Talk:Glaucine: Difference between revisions

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{{SummarySheet}}
{{SummarySheet}}
Glaucine is a naturally occurring novel [[psychedelic]] substance of the [[aporphine]] class found in ''[[Glaucium Flavum]]''.<ref>https://link.springer.com/article/10.1023/B:PHAC.0000048907.58847.c6</ref> Glaucine has one stereocenter, therefore it has two stereoisomers, where (S)-Glaucine is a 5-HT<sub>2A</sub>  [[agonist]] and (R)-Glaucine is a 5-HT<sub>2</sub> positive allosteric modulator.<ref>https://onlinelibrary.wiley.com/doi/10.1111/cbdd.13390</ref> Its psychedelic effects are believed to be produced by its interaction with [[serotonin]] [[Receptor|receptors]] like most psychedelics do, but also has clinically significant interactions at D1,<ref>https://www.sciencedirect.com/science/article/abs/pii/S0968089605002312?via%3Dihub</ref> α1, and benzothiazepine receptors as an [[antagonist]], and inhibits MOA to a moderate degree.<ref>https://www.sciencedirect.com/science/article/abs/pii/S0021967319301104?via%3Dihub</ref> Glaucine has a close relative found in [[Blue Lotus]] (''Nymphaea nouchali)'' called [[apomorphine]]. It is both psychedelic as well as sedating, but the [[sedation]] is more similar to that of [[opioids]] than [[Psilocybin mushrooms|psilocybin]], a generally sedating psychedelic. It is most commonly consumed [[Routes of administration|orally]].
 
Glaucine is a naturally occurring novel [[psychedelic]] substance of the [[aporphine]] class found in ''[[Glaucium Flavum]]''.<ref>https://link.springer.com/article/10.1023/B:PHAC.0000048907.58847.c6</ref> Glaucine has one stereocenter, therefore it has two stereoisomers, where (S)-Glaucine is a 5-HT<sub>2A</sub>  [[agonist]] and (R)-Glaucine is a 5-HT<sub>2</sub> positive allosteric modulator.<ref name=":1">https://onlinelibrary.wiley.com/doi/10.1111/cbdd.13390</ref> Its psychedelic effects are believed to be produced by its interaction with [[serotonin]] [[Receptor|receptors]] like most psychedelics do, but also has clinically significant interactions at D1<ref>https://www.sciencedirect.com/science/article/abs/pii/S0968089605002312?via%3Dihub</ref> and α1<ref name=":2">https://pubmed.ncbi.nlm.nih.gov/30216681/</ref> receptors as an [[antagonist]], and inhibits MOA to a moderate degree.<ref>https://www.sciencedirect.com/science/article/abs/pii/S0021967319301104?via%3Dihub</ref> Glaucine has a close relative found in [[Blue Lotus]] (''Nymphaea nouchali)'' called [[apomorphine]]. It is both psychedelic as well as sedating, but the [[sedation]] is more similar to that of [[opioids]] than [[Psilocybin mushrooms|psilocybin]], a generally sedating psychedelic. It is most commonly consumed [[Routes of administration|orally]].
 
{{SubstanceBox/Glaucine}}


Glaucine is rarely sold on the streets and almost exclusively distributed as a legal alternative to more common psychedelics, where it is commonly used for recreational and entheogenic purposes. It was and still is a very uncommon and unheard of substance with sparing experiences on the internet.
Glaucine is rarely sold on the streets and almost exclusively distributed as a legal alternative to more common psychedelics, where it is commonly used for recreational and entheogenic purposes. It was and still is a very uncommon and unheard of substance with sparing experiences on the internet.


Due to its potent sedating effects as well as unknown toxicity profile, it is strongly recommended that one use proper [[Responsible drug use|harm reduction practices]] if choosing to use this substance.{{SubstanceBox/Example}}
Due to its potent sedating effects as well as unknown toxicity profile, it is strongly recommended that one use proper [[Responsible drug use|harm reduction practices]] if choosing to use this substance.
 
