Evidence map›Paper›PMID 35016263›Full record

ArticleDevelopmental neurobiology2022

Influence of developmental nicotine exposure on serotonergic control of breathing-related motor output.

Lila Wollman, Andrew Hill, Brady Hasse, Christina Young, Giovanni Hernandez-De La Pena, Richard B Levine, Ralph F Fregosi

Open access · greenAbstract read
In one paragraph

Article in Developmental neurobiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 52% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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 1 institution in 1 country.

Lila WollmanDepartment of Physiology, University of Arizona College of Medicine, Tucson, Arizona, USA.
Andrew HillDepartment of Physiology, University of Arizona College of Medicine, Tucson, Arizona, USA.
Brady HasseDepartment of Neuroscience, University of Arizona, Tucson, Arizona, USA.
Christina YoungDepartment of Physiology, University of Arizona College of Medicine, Tucson, Arizona, USA.
Giovanni Hernandez-De La PenaDepartment of Physiology, University of Arizona College of Medicine, Tucson, Arizona, USA.
Richard B LevineDepartment of Physiology, University of Arizona College of Medicine, Tucson, Arizona, USA.
Ralph F FregosiDepartment of Physiology, University of Arizona College of Medicine, Tucson, Arizona, USA.ORCID 0000-0002-6849-7530
University of Arizona · US

Funding

Chronic nicotine and synaptic transmission in brainstem respiratory neuronsR01HD071302 · NICHD · UNIVERSITY OF ARIZONA · PI FREGOSI, RALPH FRANK · 2012 to 2022
$3.5M
NICHD NIH HHS R01 HD071302
6 · The paper itself

Abstract

Serotonin plays an important role in the development of brainstem circuits that control breathing. Here, we test the hypothesis that developmental nicotine exposure (DNE) alters the breathing-related motor response to serotonin (5HT). Pregnant rats were exposed to nicotine or saline, and brainstem-spinal cord preparations from 1- to 5-day-old pups were studied in a split-bath configuration, allowing drugs to be applied selectively to the medulla or spinal cord. The activity of the fourth cervical ventral nerve roots (C4VR), which contain axons of phrenic motoneurons, was recorded. We applied 5HT alone or together with antagonists of 5HT1A, 5HT2A, or 5HT7 receptor subtypes. In control preparations, 5HT applied to the medulla consistently reduced C4VR frequency and this reduction could not be blocked by any of the three antagonists. In DNE preparations, medullary 5HT caused a large and sustained frequency increase (10 min), followed by a sustained decrease. Notably, the transient increase in frequency could be blocked by the independent addition of any of the antagonists. Experiments with subtype-specific agonists suggest that the 5HT7 subtype may contribute to the increased frequency response in the DNE preparations. Changes in C4VR burst amplitude in response to brainstem 5HT were uninfluenced by DNE. Addition of 5HT to the caudal chamber modestly increased phasic and greatly increased tonic C4VR activity, but there were no effects of DNE. The data show that DNE alters serotonergic signaling within brainstem circuits that control respiratory frequency but does not functionally alter serotonin signaling in the phrenic motoneuron pool.

Indexed as

NicotinePrenatal Exposure Delayed EffectsAnimalsAnimals, NewbornFemalePregnancyRatsRats, Sprague-DawleySynaptic TransmissionNicotinebrainstemcontrol of breathingphrenic motoneuronserotonin receptorsspinal cord

Identifiers

PMID35016263
PMCPMC8940681
OpenAlexW4206818193

What OpenQuestion holds

Textmetadata
LicenceTDM
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.