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{{headerpanel|{{Approval}}{{DepressantOD|GABAergics}}}}
{{headerpanel|{{DepressantOD|GABAergics|Opioids}}}}
{{SubstanceBox/Progesterone}}
{{SummarySheet}}
{{SummarySheet}}
{{Talk:SubstanceBox/Progesterone}}
'''Pregn-4-ene-3,20-dione''', also known as '''Progesterone''' or '''P4''' is a [[wikipedia:steroid|steroid]] sex [[hormone]] of the [[wikipedia:progestogen|progestogen]] class. It occurs naturally and is the bodies major progestogen.
'''Pregn-4-ene-3,20-dione''', also known as '''Progesterone''' or '''P4''' is a [[wikipedia:steroid|steroid]] sex [[hormone]] of the [[wikipedia:progestogen|progestogen]] class. It occurs naturally and is the bodies major progestogen.


Progesterone can be taken orally, vaginal, rectal and by subcutaneous or intramuscular injection.
Progesterone can be taken [[orally]], [[wikipedia:vaginal|vaginal]], [[rectal]] and by [[subcutaneous]] or [[intramuscular]] [[injection]].


Progetserone is commonly used as a part of [[wikipedia:Transgender_hormone_therapy|trans-feminising hormone therapy]] or [[wikipedia:Menopause|post menopausal]] [[wikipedia:Hormone replacement therapy|Hormone replacement therapy]].
Progesterone is commonly used as a part of [[wikipedia:Transgender_hormone_therapy|trans-feminising hormone therapy]] or [[wikipedia:Menopause|post menopausal]] [[wikipedia:Hormone replacement therapy|Hormone replacement therapy]].
[[File:Progesterone Blister.jpg|thumb|Progesterone Besins 200mg]]


==History and culture==
==History and culture==
{{historyStub}}
Progesterone was first discovered in 1929 by George W. Corner and Willard M. Allen. By 1934 pure crystalline material was achieved by Adolf Butenandt at the ''[[wikipedia:Gdańsk_University_of_Technology|Chemisches Institut of Technical University]]'' in [[wikipedia:Gdańsk]]. Synthesis was accomplished later that year.
Progesterone was first discovered in 1929 by George W. Corner and Willard M. Allen. By 1934 pure crystalline material was achieved by Adolf Butenandt at the ''Chemisches Institut of Technical University'' in Gdańsk. Synthesis was accomplished later that year.
<ref name="Josimovich 2013 p.">{{cite book | last=Josimovich | first=J.B. | title=Gynecologic Endocrinology | publisher=Springer Science & Business Media |url=https://books.google.com/books?id=9vv2BwAAQBAJ&pg=PA25 |date=11 November 2013 |access-date=1 February 2016 |archive-date=14 January 2023 |archive-url=https://web.archive.org/web/20230114024947/https://books.google.com/books?id=9vv2BwAAQBAJ&pg=PA25| isbn=978-1-4613-2157-6 |pages=9, 25–29 }}</ref>


