Evidence map›Paper›PMID 18309234›Full record

ArticleNeuroendocrinology2008

The recreational drug ecstasy disrupts the hypothalamic-pituitary-gonadal reproductive axis in adult male rats.

Sarah M Dickerson, Deena M Walker, Maria E Reveron, Christine L Duvauchelle, Andrea C Gore

Open access · bronzeAbstract readEvaluation Study
In one paragraph

Article in Neuroendocrinology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 27% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Psychoactive drugs and male fertility: impacts and mechanisms.Reproductive biology and endocrinology : RB&E · 2023
    Review
  7. Article
  8. Article
  9. Substance Abuse and Male Hypogonadism.Journal of clinical medicine · 2019
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
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.

Sarah M DickersonDivision of Pharmacology and Toxicology, The University of Texas at Austin, Austin, Tex. 78712-0125, USA.
Deena M Walker
Maria E Reveron
Christine L Duvauchelle
Andrea C Gore
Society for Neuroscience · USThe University of Texas at Austin · US

Funding

Training in Molecular Toxicology/Environmental DiseaseT32ES007247 · NIEHS · UNIVERSITY OF TEXAS AUSTIN · PI RICHBURG, JOHN H · 1990 to 2014
$2.9M
Cocaine &Brain: Progressive Changes in Behavior/DA/FosR01DA014640 · NIDA · UNIVERSITY OF TEXAS AUSTIN · PI DUVAUCHELLE, CHRISTINE LEILANI · 2003 to 2009
$1.3M
Neuroendocrine outcomes of prenatal PCB exposuresR21ES012272 · NIEHS · UNIVERSITY OF TEXAS AUSTIN · PI GORE, ANDREA C · 2003 to 2005
$419k
NIDA NIH HHS DA14640NIDA NIH HHS R01 DA014640NIEHS NIH HHS ES012272NIEHS NIH HHS R21 ES012272NIEHS NIH HHS T32 ES007247NIEHS NIH HHS T32 ES07247
6 · The paper itself

Abstract

Reproductive function involves an interaction of three regulatory levels: hypothalamus, pituitary, and gonad. The primary drive upon this system comes from hypothalamic gonadotropin-releasing hormone (GnRH) neurosecretory cells, which receive afferent inputs from other neurotransmitter systems in the central nervous system to result in the proper coordination of reproduction and the environment. Here, we hypothesized that the recreational drug (+/-)-3,4-methylenedioxymethamphetamine (MDMA; 'ecstasy'), which acts through several of the neurotransmitter systems that affect GnRH neurons, suppresses the hypothalamic-pituitary-gonadal reproductive axis of male rats. Adult male Sprague-Dawley rats self-administered saline or MDMA either once (acute) or for 20 days (chronic) and were euthanized 7 days following the last administration. We quantified hypothalamic GnRH mRNA, serum luteinizing hormone concentrations, and serum testosterone levels as indices of hypothalamic, pituitary, and gonadal functions, respectively. The results indicate that the hypothalamic and gonadal levels of the hypothalamic-pituitary-gonadal axis are significantly altered by MDMA, with GnRH mRNA and serum testosterone levels suppressed in rats administered MDMA compared to saline. Furthermore, our finding that hypothalamic GnRH mRNA levels are suppressed in the context of low testosterone concentrations suggests that the central GnRH neurosecretory system may be a primary target of inhibitory regulation by MDMA usage.

Indexed as

AnimalsEndocrine DisruptorsGene ExpressionGonadotropin-Releasing HormoneHypothalamic DiseasesHypothalamo-Hypophyseal SystemHypothalamusIllicit DrugsLuteinizing HormoneMaleN-Methyl-3,4-methylenedioxyamphetamineOrgan SizeRatsRats, Sprague-DawleyReproductionTestisEndocrine DisruptorsGonadotropin-Releasing HormoneIllicit DrugsLuteinizing HormoneN-Methyl-3,4-methylenedioxyamphetamineTestosterone

Identifiers

PMID18309234
PMCPMC2753463
OpenAlexW2022566604

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.