Evidence map›Paper›PMID 8860234›Full record

ArticleJournal of molecular neuroscience : MN1995

Human and monkey cholinergic neurons visualized in paraffin-embedded tissues by immunoreactivity for VAChT, the vesicular acetylcholine transporter.

M K Schafer, E Weihe, J D Erickson, L E Eiden

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Journal of molecular neuroscience : MN, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

20 citing papers in PubMed, 80 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Molecular Imaging of the Heart.Comprehensive Physiology · 2019
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. A novel population of cholinergic neurons in the macaque spinal dorsal horn of potential clinical relevance for pain therapy.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  13. Article
  14. Article
  15. Article
  16. Cholinergic modulation of spindle bursts in the neonatal rat visual cortex in vivo.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2007
    Article
  17. Article
  18. Elevation of nerve growth factor and antisense knockdown of TrkA receptor during contextual memory consolidation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2001
    Article
  19. Article
  20. 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

4 authors at 2 institutions in 2 countries.

M K SchaferDepartment of Anatomy and Cell Biology, Philipps University, Marburg, FRG.
E Weihe
J D Erickson
L E Eiden
National Institute of Mental Health · USPhilipps University of Marburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The predicted C-terminal dodecapeptide of the human vesicular acetylcholine transporter (VAChT), deduced from the unique open reading frame of the recently cloned human VAChT cDNA, was conjugated through an N-terminal cysteine to keyhole limpet hemocyanin and used as an immunogen to generate polyclonal antihuman VAChT antibodies in rabbits. The distribution of the VAChT antigen in representative regions of the cholinergic nervous system was examined and compared to that of the acetylcholine biosynthetic enzyme choline acetyltransferase (ChAT), a specific marker for cholinergic neurons. VAChT immunoreactivity was localized in cell bodies of neurons in the basal forebrain and ventral horn of the spinal cord, regions in which major cholinergic projection systems to the cerebral cortex and to skeletal muscle, respectively, originate. The primate caudate nucleus contained numerous VAChT-positive interneurons. VAChT immunoreactivity was visualized in both cell bodies and extensive terminals in striatal interneurons, in contrast to formalin-fixed, deparaffinized sections stained for ChAT, in which cell bodies and fibers were stained but nerve terminals were less well visualized than with the VAChT antiserum. VAChT-positive nerve fibers were visualized in routinely immersion-fixed, paraffin-embedded human cerebral cortex, comparable to the density of fibers observed in perfusion-fixed Bouin's-postfixed monkey cerebral cortex. Extensive investment of virtually all principal ganglion cells of thoracic sympathetic ganglia of monkey and human with VAChT-positive nerve terminals was observed. VAChT-positive cell bodies, presumably corresponding to cholinergic sympathetic sudomotor neurons, were a significant fraction of the total principal cell population in monkey and human thoracic sympathetic ganglia.

Indexed as

Membrane Transport ProteinsVesicular Transport ProteinsAcetylcholineAnimalsAntibody SpecificityCarrier ProteinsCholine O-AcetyltransferaseCholinergic FibersGanglia, SympatheticHumansImmunohistochemistryMacaca mulattaMaleMotor NeuronsNeuronsParaffin EmbeddingAcetylcholineCarrier ProteinsCholine O-AcetyltransferaseMembrane Transport ProteinsSLC18A3 protein, humanVesicular Acetylcholine Transport ProteinsVesicular Transport Proteins

Identifiers

PMID8860234
OpenAlexW2020664594

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.