N-Acetylcysteine |
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This article requires proofreading. As such, it likely contains incorrect grammar, spelling, and punctuation. |
| N-Acetylcysteine | |||||||||||||||||||||||||
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| Molecular structure of N-Acetylcysteine | |||||||||||||||||||||||||
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| Common names | N-Acetylcysteine | ||||||||||||||||||||||||
| Substitutive name | (2R)-2-acetamido-3-sulfanylpropanoic acid | ||||||||||||||||||||||||
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| Summary sheet: N-Acetylcysteine |
Acetylcysteine, also known as N-acetylcysteine or N-acetyl-L-cysteine (NAC), is a substituted amino acid with nootropic properties which is used as a medication for treating paracetamol (acetaminophen) overdose and to loosen thick mucus such as in cystic fibrosis or chronic obstructive pulmonary disease.[1]
This compound was initially patented in 1960 and licensed for use in 1968.[2] It is on the World Health Organization's List of Essential Medicines needed in a basic health system.[3] It is available as a generic medication and is available over the counter in many countries.[4]
N-acetylcysteine (NAC) is emerging as a useful agent in the treatment of psychiatric disorders.[5] It currently being explored in it's effect and relief of a wide variety of cognitive disorders including, but not limited to addiction, autism, compulsive and grooming disorders, schizophrenia and bipolar disorder. N-acetylcysteine has shown promising results in populations with these disorders and others whom treatment efficacy has previously been limited.
The recommended safe oral dosage range of N-acetylcysteine ranges between 300mg and 3000mg.
Contents
Chemistry
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N-Acetylcysteine is similar to both L-Cysteine (NAC being but an acetylated form of it) and the glutathione enzyme itself (being the direct precursor to glutathione synthesis); both L-cysteine and glutathione have also been explored for their usage as supplements.
Pharmacology
Acetylcysteine serves as a prodrug to L-cysteine. L-cysteine is a precursor to the biologic antioxidant glutathione. Hence administration of acetylcysteine replenishes glutathione stores.[6] This is why N-acetylcysteine is used in the event of a parcetomol overdose, as it works by increasing glutathione levels and binding with the toxic break down products of paracetamol.[7]
In terms of its psychologically beneficial effects, N-acetylcysteine targets glutaminergic and dopaminergic pathways.[8] This could potentially account for its stimulating properties. It is also thought that provision of additional cysteine (an endogenous amino acid), via N-acetylcysteine supplementation, reverses function disturbed with usage of drugs in the pathology of addiction.[9]
Subjective effects
The effects listed below are based upon the subjective effects index and personal experiences of PsychonautWiki contributors. The listed effects will rarely (if ever) occur all at once, but heavier dosages will increase the chances and are more likely to induce a full range of effects.
In comparison to other commonly used nootropics, N-acetylcysteine has considerably stronger stimulation and motivation enhancement but with a greater amount of side effects such as dehydration and nausea. However, unlike other stimulants this compound does not seem to induce a "crash" or "come down" during the offset of its experience.
Cognitive effects
- Addiction suppression - N-acetylcysteine's action on glutaminergic and dopaminergic pathways is thought to reverse brain functions which have become disturbed by heavy drug addiction.[10] This mechanism has been shown to provide relief for those who struggle with compulsive redosing, reward behaviors and psychological cravings, and has been shown to positively reverse nicotine addiction[11], cocaine addiction[12], marijuana dependence.[13], and many other compulsive behaviors[14]. Annecdotal reports suggest that one can take this compound over their addictive drug of choice for the purpose of quickly suppressing their cravings.
- Motivation enhancement
- Anxiety suppression
- Focus enhancement
- Thought acceleration
- Rejuvenation
- Mindfulness
Physical effects
- Dehydration
- Stimulation
- Euphoria
- Cough suppression
- Bronchodilation
- Headaches
- Increased blood pressure
- Nausea
- Itchiness
- Nose bleeds - A certain subset of people may experience minor nosebleeds which is likely due to this compounds mechanism as a blood thinner.[15]
Toxicity and harm potential
N-Acetylcysteine is considered to be safe for most adults when used as a prescription medication although the exact toxic dosage is unknown. However, dosage ranges in excess of twenty grams over an extended period of time may inversely affect heart and lung function.[16]
This compound can also rarely cause rashes, fever, headache, drowsiness, nose bleeds, low blood pressure, and liver problems.[17]
It is strongly recommended that one use harm reduction practices when using this drug.
