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'''Myristicin''' is a [[naturally-occurring]] [[psychoactive class::deliriant]] substance of the [[Chemical class::phenylpropene]] class. It is present in small amounts in the essential oil of nutmeg and, to a lesser extent, in other spices such as [[parsley]] and [[dill]].<ref>http://www.lktlabs.com/products/Myristicin-126-50.html</ref> It acts as an [[Deliriant|anticholinergic]] in very high doses{{citation needed}}, and has been shown to act on the [[Cannabinoid|endocannabinoid system]].<ref>https://onlinelibrary.wiley.com/doi/full/10.1111/jphp.13174?casa_token=3G00LOa4HdYAAAAA%3ARWt2lo3lt5JWDQRjsghMId1Fih01Jn_t5HJWoz43jAGnVzVpjxkeyg9kwtiiSqN9dGkH7hO4EwYocyc#jphp13174-bib-0013</ref>
'''Myristicin''' is a [[naturally-occurring]] [[psychoactive class::deliriant]] substance of the [[Chemical class::phenylpropene]] class. It is present in small amounts in the essential oil of nutmeg and, to a lesser extent, in other spices such as [[parsley]] and [[dill]].<ref>http://www.lktlabs.com/products/Myristicin-126-50.html</ref> It has been shown to act on the [[Cannabinoid|endocannabinoid system]].<ref>{{cite journal | vauthors=((El-Alfy, A. T.)), ((Abourashed, E. A.)), ((Patel, C.)), ((Mazhari, N.)), ((An, H.)), ((Jeon, A.)) | journal=Journal of Pharmacy and Pharmacology | title=Phenolic compounds from nutmeg ( Myristica fragrans Houtt.) inhibit the endocannabinoid-modulating enzyme fatty acid amide hydrolase | volume=71 | issue=12 | pages=1879–1889 | date=8 November 2019 | url=https://academic.oup.com/jpp/article/71/12/1879-1889/6122229 | issn=2042-7158 | doi=10.1111/jphp.13174}}</ref>
Myristicin, along with [[elemicin]], is thought to be the main psychoactive constituent of nutmeg.{{citation needed}} Additionally, myristicin is the traditional precursor for the [[psychedelic]] and [[empathogenic]] drug [[MMDA]].{{citation needed}}
Myristicin, along with [[elemicin]], is thought to be the main psychoactive constituent of nutmeg.{{citation needed}} When oxidized with Potassium permanganate, Myristicin can be converted into Myristicinaldehyde, which can then be used to synthesize MMDPEA (Lophophine) via reductive amination.{{citation needed}} Additionally, myristicin is the traditional precursor for the [[psychedelic]] and [[empathogenic]] drug [[MMDA]].{{citation needed}}
Nutmeg is reported to induce hallucinogenic effects, such as visual distortions and paranoid ideation. In the reports, nutmeg intoxication took several hours before maximum effect was reached. Effects and after-effects lasted up to several days. Raw nutmeg consists of 5-15% essential oil by mass. 4-8.5% of nutmeg essential oil, or 0.2-1.3% of raw nutmeg, is myristicin. One study found 20 grams of nutmeg to contain 210 mg myristicin.<ref>https://bitnest.netfirms.com/external.php?id=%250E%253D9%250F%2524G%252F%2518B%255B%255B4%2522.FXQ%255CO%2500TK</ref>
Nutmeg is reported to induce hallucinogenic effects, such as visual distortions and paranoid ideation. In the reports, nutmeg intoxication took several hours before maximum effect was reached. Effects and after-effects lasted up to several days. Raw nutmeg consists of 5-15% essential oil by mass. 4-8.5% of nutmeg essential oil, or 0.2-1.3% of raw nutmeg, is myristicin. One study found 20 grams of nutmeg to contain 210 mg myristicin.
