Evidence map›Paper›PMID 23357530›Full record

ReviewMetabolism: clinical and experimental2013

Cellular mechanisms regulating fuel metabolism in mammals: role of adipose tissue and lipids during prolonged food deprivation.

Jose Abraham Viscarra, Rudy Martin Ortiz

Abstract readReview
In one paragraph

Review in Metabolism: clinical and experimental, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.2field-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

30 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. An Overview of Hormone-Sensitive Lipase (HSL).TheScientificWorldJournal · 2022
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Metabolic Complications in Cardiac Aging.Frontiers in physiology · 2021
    Review
  13. Article
  14. Frontiers in physiology · 2020
    Article
  15. Article
  16. Article
  17. Article
  18. The Role of Leptin in Maintaining Plasma Glucose During Starvation.Postdoc journal : a journal of postdoctoral research and postdoctoral affairs · 2018
    Article
  19. Article
  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

2 authors at 1 institution in 1 country.

Jose Abraham ViscarraDepartment of Molecular and Cellular Biology, University of California, Merced, 5200 N Lake Rd., Merced, CA 95343, USA. jviscarra@ucmerced.edu
Rudy Martin Ortiz
University of California, Merced · US

Funding

Mechanisms of Oxidative Stress and Inflammation during Prolonged Fasting and SleeR01HL091767 · NHLBI · UNIVERSITY OF CALIFORNIA, MERCED · PI ORTIZ, RUDY M · 2009 to 2013
$1.9M
Independent Scientist Development Award in Oxidative Stress and ApneaK02HL103787 · NHLBI · UNIVERSITY OF CALIFORNIA, MERCED · PI ORTIZ, RUDY M · 2010 to 2013
$415k
NHLBI NIH HHS HL091767-S4NHLBI NIH HHS K02 HL103787NHLBI NIH HHS K02HL103787NHLBI NIH HHS R01 HL091767
6 · The paper itself

Abstract

Food deprivation in mammals results in profound changes in fuel metabolism and substrate regulation. Among these changes are decreased reliance on the counter-regulatory dynamics by insulin-glucagon due to reduced glucose utilization, and increased concentrations of lipid substrates in plasma to meet the energetic demands of peripheral tissues. As the primary storage site of lipid substrates, adipose tissue must then be a primary contributor to the regulation of metabolism in food deprived states. Through its regulation of lipolysis, adipose tissue influences the availability of carbohydrate, lipid, and protein substrates. Additionally, lipid substrates can act as ligands to various nuclear receptors (retinoid x receptor (RXR), liver x receptor (LXR), and peroxisome proliferator-activated receptor (PPAR)) and exhibit prominent regulatory capabilities over the expression of genes involved in substrate metabolism within various tissues. Therefore, through its control of lipolysis, adipose tissue also indirectly regulates the utilization of metabolic substrates within peripheral tissues. In this review, these processes are described in greater detail and the extent to which adipose tissue and lipid substrates regulate metabolism in food deprived mammals is explored with comments on future directions to better assess the contribution of adipose tissue to metabolism.

Indexed as

Energy MetabolismLipolysisAdipose TissueAnimalsFood DeprivationGene Expression RegulationHumansLipid MetabolismLiver X ReceptorsMammalsOrphan Nuclear ReceptorsPeroxisome Proliferator-Activated ReceptorsRetinoid X ReceptorsStarvationLiver X ReceptorsOrphan Nuclear ReceptorsPeroxisome Proliferator-Activated ReceptorsRetinoid X Receptors

Identifiers

PMID23357530
PMCPMC3640658
OpenAlexW1984438362

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.