Salvinorin A: Difference between revisions

>MountainTraveler
Grammar
>Awberry
mNo edit summary
 
(69 intermediate revisions by 25 users not shown)
Line 2: Line 2:
{{SubstanceBox/Salvia}}
{{SubstanceBox/Salvia}}


'''Salvinorin A''' is the main active psychoactive molecule within [[Salvia divinorum (botany)|''salvia divinorum'']], a Mexican plant which has a long history of use as an [[entheogen]] by indigenous Mazatec shamans. It is structurally distinct from other naturally occurring [[hallucinogens]] (such as [[DMT]], [[psilocin]] and [[mescaline]]) because it contains no nitrogen atoms; which is why it is a [[Chemical class::terpenoid]] and not an [[alkaloid]] and cannot be rendered as a salt.  
'''Salvinorin A''' is the main active psychoactive molecule within [[Salvia divinorum (botany)|''Salvia Divinorum'']], a Mexican plant which has a long history of use as an [[entheogen]] by indigenous Mazatec shamans. It is structurally distinct from other naturally occurring [[hallucinogens]] (such as [[DMT]], [[psilocin]] and [[mescaline]]) because it contains no nitrogen atoms, making it a [[Chemical class::terpenoid]] and not an [[alkaloid]] as is the norm. This means it cannot be rendered as a salt.  


It also differs in subjective experience compared to other [[Psychoactive class::hallucinogen]]s, and has been described as an atypical [[dissociative]] although this formal classification is debatable.
It also differs in subjective experience compared to other [[Psychoactive class::hallucinogen]]s, and has been described as an atypical [[psychedelic]] although this formal classification is debatable.{{citation needed}}


==Chemistry==
==Chemistry==
Salvinorin A is a neoclerodane molecule, an oxygenated cyclic diterpenoid. It contains four isoprene groups bound to its oxygenated polycyclic rings. Salvinorin A is unique as it is not an alkaloid; it contains no nitrogen atoms unlike classical, natural, or synthetic hallucinogens.
Salvinorin A is a neoclerodane molecule, an oxygenated cyclic diterpenoid. It contains four isoprene groups bound to its oxygenated polycyclic rings. Salvinorin A is unique as it is not an [[alkaloid]]; it contains no nitrogen atoms unlike almost all known classical, natural, or synthetic [[hallucinogens]].


==Pharmacology==
==Pharmacology==
Salvinorin A is a potent [[Opioid#Kappa_.28.CE.BA.29|κ-opioid]] receptor [[agonist]]. It does not have any effect on the 5-HT<sub>2A</sub> receptor, the receptor targeted by most [[psychedelic]] drugs, nor does it function as an NMDA receptor antagonist as most dissociatives do. Its unique structure lacks features commonly associated with opioid ligand binding, namely it doesn't contain a quaternary carbon atom linked to a tertiary amine group by two other carbon atoms. Unlike traditional opioid agonists, salvinorin A targets the [[Opioid#Kappa_.28.CE.BA.29|κ-opioid]] receptor rather than the [[Opioid#Mu_.28.CE.BC.29|μ-opioid]] receptor. Salvinorin A is currently being researched in relation to its properties as an anti-addiction drug, and several analogs with improved pharmacokinetic profiles have been shown to have anti-addictive effects as well.<ref>http://www.ncbi.nlm.nih.gov/pubmed/24484985</ref>
Salvinorin A is a potent [[Opioid#Kappa_.28.CE.BA.29|κ-opioid]] receptor [[agonist]]. It does not have any effect on the 5-HT<sub>2A</sub> receptor, the receptor targeted by most [[psychedelic]] substances, nor does it act as an NMDA receptor antagonist as dissociatives do. The unique structure of salvinorin A lacks features commonly associated with opioid ligand binding such as a guaternary carbon atom linked to a tertiary amine group by two other carbon atoms. Unlike traditional opioid agonists, salvinorin A targets the [[Opioid#Kappa_.28.CE.BA.29|κ-opioid]] receptor rather than the [[Opioid#Mu_.28.CE.BC.29|μ-opioid]] receptor.


However, the role of these interactions and how they result in a [[hallucinogen]]ic experience continues to remain elusive.
Salvinorin A also acts as a potent agonist at [[dopamine|D<sub>2</sub>]] receptors,<ref name="d2">{{cite journal | vauthors=((Seeman, P.)), ((Guan, H.-C.)), ((Hirbec, H.)) | journal=Synapse | title=Dopamine D2 High receptors stimulated by phencyclidines, lysergic acid diethylamide, salvinorin A, and modafinil | volume=63 | issue=8 | pages=698–704 | date= August 2009 | url=https://onlinelibrary.wiley.com/doi/10.1002/syn.20647 | issn=08874476 | doi=10.1002/syn.20647}}</ref> which may be partially responsible for its hallucinogenic effects.