In a 2012 study higher levels of progesterone were linked to lower affinity to competitive behavior in women.<ref name="Buser-2012">{{Cite journal|vauthors=Buser T|date=1 June 2012|title=The impact of the menstrual cycle and hormonal contraceptives on competitiveness|journal=Journal of Economic Behavior & Organization|series=Gender Differences in Risk Aversion and Competition|volume=83|issue=1|pages=1–10|doi=10.1016/j.jebo.2011.06.006|issn=0167-2681|url=https://pure.uva.nl/ws/files/1864146/117489_376503.pdf|access-date=2 February 2024|archive-date=2 February 2024|archive-url=https://web.archive.org/web/20240202143019/https://pure.uva.nl/ws/files/1864146/117489_376503.pdf|url-status=live}}</ref>
In a 2012 study higher levels of progesterone were linked to lower affinity to competitive behavior in women.<ref name="Buser 2012 pp. 1–10">{{cite journal | last=Buser | first=Thomas | title=The impact of the menstrual cycle and hormonal contraceptives on competitiveness|journal=Journal of Economic Behavior & Organization|series=Gender Differences in Risk Aversion and Competition|volume=83|issue=1|pages=1–10|doi=10.1016/j.jebo.2011.06.006|issn=0167-2681|url=https://pure.uva.nl/ws/files/1864146/117489_376503.pdf|access-date=2 February 2024|archive-date=2 February 2024|archive-url=https://web.archive.org/web/20240202143019/https://pure.uva.nl/ws/files/1864146/117489_376503.pdf}}</ref><ref name="Piosik 2003 pp. 135–138">{{cite journal | last=Piosik | first=Romuald | title=Adolf Butenandt und sein Wirken an der Technischen Hochschule Danzig | journal=CHEMKON | volume=10 | issue=3 | date=2003 | issn=0944-5846 | doi=10.1002/ckon.200390038 | pages=135–138}}</ref>


==Chemistry==
==Chemistry==
{{chemistry}}
Progesterone is a naturally occurring pregnane steroid and is also known as pregn-4-ene-3,20-dione. It has a double bond (4-ene) between the C4 and C5 positions and two ketone groups (3,20-dione), one at the C3 position and the other at the C20 position.<ref name="Pubchem">{{Cite web|date= 12 March 2024|title= Compound Summary Progesterone| publisher=National Library of Medicine|access-date=12 March 2024|url=https://pubchem.ncbi.nlm.nih.gov/compound/progesterone}}</ref>
Progesterone is a naturally occurring pregnane steroid and is also known as pregn-4-ene-3,20-dione. It has a double bond (4-ene) between the C4 and C5 positions and two ketone groups (3,20-dione), one at the C3 position and the other at the C20 position.<ref>Compound Summary Progesterone|https://pubchem.ncbi.nlm.nih.gov/compound/progesterone</ref>
 
==Pharmacology==
==Pharmacology==
{{pharmacology}}
Progesterone on it's own acts as a [[antagonist]] on the [[wikipedia:Sigma-2 receptor|'''σ<sub>2</sub>''' receptor]] and as a [[wikipedia:negative allosteric modulator|negative allosteric modulator]] on [[wikipedia:nicotinic acetylcholine receptors|nicotinic acetylcholine receptors]]. However most of the psychoactive effects of progesterone are induced by it's metabolites.<ref name="Gonzalez 2020 p. 1846">{{cite journal | last=Gonzalez | first=Susana Laura | title=Progesterone for the treatment of central nervous system disorders: the many signaling roads for a single molecule | journal=Neural Regeneration Research | volume=15 | issue=10 | date=2020 | issn=1673-5374 | pmid=32246629 | pmc=7513974 | doi=10.4103/1673-5374.280314 | doi-access=free | page=1846}}</ref>
Progesterone on it's own acts as a antagonist on the '''σ<sub>2</sub>''' receptor and as a negative allosteric modulator on nicotinic acetylcholine receptors. However most of the psychoactive effects of progesterone are induced by it's metabolites.<ref>Progesterone for the treatment of central nervous system disorders: the many signaling roads for a single molecule|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7513974/</ref>
 
===Metabolism===
===Metabolism===
Progesterone is mainly metabolised in the liver, therefore the route of administration significantly influences the intensity of experienced effects. The most important metabolites are allopregnanolone, pregnanolone, isopregnanolone and epipregnanolone.  
Progesterone is mainly metabolised in the liver, therefore the route of administration significantly influences the intensity of experienced effects. The most important metabolites are [[wikipedia:allopregnanolone|allopregnanolone]], [[wikipedia:pregnanolone|pregnanolone]], [[wikipedia:isopregnanolone|isopregnanolone]] and [[wikipedia:epipregnanolone|epipregnanolone]].<ref name="Kolatorova Vitku Suchopar Hill 2022 p. 7989">{{cite journal | last=Kolatorova | first=Lucie | last2=Vitku | first2=Jana | last3=Suchopar | first3=Josef | last4=Hill | first4=Martin | last5=Parizek | first5=Antonin | title=Progesterone: A Steroid with Wide Range of Effects in Physiology as Well as Human Medicine | journal=International Journal of Molecular Sciences | volume=23 | issue=14 | date=2022-07-20 | issn=1422-0067 | pmid=35887338 | doi=10.3390/ijms23147989 | doi-access=free | page=7989}}</ref>
 