It should be noted that the dosage listed on this page assumes that one is using nutmeg powder and not pure myristicin, as this is extremely uncommon. It is highly advised to use [[harm reduction practices]] if using this substance.
It should be noted that the dosage listed on this page assumes that one is using nutmeg powder and not pure myristicin, as this is extremely uncommon. It is highly advised to use [[harm reduction practices]] if using this substance.
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==Pharmacology==
==Pharmacology==
{{pharmacology}}
In 1963, [[Alexander Shulgin]] speculated myristicin could be metabolized to [[MMDA]], a psychoactive drug related to [[MDA]], in the liver.<ref>{{Citation | title=UNODC - Bulletin on Narcotics - 1966 Issue 4 - 002 | url=//www.unodc.org/unodc/en/data-and-analysis/bulletin/bulletin_1966-01-01_4_page003.html}}</ref> This, however, is unlikely due to the fact that no [[amphetamine]] metabolites were found in urine after the ingestion of myristicin. It is believed that myristicin is an [[deliriant|anticholinergic]], since, in overdose, it produces effects similar to anticholinergics<ref>{{cite journal | vauthors=((McKenna, A.)), ((Nordt, S. P.)), ((Ryan, J.)) | journal=European Journal of Emergency Medicine | title=Acute nutmeg poisoning: | volume=11 | issue=4 | pages=240–241 | date= August 2004 | url=http://journals.lww.com/00063110-200408000-00017 | issn=0969-9546 | doi=10.1097/01.mej.0000127649.69328.a5}}</ref><ref>{{cite journal | vauthors=((Abernethy, M. K.)), ((Becker, L. B.)) | journal=The American Journal of Emergency Medicine | title=Acute nutmeg intoxication | volume=10 | issue=5 | pages=429–430 | date= September 1992 | url=https://linkinghub.elsevier.com/retrieve/pii/073567579290069A | issn=07356757 | doi=10.1016/0735-6757(92)90069-A}}</ref>, but the exact mechanism of action has not been established. Myristicin is also found to be a [[serotonin]] [[receptor]] [[antagonist]], while simultaneously acting as a weak [[MAO inhibitor]].{{citation needed}}
In 1963, [[Alexander Shulgin]] speculated myristicin could be metabolized to [[MMDA]], a psychoactive drug related to [[MDA]], in the liver.<ref>http://www.unodc.org/unodc/en/data-and-analysis/bulletin/bulletin_1966-01-01_4_page003.html</ref> This, however, is unlikely due to the fact that no [[amphetamine]] metabolites were found in urine after the ingestion of myristicin.<ref>https://www.scopus.com/record/display.uri?eid=2-s2.0-33746309901&origin=inward&txGid=1371ffb081f561831f7dc88c134165eb</ref> It is believed that myristicin is an [[deliriant|anticholinergic]], since, in overdose, it produces effects similar to anticholinergics<ref>McKenna, A., Nordt, S. P., & Ryan, J. (2004). Acute nutmeg poisoning. European Journal of Emergency Medicine, 11(4), 240-241. https://doi.org/10.1097/01.mej.0000127649.69328.a5</ref><ref>Abernethy, M. K., & Becker, L. B. (1992). Acute nutmeg intoxication. The American journal of emergency medicine, 10(5), 429-430. https://doi.org/10.1016/0735-6757(92)90069-A</ref>, but the exact mechanism of action has not been established. Myristicin is also found to be a [[serotonin]] [[receptor]] [[antagonist]], while simultaneously acting as a weak [[MAO inhibitor]].{{citation needed}}
====Elemicin====
====Elemicin====
Elemicin is found in nutmeg alongside myristicin and contributes to its [[hallucinogenic]] effects. Elemicin is likely to have similar effects to myristicin. It is also the traditional precursor in synthesizing the alkaloid [[mescaline]].{{citation needed}}
Elemicin is found in nutmeg alongside myristicin and contributes to its [[hallucinogenic]] effects. Elemicin is likely to have similar effects to myristicin. It is also the traditional precursor in synthesizing the alkaloid [[mescaline]].{{citation needed}}
==== Cannabinoids ====
people who have ingested Elemi oil, (a source of elemicin that exists without high amounts of Myristicin) have claimed the visual effects the oil produce seem to be more similar to classical hallucinogens than the visual effects of nutmeg oil, (which seem to be more delirious and sedating in nature)
Three compounds in nutmeg (Malabaricone C, Licarin A, 5-Methoxylicarin A) have been proven to act as endo-cannabinoid enhancing agents by inhibiting the enzyme FAAH which is responsible for the breakdown of the endocannabinoid Anandamide. <ref>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7938946/</ref>The decrease in the activity of FAAH causes a significant increase in Anandamide levels. This leads to increased CB1 receptor activity which causes cannabimimetic effects, and is believed to be the main cause behind the nutmeg high.
