Evidence map›Paper›PMID 27168363›Full record

ArticleAging cell2016

Deterioration of autonomic neuronal receptor signaling and mechanisms intrinsic to heart pacemaker cells contribute to age-associated alterations in heart rate variability in vivo.

Yael Yaniv, Ismayil Ahmet, Kenta Tsutsui, Joachim Behar, Jack M Moen, Yosuke Okamoto, Toni-Rose Guiriba, Jie Liu, Rostislav Bychkov, Edward G Lakatta

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

35 citing papers in PubMed, 52 citations in OpenAlex.

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  13. Loss of Natriuretic Peptide Receptor C Enhances Sinoatrial Node Dysfunction in Aging and Frail Mice.The journals of gerontology. Series A, Biological sciences and medical sciences · 2022
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  16. Increase in CaFrontiers in physiology · 2022
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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

10 authors at 3 institutions in 2 countries.

Yael YanivBiomedical Engineering Faculty, Technion-IIT, Haifa, Israel.
Ismayil AhmetLaboratory of Cardiovascular Science, Biomedical Research Center, Intramural Research Program, National Institute on Aging, NIH, Baltimore, MD, USA.
Kenta TsutsuiLaboratory of Cardiovascular Science, Biomedical Research Center, Intramural Research Program, National Institute on Aging, NIH, Baltimore, MD, USA.
Joachim BeharBiomedical Engineering Faculty, Technion-IIT, Haifa, Israel.
Jack M MoenLaboratory of Cardiovascular Science, Biomedical Research Center, Intramural Research Program, National Institute on Aging, NIH, Baltimore, MD, USA.
Yosuke OkamotoLaboratory of Cardiovascular Science, Biomedical Research Center, Intramural Research Program, National Institute on Aging, NIH, Baltimore, MD, USA.
Toni-Rose GuiribaLaboratory of Cardiovascular Science, Biomedical Research Center, Intramural Research Program, National Institute on Aging, NIH, Baltimore, MD, USA.
Jie LiuLaboratory of Cardiovascular Science, Biomedical Research Center, Intramural Research Program, National Institute on Aging, NIH, Baltimore, MD, USA.
Rostislav BychkovLaboratory of Cardiovascular Science, Biomedical Research Center, Intramural Research Program, National Institute on Aging, NIH, Baltimore, MD, USA.
Edward G LakattaLaboratory of Cardiovascular Science, Biomedical Research Center, Intramural Research Program, National Institute on Aging, NIH, Baltimore, MD, USA.
Institute on Aging · USNational Institute on Aging · USTechnion – Israel Institute of Technology · IL

Funding

Baltimore Longitudinal Study of Mice AgingZIAAG000298 · NIA · NATIONAL INSTITUTE ON AGING · PI LAKATTA, EDWARD · 2016 to 2025
$1.2M
CLINICAL PROJECT: Biomarkers of Cardiovascular AgingZIAAG000891 · NIA · NATIONAL INSTITUTE ON AGING · PI LAKATTA, EDWARD · 2016 to 2025
$740k
6 · The paper itself

Abstract

We aimed to determine how age-associated changes in mechanisms extrinsic and intrinsic to pacemaker cells relate to basal beating interval variability (BIV) reduction in vivo. Beating intervals (BIs) were measured in aged (23-25 months) and adult (3-4 months) C57BL/6 male mice (i) via ECG in vivo during light anesthesia in the basal state, or in the presence of 0.5 mg mL(-1) atropine + 1 mg mL(-1) propranolol (in vivo intrinsic conditions), and (ii) via a surface electrogram, in intact isolated pacemaker tissue. BIV was quantified in both time and frequency domains using linear and nonlinear indices. Although the average basal BI did not significantly change with age under intrinsic conditions in vivo and in the intact isolated pacemaker tissue, the average BI was prolonged in advanced age. In vivo basal BIV indices were found to be reduced with age, but this reduction diminished in the intrinsic state. However, in pacemaker tissue BIV indices increased in advanced age vs. adults. In the isolated pacemaker tissue, the sensitivity of the average BI and BIV in response to autonomic receptor stimulation or activation of mechanisms intrinsic to pacemaker cells by broad-spectrum phosphodiesterase inhibition declined in advanced age. Thus, changes in mechanisms intrinsic to pacemaker cells increase the average BIs and BIV in the mice of advanced age. Autonomic neural input to pacemaker tissue compensates for failure of molecular intrinsic mechanisms to preserve average BI. But this compensation reduces the BIV due to both the imbalance of autonomic neural input to the pacemaker cells and altered pacemaker cell responses to neural input.

Indexed as

AgingAnimalsAutonomic Nervous SystemCarbacholHeart RateIsoproterenolLongevityMice, Inbred C57BLNeuronsPacemaker, ArtificialPhosphodiesterase InhibitorsReceptors, Adrenergic, betaReceptors, Cell SurfaceSinoatrial NodeCarbacholIsoproterenolPhosphodiesterase InhibitorsReceptors, Adrenergic, betaReceptors, Cell Surfaceautonomic neural impulseschaotic systemsheart rate variabilityintrinsic heart ratepacemaker cellssinoatrial nodal

Identifiers

PMID27168363
PMCPMC4933656
OpenAlexW2383759838

What OpenQuestion holds

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LicenceCC BY
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.