Allopregnanolone and Pregnanolone are documented to have [[antidepressant]], [[anxiolytic]], stress reducing, antiagressive, [[sedative]], sleep aiding, [[analgesic]], [[amnesic]], [[wikipedia:anesthetic|anesthetic]], [[anticonvulsant]] & [[wikipedia:neuroprotective|neuroprotective]] effects.<ref name="Diviccaro Cioffi Falvo Giatti 2022 p.">{{cite journal | last=Diviccaro | first=Silvia | last2=Cioffi | first2=Lucia | last3=Falvo | first3=Eva | last4=Giatti | first4=Silvia | last5=Melcangi | first5=Roberto Cosimo | title=Allopregnanolone: An overview on its synthesis and effects | journal=Journal of Neuroendocrinology | volume=34 | issue=2 | date=2022 | issn=0953-8194 | pmid=34189791 | doi=10.1111/jne.12996 | page=}}</ref><ref name="PubChem p788">{{cite web | title=Brexanolone | website=PubChem | url=https://pubchem.ncbi.nlm.nih.gov/compound/92786 | access-date=2024-03-12}}</ref>Allopregnanolone and Pregnanolone act as positive allosteric modulators of [[GABA]]<sub>A</sub> whereas isopregnanolone and epipregnanolone selectively counteract GABA<sub>A</sub> as well as the sedative and anesthetic effects.<ref name="Kolatorova Vitku Suchopar Hill 2022 p. 7989">{{cite journal | last=Kolatorova | first=Lucie | last2=Vitku | first2=Jana | last3=Suchopar | first3=Josef | last4=Hill | first4=Martin | last5=Parizek | first5=Antonin | title=Progesterone: A Steroid with Wide Range of Effects in Physiology as Well as Human Medicine | journal=International Journal of Molecular Sciences | volume=23 | issue=14 | date=2022-07-20 | issn=1422-0067 | pmid=35887338 | doi=10.3390/ijms23147989 | doi-access=free | page=7989}}</ref>
Allopregnanolone and Pregnanolone are documented to have antidepressant, anxiolytic, stress reducing, antiagressive, sedative, sleep aiding, analgesic, amnesic, anesthetic, anticonvulsant & neuroprotective effects.<ref>Allopregnanolone: An overview on its synthesis and effects|https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9285581/</ref><ref>Compound Summary Pregnanolone|https://pubchem.ncbi.nlm.nih.gov/compound/31402</ref><ref>Compound Summary Brexanolone|https://pubchem.ncbi.nlm.nih.gov/compound/92786</ref>
Allopregnanolone and Pregnanolone act as positive allosteric modulators of GABA<sub>A</sub> whereas isopregnanolone and epipregnanolone selectively counteract GABA<sub>A</sub> as well as the sedative and anesthetic effects.
 


==Subjective effects==
==Subjective effects==
{{EffectStub}}
{{Preamble/SubjectiveEffects}}
{{Preamble/SubjectiveEffects}}
{{effects/base
{{effects/base


|{{effects/physical|
|{{effects/physical|
If applicable, a brief paragraph summary of the substance's physical effects may be included here.  
If applicable, a brief paragraph summary of the substance's physical effects may be included here.


You may select physical effects to add below [[Subjective effect index#Physical effects|here]].
You may select physical effects to add below [[Subjective effect index#Physical effects|here]].


