Evidence map›Paper›PMID 22683097›Full record

ArticleMetabolism: clinical and experimental2012

Shc proteins influence the activities of enzymes involved in fatty acid oxidation and ketogenesis.

Kevork Hagopian, Alexey A Tomilov, Natalia Tomilova, Kyoungmi Kim, Sandra L Taylor, Adam K Lam, Gino A Cortopassi, Roger B McDonald, Jon J Ramsey

Abstract read
In one paragraph

Article in Metabolism: clinical and experimental, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. The ketone body β-hydroxybutyrate shifts microglial metabolism and suppresses amyloid-β oligomer-induced inflammation in human microglia.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
  2. Emerging Targets in Type 2 Diabetes and Diabetic Complications.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Review
  3. Article
  4. Article
  5. p46Shc Inhibits Thiolase and Lipid Oxidation in Mitochondria.The Journal of biological chemistry · 2016
    Article
  6. Article
  7. The influence of Shc proteins on life span in mice.The journals of gerontology. Series A, Biological sciences and medical sciences · 2014
    Article
  8. Article
  9. Article
  10. 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

9 authors at 1 institution in 1 country.

Kevork HagopianDepartment of Molecular Biosciences, School of Veterinary Medicine, University of California, Davis, CA 95616, USA.
Alexey A Tomilov
Natalia Tomilova
Kyoungmi Kim
Sandra L Taylor
Adam K Lam
Gino A Cortopassi
Roger B McDonald
Jon J Ramsey
University of California, Davis · US

Funding

TRANSLOCATION OF p66Shc: KINETICS, FUNCTION, APOPTOSISP01AG025532 · NIA · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KIM, KYOUNGMI · 2007 to 2017
$12.1M
Mouse Metabolic Phenotyping Center (MMPC) at UC DavisU24DK092993 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LLOYD, KC KENT · 2011 to 2015
$4.1M
NIA NIH HHS P01 AG025532NIDDK NIH HHS U24 DK092993
6 · The paper itself

Abstract

objectivesShcKO mice have low body fat and resist weight gain on a high fat diet, indicating that Shc proteins may influence enzymes involved in β-oxidation. To investigate this idea, the activities of β-oxidation and ketone body metabolism enzymes were measured.

methodsThe activities of β-oxidation enzymes (acyl-CoA dehydrogenase, 3-hydroxyacyl-CoA dehydrogenase and ketoacyl-CoA thiolase) in liver and hindlimb skeletal muscle, ketolytic enzymes (acetoacetyl-CoA thiolase, β-hydroxybutyrate dehydrogenase and 3-oxoacid-CoA transferase) in skeletal muscle, and ketogenic enzymes (acetoacetyl-CoA thiolase and β-hydroxybutyrate dehydrogenase) in liver were measured from wild-type and ShcKO mice.

resultsThe activities of β-oxidation enzymes were increased (P<.05) in the ShcKO compared to wild-type mice in the fasted but not the fed state. In contrast, no uniform increases in the ketolytic enzyme activities were observed between ShcKO and wild-type mice. In liver, the activities of ketogenic enzymes were increased (P<.05) in ShcKO compared to wild-type mice in both the fed and fasted states. Levels of phosphorylated hormone sensitive lipase from adipocytes were also increased (P<.05) in fasted ShcKO mice.

conclusionThese studies indicate that the low Shc levels in ShcKO mice result in increased liver and muscle β-oxidation enzyme activities in response to fasting and induce chronic increases in the activity of liver ketogenic enzymes. Decreases in the level of Shc proteins should be considered as possible contributors to the increase in activity of fatty acid oxidation enzymes in response to physiological conditions which increase reliance on fatty acids as a source of energy.

Indexed as

3-Hydroxyacyl CoA DehydrogenasesAcetyl-CoA C-AcetyltransferaseAcyl-CoA DehydrogenaseAnimalsBlotting, WesternCell RespirationCoenzyme A-TransferasesDNA, MitochondrialEatingElectrophoresisFastingHindlimbHydroxybutyrate DehydrogenaseKetone BodiesLipaseLiver3-Hydroxyacyl CoA Dehydrogenases3-ketoacid CoA-transferaseAcetyl-CoA C-AcetyltransferaseAcyl-CoA DehydrogenaseCoenzyme A-TransferasesDNA, MitochondrialHydroxybutyrate DehydrogenaseKetone BodiesLipaseShc Signaling Adaptor Proteins

Identifiers

PMID22683097
PMCPMC3442136
OpenAlexW2040490002

What OpenQuestion holds

Textmetadata
LicenceTDM
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.