
MDPV
MDPV | |||||||||||||||||||||||||||||||
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Chemical Nomenclature | |||||||||||||||||||||||||||||||
Common names | MDPV, Bath Salts, NRG-1 | ||||||||||||||||||||||||||||||
Substitutive name | 3,4-Methylenedioxypyrovalerone | ||||||||||||||||||||||||||||||
Systematic name | 1-(1,3-Benzodioxol-5-yl)-2-(pyrrolidin-1-yl)pentan-1-one | ||||||||||||||||||||||||||||||
Class Membership | |||||||||||||||||||||||||||||||
Psychoactive class | Stimulant / Entactogen | ||||||||||||||||||||||||||||||
Chemical class | Cathinone / MDxx / Pyrrolidinophenone | ||||||||||||||||||||||||||||||
Routes of Administration | |||||||||||||||||||||||||||||||
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Interactions | |||||||||||||||||||||||||||||||
This article is a stub. As such, it may contain incomplete or wrong information. You can help by expanding it. |
Methylenedioxypyrovalerone (commonly known as MDPV or bath salts) is a potent euphoric stimulant with a short history of human use. MDPV acts as a norepinephrine-dopamine reuptake inhibitor (NDRI) and possesses stimulant qualities. It was first developed in the 1960s by a team at Boehringer Ingelheim. MDPV remained an obscure stimulant until around 2004, when it was reportedly first sold as a designer drug available to the public. Products labeled as "bath salts" containing MDPV were previously sold as recreational drugs in gas stations and convenience stores in the United States, similar to the marketing strategy of Spice and K2 as incense.
Historical reports show records of the preparation of MDPV for potential use as a CNS stimulant. It was claimed to have potential to be an alternative for racemic amphetamine and, although showing some desirable qualities such as reduced toxicity as compared to amphetamine, MDPV was not developed as a medicinal drug.[1]
Incidents of psychological and physical harm have been attributed to MDPV use.
Chemistry
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MDPV, or 3,4-Methylenedioxypyrovalerone, is a cathinone-class stimulant. Specifically, MDPV possesses a 2-amino-1-phenylpropan-1-one nucleus. Many, but not all, cathinone-based substances also possess this nucleus. Cathinone, and by extension MDPV, differs from most stimulants due it containing a ketone functional group.
Pharmacology
MDPV acts as a norepinephrine-dopamine reuptake inhibitor. Reduced re-uptake of norepinephrine and dopamine results in higher concentrations of the two neurotransmitters in the synapse, or junction between neurons. The result of this inhibition is an enhanced and prolonged post-synaptic effect of dopaminergic and noradrenaline signaling at dopamine and norepinephrine receptors on the receiving neuron. Serotonin transmitters also experience a similar effect, although to a much lesser degree. This sudden increase in neurotransmitter levels in the brain is responsible for the high that MDPV provides. Mainly possessing re-uptake inhibiting qualities, MDPV could be considered more like cocaine than amphetamine in method of action.[2] Amphetamine acts primarily as an agonist to release dopamine and noradrenaline indirectly via activation of the TAAR1 receptor.
Subjective effects
The effects listed below are based upon the subjective effects index and personal experiences of PsychonautWiki contributors. The listed effects will rarely (if ever) occur all at once, but heavier dosages will increase the chances and are more likely to induce a full range of effects.
Physical effects
- Abnormal heartbeat
- Appetite suppression
- Diarrhea or nausea - Some experience reports describe individuals who have experienced one or more types of gastrointestinal disturbance while under the influence of MDPV.
- Gustatory hallucinations
- Headaches
- Increased heart rate - Higher doses of MDPV can create a significant and sometimes serious rise in heart rate.
- Muscle contractions
- Muscle spasms
- Restless leg syndrome
- Stamina enhancement
- Stimulation
Cognitive effects
The general cognitive effects of MDPV can be described as being similar to those of other typical stimulants. At common dosages, the MDPV high is described as being euphoric and slightly empatheogenic in its effects, causing increased motivation, sociability, sexual desire and concentration. Higher doses of MDPV, however, can intensify numerous negative effects such as anxiety and disorganized thoughts; at extremely high doses or continued use, delusions and psychosis become likely.[3]
- Anxiety
- Cognitive euphoria
- Compulsive redosing - MDPV is extremely potent in this effect; it been shown to sometimes cause users to redose even without planning to do so.
- Confusion - This effect is intensified at higher doses.
- Creativity enhancement
- Delusions - This effect can also manifest with high doses.