==Subjective effects==
==Subjective effects==
{{Preamble/SubjectiveEffects}}
{{Preamble/SubjectiveEffects}}
===Physical effects===
 
*'''[[Effect::Changes in gravity]]''' - The most prominent physical sensation of a salvinorin A trip is known by many people as “salvia gravity.” This is at least partially present during the mildest of trips and increases proportionally with dose until it is all-encompassing. It begins with a heavy sensation that pulls and tugs at the body. As this increases, it inevitably becomes so powerful that it swiftly lifts the tripper up and out of their body at extremely high speeds and over vast distances in a direction that often doesn't quite make sense. This feels as if the user is being pushed or pulled into a space vastly different from anything found on the classic hallucinogens.
{{effects/base
|{{effects/physical|
*'''[[Effect::Sedation]]''' - Salvia tends to produce a strong sedative effect in a dose-dependent manner.
*'''[[Effect::Changes in felt gravity]]''' - The most prominent physical sensation of a salvinorin A trip is known by many people as “salvia gravity.” This is at least partially present during the mildest of trips and increases proportionally with dose until it is all-encompassing. It begins with a heavy sensation that pulls and tugs at the body. As this increases, it inevitably becomes so powerful that it swiftly lifts the user up and out of their body at extremely high speeds and over vast distances in a direction that often doesn't quite make sense. This feels as if the user is being pushed or pulled into a space vastly different from anything found on the classic hallucinogens.
*'''[[Effect::Changes in felt bodily form]]''' - This effect often accompanies the onset of powerful salvinorin A gravity and can be described as non-painful sensations of being stretched horizontally or vertically into infinity, splitting into two halves, and a variety of other sudden changes. This can even include the user feeling as if they have actually become an inanimate object within their current setting.   
*'''[[Effect::Changes in felt bodily form]]''' - This effect often accompanies the onset of powerful salvinorin A gravity and can be described as non-painful sensations of being stretched horizontally or vertically into infinity, splitting into two halves, and a variety of other sudden changes. This can even include the user feeling as if they have actually become an inanimate object within their current setting.   
*'''[[Effect::Spontaneous physical sensations]]''' - For some unlucky people, this is sometimes accompanied by the sensation of intense, sharp and cold pins and needles all over a person's skin which can quickly become very uncomfortable. Most people, however, will never experience this feeling.
*'''[[Effect::Spontaneous bodily sensations]]''' - For some unlucky people, this is sometimes accompanied by the sensation of intense, sharp and cold pins and needles all over a person's skin which can quickly become very uncomfortable. Most people, however, will never experience this feeling.
*'''[[Effect::Spatial disorientation]]'''
*'''[[Effect::Spatial disorientation]]'''
*'''[[Effect::Motor control loss|Motor control loss (''Ataxia'')]]'''
*'''[[Effect::Motor control loss]]'''
 
*'''[[Effect::Pain relief]]'''
===Cognitive effects===
}}
The cognitive effects of salvinorin A can be broken down into several components which progressively intensify proportional to dosage. The general head space of salvia is described by many as one of extreme cognitive suppression and strong feelings of [[confusion]]. It’s these effects which create an experience devoid of personal introspection. This substance is best described as a drug that does not create profound personal insights, but simply creates powerful and interesting experiences.
 
The most prominent of these cognitive effects generally include:
 
*'''[[Effect::Anxiety]]''' - General paranoia, anxiety and panic are very common for the unprepared and this can be accounted for by the fact that k-opioid [[agonist|agonists]] have been shown to cause such feelings in people.
*'''[[Effect::Amnesia]]'''
*'''[[Effect::Cognitive dysphoria]]'''
*'''[[Effect::Confusion]]'''
*'''[[Effect::Delusions]]'''
*'''[[Effect::Depersonalization]]'''
*'''[[Effect::Ego replacement]]''' - This effect differs qualitatively from [[psychedelics]] in that it usually comes about in the form of another human being, animal or even plant.
*'''[[Effect::Feelings of impending doom]]'''
*'''[[Effect::Increased music appreciation]]'''
*'''[[Effect::Information processing suppression]]'''
*'''[[Effect::Language suppression]]'''
*'''[[Effect::Laughter]]''' - The average first time salvia user generally experiences a mixture of extreme giggles and confusion.
*'''[[Effect::Memory suppression]]''' - This substance is particularly intense in its cognitive effects due to the near instant transition from sobriety into [[Effect::ego death]] (complete memory failure) which can occur very suddenly at moderate to high doses. Throughout the experience, this feels as if the user is receiving the sensory input of their trip but are not fully conscious enough to process the implications of it until the offset.
*'''[[Effect::Thought deceleration]]'''
*'''[[Effect::Time distortion]]'''
*'''[[Effect::Unity and interconnectedness]]'''