==History and culture==
==History and culture==
Glaucine was first described in 1839 by Probst, defined as an 'acrid [[alkaloid]], and was first isolated by Richard Fischer in 1901.<ref name=":0">https://minds.wisconsin.edu/bitstream/handle/1793/71908/KETCHAM.pdf?sequence=1&isAllowed=y#:~:text=(1)%20The%20earliest%20chemical%20investigation,which%20he%20called%20Glaucopicrin%2C%203.</ref> It has been used used for millennia, where records back to the year 131 claim it was used for aches and sores as well as abscess' in present-day Turkey.<ref name=":0" /> In an overview study in 2007, glaucine's antitussive effectiveness was confirmed along with its potent [[bronchodilation]] effects, but lacked the [[Respiratory depression|respiratory depression]] and habit-forming use associated with opioid antitussives.<ref>https://www.sciencedirect.com/science/article/abs/pii/B9780080552323618252?via%3Dihub</ref> Today, it is sold as an antitussive medicine in Iceland and eastern European countries, as well as being used off-label for asthma.<ref>https://link.springer.com/article/10.1007/s00228-007-0451-9</ref>{{historyStub}}
Glaucine was first described in 1839 by Probst, defined as an 'acrid [[alkaloid]], and was first isolated by Richard Fischer in 1901.<ref name=":0">https://minds.wisconsin.edu/bitstream/handle/1793/71908/KETCHAM.pdf?sequence=1&isAllowed=y#:~:text=(1)%20The%20earliest%20chemical%20investigation,which%20he%20called%20Glaucopicrin%2C%203.</ref> It has been used used for millennia, where records back to the year 131 claim it was used for aches and sores as well as abscess' in present-day Turkey.<ref name=":0" /> In an overview study in 2007, glaucine's antitussive effectiveness was confirmed along with its potent [[bronchodilation]] effects, but lacked the [[Respiratory depression|respiratory depression]] and habit-forming use associated with opioid antitussives.<ref>https://www.sciencedirect.com/science/article/abs/pii/B9780080552323618252?via%3Dihub</ref> Today, it is sold as an antitussive medicine in Iceland and eastern European countries, as well as being used off-label for asthma.<ref>https://link.springer.com/article/10.1007/s00228-007-0451-9</ref> It has very few written experiences online, but the earliest found is from 2009.<ref>https://www.erowid.org/experiences/subs/exp_Glaucine.shtml</ref>{{historyStub}}


==Chemistry==
==Chemistry==
Glaucine is an aporphine, meaning 'not [[morphine]].' It is named this because despite similar structure to morphine, it is in fact not morphine. Aporphine is the parent compound of glaucine, where glaucine has methoxy groups substituted at the 1, 2, 9, and 10 positions. Glaucine has one stereocenter, meaning it has two stereoisomers. Both stereoisomers are found in nature, albeit in different plants.<ref>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9174169</ref>{{chemistry}}
Glaucine is an aporphine, meaning 'not [[morphine]].' It is named this because despite similar structure to morphine, it is in fact not morphine. Aporphine is the parent compound of glaucine, where glaucine has methoxy groups substituted at the 1, 2, 9, and 10 positions. Glaucine has one stereocenter, meaning it has two stereoisomers. Both stereoisomers are found in nature, albeit in different plants.<ref>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9174169</ref>{{chemistry}}
==Pharmacology==
==Pharmacology==
Glaucine is a sedative-psychedelic. The psychedelic effects perceived from glaucine are in fact from interaction of 5-HT<sub>2A</sub> receptors, but both stereoisomers of glaucine interact with the receptor differently. (S)-glaucine is an agonist of the receptor, the same action performed by psychedelics like [[LSD]] and [[mescaline]], but (R)-glaucine is a positive allosteric modulator, meaning it boosts the signaling and activity at the receptor.{{pharmacology}}
Glaucine is a sedative-psychedelic. The psychedelic effects perceived from glaucine are in fact from interaction of 5-HT<sub>2A</sub> receptors, but both stereoisomers of glaucine interact with the receptor differently. (S)-glaucine is an agonist of the receptor, the same action performed by psychedelics like [[LSD]] and [[mescaline]], but (R)-glaucine is a positive allosteric modulator, meaning it boosts the signaling and activity at the receptor.<ref name=":1" /> Its sedating effects are believed to come from its strong antagonism at α1 receptors, the same receptors that the stimulant [[caffeine]] agonizes.<ref name=":2" /> D1 antagonism is common amongst aporphines such as apomorphine, and might be a cause of reduction in drug-seeking behaviors following administration such as seen with apomorphine.<ref>https://apomorphine.info/</ref>{{pharmacology}}


==Subjective effects==
==Subjective effects==
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|{{effects/physical|
|{{effects/physical|
If applicable, a brief paragraph summary of the substance's physical effects may be included here.
Glaucine can be described as a warm and encompassing body high with an especially prominent euphoria. The body high can be described as more opiate-like than psychedelic, preferring physical euphoria over tactile sensations.
 