- Ego inflation
- Empathy, love, and sociability enhancement - MDPV's effects in this regard are similar to, but weaker than, those of MDMA.
- Focus enhancement
- Increased libido
- Motivation enhancement
- Paranoia
- Stamina enhancement
- Psychosis - High doses of MDPV have been known to induce states of psychosis at a more frequent rate than most other stimulants.[citation needed]
- Thought acceleration
- Thought organization - Mainly observed with low to common doses.
- Thought disorganization - This effect manifests and is also intensified with higher doses.
- Wakefulness
After effects
The effects which occur during the offset of a stimulant experience generally feel negative and uncomfortable in comparison to the effects which occurred during its peak. This is often referred to as a "comedown" and occurs because of neurotransmitter depletion. Its effects commonly include:
- Anxiety
- Cognitive fatigue
- Depression
- Irritability
- Motivation suppression
- Thought deceleration
- Wakefulness
It should be noted that many users consider the after effects of MDPV to be significantly more unpleasant if compulsively redosed.[4][5]
Toxicity and harm potential
MDPV has a relatively short history of human use, with very few mentions concerning the use thereof before 2004. Although once considered a potential alternative to existing stimulants with a lower risk for toxicity, human MDPV administration has not been extensively studied in a clinical setting for quite some time. Despite this, several recent studies on cases of persisting psychosis caused by chronic use of MDPV show promising rates of recovery among individuals who are treated with certain antipsychotics and first-line antihistamines.[6] There has been no conclusive data concerning the neurotoxicity of MDPV in the human brain as of 2016. Anecdotal evidence from those who have tried MDPV in the online community suggest that there are no negative health effects associated with the drug if simply taken at low doses by itself and when used sparingly (but nothing can be completely guaranteed).
Data taken from in-vitro and in-vivo studies have indicated that MDPV shares similar properties to methamphetamine and cocaine; in fact, MDPV is more potent than these two stimulants in a number of varying ways.[7] The over-excitation of dopamine and noradrenaline caused by MDPV use, combined with MDPV's potential inability to create compensatory serotonergic activity, sets the stage for a number of hostile and psychotic reactions to the drug. These hostile tendencies have been witnessed in emergency response situations, and have also seen wide television coverage in the past, after an individual under the influence of MDPV viciously assaulted an innocent bystander. It is uncertain if the individual had any pre-existing mental disorders or if he was under the influence of any other drugs.
Lethal dosage
The exact lethal dosage of MDPV is unknown and no formal studies have been carried out in humans. For sake of reference, one report placed the lethal dosage for a 39 year old male at 0.4 micrograms per millilitre or greater following the results of a post mortem,[8] but this data is far too individually unique and the variables simply too diverse to derive any kind of meaningful information from it. It is strongly recommended that one use harm reduction practices when using this drug.
Tolerance and addiction potential
As with other stimulants, the chronic use of MDPV can be considered moderately addicting with a high potential for abuse and is capable of causing psychological dependence among certain users. When addiction has developed, cravings and withdrawal effects may occur if a person suddenly stops their usage. Addiction is a serious risk among users of MDPV as it easily causes compulsive redosing and causes highly unpleasant comedown symptoms.
Dangerous interactions
References
- ↑ MDPV Summary | http://www.who.int/medicines/areas/quality_safety/4_13_Review.pdf?ua=1
- ↑ http://www.who.int/medicines/areas/quality_safety/4_13_Review.pdf?ua=1
- ↑ Some Guy. "Psychosis: An Experience with MDPV (ID 78382)". Erowid.org. Mar 22, 2010. erowid.org/exp/78382 | https://www.erowid.org/experiences/exp.php?ID=78382
- ↑ InnerExplorer. "Personal Research Comedown Guide: An Experience with MDPV (ID 98601)". Erowid.org. Feb 21, 2013. erowid.org/exp/98601 | https://erowid.org/experiences/exp.php?ID=98601
- ↑ Trippy. "Seemingly Real Paranoid Hallucination Hell: An Experience with MDPV (ID 91741)". Erowid.org. Jun 30, 2011. erowid.org/exp/91741 | https://erowid.org/experiences/exp.php?ID=91741
- ↑ Studies concerning MDPV hospitalization, pages 19 to 25. | http://www.who.int/medicines/areas/quality_safety/4_13_Review.pdf?ua=1
- ↑ MDPV In-vivo statistics | http://www.who.int/medicines/areas/quality_safety/4_13_Review.pdf?ua=1
- ↑ http://jat.oxfordjournals.org/content/37/3/182.full