===Visual effects===
{{effects/visual|
====Distortions====
====Distortions====
When a user of this substance keeps their eyes open throughout the duration of a moderate to strong trip, a number of open eye distortions and alterations are usually present. These are significantly more simplistic from that of open eye distortions found with other classes of [[hallucinogen]]s. They seem to play heavily on different sections of the user's vision and generally include:
When a user of this substance keeps their eyes open throughout the duration of a moderate to strong trip, a number of open eye distortions and alterations are usually present. These are significantly more simplistic from that of open eye distortions found with other classes of [[hallucinogen]]s. They seem to play heavily on different sections of the user's vision and generally include:
Line 69: Line 52:
*'''[[Effect::Machinescapes]]'''  
*'''[[Effect::Machinescapes]]'''  
*'''[[Effect::Transformations]]''' - In comparison to psychedelics, the transformations found within salvinorin A are significantly more solid, believable and realistic in appearance. They are commonly manifested as objects within the external environment coming alive or changing in some way.
*'''[[Effect::Transformations]]''' - In comparison to psychedelics, the transformations found within salvinorin A are significantly more solid, believable and realistic in appearance. They are commonly manifested as objects within the external environment coming alive or changing in some way.
*'''[[Effect::Internal hallucinations]]''' - The imagery on salvia is described as more solid than psychedelics and does not seem to be composed of condensed visual [[geometry]] as with the imagery found within psychedelics. It is often embedded within and across structures which often become solid fractal representations of the original image. At higher doses, this particular effect commonly contains a full array of hallucinations with [[Scenarios and plots|plots, scenarios]], [[Settings, sceneries, and landscapes|settings]] and [[autonomous entity]] contact. They can be described as both lucid and delirious in their believability, fixed in style and often ominous or sinister in nature. A unique aspect to the hallucinatory scenarios found within salvia are how commonly they are manifested with a 2nd person perspective in comparison to other classes of hallucinogens. This is commonly described as suddenly becoming a random object with common examples often including a conveyor belt, a wall, a book or a specific part of a building.
*'''[[Effect::Internal hallucination]]''' - The imagery on salvia is described as more solid than psychedelics and does not seem to be composed of condensed visual [[geometry]] as with the imagery found within psychedelics. It is often embedded within and across structures which often become solid fractal representations of the original image. At higher doses, this particular effect commonly contains a full array of hallucinations with [[Scenarios and plots|plots, scenarios]], [[Settings, sceneries, and landscapes|settings]] and [[autonomous entity]] contact. They can be described as both lucid and delirious in their believability, fixed in style and often ominous or sinister in nature. A unique aspect to the hallucinatory scenarios found within salvia are how commonly they are manifested with a 2nd person perspective in comparison to other classes of hallucinogens. This is commonly described as suddenly becoming a random object with common examples often including a conveyor belt, a wall, a book or a specific part of a building.
 
}}
 
|{{effects/cognitive|
The cognitive effects of salvinorin A can be broken down into several components which progressively intensify proportional to dosage. The general head space of salvia is described by many as one of extreme cognitive suppression and strong feelings of [[confusion]]. It’s these effects which create an experience devoid of personal introspection. This substance is best described as a drug that does not create profound personal insights, but simply creates powerful and interesting experiences.
 
The most prominent of these cognitive effects generally include:


===Auditory effects===
*'''[[Effect::Anxiety]]''' - General paranoia, anxiety and panic are very common for the unprepared and this can be accounted for by the fact that k-opioid [[agonist|agonists]] have been shown to cause such feelings in people.
*'''[[Effect::Amnesia]]'''
*'''[[Effect::Cognitive dysphoria]]'''
*'''[[Effect::Confusion]]'''
*'''[[Effect::Delusion]]'''
*'''[[Effect::Depersonalization]]'''
*'''[[Effect::Ego replacement]]''' - This effect differs qualitatively from [[psychedelics]] in that it usually comes about in the form of another human being, animal or even plant.
*'''[[Effect::Feelings of impending doom]]'''
*'''[[Effect::Increased music appreciation]]'''
*'''[[Effect::Analysis suppression]]'''
*'''[[Effect::Language suppression]]'''
*'''[[Effect::Laughter fits]]''' - The average first time salvia user generally experiences a mixture of extreme giggles and confusion.
*'''[[Effect::Memory suppression]]''' - This substance is particularly intense in its cognitive effects due to the near instant transition from sobriety into [[Effect::ego death]] (complete memory failure) which can occur very suddenly at moderate to high doses. Throughout the experience, this feels as if the user is receiving the sensory input of their trip but are not fully conscious enough to process the implications of it until the offset.
*'''[[Effect::Thought deceleration]]'''
*'''[[Effect::Time distortion]]'''
 
