Evidence map›Paper›PMID 30217819›Full record

ArticleThe Journal of biological chemistry2018

Impact of 17β-estradiol on complex I kinetics and H

Maria J Torres, Terence E Ryan, Chien-Te Lin, Tonya N Zeczycki, P Darrell Neufer

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.6field-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

21 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Loss of ovarian function prevents exercise-induced activation of hepatic mitophagic flux.American journal of physiology. Endocrinology and metabolism · 2025
    Article
  4. Mitochondrial Biogenesis in Skeletal Muscle.Advances in experimental medicine and biology · 2025
    Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Skeletal muscle wasting: the estrogen side of sexual dimorphism.American journal of physiology. Cell physiology · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. 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 1 institution in 1 country.

Maria J TorresFrom the East Carolina Diabetes and Obesity Institute.
Terence E RyanFrom the East Carolina Diabetes and Obesity Institute.
Chien-Te LinFrom the East Carolina Diabetes and Obesity Institute.
Tonya N ZeczyckiFrom the East Carolina Diabetes and Obesity Institute, zeczyckit@ecu.edu.
P Darrell NeuferFrom the East Carolina Diabetes and Obesity Institute, neuferp@ecu.edu.
East Carolina University · US

Funding

Impact of organic cations on mitochondrial energetic driving forces and metabolic efficiencyR01DK110656 · NIDDK · EAST CAROLINA UNIVERSITY · PI NEUFER, P DARRELL · 2016 to 2019
$1.8M
Redox Biology and Muscle Insulin SensitivityR01DK096907 · NIDDK · EAST CAROLINA UNIVERSITY · PI NEUFER, P DARRELL · 2012 to 2015
$1.4M
NIDDK NIH HHS R01 DK096907NIDDK NIH HHS R01 DK110656
6 · The paper itself

Abstract

Naturally or surgically induced postmenopausal women are widely prescribed estrogen therapies to alleviate symptoms associated with estrogen loss and to lower the subsequent risk of developing metabolic diseases, including diabetes and nonalcoholic fatty liver disease. However, the molecular mechanisms by which estrogens modulate metabolism across tissues remain ill-defined. We have previously reported that 17β-estradiol (E2) exerts antidiabetogenic effects in ovariectomized (OVX) mice by protecting mitochondrial and cellular redox function in skeletal muscle. The liver is another key tissue for glucose homeostasis and a target of E2 therapy. Thus, in the present study we determined the effects of acute loss of ovarian E2 and E2 administration on liver mitochondria. In contrast to skeletal muscle mitochondria, E2 depletion via OVX did not alter liver mitochondrial respiratory function or complex I (CI) specific activities (NADH oxidation, quinone reduction, and H

Indexed as

AnimalsElectron Transport Complex IEstradiolEstrogensFemaleGene Expression RegulationHydrogen PeroxideKineticsMiceMice, Inbred C57BLMitochondria, LiverMitochondria, MuscleOxidation-ReductionElectron Transport Complex IEstradiolEstrogensHydrogen Peroxidecomplex Iestrogenhydrogen peroxidelivermitochondrial functionmitochondrial respiratory chain complexovariectomyskeletal muscle

Identifiers

PMID30217819
PMCPMC6204892
OpenAlexW2891358884

What OpenQuestion holds

Textmetadata
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.