Evidence map›Paper›PMID 34875198›Full record

ArticleProceedings. Biological sciences2021

Prenatal acoustic programming of mitochondrial function for high temperatures in an arid-adapted bird.

Eve Udino, Julia M George, Matthew McKenzie, Anaïs Pessato, Ondi L Crino, Katherine L Buchanan, Mylene M Mariette

Open access · hybridAbstract read
In one paragraph

Article in Proceedings. Biological sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

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  11. Neurobiology and Changing Ecosystems: Mechanisms Underlying Responses to Human-Generated Environmental Impacts.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
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  14. Plasticity of mitochondrial function safeguards phosphorylating respiration during in vitro simulation of rest-phase hypothermia.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
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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 2 institutions in 3 countries.

Eve UdinoSchool of Life and Environmental Sciences, Deakin University, Waurn Ponds, Victoria 3288, Australia.ORCID 0000-0002-9794-2795
Julia M GeorgeDepartment of Biological Sciences, Clemson University, Clemson, SC 29634, USA.ORCID 0000-0001-6194-6914
Matthew McKenzieSchool of Life and Environmental Sciences, Deakin University, Waurn Ponds, Victoria 3288, Australia.ORCID 0000-0001-7508-1800
Anaïs PessatoSchool of Life and Environmental Sciences, Deakin University, Waurn Ponds, Victoria 3288, Australia.ORCID 0000-0002-9694-2013
Ondi L CrinoSchool of Life and Environmental Sciences, Deakin University, Waurn Ponds, Victoria 3288, Australia.ORCID 0000-0001-5700-1387
Katherine L BuchananSchool of Life and Environmental Sciences, Deakin University, Waurn Ponds, Victoria 3288, Australia.ORCID 0000-0002-6648-5819
Mylene M MarietteSchool of Life and Environmental Sciences, Deakin University, Waurn Ponds, Victoria 3288, Australia.ORCID 0000-0003-0567-4111
Deakin University · AUClemson University · US

Funding

Biotechnology and Biological Sciences Research Council BB/S003223/1
6 · The paper itself

Abstract

Sound is an essential source of information in many taxa and can notably be used by embryos to programme their phenotypes for postnatal environments. While underlying mechanisms are mostly unknown, there is growing evidence for the involvement of mitochondria-main source of cellular energy (i.e. ATP)-in developmental programming processes. Here, we tested whether prenatal sound programmes mitochondrial metabolism. In the arid-adapted zebra finch, prenatal exposure to 'heat-calls'-produced by parents incubating at high temperatures-adaptively alters nestling growth in the heat. We measured red blood cell mitochondrial function, in nestlings exposed prenatally to heat- or control-calls, and reared in contrasting thermal environments. Exposure to high temperatures always reduced mitochondrial ATP production efficiency. However, as expected to reduce heat production, prenatal exposure to heat-calls improved mitochondrial efficiency under mild heat conditions. In addition, when exposed to an acute heat-challenge,

Indexed as

FinchesPrenatal Exposure Delayed EffectsAcclimatizationAcousticsAdenosine TriphosphateAnimalsHot TemperatureMitochondriaTemperatureAdenosine Triphosphatecellular respirationclimate changedevelopmental plasticityheat-stressOroborosthermal acclimation

Identifiers

PMID34875198
PMCPMC8651415
OpenAlexW4200141215

What OpenQuestion holds

Textmetadata
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.