This distinction seems to paint Myristicin as a more sedating and mind-dulling drug, while Elemicin seems to be more-visually active and stimulating. this assumption is further supported by the fact that while Elemicin has direct structural ties to Mescaline, Myristicin has ties to [[MDxx|MDXX]] compounds such as [[MDMA]].
The chemical structure of Elemicin appears to be a carbon-based analogue of [[Mescaline]] while Myristicin itself appears to be a carbon analogue of Lophophine, these structural differences may be indicators of the slightly different psychoactive effects both Elemicin and Myristicin have.
====Cannabinoids====
No compound has been found in nutmeg to directly bind to CB1 or CB2 receptors. Three compounds in nutmeg (Malabaricone C, Licarin A, 5-Methoxylicarin A) have been shown to act as endo-cannabinoid modulating agents by inhibiting the enzymes FAAH and MAGL.<ref>{{cite journal | vauthors=((El-Alfy, A. T.)), ((Abourashed, E. A.)), ((Patel, C.)), ((Mazhari, N.)), ((An, H.)), ((Jeon, A.)) | journal=The Journal of Pharmacy and Pharmacology | title=Phenolic compounds from nutmeg (Myristica fragrans Houtt.) inhibit the endocannabinoid-modulating enzyme fatty acid amide hydrolase | volume=71 | issue=12 | pages=1879–1889 | date=8 October 2019 | url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7938946/ | issn=0022-3573 | doi=10.1111/jphp.13174}}</ref>
==Subjective effects==
==Subjective effects==
{{effectStub}}
In comparison to [[datura]] or [[diphenhydramine]], myristicin's effects tend to be milder and can be pleasant and euphoric depending on dose. It has unique effects compared to other [[deliriants]] or [[hallucinogens]]. It also has a long, smooth, and enjoyable come-up, where the effects build in a similar manner to [[cannabis]]. In addition to this, [[cannabis]] like effects throughout the duration have been reported among users of the substance which is possibly due to its activity on [[cannabinoid]] receptors. With higher doses, however, the [[deliriant]] effects become more pronounced.
In comparison to [[datura]] or [[diphenhydramine]], myristicin's effects tend to be milder and can be pleasant and euphoric depending on dose. It has unique effects compared to other [[deliriants]] or [[hallucinogens]]. It also has a long, smooth, and enjoyable come-up, where the effects build in a similar manner to [[cannabis]]. In addition to this, [[cannabis]] like effects throughout the duration have been reported among users of the substance which is possibly due to its activity on [[cannabinoid]] receptors. With higher doses, however, the [[deliriant]] effects become more pronounced.
{{Preamble/SubjectiveEffects}}
{{Preamble/SubjectiveEffects}}
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*'''[[Effect::Nausea]]''' - This effect is usually caused by the unpleasurable taste rather than the compounds themselves.
*'''[[Effect::Nausea]]''' - This effect is usually caused by the unpleasurable taste rather than the compounds themselves.