You may select physical effects to add below [[Subjective effect index#Physical effects|here]].


*'''[[Effect::Physical effect]]'''  
*'''[[Effect::Increased respiration]]''' - Potent bronchodilation allows for a more vast airflow, though the feeling is uncomfortable and might feel like one is suffocating.
*'''[[Effect::Physical effect2]]'''
*'''[[Effect::Cough suppression]]''' - Glaucine is known to be an antitussive with the same effectiveness as codeine.
*'''[[Effect::Physical effect3]]'''
*'''[[Effect::Motor control loss]]''' - Strong sedation leads to a decrease in coordination and motivation to move.
*'''[[Effect::Pain relief]]''' - Glaucine has been reported to reduce the signaling of pain receptors.
*'''[[Effect::Sedation]]''' - Glaucine is known for its strong sedation due to α1 antagonism.
*'''[[Effect::Bronchodilation]]''' This is caused by antagonism of benzothiazepine sites in the brain.
*'''[[Effect::Changes in felt bodily forms]]''' - This usually manifests as one becoming with the object they are resting on.
*'''[[Effect::Excessive yawning]]'''
*'''[[Effect::Muscle relaxation]]'''
*'''[[Effect::Perception of bodily heaviness]]'''
*'''[[Effect::Physical euphoria]]''' - It is usually felt as a warm encompassment of the body.
*'''[[Effect::Pupil dilation]]''' - Serotonergic substances are known to cause pupil dilation.


}}
}}
{{effects/visual|
{{effects/visual|
If applicable, a brief paragraph summary of the substance's visual effects may be included here.
Glaucine visuals are subtle, slow, encompassing, and conform to current patterns and scenery.
 
You may select visual effects to add below [[Subjective effect index#Visual effects|here]].


====Enhancements====
====Enhancements====
*'''[[Effect::Visual acuity effect1]]'''
*'''[[Effect::Pattern recognition enhancement]]'''
 
====Distortions====
*'''[[Effect::Visual distortion effect1]]'''
 
====[[Effect::Geometry]]====
If applicable, a brief paragraph summary describing the visual geometry produced by the substance may be included here.
====Hallucinatory states====
If applicable, a brief summary of the substance's visual effects profile may be written here.
 
*'''[[Effect::Hallucinatory states1]]'''
 
}}
 
|{{effects/cognitive|
If applicable, a brief paragraph summary of the substance's cognitive effects may be included here.
 
You may select from a list of cognitive effects to add below [[Subjective effect index#Cognitive effects|here]].
 
*'''[[Effect::Cognitive effect1]]'''
*'''[[Effect::Cognitive effect2]]'''
*'''[[Effect::Cognitive effect3]]'''
 
}}
{{effects/auditory|
If applicable, a brief paragraph summary of the substance's auditory effects may be included here.
 
You may select from a list of auditory effects to add below [[Subjective effect index#Auditory effects|here]].
 
*'''[[Effect::Auditory effect1]]'''
*'''[[Effect::Auditory effect2]]'''
 
}}
{{effects/multisensory|
If applicable, a brief paragraph summary of the substance's multisensory effects may be included here.
 
You may select from a list of multisensory effects to add below [[Subjective effect index#Multisensory effects|here]].
 
*'''[[Effect::Multisensory effect1]]'''
*'''[[Effect::Multisensory effect2]]'''
 
}}
{{effects/transpersonal|
If applicable, a brief paragraph summary of the substance's transpersonal effects may be included here.
 
You may select from a list of transpersonal effects to add below [[Subjective effect index#Transpersonal effects|here]].
 
*'''[[Effect::Transpersonal effect1]]'''
*'''[[Effect::Transpersonal effect2]]'''


}}
}}
}}
}}
===Experience reports===
===Experience reports===
There are currently {{#ask:[[Category:SUBSTANCE]][[Category:Experience]] | format=count}} experience reports which describe the effects of this substance in our [[experience index]].
There are currently {{#ask:[[Category:Glaucine]][[Category:Experience]] | format=count}} experience reports which describe the effects of this substance in our [[experience index]]. Additional experience reports can be found here:
{{#ask: [[Category:SUBSTANCE]][[Category:Experience]]|format=ul|Columns=1}}
Additional experience reports can be found here:


*[https://www.erowid.org/experiences/subs/exp_SUBSTANCE.shtml Erowid Experience Vaults: SUBSTANCE]<!-- Check the link to see if it exists -->
*[https://www.erowid.org/experiences/subs/exp_Glaucine.shtml Erowid Experience Vaults: Glaucine]


