other depressants
  • 2-3 uses a week should be the maximum
  • High addiction potential

Chemistry and Pharmacology

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

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

Dopamine Rebound

GHB will reduce dopamine levels in high amounts, but increase dopamine levels in the brain in low amounts[1]. This leads to what is known as dopamine rebound among users. Users can experience strong wakefullness about 4 hours after the last dose was consumed. This is often strong enough to wake the user up from sleep, and may be accompanied by a strong redose compulsion. The longer and higher the dose of GHB used, the more pronounced the effect may become.

Production

Production of GHB consists simply of mixing "lactone" (short for gamma butyrlactone) and lye (sodium hydroxide) in the proper amounts. It can also be converted from GBL.

Legal status

GHB is illegal in most parts of the world, GBL is legal in parts of Europe.

Links

Wikipedia

Erowid

References