Evidence map›Paper›PMID 18310125›Full record

ArticleThe Journal of experimental biology2008

A newly identified extrinsic input triggers a distinct gastric mill rhythm via activation of modulatory projection neurons.

Dawn M Blitz, Rachel S White, Shari R Saideman, Aaron Cook, Andrew E Christie, Farzan Nadim, Michael P Nusbaum

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

43 citing papers in PubMed, 62 citations in OpenAlex.

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  11. Neuronal Switching between Single- and Dual-Network Activity via Modulation of Intrinsic Membrane Properties.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
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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

7 authors at 3 institutions in 1 country.

Dawn M BlitzDepartment of Neuroscience, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.
Rachel S White
Shari R Saideman
Aaron Cook
Andrew E Christie
Farzan Nadim
Michael P Nusbaum
University of Pennsylvania · USMount Desert Island Biological Laboratory · USNew Jersey Institute of Technology · US

Funding

REGULATION OF NEURONAL OSCILLATIONS BY SYNAPTIC DYNAMICSR01MH060605 · NIMH · NEW JERSEY INSTITUTE OF TECHNOLOGY · PI Dirk Martin Bucher, Farzan Nadim · 2001 to 2026
$6.6M
Motor pattern selection from a multifunctional motor circuitR01NS042813 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI NUSBAUM, MICHAEL P · 2002 to 2009
$2.6M
NIMH NIH HHS R01 MH060605NINDS NIH HHS NS42813NINDS NIH HHS R01 NS042813
6 · The paper itself

Abstract

Neuronal network flexibility enables animals to respond appropriately to changes in their internal and external states. We are using the isolated crab stomatogastric nervous system to determine how extrinsic inputs contribute to network flexibility. The stomatogastric system includes the well-characterized gastric mill (chewing) and pyloric (filtering of chewed food) motor circuits in the stomatogastric ganglion. Projection neurons with somata in the commissural ganglia (CoGs) regulate these rhythms. Previous work characterized a unique gastric mill rhythm that occurred spontaneously in some preparations, but whose origin remained undetermined. This rhythm includes a distinct protractor phase activity pattern, during which a key gastric mill circuit neuron (LG neuron) and the projection neurons MCN1 and CPN2 fire in a pyloric rhythm-timed activity pattern instead of the tonic firing pattern exhibited by these neurons during previously studied gastric mill rhythms. Here we identify a new extrinsic input, the post-oesophageal commissure (POC) neurons, relatively brief stimulation (30 s) of which triggers a long-lasting (tens of minutes) activation of this novel gastric mill rhythm at least in part via its lasting activation of MCN1 and CPN2. Immunocytochemical and electrophysiological data suggest that the POC neurons excite MCN1 and CPN2 by release of the neuropeptide Cancer borealis tachykinin-related peptide Ia (CabTRP Ia). These data further suggest that the CoG arborization of the POC neurons comprises the previously identified anterior commissural organ (ACO), a CabTRP Ia-containing neurohemal organ. This endocrine organ thus appears to also have paracrine actions, including activation of a novel and lasting gastric mill rhythm.

Indexed as

AnimalsBrachyuraElectric StimulationEnteric Nervous SystemIn Vitro TechniquesMaleMasticationModels, NeurologicalNeuronsNeuropeptidesStomachNeuropeptides

Identifiers

PMID18310125
PMCPMC2430018
OpenAlexW2167488505

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.