Evidence map›Paper›PMID 28384162›Full record

ArticlePloS one2017

Responses of Nucleus Tractus Solitarius (NTS) early and late neurons to blood pressure changes in anesthetized F344 rats.

Jenya Kolpakova, Liang Li, Jeffrey T Hatcher, He Gu, Xueguo Zhang, Jin Chen, Zixi Jack Cheng

Abstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. The protective role of SOD1 overexpression in central mediation of bradycardia following chronic intermittent hypoxia in mice.American journal of physiology. Regulatory, integrative and comparative physiology · 2021
    Article
  4. 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

7 authors.

Jenya KolpakovaBurnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando FL, United States of America.
Liang LiBurnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando FL, United States of America.
Jeffrey T HatcherBurnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando FL, United States of America.
He GuBurnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando FL, United States of America.
Xueguo ZhangDepartment of Neurology, Henry Ford Hospital, Detroit, Michigan, United States of America.
Jin ChenBurnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando FL, United States of America.
Zixi Jack ChengBurnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando FL, United States of America.

Funding

Aging, Episodic Hypoxia, and Vagal Cardiac Projections.R01AG021020 · NIA · UNIVERSITY OF LOUISVILLE · PI CHENG, ZIXI JACK · 2003 to 2007
$1.7M
Chronic Intermittent Hypoxia: Sympathetic and Intrinsic Cardiac GanglionicInnervationR15HL137143 · NHLBI · UNIVERSITY OF CENTRAL FLORIDA · PI CHENG, ZIXI JACK · 2018 to 2018
$431k
NHLBI NIH HHS R15 HL137143NIA NIH HHS R01 AG021020
6 · The paper itself

Abstract

Previously, many different types of NTS barosensitive neurons were identified. However, the time course of NTS barosensitive neuronal activity (NA) in response to arterial pressure (AP) changes, and the relationship of NA-AP changes, have not yet been fully quantified. In this study, we made extracellular recordings of single NTS neurons firing in response to AP elevation induced by occlusion of the descending aorta in anesthetized rats. Our findings were that: 1) Thirty-five neurons (from 46 neurons) increased firing, whereas others neurons either decreased firing upon AP elevation, or were biphasic: first decreased firing upon AP elevation and then increased firing during AP decrease. 2) Fourteen neurons with excitatory responses were activated and rapidly increased their firing during the early phase of AP increase (early neurons); whereas 21 neurons did not increase firing until the mean arterial pressure changes (ΔMAP) reached near/after the peak (late neurons). 3) The early neurons had a significantly higher firing rate than late neurons during AP elevation at a similar rate. 4) Early neuron NA-ΔMAP relationship could be well fitted and characterized by the sigmoid logistic function with the maximal gain of 29.3. 5) The increase of early NA correlated linearly with the initial heart rate (HR) reduction. 6) The late neurons did not contribute to the initial HR reduction. However, the late NA could be well correlated with HR reduction during the late phase. Altogether, our study demonstrated that the NTS excitatory neurons could be grouped into early and late neurons based on their firing patterns. The early neurons could be characterized by the sigmoid logistic function, and different neurons may differently contribute to HR regulation. Importantly, the grouping and quantitative methods used in this study may provide a useful tool for future assessment of functional changes of early and late neurons in disease models.

Indexed as

Blood PressureAction PotentialsAnimalsMaleNeuronsRatsRats, Inbred F344Solitary Nucleus

Identifiers

PMID28384162
PMCPMC5383029

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Registered trials

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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.