 
}}
{{effects/auditory|
*'''[[Effect::Auditory distortion|Distortions]]'''
*'''[[Effect::Auditory distortion|Distortions]]'''
*'''[[Effect::Auditory hallucinations|Hallucinations]]'''
*'''[[Effect::Auditory hallucinations|Hallucinations]]'''


===Multi-sensory effects===
}}
{{effects/multisensory|
*'''[[Effect::Synaesthesia]]'''
*'''[[Effect::Synaesthesia]]'''


===Classification===
}}
At the present moment, the scientific literature is currently classing salvinorin A as a [[hallucinogen]] and it has been referred in varying contexts as either solely a [[dissociative]] or an atypical dissociative with some [[psychedelic]] and even [[deliriant|delirious]] qualities.{{citation needed}}
{{effects/transpersonal|
 
*'''[[Effect::Spirituality enhancement]]'''
Although salvia shares states of hallucinatory structures and out-of-body experiences commonly reported with typical dissociatives ([[NMDA receptor antagonist]]s), this is arguably not sufficient so that it falls under the same classification. For example, the hallucinatory structures (although similar) are vastly different in their style and complexity. Alongside of this, the out-of-body experiences commonly reported with dissociatives are presumed to be triggered by the way in which NMDA receptor antagonists block signals to the conscious mind from other parts of the brain. This is accompanied by a distinctive feeling of dissociation, disconnection and detachment which is not present on salvia as it works on an entirely different set of receptors, the function of which in the human brain is almost entirely unknown.{{citation needed}}
*'''[[Effect::Near-death experience]]'''<ref name="pmid=30711788" />
 
*'''[[Effect::Unity and interconnectedness]]'''
The effects of salvia have a subjectively unique style and pharmacology that is not found within any other category of [[hallucinogen]], this has led many within the [[psychonaut]] community assert that it deserves recognition for falling into an entirely new class of its own. Any compound within this subjective and pharmacological class could potentially be referred to as a "salviagenic". This would also include various other similar analogues such as [[Salvinorin B methoxymethyl ether|Salvinorin B]] and many others.<ref>
}}
Salvinorin Analogues; Beyond Salvinorin A (DMT Nexus) | https://www.dmt-nexus.me/forum/default.aspx?g=posts&t=4823</ref>
}}
 
===Experience reports===
===Experience reports===
Anecdotal reports which describe the effects of this compound within our [[experience index]] include:
Anecdotal reports which describe the effects of this compound within our [[experience index]] include:
{{#ask: [[Category:Salvia]][[Category:Experience]]|format=ul|Columns=1}}
{{#ask: [[Category:Salvia]][[Category:Experience]]|format=ul|Columns=1}}
{{#ask: [[Category:Salvinorin A]][[Category:Experience]]|format=ul|Columns=1}}
Additional experience reports can be found here:
Additional experience reports can be found here:
* [https://www.erowid.org/experiences/subs/exp_Salvia_divinorum.shtml Erowid Experience Vaults: Salvia]


==Salvia divinorum==
*[https://www.erowid.org/experiences/subs/exp_Salvia_divinorum.shtml Erowid Experience Vaults: Salvia]
 
==Salvia Divinorum==
[[File:Salvia-divinorum-plants.jpg|300px|thumb|right|The leaves of a Salvia divinorum plant]]
[[File:Salvia-divinorum-plants.jpg|300px|thumb|right|The leaves of a Salvia divinorum plant]]
'''''Salvia divinorum''''' (also known as '''Diviner's Sage''', '''Ska María Pastora''', '''Seer's Sage''', and by its genus name '''''Salvia''''') is a psychoactive plant which is a potent producer of "visions" and other hallucinatory experiences. Its native habitat is within Cloud Forest in the isolated Sierra Mazateca of Oaxaca, Mexico where it grows in shady and moist locations. The plant grows to over a meter high and has hollow square stems, large leaves, and occasional white flowers with violet calyxes. {{citation needed}}
'''''Salvia Divinorum''''' (also known as '''Diviner's Sage''', '''Ska María Pastora''', '''Seer's Sage''', and by its genus name '''''Salvia''''') is a psychoactive plant which is a potent producer of "visions" and other hallucinatory experiences. Its native habitat is within Cloud Forest in the isolated Sierra Mazateca of Oaxaca, Mexico where it grows in shady and moist locations. The plant grows to over a meter high and has hollow square stems, large leaves, and occasional white flowers with violet calyxes. {{citation needed}}


===Forms of salvia divinorum===
===Forms of Salvia Divinorum===
====='''Fresh leaf'''=====
====='''Fresh leaf''' (sublingual)=====
The fresh leaf is typically used for making a quid of leaves and is held under the tongue for [[Routes of administration#Sublingual|sublingual absorption]]. Fresh leaf is preferred for sublingual absorption because it doesn't break up in one's mouth and is easier to chew.
The fresh leaf is typically used for making a quid of leaves and is held under the tongue for [[Routes of administration#Sublingual|sublingual absorption]]. Fresh leaf is preferred for sublingual absorption because it does not break up in one's mouth and is easier to chew. If one plans to use dried leaf for a quid, they should soak them in water for at least ten minutes otherwise ingestion can become highly unpleasant. Soaking the dried leaf in water can also cause it to lose potency.