*'''[[Effect::Sedation]]''' - This effect can be extremely strong at higher dosage, leaving the user in a near sleep state during the experience.
*'''[[Effect::Sedation]]''' - This effect can be extremely strong at higher dosage, leaving the user in a near sleep state during the experience.
*'''[[Effect::Stimulation]]''' - this effect occurs on lower doses.
*'''[[Effect::Stimulation]]''' - This effect occurs on lower doses.
*'''[[Effect::Motor control loss]]''' - This effect is very similar in effect to alcohol.
*'''[[Effect::Motor control loss]]'''
*'''[[Effect::Muscle relaxation]]''' - This effect is similar to alcohol and tends to occur at lower doses.
*'''[[Effect::Muscle relaxation]]'''
*'''[[Effect::Perception of bodily heaviness]]''' - This effect is similar to alcohol.
*'''[[Effect::Perception of bodily heaviness]]'''
*'''[[Effect::Photophobia]]'''
*'''[[Effect::Photophobia]]'''
*'''[[Effect::Pupil dilation]]''' - This effect is usually extremely rare and only occurs at very high doses. Nutmeg is more likely to cause bloodshot eyes due to its vasodilating properties.
*'''[[Effect::Spontaneous tactile sensations]]'''
*'''[[Effect::Spontaneous tactile sensations]]'''
*'''[[Effect::Tactile enhancement]]''' or '''[[Effect::Tactile suppression]]''' at higher doses.
*'''[[Effect::Tactile enhancement]]''' or '''[[Effect::Tactile suppression]]''' at higher doses.
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*'''[[Effect::Drifting]]''' - Breathing, objects having their size altered
*'''[[Effect::Drifting]]''' - Breathing, objects having their size altered
*'''[[Effect::Environmental patterning]]''' - You may see lines around and inside objects, essentially everything will have structure - You may see eyes like you would on psilocybin but to a lesser intensity
*'''[[Effect::Environmental patterning]]''' - You may see lines around and inside objects, essentially everything will have structure - You may see eyes like you would on psilocybin but to a lesser intensity
*'''[[Effect::Tracers]]''' - Tracers can reach up to intense (3.) level.
*'''[[Effect::Tracers]]''' - Tracers can reach up to 3. level.
*'''[[Effect::Frame rate suppression]]''' - Combined with time distortion nutmeg could make movies and videos feel more dissociative. This effect is similar to DXM
*'''[[Effect::Frame rate suppression]]''' - Combined with time distortion nutmeg could make movies and videos feel more dissociative. This effect is similar to DXM
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*'''[[Effect::Internal hallucination]]''' (''[[effect::autonomous entities]]''; ''[[effect::settings, sceneries, and landscapes]]''; ''[[effect::perspective hallucinations]]'' and ''[[effect::scenarios and plots]]'') - In comparison to other classes of [[hallucinogen]], this effect occurs briefly and spontaneously at moderate doses but becomes progressively extended in its occurrence and duration proportional to dosage before eventually becoming all-encompassing. It can be comprehensively described through its [[Internal_hallucinations#Variations|variations]] as delirious in believability, interactive in style, equal in new experiences and memory replays in content, autonomous in controllability and solid in style.
*'''[[Effect::Internal hallucination]]''' (''[[effect::autonomous entities]]''; ''[[effect::settings, sceneries, and landscapes]]''; ''[[effect::perspective hallucinations]]'' and ''[[effect::scenarios and plots]]'') - In comparison to other classes of [[hallucinogen]], this effect occurs briefly and spontaneously at moderate doses but becomes progressively extended in its occurrence and duration proportional to dosage before eventually becoming all-encompassing. It can be comprehensively described through its [[Internal_hallucinations#Variations|variations]] as delirious in believability, interactive in style, equal in new experiences and memory replays in content, autonomous in controllability and solid in style.
