Evidence map›Paper›PMID 20600198›Full record

ArticlePhysiology & behavior2010

Differential effects of sucrose and fructose on dietary obesity in four mouse strains.

John I Glendinning, Lindsey Breinager, Emily Kyrillou, Kristine Lacuna, Rotsen Rocha, Anthony Sclafani

Abstract readComparative Study
In one paragraph

Article in Physiology & behavior, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.6field-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

29 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Differential effects of acute versus chronic dietary fructose consumption on metabolic responses in FVB/N mice.American journal of physiology. Regulatory, integrative and comparative physiology · 2022
    Article
  7. Article
  8. Article
  9. Genetic controls of Tas1r3-independent sucrose consumption in mice.Mammalian genome : official journal of the International Mammalian Genome Society · 2021
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Microglia Play an Active Role in Obesity-Associated Cognitive Decline.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

6 authors at 3 institutions in 1 country.

John I GlendinningDepartment of Biological Sciences, Barnard College, Columbia University, New York, NY 10027, United States. jglendinning@barnard.edu
Lindsey Breinager
Emily Kyrillou
Kristine Lacuna
Rotsen Rocha
Anthony Sclafani
Barnard College · USColumbia University · USBrooklyn College · US

Funding

Carbohydrate Appetite, Fat Appetite and ObesityR37DK031135 · NIDDK · BROOKLYN COLLEGE · PI SCLAFANI, ANTHONY · 2001 to 2010
$2.9M
CARBOHYDRATE APPETITE, FAT APPETITE, AND OBESITYR01DK031135 · NIDDK · BROOKLYN COLLEGE · PI ACKROFF, KAREN, SCLAFANI, ANTHONY · 1986 to 2015
$2.0M
Discovery of Natural Products and Natural Product-Like InhibitorsZ01DK031135 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI BEWLEY, CAROLE · 2007 to 2008
$844k
Intramural NIH HHS Z01 DK031135NIDDK NIH HHS DK-031135NIDDK NIH HHS R01 DK031135NIDDK NIH HHS R37 DK031135
6 · The paper itself

Abstract

We examined sugar-induced obesity in mouse strains polymorphic for Tas1r3, a gene that codes for the T1R3 sugar taste receptor. The T1R3 receptor in the FVB and B6 strains has a higher affinity for sugars than that in the AKR and 129P3 strains. In Experiment 1, mice had 40days of access to lab chow plus water, sucrose (10 or 34%), or fructose (10 or 34%) solutions. The strains consumed more of the sucrose than isocaloric fructose solutions. The pattern of strain differences in caloric intake from the 10% sugar solutions was FVB>129P3=B6>AKR; and that from the 34% sugar solutions was FVB>129P3>B6>/=AKR. Despite consuming more sugar calories, the FVB mice resisted obesity altogether. The AKR and 129P3 mice became obese exclusively on the 34% sucrose diet, while the B6 mice did so on the 34% sucrose and 34% fructose diets. In Experiment 2, we compared total caloric intake from diets containing chow versus chow plus 34% sucrose. All strains consumed between 11 and 25% more calories from the sucrose-supplemented diet. In Experiment 3, we compared the oral acceptability of the sucrose and fructose solutions, using lick tests. All strains licked more avidly for the 10% sucrose solutions. The results indicate that in mice (a) Tas1r3 genotype does not predict sugar-induced hyperphagia or obesity; (b) sucrose solutions stimulate higher daily intakes than isocaloric fructose solutions; and (c) susceptibility to sugar-induced obesity varies with strain, sugar concentration and sugar type.

Indexed as

FructoseSucroseAdministration, OralAnalysis of VarianceAnimalsDose-Response Relationship, DrugEatingEnergy IntakeFemaleFood PreferencesHyperphagiaMaleMiceMice, 129 StrainMice, Inbred AKRMice, Inbred C57BLFructoseReceptors, G-Protein-CoupledSucrosetaste receptors, type 1

Identifiers

PMID20600198
PMCPMC2930118
OpenAlexW1984664636

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.