*'''[[Effect::Physical effect]]'''  
*'''[[Effect::Increased bodily temperature]]''' - at high concentration progesterone elevates body temperature for ~1°C
*'''[[Effect::Physical effect2]]'''
*'''[[Effect::Sedation]]'''
*'''[[Effect::Physical effect3]]'''
*'''[[Effect::Pain relief]]'''
 
*'''[[Effect::Motor control loss]]'''
}}
}}
{{effects/visual|
<!--{{effects/visual|
If applicable, a brief paragraph summary of the substance's visual effects may be included here.  
If applicable, a brief paragraph summary of the substance's visual effects may be included here.


You may select visual effects to add below [[Subjective effect index#Visual effects|here]].
You may select visual effects to add below [[Subjective effect index#Visual effects|here]].
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*'''[[Effect::Hallucinatory states1]]'''
*'''[[Effect::Hallucinatory states1]]'''


}}
}}-->


|{{effects/cognitive|
|{{effects/cognitive|
If applicable, a brief paragraph summary of the substance's cognitive effects may be included here.  
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]].
You may select from a list of cognitive effects to add below [[Subjective effect index#Cognitive effects|here]].


*'''[[Effect::Cognitive effect1]]'''  
*'''[[Effect::Thought deceleration]]'''
*'''[[Effect::Cognitive effect2]]'''  
*'''[[Effect::Amnesia]]'''
*'''[[Effect::Cognitive effect3]]'''  
*'''[[Effect::Dizziness]]'''
 
*'''[[Effect::Sleepiness]]'''
*'''[[Effect::Anxiety suppression]]'''
*'''[[Effect::Physical euphoria]]'''
*'''[[Effect::Increased libido]]'''
*'''[[Effect::Mindfulness]]'''
}}
}}
{{effects/auditory|
<!--{{effects/auditory|
If applicable, a brief paragraph summary of the substance's auditory effects may be included here.  
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]].
You may select from a list of auditory effects to add below [[Subjective effect index#Auditory effects|here]].
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*'''[[Effect::Auditory effect2]]'''
*'''[[Effect::Auditory effect2]]'''


}}
}}-->
{{effects/multisensory|
<!--{{effects/multisensory|
If applicable, a brief paragraph summary of the substance's multisensory effects may be included here.  
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]].
You may select from a list of multisensory effects to add below [[Subjective effect index#Multisensory effects|here]].


*'''[[Effect::Multisensory effect1]]'''  
*'''[[Effect::Multisensory effect1]]'''
*'''[[Effect::Multisensory effect2]]'''  
*'''[[Effect::Multisensory effect2]]'''


}}
}}-->
{{effects/transpersonal|
<!--{{effects/transpersonal|
If applicable, a brief paragraph summary of the substance's transpersonal effects may be included here.  
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]].
You may select from a list of transpersonal effects to add below [[Subjective effect index#Transpersonal effects|here]].
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*'''[[Effect::Transpersonal effect1]]'''
*'''[[Effect::Transpersonal effect1]]'''
*'''[[Effect::Transpersonal effect2]]'''
*'''[[Effect::Transpersonal effect2]]'''
}}-->
{{effects/aftereffects|
*'''[[Effect::Increased libido]]'''
*'''[[Effect::Sleepiness]]'''


}}
}}
}}
}}
===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:Progesterone]][[Category:Experience]] | format=count}} experience reports which describe the effects of this substance in our [[experience index]].
{{#ask: [[Category:SUBSTANCE]][[Category:Experience]]|format=ul|Columns=1}}
{{#ask: [[Category:Progesterone]][[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_SUBSTANCE.shtml Erowid Experience Vaults: SUBSTANCE] <!-- Check the link to see if it exists -->
* [https://www.erowid.org/experiences/subs/exp_SUBSTANCE.shtml Erowid Experience Vaults: SUBSTANCE] <!-- Check the link to see if it exists -->


==Toxicity and harm potential==
==Toxicity and harm potential==
{{toxicity}}
'''Warning:''' Progesterone is a naturally occuring sex hormone, changing its levels might induce gender dysphoria or premenstrual syndrome.
'''Warning:''' Progesterone is a naturally occuring sex hormone, changing its levels might induce gender dysphoria or premenstrual syndrome.