*'''Light -''' 10 g fresh / 2 g dried
*'''Light -''' 10 g fresh / 2 g dried
Line 104: Line 114:
*'''Strong -''' 50 g fresh / 10 g dried
*'''Strong -''' 50 g fresh / 10 g dried


====='''Dried leaf'''=====
====='''Dried leaf''' (smoked)=====
Dried leaf is usually prepared by simply taking the leaf and leaving it out in the sun. The leaf can also be dried in the oven at about 150 degrees Fahrenheit for however long it takes until it becomes crispy. Dried salvia leaf is used for smoking. If one plans to use dried leaf for a quid, they should soak them in water for at least ten minutes otherwise [[Routes of administration#Sublingual|sublingual administration]] can become highly unpleasant. Soaking the dried leaf in water can also cause it to lose potency.
Dried leaf is usually prepared by simply taking the leaf and leaving it out in the sun. The leaf can also be dried in the oven at about 150 degrees Fahrenheit until it becomes crispy. Dried salvia leaf is used for smoking.


*'''Light -''' 0.25&nbsp;g
*'''Light -''' 0.25&nbsp;g dried
*'''Common -''' 0.5&nbsp;g
*'''Common -''' 0.5&nbsp;g dried
*'''Strong -''' 0.75&ndash;1.00&nbsp;g
*'''Strong -''' 0.75&ndash;1.00&nbsp;g dried


====='''Extracts'''=====
====='''Extracts'''=====
Line 119: Line 129:
====='''Tea'''=====
====='''Tea'''=====
A [[Hot water extraction from dried Salvia Divinorum leaves|tea]] can be made by crushing 3&ndash;4&nbsp;g of dried leaves and boiling them for 5 minutes. Afterwards, let it simmer for around 15 minutes. Salvinorin A is not orally active, so the tea has to be kept in the mouth for around 15&ndash;20 seconds for each sip. This tea, if properly brewed and ingested, can produce a trance-like state when closing the eyes and up to an entire night of vivid and intense dreams along with occasional closed eye visuals.
A [[Hot water extraction from dried Salvia Divinorum leaves|tea]] can be made by crushing 3&ndash;4&nbsp;g of dried leaves and boiling them for 5 minutes. Afterwards, let it simmer for around 15 minutes. Salvinorin A is not orally active, so the tea has to be kept in the mouth for around 15&ndash;20 seconds for each sip. This tea, if properly brewed and ingested, can produce a trance-like state when closing the eyes and up to an entire night of vivid and intense dreams along with occasional closed eye visuals.
==Other salvinorin A containing plants==
[[File:Salvia Recognita.jpg|thumb|Salvia Recognita]]
*'''''Salvia Recognita''''' (also known as '''Turkish Cliff Sage''') is a psychoactive plant which is 10 times less potent than its relative ''Salvia Divinorum''. Its native habitat is at the base of cliffs in the  central Turkey, where it grows in light shade at elevations of 4,000 feet. The plant grows up to a meter high and leafs that span from 3-4 inches to nearly 1 foot long, and occasional white flowers with many whorls of widely spaced flowers.
*'''''Salvia Glutinosa''''' (also known as '''Jupiter's Sage''') is a psychoactive plant which is far less potent than Salvia Recognita. Its native habitat is in forested areas located around Central and East Europe and West Asia, where it grows in partial shade in calcareous soils, at elevations of 330 - 5,250 feet (100 - 1,600 metres) above sea level. The plant grows up to a 16-24 inches (40 - 60 cm) tall and hairy leafs that span from 5.1 inches (13 cm) inches with petioles of about 3.1 - 3.9 inches (7.9 - 9.9 centimetres), and occasional white flowers with many whorls of widely spaced flowers.
==Classification==
Currently, the scientific literature classifies salvinorin A as a [[hallucinogen]]. However, there is additional debate as to whether it can correctly be labeled as a [[dissociative]] or an atypical dissociative with some [[psychedelic]] and even [[deliriant|delirious]] qualities.{{citation needed}}
Although salvia shares states of hallucinatory structures and out-of-body experiences commonly reported with typical dissociatives ([[NMDA receptor antagonist]]s), this is arguably not sufficient so that it falls under the same classification. For example, the hallucinatory structures (although similar) are vastly different in their style and complexity. Alongside this, the out-of-body experiences commonly reported with dissociatives are presumed to be triggered by the way in which NMDA receptor antagonists block signals to the conscious mind from other parts of the brain. This is accompanied by a distinctive feeling of dissociation, disconnection and detachment which is not present on salvia as it works on an entirely different set of receptors, the function of which in the human brain is almost entirely unknown.{{citation needed}}
The effects of salvia have a subjectively unique style and pharmacology that is not found within any other category of [[hallucinogen]], this has led many within the [[psychonaut]] community assert that it deserves recognition for falling into an entirely new class of its own. Any compound within this subjective and pharmacological class could potentially be referred to as a "salviagenic". This would also include various other similar analogues such as [[Salvinorin B methoxymethyl ether|Salvinorin B]] and many others.<ref>{{Citation | title=Salvinorin Analogues; Beyond Salvinorin A - Salvia Divinorum - Welcome to the DMT-Nexus | url=https://www.dmt-nexus.me/forum/default.aspx?g=posts&t=4823}}</ref>
==Research==
Salvinorin A is currently being researched in relation to its properties as an anti-addiction drug, and several analogs with improved pharmacokinetic profiles have been shown to have anti-addictive effects as well.<ref>{{cite journal | vauthors=((Kivell, B. M.)), ((Ewald, A. W. M.)), ((Prisinzano, T. E.)) | journal=Advances in Pharmacology (San Diego, Calif.) | title=Salvinorin A analogs and other κ-opioid receptor compounds as treatments for cocaine abuse | volume=69 | pages=481–511 | date= 2014 | issn=1557-8925 | doi=10.1016/B978-0-12-420118-7.00012-3}}</ref>
===Near-death experience===
A 2019 large-scale study found that [[ketamine]], ''Salvia divinorum'', and [[DMT]] (and other classical psychedelic substances) are linked to [[near-death experience]]s.<ref name="pmid=30711788">{{cite journal |last1=Martial |first1=C |last2=Cassol |first2=H |last3=Charland-Verville |first3=V |last4=Pallavicini |first4=C |last5=Sanz |first5=C |last6=Zamberlan |first6=F |last7=Vivot |first7=RM |last8=Erowid |first8=F |last9=Erowid |first9=E |last10=Laureys |first10=S |last11=Greyson |first11=B |last12=Tagliazucchi |first12=E |title=Neurochemical models of near-death experiences: A large-scale study based on the semantic similarity of written reports. |journal=Consciousness and cognition |date=March 2019 |volume=69 |pages=52-69 |doi=10.1016/j.concog.2019.01.011 |pmid=30711788}}</ref>