*'''[[Effect::Peripheral information misinterpretation]]
*'''[[Effect::Peripheral information misinterpretation]]
*'''[[Effect::Shadow people]]''' - Nutmeg is rarely reported to induce full-on psychosis-like delirium with shadow figures but at higher doses combined with dehydration, it is possible.
}}
}}
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*'''[[Effect::Empathy, affection and sociability enhancement]]'''
*'''[[Effect::Empathy, affection and sociability enhancement]]'''
*'''[[Effect::Anxiety]]''' at higher doses or '''[[Effect::Anxiety suppression]]''' on lower doses with a positive setting
*'''[[Effect::Anxiety]]''' at higher doses or '''[[Effect::Anxiety suppression]]''' on lower doses with a positive setting
**'''[[Effect::Paranoia]]''' - This effect is common at high doses.
**'''[[Effect::Feelings of impending doom]]
*'''[[Effect::Confusion]]''' - This effect is more common at higher doses and when the user is dehydrated
*'''[[Effect::Confusion]]''' - This effect is more common at higher doses and when the user is dehydrated
*'''[[Effect::Depersonalization]]]''' and '''[[Effect::Derealization]]''' - This effect differs from classic disscoatives and tends to be more dream like and results more often in anxiety due to the unpleasant body load nutmeg offers. This effect appears at higher doses only and is similar to the DPDR produced by THC and synthetic cannabinoids.
*'''[[Effect::Depersonalization]]]''' and '''[[Effect::Derealization]]''' - This effect differs from classic disscoatives and tends to be more dream like and results more often in anxiety due to the unpleasant body load nutmeg offers. This effect appears at higher doses only and is similar to the DPDR produced by THC and synthetic cannabinoids.
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*'''[[Effect::Immersion enhancement]]''' - This effect is similar to cannabis and usually does not increase that much as the dose gets higher
*'''[[Effect::Immersion enhancement]]''' - This effect is similar to cannabis and usually does not increase that much as the dose gets higher
*'''[[Effect::Focus suppression]]''' or '''[[Effect::Focus enhancement]]''' - This depends on the dose, user, dehydration and genetic factors.
*'''[[Effect::Focus suppression]]''' or '''[[Effect::Focus enhancement]]''' - This depends on the dose, user, dehydration and genetic factors.
*'''[[Effect::Paranoia]]''' - This effect is common at high doses.
*'''[[Effect::Psychosis]]''' - This effect is common at high or strong doses
*'''[[Effect::Psychosis]]''' - This effect is common at high or strong doses
*'''[[Effect::Sleepiness]]''' - This effect gets stronger as the dose increases
*'''[[Effect::Sleepiness]]''' - This effect gets stronger as the dose increases
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{{toxicity}}
{{toxicity}}
{{further|Research chemicals#Toxicity and harm potential|Responsible use #Hallucinogens}}
{{further|Research chemicals#Toxicity and harm potential|Responsible use #Hallucinogens}}
Myristicin [[Toxicity::is neurotoxic]] and [[Toxicity::can be fatal in extremely high doses]].<ref>Myristicin-induced neurotoxicity in human neuroblastoma SK-N-SH cells. (PubMed.gov / NCBI) | https://www.ncbi.nlm.nih.gov/pubmed/15795093</ref> Also myristicin causes severe dehydration. It increases side effects of myristicin.
Myristicin [[Toxicity::is neurotoxic]] and [[Toxicity::can be fatal in extremely high doses]].<ref>{{cite journal | vauthors=((Lee, B. K.)), ((Kim, J. H.)), ((Jung, J. W.)), ((Choi, J. W.)), ((Han, E. S.)), ((Lee, S. H.)), ((Ko, K. H.)), ((Ryu, J. H.)) | journal=Toxicology Letters | title=Myristicin-induced neurotoxicity in human neuroblastoma SK-N-SH cells | volume=157 | issue=1 | pages=49–56 | date=16 May 2005 | issn=0378-4274 | doi=10.1016/j.toxlet.2005.01.012}}</ref> Also myristicin causes severe dehydration. It increases side effects of myristicin.
