Evidence map›Paper›PMID 24899699›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Critical role of peripheral vasoconstriction in fatal brain hyperthermia induced by MDMA (Ecstasy) under conditions that mimic human drug use.

Eugene A Kiyatkin, Albert H Kim, Ken T Wakabayashi, Michael H Baumann, Yavin Shaham

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
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  6. Worsening of the Toxic Effects of (±)International journal of molecular sciences · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Eugene A KiyatkinIntramural Research Program, National Institute on Drug Abuse-National Institutes of Health, Baltimore, Maryland 21224 ekiyatki@intra.nida.nih.gov.
Albert H KimIntramural Research Program, National Institute on Drug Abuse-National Institutes of Health, Baltimore, Maryland 21224.
Ken T WakabayashiIntramural Research Program, National Institute on Drug Abuse-National Institutes of Health, Baltimore, Maryland 21224.
Michael H BaumannIntramural Research Program, National Institute on Drug Abuse-National Institutes of Health, Baltimore, Maryland 21224.
Yavin ShahamIntramural Research Program, National Institute on Drug Abuse-National Institutes of Health, Baltimore, Maryland 21224.
National Institute on Drug Abuse · USNational Institutes of Health · US

Funding

Neurobiology Of Relapse To Opiate and Psychostimulant DrugsZIADA000434 · NIDA · NATIONAL INSTITUTE ON DRUG ABUSE · PI SHAHAM, YAVIN · 2009 to 2025
$39.8M
Studies on MDMA and Related CompoundsZIADA000523 · NIDA · NATIONAL INSTITUTE ON DRUG ABUSE · PI BAUMANN, MICHAEL · 2009 to 2025
$16.4M
Brain Temperature, Reward, And Drugs Of AbuseZIADA000445 · NIDA · NATIONAL INSTITUTE ON DRUG ABUSE · PI KIYATKIN, EUGENE A · 2009 to 2020
$4.1M
Intramural NIH HHS
6 · The paper itself

Abstract

MDMA (Ecstasy) is an illicit drug used by young adults at hot, crowed "rave" parties, yet the data on potential health hazards of its abuse remain controversial. Here, we examined the effect of MDMA on temperature homeostasis in male rats under standard laboratory conditions and under conditions that simulate drug use in humans. We chronically implanted thermocouple microsensors in the nucleus accumbens (a brain reward area), temporal muscle, and facial skin to measure temperature continuously from freely moving rats. While focusing on brain hyperthermia, temperature monitoring from the two peripheral locations allowed us to evaluate the physiological mechanisms (i.e., intracerebral heat production and heat loss via skin surfaces) that underlie MDMA-induced brain temperature responses. Our data confirm previous reports on high individual variability and relatively weak brain hyperthermic effects of MDMA under standard control conditions (quiet rest, 22-23°C), but demonstrate dramatic enhancements of drug-induced brain hyperthermia during social interaction (exposure to male conspecific) and in warm environments (29°C). Importantly, we identified peripheral vasoconstriction as a critical mechanism underlying the activity- and state-dependent potentiation of MDMA-induced brain hyperthermia. Through this mechanism, which prevents proper heat dissipation to the external environment, MDMA at a moderate nontoxic dose (9 mg/kg or ~1/5 of LD50 in rats) can cause fatal hyperthermia under environmental conditions commonly encountered by humans. Our results demonstrate that doses of MDMA that are nontoxic under cool, quiet conditions can become highly dangerous under conditions that mimic recreational use of MDMA at rave parties or other hot, crowded venues.

Indexed as

AnimalsBody TemperatureBrainDisease Models, AnimalDose-Response Relationship, DrugFeverHallucinogensInterpersonal RelationsLocomotionMuscle, SkeletalN-Methyl-3,4-methylenedioxyamphetamineNucleus AccumbensRatsRats, Long-EvansSkinVasoconstrictionHallucinogensN-Methyl-3,4-methylenedioxyamphetamineacute intoxicationbrain temperatureMDMAperipheral vasoconstrictionsocial interactionwarm environment

Identifiers

PMID24899699
PMCPMC4044242
OpenAlexW1969475346

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.