==Toxicity and harm potential==
==Toxicity and harm potential==
The toxicity and long-term health effects of recreational salvinorin A use do not seem to have been studied in any scientific context and the exact [[Toxicity::toxic dose is unknown]]. This is because salvinorin A is a [[research chemical]] with very little history of human usage. Anecdotal evidence from people within the psychonaut community who have tried salvinorin A suggests that there are no negative health effects attributed to simply trying the drug by itself at low to moderate doses and using it very sparingly (but nothing can be completely guaranteed). [https://www.google.com/ Independent research] should always be done to ensure that a combination of two or more substances is safe before consumption.
{{toxicity}}
{{Further|Responsible use#Hallucinogens}}
The toxicity and long-term health effects of recreational salvinorin A use do not seem to have been studied in any scientific context and the exact [[Toxicity::toxic dose is unknown]]. This is because salvinorin A is a [[research chemical]] with very little history of human usage.  
 
Anecdotal evidence suggests that there are no negative health effects attributed to simply trying it by itself at low to moderate doses and using it very sparingly (but nothing can be completely guaranteed). [https://www.google.com/ Independent research] should always be done to ensure that a combination of two or more substances is safe before consumption.
 
Due to its unusually potent and potentially overwhelming effects, it is strongly recommended that one use [[responsible drug use|harm reduction practices]] when using this substance.


Due to its unusually potent and debilitating psychoactivity, it is strongly recommended that one use [[responsible drug use|harm reduction practices]] when using this drug.
Please see Research Articles below in External Links section for dose related scientific research on Salvinorin A.


===Tolerance and addiction potential===
===Tolerance and addiction potential===
Line 130: Line 165:
Tolerance to the effects of salvinorin A does not occur. In fact, many users report that the effects of this substance can actually become stronger over time and with repeated usage (a phenomenon known as "[[reverse tolerance]]"). Due to its unique set of target receptors, salvinorin A presents cross-tolerance with [[Cross-tolerance::no other [[hallucinogen]]s]].
Tolerance to the effects of salvinorin A does not occur. In fact, many users report that the effects of this substance can actually become stronger over time and with repeated usage (a phenomenon known as "[[reverse tolerance]]"). Due to its unique set of target receptors, salvinorin A presents cross-tolerance with [[Cross-tolerance::no other [[hallucinogen]]s]].


