Evidence map›Paper›PMID 17100844›Full record

ArticleThe European journal of neuroscience2006

Mechanism of progesterone neuroprotection of rat cerebellar Purkinje cells following oxygen-glucose deprivation.

A Ardeshiri, M H Kelley, I P Korner, P D Hurn, P S Herson

Open access · greenAbstract read
In one paragraph

Article in The European journal of neuroscience, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
1.9field-weighted citation impact, top 17% 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

45 citing papers in PubMed, 84 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Progesterone: The Key Factor of the Beginning of Life.International journal of molecular sciences · 2022
    Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. A Light-Controlled Allosteric Modulator Unveils a Role for mGluFrontiers in cellular neuroscience · 2018
    Article
  17. Article
  18. Article
  19. Review
  20. Progesterone treatment in two rat models of ocular ischemia.Investigative ophthalmology & visual science · 2015
    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 1 institution in 1 country.

A ArdeshiriDepartment of Anesthesioloy and Peri-Operative Medicine, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97201, USA.
M H Kelley
I P Korner
P D Hurn
P S Herson
Oregon Health & Science University · US

Funding

GABA-A Receptor Rescue as a Neuroprotective Strategy in Cerebral IschemiaR01NS058792 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI ADELMAN, JOHN P · 2007 to 2011
$1.8M
Sex differences in Purkinje cell sensitivity to ischemiaR21NS052591 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI HERSON, PACO S · 2005 to 2006
$402k
NINDS NIH HHS 1 R21 NS052591NINDS NIH HHS R01 NS058792NINDS NIH HHS R21 NS052591
6 · The paper itself

Abstract

The survival of rat Purkinje cell (PCs) cerebellar cultures was used to test the hypothesis that progesterone is protective against oxygen-glucose deprivation through potentiation of GABA(A) receptor activity. Electrophysiological recordings confirm that PCs develop robust excitatory and inhibitory synapses in culture. Exposure of cultured PCs to increasing concentrations of progesterone during oxygen-glucose deprivation revealed a concentration-dependent protection by progesterone, with significant protection observed at physiological concentrations, as low as 10 nm. The concurrent application of the GABA(A) receptor antagonist picrotoxin (100 microm) completely abolished the neuroprotection afforded by progesterone, indicating that progesterone is neuroprotective through activation of GABA(A) receptors. Progesterone potentiates GABA(A) receptor activity indirectly through its metabolites, such as allopregnanolone (ALLO). Therefore, ALLO was applied to PC cultures and was observed to produce significant protection at all concentrations tested, from 10 to 1000 nm. Finally, the inhibition of progesterone metabolism with finasteride abolished the protection afforded by progesterone without having any effect on the neuroprotection caused by ALLO. These data indicate that progesterone protects cerebellar PCs at physiological concentrations through a GABA-active metabolite.

Indexed as

AnimalsApoptosisCell HypoxiaCells, CulturedCerebellumExcitatory Postsynaptic PotentialsFemaleGlucoseHypoxia-Ischemia, BrainImmunohistochemistryIn Situ Nick-End LabelingMaleOxygenPatch-Clamp TechniquesProgesteronePurkinje CellsGlucoseOxygenProgesterone

Identifiers

PMID17100844
PMCPMC2831653
OpenAlexW1525886046

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.