Evidence map›Paper›PMID 16973697›Full record

ArticleThe Journal of physiology2006

Inactivation of nitric oxide by rat cerebellar slices.

C N Hall, J Garthwaite

Abstract read
In one paragraph

Article in The Journal of physiology, 2006. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. NChemical biology & drug design · 2019
    Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Nitric oxide donors enhance the frequency dependence of dopamine release in nucleus accumbens.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2011
    Article
  14. Article
  15. Article
  16. Article
  17. What is the real physiological NO concentration in vivo?Nitric oxide : biology and chemistry · 2009
    Review
  18. Article
  19. Article
  20. Concepts of neural nitric oxide-mediated transmission.The European journal of neuroscience · 2008
    Review
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.

C N HallWolfson Institute for Biomedical Research, University College London, Cruciform Building, Gower Street, London WC1E 6BT, UK. catherine.hall@ucl.ac.uk
J Garthwaite

Funding

Wellcome Trust
6 · The paper itself

Abstract

Nitric oxide (NO) functions as an intercellular messenger throughout the brain. For this role to be performed efficiently, there must be a mechanism for neutralizing NO, but whether an active biological process exists, or whether NO is lost mainly through diffusion is unclear. To investigate this issue, rat cerebellar slices were exposed to constant levels of NO and the cGMP generated within the slice used as an indicator of NO concentrations therein. NO was about 1000-fold less potent in slices (EC50, 1 microM) than in separated cells from the same tissue (EC50, 1.6 nM), consistent with access of NO to the slice interior being greatly hindered by inactivation. Supporting this interpretation, immunohistochemical analysis indicated a marked concentration gradient of cGMP across the thickness of slices exposed to subsaturating NO concentrations, signifying a marked NO gradient. Several known NO-degrading processes, including reaction with lipid peroxyl radicals, erythrocytes and superoxide ions, were eliminated as contributing factors, indicating a novel mechanism. A diffusion-inactivation model was used to estimate the kinetics of NO consumption by the slices. The best fits to experimental data indicated a Michaelis-Menten-type reaction having a Vmax of 1-2 microM s-1 and a Km of around 10 nM. The rates predict that inactivation would impose a very short half-life (<10 ms) on NO in physiological concentrations (up to 10 nM) and that it would play an important role in shaping the NO concentration profiles when it is synthesized by multiple nearby sites.

Indexed as

Signal TransductionAnimalsAntioxidantsCerebellumCyclic GMPCyclooxygenase InhibitorsDiethylaminesDiffusionDose-Response Relationship, DrugEnzyme InhibitorsErythrocytesHalf-LifeIn Vitro TechniquesKineticsLipid PeroxidationLipoxygenase InhibitorsAntioxidantsCyclic GMPCyclooxygenase Inhibitorsdiethylamine dinitric oxide adductDiethylaminesEnzyme InhibitorsLipoxygenase InhibitorsNitric OxideNitric Oxide DonorsNitric Oxide SynthaseSperminespermine nitric oxide complexSuperoxides

Identifiers

PMID16973697
PMCPMC1890435

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.