===Dependence and abuse potential===
===Dependence and abuse potential===
Although there hasn't been any studies confirming this, nutmeg has been reported by some users to cause mild psychological dependence, similarly to cannabis but to a lesser degree.
Myristicin [[Addiction potential::is not known to be addictive]] and the desire to use it can actually decrease with use.
Although there have not been any scientific studies on nutmeg tolerance, it has been reported to exhibit cross-tolerance with cannabis, as well as other cannabinoids.
WARNING: Always start with lower doses due to differences between individual body weight, tolerance, metabolism, and personal sensitivity. See responsible use section.
DISCLAIMER: PW's dosage information is gathered from users and resources for educational purposes only. It is not a recommendation and should be verified with other sources for accuracy.
Myristicin, along with elemicin, is thought to be the main psychoactive constituent of nutmeg.[citation needed] When oxidized with Potassium permanganate, Myristicin can be converted into Myristicinaldehyde, which can then be used to synthesize MMDPEA (Lophophine) via reductive amination.[citation needed] Additionally, myristicin is the traditional precursor for the psychedelic and empathogenic drug MMDA.[citation needed]
Nutmeg is reported to induce hallucinogenic effects, such as visual distortions and paranoid ideation. In the reports, nutmeg intoxication took several hours before maximum effect was reached. Effects and after-effects lasted up to several days. Raw nutmeg consists of 5-15% essential oil by mass. 4-8.5% of nutmeg essential oil, or 0.2-1.3% of raw nutmeg, is myristicin. One study found 20 grams of nutmeg to contain 210 mg myristicin.
It should be noted that the dosage listed on this page assumes that one is using nutmeg powder and not pure myristicin, as this is extremely uncommon. It is highly advised to use harm reduction practices if using this substance.
Myristicin, also known as 3-methoxy,4,5-methylenedioxyallylbenzene, is a naturally occurring substance that belongs to a chemical class known as the phenylpropenes. It features a methylenedioxy ring at carbons R4 and R5 of the benzene ring. The benzene ring is also substituted with a separate methoxy group at the R3 carbon, and an allyl chain at R6 to make the main phenylpropene group.
Pharmacology
In 1963, Alexander Shulgin speculated myristicin could be metabolized to MMDA, a psychoactive drug related to MDA, in the liver.[3] This, however, is unlikely due to the fact that no amphetamine metabolites were found in urine after the ingestion of myristicin. It is believed that myristicin is an anticholinergic, since, in overdose, it produces effects similar to anticholinergics[4][5], but the exact mechanism of action has not been established. Myristicin is also found to be a serotoninreceptorantagonist, while simultaneously acting as a weak MAO inhibitor.[citation needed]
Elemicin
Elemicin is found in nutmeg alongside myristicin and contributes to its hallucinogenic effects. Elemicin is likely to have similar effects to myristicin. It is also the traditional precursor in synthesizing the alkaloid mescaline.[citation needed]
people who have ingested Elemi oil, (a source of elemicin that exists without high amounts of Myristicin) have claimed the visual effects the oil produce seem to be more similar to classical hallucinogens than the visual effects of nutmeg oil, (which seem to be more delirious and sedating in nature)
This distinction seems to paint Myristicin as a more sedating and mind-dulling drug, while Elemicin seems to be more-visually active and stimulating. this assumption is further supported by the fact that while Elemicin has direct structural ties to Mescaline, Myristicin has ties to MDXX compounds such as MDMA.
The chemical structure of Elemicin appears to be a carbon-based analogue of Mescaline while Myristicin itself appears to be a carbon analogue of Lophophine, these structural differences may be indicators of the slightly different psychoactive effects both Elemicin and Myristicin have.
