Evidence map›Paper›PMID 8987781›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience1997

Heterogeneity of nicotinic receptor class and subunit mRNA expression among individual parasympathetic neurons from rat intracardiac ganglia.

K Poth, T J Nutter, J Cuevas, M J Parker, D J Adams, C W Luetje

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

34 citing papers in PubMed, 121 citations in OpenAlex.

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  12. Quantitative biology of single neurons.Journal of the Royal Society, Interface · 2012
    Review
  13. AT-1001: a high affinity and selective α3β4 nicotinic acetylcholine receptor antagonist blocks nicotine self-administration in rats.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2012
    Article
  14. Article
  15. Review
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  18. Article
  19. Feasibility of 2-deoxy-2-[18F]fluoro-D-glucose- A85380-PET for imaging of human cardiac nicotinic acetylcholine receptors in vivo.Clinical research in cardiology : official journal of the German Cardiac Society · 2006
    Article
  20. Selective modulation of neuronal nicotinic acetylcholine receptor channel subunits by Go-protein subunits.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2005
    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

6 authors at 1 institution in 1 country.

K PothDepartment of Molecular and Cellular Pharmacology, University of Miami School of Medicine, Florida 33101, USA.
T J Nutter
J Cuevas
M J Parker
D J Adams
C W Luetje
University of Miami · US

Funding

BINDING SITE STRUCTURE OF NEURONAL NICOTINIC RECEPTORSR01DA008102 · NIDA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI LUETJE, CHARLES WARD · 1994 to 2002
$963k
IONIC BASIS OF EXCITABILITY IN INTRINSIC CARDIAC NEURONSR01HL035422 · NHLBI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ADAMS, DAVID J · 1986 to 1995
–
NHLBI NIH HHS HL35422NIDA NIH HHS DA08102NIDA NIH HHS R01 DA008102
6 · The paper itself

Abstract

Neurons have the potential to form thousands of distinct neuronal nicotinic receptors from the eight alpha and three beta subunits that currently are known. In an effort to determine how much of this potential complexity is realized among individual neurons, we examined the nicotinic pharmacological and biophysical properties and receptor subunit mRNA expression patterns in individual neurons cultured from rat epicardial ganglia. Analysis of the whole-cell pharmacology of these neurons showed a diversity of responses to the agonists acetylcholine, nicotine, cytisine, and 1,1-dimethyl-4-phenylpiperazinium, suggesting that a heterogeneous population of nicotinic receptor classes, or subtypes, is expressed by individual neurons. Single-channel analysis demonstrated three distinct conductances (18, 24, and 31 pS), with patches from different neurons containing different combinations of these channel classes. We used single-cell RT-PCR to examine nicotinic acetylcholine receptor (nAChR) subunit mRNA expression by individual neurons. Although mRNAs encoding all eight neuronal nAChR subunits for which we probed (alpha 2-alpha 5, alpha 7, beta 2-beta 4) were present in multicellular cultures, we found that individual epicardial neurons express distinct subsets of these nAChR subunit mRNAs. These results suggest that individual epicardial neurons express distinct arrays of nAChR subunits and that these subunits may assemble into functional receptors with distinct and variable subunit composition. This variable receptor subunit expression provides an explanation for the diversity of pharmacological and single-channel responses we have observed in individual neurons.

Indexed as

Action PotentialsAnimalsGanglia, ParasympatheticGene Expression RegulationHeartHeart AtriaNerve Tissue ProteinsNeuronsNicotinic AgonistsNicotinic AntagonistsPatch-Clamp TechniquesPolymerase Chain ReactionProtein ConformationRatsReceptors, NicotinicRNA, MessengerNerve Tissue ProteinsNicotinic AgonistsNicotinic AntagonistsReceptors, NicotinicRNA, Messenger

Identifiers

PMID8987781
PMCPMC6573231
OpenAlexW2130456914

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.