==Toxicity and harm potential==
==Toxicity and harm potential==
{{toxicity}}
Intragastrical administration of glaucine to rats in doses of 5, 25 and 75 mg/kg bodyweight daily for 3 months did not produce any detectable harm to any organ. It has also been concluded that it is not an allergen, mutagenic, or toxic to embryos.<ref>https://pubmed.ncbi.nlm.nih.gov/6617832/</ref>{{toxicity}}
It is strongly recommended that one use [[responsible use|harm reduction practices]] when using this substance.
It is strongly recommended that one use [[responsible use|harm reduction practices]] when using this substance.
===Lethal dosage===
===Lethal dosage===
Intraperitoneal LD50 in mice was found to be between 150-180mg/kg bodyweight. Intragastrical route was 510-610mg/kg bodyweight.<ref>https://pubmed.ncbi.nlm.nih.gov/35394081/#:~:text=Bioavailability%20following%20oral%20administration%20was,16%20and%2048%20h%2C%20respectively.</ref>
===Tolerance and addiction potential===
===Tolerance and addiction potential===
Like other serotonergic psychedelics, glaucine has been found to not produce dependency with humans, even after prolonged use.<ref>https://www.researchgate.net/publication/288395199_Glaucine_as_a_non-declared_active_component_of_legal_highs</ref>
===Dangerous interactions===
===Dangerous interactions===
{{DangerousInteractions}}
{{DangerousInteractions}}
{{DangerousInteractions/Intro}}
{{DangerousInteractions/Intro}}
*'''Lithium''': Lithium is commonly prescribed in the treatment of bipolar disorder; however, there is a large body of anecdotal evidence that suggests taking it with psychedelics can significantly increase the risk of [[psychosis]] and [[seizures]]. As a result, this combination should be '''strictly avoided.'''
*'''[[Tramadol]]''': Tramadol is well documented to lower the seizure threshold in individuals and psychedelics also has the potential to induce seizures in susceptible individuals.<ref>https://www.sciencedirect.com/science/article/pii/S0376871622003234?via%3Dihub</ref>
*'''[[Deliriants]]''' (e.g. '''''[[diphenhydramine]], [[scopolamine]]'''''): Deliriants should generally not be combined with other substances, but may have additional risks when taken with psychedelics. May increase the risk of [[anxiety]], [[delusions]], [[mania]], psychosis, and [[Serotonin syndrome|serotonin syndrome]].
*'''[[Cannabis]]''': Cannabis has a strong, volatile synergy with psychedelics. While often used to intensify or prolong psychedelic effects, the combination increases the risk of adverse psychological effects like anxiety, [[paranoia]], [[Panic attacks|panic attacks]], and psychosis. Anecdotal reports often describe cannabis use as the triggering event for a [[Bad trip|bad trip]] or [[psychosis]]. Caution is advised.
*[[Depressant|'''Depressants''']] (e.g. '''''[[GHB]]''''', [[Alprazolam|'''''alprazolam''''']], [[Hydrocodone|'''''hydrocodone''''']]): While respiratory depression isn't a problem with glaucine alone, due to the nature of the drug reducing blood pressure and heart contraction force, adding depressants could dangerously amplify the effects of a depressed CNS, leading to dangerous bradycardia, [[Decreased blood pressure|low blood pressure]], and asphyxiation. Caution is advised.
*'''[[Stimulants]]''': (e.g. [[Amphetamine|'''''amphetamine''''']], [[Project talk:Methcathinone|'''''methcathinone''''']]): Due to a moderate inhibition of MAO-B, stimulants in combination with glaucine will cause a massive spike in blood pressure leading to hypertensive crisis as well as prolonged and more intense effects of stimulants. This combination should be '''strictly avoided.'''
*'''Tyramine''': Any food with a high level of tyramine should be avoided for two weeks after use. MAO-B inhibition can lead to a buildup of tyramine in the body, leading to a hypertensive crisis.


==Legal status==
==Legal status==
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==External links==
==External links==
(List along order below)
*[https://en.wikipedia.org/wiki/SUBSTANCE SUBSTANCE (Wikipedia)]
*SUBSTANCE (Erowid Vault)
*SUBSTANCE ([''PiHKAL'' or ''TiHKAL''] / Isomer Design)
==Literature==
*APA formatted reference


Please see the [[citation formatting guide]] if you need assistance properly formatting citations.
*[https://en.wikipedia.org/wiki/Glaucine Glaucine (Wikipedia)]


==References==
==References==
Return to "Glaucine" page.