Evidence map›Paper›PMID 17714791›Full record

ArticleJournal of neuroscience methods2007

Matching native electrical stimulation by graded chemical stimulation in isolated mouse adrenal chromaffin cells.

Tiberiu Fulop, Corey Smith

Open access · greenAbstract read
In one paragraph

Article in Journal of neuroscience methods, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

18 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Influence of Fimasartan (a Novel AT(1) Receptor Blocker) on Catecholamine Release in the Adrenal Medulla of Spontaneously Hypertensive Rats.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2013
    Article
  10. Review
  11. Article
  12. Article
  13. A Microfluidic Approach to Pulsatile Delivery of Drugs for Neurobiological Studies.Journal of microelectromechanical systems : a joint IEEE and ASME publication on microstructures, microactuators, microsensors, and microsystems · 2012
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Myosin II activation and actin reorganization regulate the mode of quantal exocytosis in mouse adrenal chromaffin cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2008
    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.

Tiberiu FulopDepartment of Physiology and Biophysics, School of Medicine, 2109 Adelbert Road, Case Western Reserve University, Cleveland, OH 44106-4970, USA. Tiberiu.Fulop@Case.Edu
Corey Smith
Case Western Reserve University · US

Funding

CLEVELAND TRAINING PROGRAM IN CARDIOVASCULAR RESEARCHT32HL007653 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI DUBYAK, GEORGE R · 1988 to 2008
$3.5M
Mechanisms of the adrenal medulla stress response.R01NS052123 · NINDS · CASE WESTERN RESERVE UNIVERSITY · PI SMITH, COREY B · 2005 to 2008
$1.2M
NHLBI NIH HHS T32 HL007653NHLBI NIH HHS T32HL07653NINDS NIH HHS 1R01NS052123NINDS NIH HHS R01 NS052123
6 · The paper itself

Abstract

Adrenal chromaffin cells release multiple transmitters in response to sympathetic stimulation. Modest cell firing, matching sympathetic tone, releases small freely soluble catecholamines. Elevated electrical firing rates matching input under sympathetic stress results in release of catecholamines as well as semi-soluble vaso- and neuro-active peptides packaged within the dense core of the secretory granule. This activity-dependent differential transmitter release has been shown to rely on a mechanistic shift in the mode of exocytosis through the regulated dilation of the secretory fusion pore between granule and cell surface membranes. However, biochemical description of the mechanism regulating fusion pore dilation remains elusive. In the experimental setting, electrical stimulation designed to mimic sympathetic input, is achieved through single-cell voltage-clamp. While precise, this approach is incompatible with biochemical and proteomic analysis, both of which require large sample sizes. We address this limitation in the current study. We describe a bulk chemical stimulation paradigm calibrated to match defined electrical activity. We utilize calcium and single-cell amperometric measurements to match extracellular potassium concentrations to physiological electrical stimulation under sympathetic tone as well as acute stress conditions. This approach provides larger samples of uniformly stimulated cells for determining molecular players in activity-dependent differential transmitter release from adrenal chromaffin cells.

Indexed as

Stimulation, ChemicalAction PotentialsAdrenal GlandsAnalysis of VarianceAnimalsCalciumCatecholaminesChromaffin CellsDose-Response Relationship, DrugDose-Response Relationship, RadiationElectric StimulationElectrochemistryMiceMice, Inbred C57BLPotassiumCalciumCatecholaminesPotassium

Identifiers

PMID17714791
PMCPMC2464294
OpenAlexW2013279676

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.