Evidence map›Paper›PMID 10725368›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2000

Antagonists of alcohol inhibition of cell adhesion.

M F Wilkemeyer, A B Sebastian, S A Smith, M E Charness

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
12.8field-weighted citation impact, top 2% 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

23 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Mitogen-activated protein kinase modulates ethanol inhibition of cell adhesion mediated by the L1 neural cell adhesion molecule.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  9. L1 cell adhesion molecule signaling is inhibited by ethanol in vivo.Alcoholism, clinical and experimental research · 2013
    Article
  10. Article
  11. Article
  12. Article
  13. Ethanol's molecular targets.Science signaling · 2008
    Review
  14. An alcohol binding site on the neural cell adhesion molecule L1.Proceedings of the National Academy of Sciences of the United States of America · 2008
    Article
  15. A systems-based computational model of alcohol's toxic effects on brain development.Alcohol research & health : the journal of the National Institute on Alcohol Abuse and Alcoholism · 2008
    Review
  16. Article
  17. Article
  18. Article
  19. Linking acquired neurodevelopmental disorders to defects in cell adhesion.Proceedings of the National Academy of Sciences of the United States of America · 2003
    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

4 authors at 3 institutions in 1 country.

M F WilkemeyerNeurology Service, Veterans Affairs Boston Healthcare System, West Roxbury, MA 02132, USA.
A B Sebastian
S A Smith
M E Charness
Harvard University · USBrigham and Women's Hospital · USVA Boston Healthcare System · US

Funding

ALCOHOL INHIBITION OF NEURONAL CELL ADHESIONR01AA009669 · NIAAA · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI CHARNESS, MICHAEL EDWARD · 1994 to 1997
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ALCOHOL INTERACTION WITH L1 CELL ADHESION MOLECULER01AA011297 · NIAAA · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI CHARNESS, MICHAEL EDWARD · 1997 to 1999
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NIAAA NIH HHS AA09669NIAAA NIH HHS AA11297
6 · The paper itself

Abstract

Increasing evidence suggests that alcohols act within specific binding pockets of selective neural proteins; however, antagonists at these sites have not been identified. 1-Alcohols from methanol through 1-butanol inhibit with increasing potency the cell-cell adhesion mediated by the immunoglobulin cell adhesion molecule L1. An abrupt cutoff exists after 1-butanol, with 1-pentanol and higher 1-alcohols showing no effect. Here, we demonstrate surprisingly strict structural requirements for alcohol inhibition of cell-cell adhesion in L1-transfected NIH 3T3 fibroblasts and in NG108-15 neuroblastoma x glioma hybrid cells treated with BMP-7, an inducer of L1 and neural cell adhesion molecule. The target site discriminates the tertiary structure of straight-chain and branched-chain alcohols and appears to comprise both a hydrophobic binding site and an adjacent hydrophilic allosteric site. Modifications to the 2- and 3-carbon positions of 1-butanol increased potency, whereas modifications that restrict movement about the 4-carbon abolished activity. The effects of ethanol and 1-butanol on cell-cell adhesion were antagonized by 1-pentanol (IC(50) = 715 microM) and 1-octanol (IC(50) = 3.6 microM). Antagonism by 1-octanol was complete, reversible, and noncompetitive. 1-Octanol also antagonized ethanol inhibition of BMP-7 morphogenesis in NG108-15 cells. 1-Octanol and related compounds may prove useful in dissecting the role of altered cell adhesion in ethanol-induced injury of the nervous system.

Indexed as

Transforming Growth Factor beta3T3 CellsAlcoholsAnimalsBone Morphogenetic Protein 7Bone Morphogenetic ProteinsCell AdhesionMiceMolecular StructureStructure-Activity RelationshipAlcoholsBone Morphogenetic Protein 7Bone Morphogenetic ProteinsTransforming Growth Factor beta

Identifiers

PMID10725368
PMCPMC16301
OpenAlexW2061163550

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.