Evidence map›Paper›PMID 12032350›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2002

Opposing actions of adrenal androgens and glucocorticoids on alternative splicing of Slo potassium channels in bovine chromaffin cells.

Guey-Jen Lai, David P McCobb

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.2field-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

22 citing papers in PubMed, 60 citations in OpenAlex.

  1. Large conductance voltage-and calcium-activated KFrontiers in pharmacology · 2024
    Review
  2. Calcium- and voltage-gated BK channels in vascular smooth muscle.Pflugers Archiv : European journal of physiology · 2018
    Review
  3. Large-conductance CaThe Journal of physiology · 2017
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Hypertension of Kcnmb1-/- is linked to deficient K secretion and aldosteronism.Proceedings of the National Academy of Sciences of the United States of America · 2009
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Age-dependent regulation of chromaffin cell proliferation by growth factors, dehydroepiandrosterone (DHEA), and DHEA sulfate.Proceedings of the National Academy of Sciences of the United States of America · 2007
    Article
  20. 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

2 authors at 1 institution in 1 country.

Guey-Jen LaiDepartment of Neurobiology and Behavior, Cornell University, Ithaca, NY 14853, USA.
David P McCobb
Cornell University · US

Funding

REGULATION OF CELLULAR EXCITABILITY BY STRESS HORMONESR01NS040790 · NINDS · CORNELL UNIVERSITY ITHACA · PI MCCOBB, DAVID P · 2000 to 2003
$1.1M
NINDS NIH HHS R01 NS040790NINDS NIH HHS R01 NS40790
6 · The paper itself

Abstract

Pituitary ablation (hypophysectomy) in rats was previously reported to cause a precipitous change in the relative abundance of two alternative splice variants of the "BK"- or "Maxi K"-encoding Slo gene in adrenal chromaffin cells. Inclusion of the optional "STREX" exon (STRess axis-regulated EXon) in a C-terminal splice site was reduced, in preference to the variant lacking an insert at this site. Adrenocorticotropic hormone (ACTH) injections prevented the drop in STREX inclusion, implicating stress-axis function, as opposed to other pituitary functions. Because ACTH promotes synthesis and release of glucocorticoids (corticosterone or cortisol, depending on species), we hypothesized that glucocorticoids applied directly would promote STREX inclusion. Contrary to predictions, we report that direct application of glucocorticoids to bovine cells in vitro decreased STREX inclusion. This effect was blocked by the glucocorticoid receptor antagonist RU38486. As with glucocorticoids, synthesis and release of the adrenal androgen dehydroepiandrosterone (DHEA) increases in response to stress or elevated ACTH levels in some species. We report that direct application of DHEA increased expression of the STREX variant in cultured bovine cells. Two other androgens, androstenedione and testosterone, had similar effects. We hypothesize that Slo splicing in adrenal chromaffin cells in vivo is differentially regulated by the integrative, concentration- and time-dependent actions of glucocorticoids and androgens, with potentially important ramifications for stress-evoked catecholamine secretion.

Indexed as

Alternative SplicingAdrenal MedullaAndrogensAnimalsCattleCells, CulturedChromaffin CellsDehydroepiandrosteroneDexamethasoneDNA PrimersGenetic VariationGlucocorticoidsKineticsLarge-Conductance Calcium-Activated Potassium ChannelsMifepristonePotassium Channels, Calcium-ActivatedAndrogensDehydroepiandrosteroneDexamethasoneDNA PrimersGlucocorticoidsLarge-Conductance Calcium-Activated Potassium ChannelsMifepristonePotassium Channels, Calcium-Activated

Identifiers

PMID12032350
PMCPMC124333
OpenAlexW2011608196

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.