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It is strongly recommended that one use [[harm reduction practices]] when using this substance.
It is strongly recommended that one use [[harm reduction practices]] when using this substance.
===Lethal dosage===
===Lethal dosage===
The observed LD50 in mice was 100mg/kg via intravenous, 327mg/kg intraperitoneal and > 200mg/kg orally, anasthetic effects were observed at 16mg/kg intraperitoneal.<ref>Evidence of developmental and repoductive toxicity of progesterone|https://oehha.ca.gov/media/downloads/proposition-65/chemicals/progeshid5.pdf</ref><ref>Progesterone Safety Data Sheet|https://sds.edqm.eu/pdf/SDS/EDQM_201600761_1.0_SDS_EN.pdf</ref>
The observed LD50 in mice was 100mg/kg via intravenous, 327mg/kg intraperitoneal and > 200mg/kg orally, anasthetic effects were observed at 16mg/kg intraperitoneal.<ref name="OEHA2004">{{cite web | publisher=Office of Environmental Health Hazard Assessment California Environmental Protection Agency | title=EVIDENCE ON THE DEVELOPMENTAL AND REPRODUCTIVE TOXICITY OF Progesterone | url=https://oehha.ca.gov/media/downloads/proposition-65/chemicals/progeshid5.pdf | access-date=2024-03-12}}</ref>
 
===Tolerance and addiction potential===
===Tolerance and addiction potential===
Dependence potential of Progesterone has been sparsely reported by transfeminine people. There is one case report of a women on post menopausal HRT that documents addiction.<ref>Progesterone abuse|https://link.springer.com/article/10.2165/00128415-199605990-00031</ref>
Dependence potential of Progesterone has been sparsely reported by transfeminine people. There is one case report of a women on post menopausal HRT that documents addiction.<ref name="React Weekly 1996 p. 9">{{cite journal | author=&Na; | title=Progesterone abuse Adverse effects: case report | journal=Reactions Weekly | volume=&NA; | issue=599 | date=1996 | issn=0114-9954 | doi=10.2165/00128415-199605990-00031 | page=9}}</ref>
 
Tolerance to the offects of Progesterone metabolites on GABA will build within a few years and return to baseline within a few months after cessation.{{Citation needed|date=March 2024|reason=from a pharma perspective this estimate makes sense, but hasn't been medically investigated}}


Tolerancde to the offects of Prog metabolites on GABA will build within a few years and return to baseline within a few months after cessation.
===Interactions===
===Interactions===
Combining oral progesterone with food leads to a two fold increase in absorptions. <ref>The absorption of oral micronized progesterone: the effect of food, dose proportionality, and comparison with intramuscular progesterone|https://pubmed.ncbi.nlm.nih.gov/8513955/</ref> Since oral progesterone is a oil soluable reports of increased effects when combined with fatty foods do seem plausible.
Combining oral progesterone with food leads to a two fold increase in absorptions. <ref name="Simon Robinson Andrews Hildebrand 1993 pp. 26–33">{{cite journal | last=Simon | first=James A. | last2=Robinson | first2=Denise E. | last3=Andrews | first3=Mason C. | last4=Hildebrand | first4=James R. | last5=Rocci | first5=Mario L. | last6=Blake | first6=Richard E. | last7=Hodgen | first7=Gary D. | title=The absorption of oral micronized progesterone: the effect of food, dose proportionality, and comparison with intramuscular progesterone | journal=Fertility and Sterility | volume=60 | issue=1 | date=1993 | doi=10.1016/S0015-0282(16)56031-2 | pages=26–33}}</ref> Since oral progesterone is a oil soluable reports of increased effects when combined with fatty foods do seem plausible.
===Dangerous interactions===
===Dangerous interactions===
{{DangerousInteractions}}
{{DangerousInteractions}}
{{DangerousInteractions/Intro}}
{{DangerousInteractions/Intro}}