Cannabinoids
No compound has been found in nutmeg to directly bind to CB1 or CB2 receptors. Three compounds in nutmeg (Malabaricone C, Licarin A, 5-Methoxylicarin A) have been shown to act as endo-cannabinoid modulating agents by inhibiting the enzymes FAAH and MAGL.[6]
Subjective effects
In comparison to datura or diphenhydramine, myristicin's effects tend to be milder and can be pleasant and euphoric depending on dose. It has unique effects compared to other deliriants or hallucinogens. It also has a long, smooth, and enjoyable come-up, where the effects build in a similar manner to cannabis. In addition to this, cannabis like effects throughout the duration have been reported among users of the substance which is possibly due to its activity on cannabinoid receptors. With higher doses, however, the deliriant effects become more pronounced.
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 PsychonautWikicontributors. 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 ☠.
Physical effects
The physical effects of myristicin are usually described as mild and tolerable, which makes them different from other deliriants. They can be uncomfortable or pleasurable, depending on the dosage. They generally include:
Difficulty urinating or / and Frequent urination - This can be described as a feeling of concrete blocking the urethra, painfully conflicting with a frequent need to urinate. However, some users report urinating perfectly fine. This effect might be dose-dependent.
Dry mouth - This effect is usually stronger than cannabis but much weaker than other deliriants like Datura.
Dehydration - Nutmeg causes a lot of dehydration and dehydration is proven to cause deliriant effects and delirium. Staying hydrated can decrease deliriant and negative effects.
Dizziness - This effect can be decreased by going for a walk or drinking ginger tea.
Nausea - This effect is usually caused by the unpleasurable taste rather than the compounds themselves.
Sedation - This effect can be extremely strong at higher dosage, leaving the user in a near sleep state during the experience.
Myristicin can both enhance and suppress visual stimuli depending on many factors that include but are not limited to; age, genetic factors, dehydration, combining nutmeg with other spices, sleep deprivation, and placebo. Some of the visual effects of nutmeg include:
Drifting - Breathing, objects having their size altered
Environmental patterning - You may see lines around and inside objects, essentially everything will have structure - You may see eyes like you would on psilocybin but to a lesser intensity
Frame rate suppression - Combined with time distortion nutmeg could make movies and videos feel more dissociative. This effect is similar to DXM
Enhancements
Colour enhancement - Visuals might be slightly more vibrant and objects might have a glow around them
Hallucinatory states
Myristicin is moderately efficient at inducing delirious hallucinations which can be broken into the categories described below:
External hallucination (autonomous entities; settings, sceneries, and landscapes; perspective hallucinations and scenarios and plots) - In comparison to other classes of hallucinogen, this effect occurs more frequently than that of any other at moderate to heavy doses and is the defining feature of the experience. It can be comprehensively described through its variations as delirious in believability, autonomous in controllability, and solid in style. The most common themes for these hallucinations include those of everyday occurrences such as smoking phantom cigarettes, talking to people who are not there, insects, and sinister, nightmarish experiences.
Internal hallucination (autonomous entities; settings, sceneries, and landscapes; perspective hallucinations and scenarios and plots) - In comparison to other classes of hallucinogen, this effect occurs briefly and spontaneously at moderate doses but becomes progressively extended in its occurrence and duration proportional to dosage before eventually becoming all-encompassing. It can be comprehensively described through its variations as delirious in believability, interactive in style, equal in new experiences and memory replays in content, autonomous in controllability and solid in style.
The cognitive effects of myristicin are described by many as mildly euphoric, but can also be dysphoric throughout the trip, primarily consisting of moderate paranoia. It can also be confusing and disorienting. Myristicin contains unique cognitive effects found almost exclusively in the deliriant class.
The most prominent of these effects include:
Confusion - This effect is more common at higher doses and when the user is dehydrated
Depersonalization] and Derealization - This effect differs from classic disscoatives and tends to be more dream like and results more often in anxiety due to the unpleasant body load nutmeg offers. This effect appears at higher doses only and is similar to the DPDR produced by THC and synthetic cannabinoids.