==Legality==
==Legal status==
*'''Australia:''' Possession and sale is illegal.
*'''Belgium:''' Possession and sale is illegal.
*'''Croatia:''' Possession and sale is illegal.
*'''Czech Republic:''' Possession and sale is illegal.
*'''Denmark:''' Salvinorin A is a Class B drug.
*'''Germany:''' Possession and sale is illegal.
*'''Ireland:''' Possession and sale is illegal.
*'''Italy:''' Possession and sale is illegal.
*'''Latvia:''' Possession and sale is illegal.
*'''Lithuania:''' Possession and sale is illegal.
*'''New Zealand:''' Possession and sale is illegal.
*'''Poland:''' Possession and sale is illegal.
*'''Romania:''' Possession and sale is illegal.
*'''Spain:''' Possession and sale is illegal.
*'''Sweden:''' Possession and sale is illegal.
*'''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.<ref>Psychoactive Substances Act 2016 (Legislation.gov.uk) | http://www.legislation.gov.uk/ukpga/2016/2/contents/enacted</ref>
*'''United States:''' Salvinorin A is illegal is some states but not all.


==Preparation methods==
*'''Australia:''' Salvinorin A is illegal to possess and sell in Australia.{{citation needed}}
Preparation methods for this compound within our [[tutorial index]] include:
*'''Austria:''' Salvinorin A is illegal to possess, produce and sell under the NPSG (Neue-Psychoaktive-Substanzen-Gesetz Österreich).{{citation needed}}
* [[Hot water extraction from dried Salvia Divinorum leaves]]
*'''Belgium:''' Salvinorin A is illegal to possess and sell in Belgium.{{citation needed}}
*'''Croatia:''' Salvinorin A is illegal to possess and sell in Croatia.{{citation needed}}
*'''Czech Republic:''' Salvinorin A is illegal to possess and sell in Czech Republic.{{citation needed}}
*'''Canada:''' Salvia divinorum and its preparations and derivatives (including Salvinorin A) are schedule IV in Canada.<ref>{{Citation | vauthors=((Branch, L. S.)) | year=2022 | title=Consolidated federal laws of Canada, Controlled Drugs and Substances Act | url=https://laws-lois.justice.gc.ca/eng/acts/c-38.8/page-15.html}}</ref>
*'''Denmark:''' Salvinorin A is a Class B drug in Denmark.{{citation needed}}
*'''Germany:''' Salvinorin A is not controlled in Germany, however Salvia Divinorum was added to BtMG Anlage I, making it illegal to grow, import, possess, sell, or transfer it as of March 1, 2008 <ref>{{Citation | title=21. BtMÄndV Einundzwanzigste Betäubungsmittelrechts-Änderungsverordnung | url=https://www.buzer.de/gesetz/8104/index.htm}}</ref>
*'''Ireland:''' Salvinorin A is illegal to possess and sell in Ireland.{{citation needed}}
*'''Italy:''' Salvinorin A is illegal to possess and sell in Italy.{{citation needed}}
*'''Latvia:''' Salvinorin A is illegal to possess and sell in Latvia.{{citation needed}}
*'''Lithuania:''' Salvinorin A is illegal to possess and sell in Lithuania.{{citation needed}}
*'''New Zealand:''' Salvinorin A is illegal to possess and sell in New Zealand.{{citation needed}}
*'''Poland:''' Salvinorin A is illegal to possess and sell in Poland.{{citation needed}}
*'''Romania:''' Salvinorin A is illegal to possess and sell in Romania.{{citation needed}}
*'''Spain:''' Salvinorin A is illegal to possess and sell in Spain.{{citation needed}}
*'''Sweden:''' Salvinorin A is illegal to possess and sell in Sweden.{{citation needed}}
*'''Switzerland''': Salvia divinorum as well as Salvinorin A are controlled substances specifically named under Verzeichnis D.<ref>{{cite web|url=https://www.admin.ch/opc/de/classified-compilation/20101220/index.html|title=Verordnung des EDI über die Verzeichnisse der Betäubungsmittel, psychotropen Stoffe, Vorläuferstoffe und Hilfschemikalien|publisher=Bundeskanzlei [Federal Chancellery of Switzerland]|access-date=January 1, 2020|language=de}}</ref>
*'''United Kingdom:''' Salvia is legal to produce, supply, or import if sold not for human consumption under the Psychoactive Substance Act, which came into effect on May 26th, 2016.<ref>{{Citation | title=Psychoactive Substances Act 2016 | url=https://www.legislation.gov.uk/ukpga/2016/2/contents/enacted}}</ref><ref>{{Citation | year=2022 | title=Legal status of Salvia divinorum | url=https://en.wikipedia.org/w/index.php?title=Legal_status_of_Salvia_divinorum&oldid=1097655490}}</ref>
*'''United States:''' Salvinorin A is illegal in certain states.{{citation needed}}


