
Naloxone: Difference between revisions
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==External links== | |||
*[https://en.wikipedia.org/wiki/Naloxone Naloxone (Drugs.com)] | |||
*[https://www.youtube.com/watch?v=ANseEroeSsg Combatting America's Opioid Crisis: Heroin's Antidote (Vice)] | |||
==References== | ==References== |
Revision as of 22:50, 20 February 2017
Naloxone | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Chemical Nomenclature | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Common names | Naloxone, Narcan, Evzio | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Substitutive name | 1-N-Allyl-14-hydroxynordihydromorphinone | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Systematic name | (4R,4aS,7aR,12bS)-4a,9-Dihydroxy-3-prop-2-enyl-2,4,5,6,7a,13-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-7-one | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Class Membership | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Psychoactive class | Opioid (Antagonist) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Chemical class | Morphinan | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Routes of Administration | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Summary sheet: Naloxone |
Naloxone, commonly sold under the brand names Narcan and Evzio, is an opioid antagonist used to reverse the effects of an opioid overdose. Like many substances that act on the opioid receptors, naloxone has a morphinan backbone. Emergency responders and law enforcement use naloxone to reverse the effects of opioid overdoses immediately. Naloxone is sold under the brand name Narcan as a nasal spray and Evzio as an auto-injector with voice instructions. Naloxone and naltrexone have also been researched in the treatment of depersonalization disorder with promising results.
Naloxone has been credited with saving an unprecedented number of opioid overdose victims. This is partially due to naloxone programs in several countries to give naloxone to people who use opioids, and the rapid deployment of naloxone by law enforcement agencies and emergency medical services.
Chemistry
Chemically, naloxone is similar in structure or many opiates and semi-synthetic opioids. Naloxone is extremely similar in structure to oxymorphone. Whereas oxymorphone has methyl group bonded to the nitrogen, naloxone has an allyl group, which is a moiety that often makes opioid agonists into opioid antagonist. The chemical formula of naloxone is C19H21NO4 and has a molar mass of 327.38g per mole[1].
Pharmacology
Naloxone acts as a potent μ-opioid receptor inverse agonist. Because of its high affinity for the μ-opioid receptor, it knocks other ligands out of the receptor. Naloxone also has a lower affinity as a κ-opioid receptor and δ-opioid receptor. If naloxone is administered without previous administration of opioids, it has few biological effects, notably a lower pain threshold. Naloxone has two isomers, (+)naloxone and (-)naloxone, with the latter being active. The liver metabolizes naloxone. It has very low oral bioavailability which is why it is administered intravenously, intramuscularly or intranasally. Small amounts of naloxone are often added to opioids like buprenorphine and pentazocine to prevent abuse. Naloxone has been noted to block a placebo based analgesic effect. For example, if an individual has been administered something that they were told was morphine and had a analgesic response to it, naloxone will block that response[2].
Subjective effects
Disclaimer: The effects listed below cite the Subjective Effect Index (SEI), an open research literature based on anecdotal user reports and the personal analyses of PsychonautWiki contributors. As a result, they should be viewed with a healthy degree of skepticism.
It is also worth noting that these effects will not necessarily occur in a predictable or reliable manner, although higher doses are more liable to induce the full spectrum of effects. Likewise, adverse effects become increasingly likely with higher doses and may include addiction, severe injury, or death ☠.
When taken by itself without the presence of other substances or an opioid overdose, naloxone causes relatively comfortable sedating effects and general emotion suppression.
Physical effects
- Sedation - Naloxone is considerably sedating. It can result in the user feeling sleepy and having difficulty keeping their eyes open.
Cognitive effects
- Emotion suppression - The emotion suppression found on naloxone is noticeably similar to the same experience found within antipsychotics although without the accompanying analysis suppression and thought deceleration.
- Identity alteration - Naloxone has been demonstrated by a pilot study to significantly reduce the symptoms of chronic long term depersonalization. Within this study, 11 patients received single doses (1.6 or 4 mg i.v.) and three others received multiple infusions, with the maximal dosage being 10 mg, and the effect of naloxone on symptom severity was then measured and determined. In most cases, the first signs of improvement were recorded soon after the naloxone infusions (within 20–40 min), and greater brightness marked the patients' perception of the world. A full reduction or disappearance of depersonalization occurred within the interval of 1–4 h and, in some patients, continued for as long as 12–24 h. This was followed by some deterioration, although the depersonalization never recurred to the initial level. Five patients showed evidence of a stable improvement.[3]
Toxicity and harm potential

Naloxone is considered not habit-forming. When naloxone is administered in an opioid overdose, the individual will go through immediate withdrawal. Opioid withdrawal may be life-threatening in serious cases. Symptoms of opioid withdrawal may include, but are not limited to agitation, nausea, psychosis, temperature regulation suppression, anxiety, physical fatigue, excessive yawning, sweating, dehydration, and pupil dilation. It has been noted that naloxone may be needed in higher dosages depending on the opioid that was consumed. It is not uncommon for several doses of naloxone in cases of fentanyl or acetylfentanyl overdoses. If an individual does not have opioids in their system when naloxone is administered, naloxone may rarely cause dehydration and nausea.
It is strongly recommended that one use harm reduction practices when using this substance.
Legal issues
Throughout the world, naloxone is not considered a controlled substance. In most countries, it is a prescription drug.
- Australia: In Australia, naloxone is considered an over the counter drug and is available at most pharmacies [4]
- Canada: In Canada, naloxone kits are distributed at many emergency rooms and clinics.
- United States: At a federal level, naloxone is a prescription drug. Many states have programs that make naloxone over the counter and available at request at most pharmacies. In the United States, most jurisdictions have programs to deploy naloxone to law enforcement and fire and rescue services.
- United Kingdom: In the United Kingdom, naloxone is considered a Prescription Only Medicine.
See also
External links
References
- ↑ PubChem | https://pubchem.ncbi.nlm.nih.gov/compound/naloxone>
- ↑ Opioids and placebo responses | http://www.jpsychores.com/article/S0022-3999(04)00515-X/abstract
- ↑ Effect of naloxone therapy on depersonalization: a pilot study | http://jop.sagepub.com/content/15/2/93.abstract / http://jop.sagepub.com.sci-hub.cc/content/15/2/93.full.pdf+html
- ↑ http://www.abc.net.au/triplej/programs/hack/how-painkiller-use-becomes-a-heroin-addiction/7129964