Emotion enhancement - This effect can enhance both negative and positive feelings, which means set and setting can alter the nutmeg experience
Myristicin is found in nutmeg, nutmeg essential oil, and to a lesser extent in parsley, dill, and other plants.
Ground nutmeg powder
Ground nutmeg powder
This is the most common form in which myristicin is sold, and it can be found in almost any supermarket as a spice.
It is worth noting that anecdotal reports suggest no clear guide on dosaging in this form. Myristicin degrades once it has been ground up, therefore it is impossible to know the potency of the powder, and the longer that the nutmeg stays as a powder, the weaker the myristicin content. When using store-bought nutmeg, the dose for oral consumption is generally considered to be:
Light:5 - 15g
Common:15 - 20g
Strong:20 - 30g
Heavy:30g+
Whole nutmeg
Whole nutmeg is also sold in most places as a spice.
Light:2 - 5g
Common:5 - 15g
Strong:15 - 20g
Heavy:20g+
Pure myristicin
Myristicin can be extracted from nutmeg powder by fractional distillation. When using pure myristicin, the dose for oral consumption is generally considered to be:
Light:50 - 200mg
Common:200 - 500mg
Strong:500 - 800mg
Heavy:800mg+
Toxicity and harm potential
This toxicity and harm potential section is a stub.
As a result, it may contain incomplete or even dangerously wrong information! You can help by expanding upon or correcting it. Note: Always conduct independent research and use harm reduction practices if using this substance.
Myristicin is neurotoxic and can be fatal in extremely high doses.[7] Also myristicin causes severe dehydration. It increases side effects of myristicin.
Dependence and abuse potential
Myristicin is not known to be addictive and the desire to use it can actually decrease with use.
Information regarding tolerance is unknown.
Dangerous Interactions
Warning:Many psychoactive substances that are reasonably safe to use on their own can suddenly become dangerous and even life-threatening when combined with certain other substances. The following list provides some known dangerous interactions (although it is not guaranteed to include all of them).
Always conduct independent research (e.g. Google, DuckDuckGo, PubMed) to ensure that a combination of two or more substances is safe to consume. Some of the listed interactions have been sourced from TripSit.
Stimulants - Nutmeg puts a fair amount of strain on the cardiovascular system, adding stimulant drugs to the mix would increase side effects.
Alcohol - Anecdotal reports suggest that small/medium amounts of alcohol can create some positive effects, however respiratory depression is a risk. Large amounts of alcohol should not be combined with myristicin in any circumstance.
Opioids - Large amounts of opioids can lead to respiratory depression when taken with myristicin.
DXM - While it is possible to take a very small dose of DXM with myristicin, it is highly risky and is generally seen to be dangerous.
DPH - DPH is cardio toxic, combining it with myristicin could be fatal.
Depressants - Respiratory depression is a risk when combining with depressant drugs, while a few anecdotal reports have shown few side effects, it is generally recommended against.
Serotonin releasers such as MDMA, 4-FA, methamphetamine, methylone and αMT will cause serotonin syndrome. If planning to combine these two, proceed with great caution.
Legal status
Myristicin and nutmeg are both unscheduled in nearly all parts of the world and are commonly bought in form of either ground spice, essential oil, or whole nuts.
United Kingdom: Nutmeg is legal to purchase as a spice in the United Kingdom, however, using it recreationally or extracting the myristicin is against the law.
↑Lee, B. K., Kim, J. H., Jung, J. W., Choi, J. W., Han, E. S., Lee, S. H., Ko, K. H., Ryu, J. H. (16 May 2005). "Myristicin-induced neurotoxicity in human neuroblastoma SK-N-SH cells". Toxicology Letters. 157 (1): 49–56. doi:10.1016/j.toxlet.2005.01.012. ISSN0378-4274.
