Evidence map›Paper›PMID 27537547›Full record

ArticlePloS one2016

Reproduction Does Not Adversely Affect Liver Mitochondrial Respiratory Function but Results in Lipid Peroxidation and Increased Antioxidants in House Mice.

Annelise V Mowry, Andreas N Kavazis, Aubrey E Sirman, Wayne K Potts, Wendy R Hood

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Mitochondrial physiology varies with parity and body mass in the laboratory mouse (Mus musculus).Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2020
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. A mitohormetic response to pro-oxidant exposure in the house mouse.American journal of physiology. Regulatory, integrative and comparative physiology · 2018
    Article
  11. Article
  12. 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

5 authors at 2 institutions in 1 country.

Annelise V MowryDepartment of Biological Sciences, Auburn University, Auburn, Alabama, United States of America.
Andreas N KavazisSchool of Kinesiology, Auburn University, Auburn, Alabama, United States of America.
Aubrey E SirmanDepartment of Biological Sciences, Auburn University, Auburn, Alabama, United States of America.
Wayne K PottsDepartment of Biology, University of Utah, Salt Lake City, Utah, United States of America.
Wendy R HoodDepartment of Biological Sciences, Auburn University, Auburn, Alabama, United States of America.
Auburn University · USUniversity of Utah · US

Funding

The role of sex in the evolution and spread of virulent infectious diseaseR01GM109500 · NIGMS · UNIVERSITY OF UTAH · PI ADLER, FREDERICK R., POTTS, WAYNE K. · 2013 to 2016
$1.6M
NIGMS NIH HHS R01 GM109500
6 · The paper itself

Abstract

Reproduction is thought to come at a cost to longevity. Based on the assumption that increased energy expenditure during reproduction is associated with increased free-radical production by mitochondria, oxidative damage has been suggested to drive this trade-off. We examined the impact of reproduction on liver mitochondrial function by utilizing post-reproductive and non-reproductive house mice (Mus musculus) living under semi-natural conditions. The age-matched post-reproductive and non-reproductive groups were compared after the reproductive females returned to a non-reproductive state, so that both groups were in the same physiological state at the time the liver was collected. Despite increased oxidative damage (p = 0.05) and elevated CuZnSOD (p = 0.002) and catalase (p = 0.04) protein levels, reproduction had no negative impacts on the respiratory function of liver mitochondria. Specifically, in a post-reproductive, maintenance state the mitochondrial coupling (i.e., respiratory control ratio) of mouse livers show no negative impacts of reproduction. In fact, there was a trend (p = 0.059) to suggest increased maximal oxygen consumption by liver mitochondria during the ADP stimulated state (i.e., state 3) in post-reproduction. These findings suggest that oxidative damage may not impair mitochondrial respiratory function and question the role of mitochondria in the trade-off between reproduction and longevity. In addition, the findings highlight the importance of quantifying the respiratory function of mitochondria in addition to measuring oxidative damage.

Indexed as

Lipid PeroxidationOxidative StressReproductionAnimalsCatalaseFemaleLongevityMaleMiceMitochondria, LiverOxidative PhosphorylationSuperoxide DismutaseCatalaseSuperoxide Dismutase

Identifiers

PMID27537547
PMCPMC4990174
OpenAlexW2515842706

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.