==See also==
==See also==
*[[Responsible use]]
*[[Responsible use]]
*[[Salvia divinorum (botany)|Salvia Divinorum]]
*[[Salvinorin B]]
*[[Salvinorin B]]
*[[Psychedelics]]
*[[Hallucinogens]]
*[[Dissociatives]]
*[[Entheogens]]
*[[Entheogens]]


==External links==
==External links==
*[https://www.erowid.org/plants/salvia/ Salvia (Erowid)]
 
*[http://en.wikipedia.org/wiki/Salvinorin_A Salvinorin A (Wikipedia)]
*[http://en.wikipedia.org/wiki/Salvinorin_A Salvinorin A (Wikipedia)]
*[http://www.bluelight.org/vb/threads/359879-The-Big-amp-Dandy-Salvia-Thread-Second-iteration Salvia (Bluelight)]
*[https://isomerdesign.com/PiHKAL/explore.php?domain=pk&id=2841 Salvinorin A (Isomer Design)]
*[http://factsheet.tripsit.me/salvia Salvia (TripSit)]
*[https://www.erowid.org/plants/salvia/ Salvia (Erowid Vault)]
*[https://en.wikipedia.org/wiki/Salvia_recognita Salvia Recognita (Wikipedia)]
 
===Discussion===
 
*[http://www.bluelight.org/vb/threads/359879-The-Big-amp-Dandy-Salvia-Thread-Second-iteration The Big & Dandy Salvia Thread - Second iteration (Bluelight)]
*[https://www.dmt-nexus.me/forum/default.aspx?g=posts&t=4823 Salvinorin Analogues; Beyond Salvinorin A (DMT Nexus)]
*[https://www.dmt-nexus.me/forum/default.aspx?g=posts&t=4823 Salvinorin Analogues; Beyond Salvinorin A (DMT Nexus)]


==Literature==
==='''Research Articles'''===
Historically, there has been very little scientific research conducted on the phenomenology and psychopharmacology of salvinorin A. This is arguably due to the evidence and investigation-suppressing effects that global [[drug prohibition]] has on scientific enterprise.{{citation needed}} However, there are signs that this is beginning to change as [[psychedelics research]] is gaining increased recognition and mainstream acceptance.


* Johnson MW, Maclean KA, Reissig CJ, Prisinzano TE, Griffiths RR. (2010) Human psychopharmacology and dose-effects of salvinorin A, a kappa opioid agonist hallucinogen present in the plant Salvia divinorum. Drug Alcohol Depend. 2010 Dec 4.
*[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089685/ Human psychopharmacology and dose-effects of salvinorin A, a kappa-opioid agonist hallucinogen present in the plant ''Salvia divinorum'']
*[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3581702/ Dose-related Effects of Salvinorin A in Humans: Dissociative, Hallucinogenic, and Memory Effects]


* Baggott MJ, Erowid E, Erowid F, Galloway GP, Mendelson J. (2010). Use patterns and self-reported effects of Salvia divinorum: An internet-based survey. Drug Alcohol Depend. 2010 Oct 1;111(3):250-6
==Literature==


* Mendelson JE, Coyle JR, Lopez JC, Baggott MJ, Flower K, Everhart ET, Munro TA, Galloway GP, Cohen BM. (2010). Lack of effect of sublingual salvinorin A, a naturally occurring kappa opioid, in humans: a placebo-controlled trial. Psychopharmacology (Berl). 2010 Dec 8. [Epub ahead of print]  
*Johnson MW, Maclean KA, Reissig CJ, Prisinzano TE, Griffiths RR. (2010) Human psychopharmacology and dose-effects of salvinorin A, a kappa opioid agonist hallucinogen present in the plant Salvia divinorum. Drug Alcohol Depend. 2010 Dec 4.
*Baggott MJ, Erowid E, Erowid F, Galloway GP, Mendelson J. (2010). Use patterns and self-reported effects of Salvia divinorum: An internet-based survey. Drug Alcohol Depend. 2010 Oct 1;111(3):250-6
*Mendelson JE, Coyle JR, Lopez JC, Baggott MJ, Flower K, Everhart ET, Munro TA, Galloway GP, Cohen BM. (2010). Lack of effect of sublingual salvinorin A, a naturally occurring kappa opioid, in humans: a placebo-controlled trial. Psychopharmacology (Berl). 2010 Dec 8. [Epub ahead of print]


==References==
<references />


==References==
[[Category:Naturally-occurring substance]]
<references/>
[[Category:Salvinorin]]
[[Category:Psychoactive substance]]
[[Category:Entheogen]]
[[Category:Psychedelic]]
[[Category:Psychedelic]]
[[Category:Dissociative]]
[[Category:Dissociative]]
[[Category:Entheogen]]
{{#set:Featured=true}}
{{#set:Featured=true}}
[[Category:Terpenoid]]