Taking oral progesterone together with alcohol will increase absorption rates and peak potentially leading to black out intervals or loss of motor control, anesthetic levels in humans are not documented, but might be reachable.  
*'''[[Depressants]]''' Taking oral progesterone together with [[alcohol]] or [[barbiturates]] will increase absorption rates and peak potentially leading to black out intervals or loss of motor control, anesthetic levels in humans are not documented, but might be reachable. Other dangerous depressants are [[benzodiazepines]] and [[opioids]] since their absorption can be increased, resulting in a higher risk of overdose.<ref name="DrugBank Online 2016 t459">{{cite web | title=Progesterone: Uses, Interactions, Mechanism of Action | website=DrugBank Online | date=2016-04-13 | url=https://go.drugbank.com/drugs/DB00396 | access-date=2024-03-12}}</ref>
 


==Legal status==
==Legal status==
{{LegalStub}}
{{LegalStub}}
Progesterone is widely available as prescription medication or in some cases over the counter and generally not controlled. Taking transgender HRT is not as widely accepted and may be prosecuted. <ref name="Drugs.com 2024 l855">{{cite web | title=Progesterone (International database) | website=Drugs.com | date=2024-03-03 | url=https://www.drugs.com/international/progesterone.html | access-date=2024-03-12}}</ref>


==See also==
==See also==
*[[Responsible use]]
*[[Responsible use]]
*[[Hormone]]
*[[GABA]]
*[[Estradiol]]


==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/Progesterone Progesterone(hormone) (Wikipedia)]
*[https://en.wikipedia.org/wiki/Progesterone_(medication) Progesterone(medication) (Wikipedia)]
*[https://go.drugbank.com/drugs/DB00396 Progesterone (DrugBank)]
*[https://www.drugs.com/progesterone.html Progesterone (Drugs.com)]


==References==
==References==
<references />
<references />


[[Category:Psychoactive substance]][[Category:Proofread]][[Category:Approval]]
[[Category:Psychoactive substance]]
[[Category:Hormone]]

Latest revision as of 11:51, 9 October 2024

Fatal overdose may occur when GABAergic substances are combined with other depressants such as opiates, benzodiazepines, barbiturates, gabapentinoids, thienodiazepines or alcohol.[1]

It is strongly discouraged to combine these substances, particularly in common to heavy doses.

Progesterone
Chemical Nomenclature
Common names P4, Pregnenedione
Substitutive name Pregn-4-ene-3,20-dione
Systematic name (1S,3aS,3bS,9aR,9bS,11aS)-1-Acetyl-9a,11a-dimethyl-1,2,3,3a,3b,4,5,8,9,9a,9b,10,11,11a-tetradecahydro-7H-cyclopenta[a]phenanthren-7-one
Class Membership
Psychoactive class Depressant
Chemical class Steroid
Routes of Administration

WARNING: Always start with lower doses due to differences between individual body weight, tolerance, metabolism, and personal sensitivity. See responsible use section.



Oral
Dosage
Bioavailability 10%
Threshold 100 mg
Light 100 - 200 mg
Common 200 - 400 mg
Strong 400 - 600 mg
Heavy 600 mg +
Duration
Total 2 - 4 hours
Onset 30 - 60 minutes
After effects 4 - 6 hours




Rectal
Dosage
Threshold 100 mg
Light 100 - 200 mg
Common 200 - 400 mg
Strong 400 - 600 mg
Heavy 600 mg +
Duration
Total 8 - 12 hours
After effects 6 - 12 hours





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.

