Evidence map›Paper›PMID 16723535›Full record

Trial reportThe Journal of neuroscience : the official journal of the Society for Neuroscience2006

Pronociceptive and antinociceptive effects of estradiol through endogenous opioid neurotransmission in women.

Yolanda R Smith, Christian S Stohler, Thomas E Nichols, Joshua A Bueller, Robert A Koeppe, Jon-Kar Zubieta

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 142 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
142citing papers in PubMed, 3 pooled it
13.1field-weighted citation impact, top 1% 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

142 citing papers in PubMed, 3 syntheses or guidelines pooled it, 378 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Stress and pain: modality-specific opioid mediation of stress-induced analgesia.Journal of neural transmission (Vienna, Austria : 1996) · 2021
    Trial
  7. Trial
  8. Trial
  9. Trial
  10. Trial
  11. Trial
  12. Trial
  13. Trial
  14. Trial
  15. Trial
  16. Trial
  17. Article
  18. Review
  19. Review
  20. Article

82 more citing papers are in PubMed but not listed here.

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

6 authors at 3 institutions in 2 countries.

Yolanda R SmithDivision of Reproductive Endocrinology, Department of Obstetrics and Gynecology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Christian S Stohler
Thomas E Nichols
Joshua A Bueller
Robert A Koeppe
Jon-Kar Zubieta
University of Michigan–Ann Arbor · USNeuroscience Institute · ITUniversity of Maryland, Baltimore · US

Funding

Neurochemical Endophenotype Responses to Pain-StressR01DA016423 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZUBIETA, JON-KAR · 2004 to 2007
$1.4M
Neurochemical mediation of placebo responses in humansR01AT001415 · NCCIH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZUBIETA, JON-KAR · 2003 to 2006
$1.2M
NEUROBIOLOGICAL EFFECT OF LONG-TERM ESTROGEN REPLACEMENTK23RR017043 · NCRR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SMITH, YOLANDA R · 2002 to 2006
$672k
NCCIH NIH HHS R01 AT 001415NCRR NIH HHS K23 RR017043NCRR NIH HHS K23 RR 17043NIDA NIH HHS R01 DA 016423
6 · The paper itself

Abstract

Prominent interindividual and sex-dependent differences have been described in responses to sustained pain and other stressful stimuli. Variations in mu-opioid receptor-mediated endogenous opioid neurotransmission may underlie some of these processes. We examined both baseline mu-opioid receptor levels and the activation of this neurotransmitter system during sustained pain using positron emission tomography in a sample of young healthy men and women. Women were studied twice, during low and high estrogen states. The high-estrogen state was associated with regional increases in baseline mu-opioid receptor availability in vivo and a greater activation of endogenous opioid neurotransmission during the pain stressor. The latter did not differ from that obtained in males. During the low estrogen condition, however, significant reductions in endogenous opioid tone were observed at the level of thalamus, nucleus accumbens, and amygdala, which were associated with hyperalgesic responses. Estrogen-associated variations in the activity of mu-opioid neurotransmission correlated with individual ratings of the sensory and affective perceptions of the pain and the subsequent recall of that experience. These data demonstrate a significant role of estrogen in modulating endogenous opioid neurotransmission and associated psychophysical responses to a pain stressor in humans.

Indexed as

AdultAnalgesicsBrainEstradiolFemaleHumansMaleNarcoticsPainReceptors, Opioid, muSex FactorsSynaptic TransmissionAnalgesicsEstradiolNarcoticsReceptors, Opioid, mu

Identifiers

PMID16723535
PMCPMC1808228
OpenAlexW2023731184

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.