Tolerance and addiction potential
The chronic use of N-Acetylcysteine does not seem to present addiction and it is not capable of causing psychological dependence among certain users. This is likely a result of its known mechanisms for reversing drug addiction.[18]
Tolerance to many of the effects of N-Acetylcysteine develops quickly with repeated use. This results in users having to administer increasingly large doses to achieve the same effects. After that, it takes about 3 - 7 days for the tolerance to be reduced to half and 1 - 2 weeks to be back at baseline (in the absence of further consumption). N-Acetylcysteine does not seem to present a cross-tolerance with other stimulants.
Legal issues
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This legality section is a stub. As such, it likely contains incomplete or wrong information. You can help by expanding it. |
N-Acetylcysteine is uncontrolled in most countries, and is legally bought and sold in pharmacies and supplement stores without a prescription.
- United Kingdom - It is illegal to produce, supply, or import this drug under the Psychoactive Substance Act, which came into effect on May 26th, 2016.[19]
See also
External links
References
- ↑ Acetylcysteine | http://www.drugs.com/monograph/acetylcysteine.html
- ↑ https://books.google.ca/books?id=FjKfqkaKkAAC&pg=PA544#v=onepage&q&f=false
- ↑ http://apps.who.int/iris/bitstream/10665/93142/1/EML_18_eng.pdf?ua=1
- ↑ https://books.google.ca/books?id=oeYjAwAAQBAJ&pg=PT44#v=onepage&q&f=false
- ↑ http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3044191/
- ↑ ACETADOTE® CONCENTRATED INJECTION Product Information | https://www.ebs.tga.gov.au/ebs/picmi/picmirepository.nsf/pdf?OpenAgent&id=CP-2010-PI-03960-3&d=2016041216114622483
- ↑ Acetylcysteine (Drugs.com) | http://www.drugs.com/monograph/acetylcysteine.html
- ↑ N-acetylcysteine in psychiatry: current therapeutic evidence and potential mechanisms of action (PubMed.gov / NCBI) | https://www.ncbi.nlm.nih.gov/pubmed/21118657
- ↑ Cystine/glutamate exchange regulates metabotropic glutamate receptor presynaptic inhibition of excitatory transmission and vulnerability to cocaine seeking (PubMed.gov / NCBI) | http://www.ncbi.nlm.nih.gov/pubmed/16000629
- ↑ Cystine/glutamate exchange regulates metabotropic glutamate receptor presynaptic inhibition of excitatory transmission and vulnerability to cocaine seeking (PubMed.gov / NCBI) | http://www.ncbi.nlm.nih.gov/pubmed/16000629
- ↑ The Role of Cystine-Glutamate Exchange in Nicotine Dependence in Rats and Humans (PubMed.gov / NCBI) | http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2756612/
- ↑ Safety and Tolerability of N-Acetylcysteine in Cocaine-Dependent Individuals (PubMed.gov / NCBI) | http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1513138/
- ↑ N-acetylcysteine (NAC) in young marijuana users: an open-label pilot study (PubMed.gov / NCBI) | http://www.ncbi.nlm.nih.gov/pubmed/20163391/
- ↑ Glutamate transmission in addiction (PubMed.gov / NCBI) | http://www.ncbi.nlm.nih.gov/pubmed/18675832/
- ↑ Review: could Acetylcysteine cause Bleeding from the nose (Nosebleed)? | http://www.ehealthme.com/ds/acetylcysteine/bleeding+from+the+nose
- ↑ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1952618/
- ↑ Acetylcysteine | http://www.drugs.com/monograph/acetylcysteine.html
- ↑ Cystine/glutamate exchange regulates metabotropic glutamate receptor presynaptic inhibition of excitatory transmission and vulnerability to cocaine seeking (PubMed.gov / NCBI) | http://www.ncbi.nlm.nih.gov/pubmed/16000629
- ↑ Psychoactive Substances Act 2016 (Legislation.gov.uk) | http://www.legislation.gov.uk/ukpga/2016/2/contents/enacted