Interactions
Summary sheet: Progesterone

Pregn-4-ene-3,20-dione, also known as Progesterone or P4 is a steroid sex hormone of the progestogen class. It occurs naturally and is the bodies major progestogen.

Progesterone can be taken orally, vaginal, rectal and by subcutaneous or intramuscular injection.

Progesterone is commonly used as a part of trans-feminising hormone therapy or post menopausal Hormone replacement therapy.

Progesterone Besins 200mg

History and culture

Progesterone was first discovered in 1929 by George W. Corner and Willard M. Allen. By 1934 pure crystalline material was achieved by Adolf Butenandt at the Chemisches Institut of Technical University in wikipedia:Gdańsk. Synthesis was accomplished later that year. [2]

In a 2012 study higher levels of progesterone were linked to lower affinity to competitive behavior in women.[3][4]

Chemistry

Progesterone is a naturally occurring pregnane steroid and is also known as pregn-4-ene-3,20-dione. It has a double bond (4-ene) between the C4 and C5 positions and two ketone groups (3,20-dione), one at the C3 position and the other at the C20 position.[5]

Pharmacology

Progesterone on it's own acts as a antagonist on the σ2 receptor and as a negative allosteric modulator on nicotinic acetylcholine receptors. However most of the psychoactive effects of progesterone are induced by it's metabolites.[6]

Metabolism

Progesterone is mainly metabolised in the liver, therefore the route of administration significantly influences the intensity of experienced effects. The most important metabolites are allopregnanolone, pregnanolone, isopregnanolone and epipregnanolone.[7] Allopregnanolone and Pregnanolone are documented to have antidepressant, anxiolytic, stress reducing, antiagressive, sedative, sleep aiding, analgesic, amnesic, anesthetic, anticonvulsant & neuroprotective effects.[8][9]Allopregnanolone and Pregnanolone act as positive allosteric modulators of GABAA whereas isopregnanolone and epipregnanolone selectively counteract GABAA as well as the sedative and anesthetic effects.[7]

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 ☠.


Physical effects

Cognitive effects


Experience reports

There are currently 0 experience reports which describe the effects of this substance in our experience index.


Toxicity and harm potential

Warning: Progesterone is a naturally occuring sex hormone, changing its levels might induce gender dysphoria or premenstrual syndrome.

Progesterone has relatively low toxicity relative to dose.

It is strongly recommended that one use harm reduction practices when using this substance.

Lethal dosage

The observed LD50 in mice was 100mg/kg via intravenous, 327mg/kg intraperitoneal and > 200mg/kg orally, anasthetic effects were observed at 16mg/kg intraperitoneal.[10]

Tolerance and addiction potential

Dependence potential of Progesterone has been sparsely reported by transfeminine people. There is one case report of a women on post menopausal HRT that documents addiction.[11]

Tolerance to the offects of Progesterone metabolites on GABA will build within a few years and return to baseline within a few months after cessation.[citation needed]

Interactions

Combining oral progesterone with food leads to a two fold increase in absorptions. [12] Since oral progesterone is a oil soluable reports of increased effects when combined with fatty foods do seem plausible.

Dangerous interactions

This dangerous interactions section is a stub.

As such, it may contain incomplete or invalid information. You can help by expanding upon or correcting it.

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.

  • Depressants Taking oral progesterone together with alcohol or barbiturates will increase absorption rates and peak potentially leading to black out intervals or loss of motor control, anesthetic levels in humans are not documented, but might be reachable. Other dangerous depressants are benzodiazepines and opioids since their absorption can be increased, resulting in a higher risk of overdose.[13]

This legality section is a stub.

As such, it may contain incomplete or wrong information. You can help by expanding it.

Progesterone is widely available as prescription medication or in some cases over the counter and generally not controlled. Taking transgender HRT is not as widely accepted and may be prosecuted. [14]

See also

References

  1. Risks of Combining Depressants - TripSit 
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