Evidence map›Paper›PMID 25446204›Full record

ArticlePhysiology & behavior2015

Hexosamine biosynthetic pathway activity in leptin resistant sucrose-drinking rats.

Ruth B S Harris, John W Apolzan

Abstract read
In one paragraph

Article in Physiology & behavior, 2015. 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
0.3field-weighted citation impact, top 50% 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, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Consuming sucrose solution promotes leptin resistance and site specifically modifies hypothalamic leptin signaling in rats.American journal of physiology. Regulatory, integrative and comparative physiology · 2021
    Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. O-GlcNAc cycling in the developing, adult and geriatric brain.Journal of bioenergetics and biomembranes · 2018
    Review
  9. Source of dietary sucrose influences development of leptin resistance in male and female rats.American journal of physiology. Regulatory, integrative and comparative physiology · 2018
    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

2 authors at 1 institution in 1 country.

Ruth B S HarrisDepartment of Physiology, Medical College of Georgia, Georgia Regents University, Augusta, GA 30912, United States. Electronic address: ruharris@gru.edu.
John W ApolzanDepartment of Physiology, Medical College of Georgia, Georgia Regents University, Augusta, GA 30912, United States.
Augusta University · US

Funding

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI JUDD E SHELLITO · 2012 to 2026
$69.1M
LEPTIN AND PERIPHERAL GLUCOSE METABOLISMR01DK053903 · NIDDK · UNIVERSITY OF GEORGIA (UGA) · PI HARRIS, RUTH B · 1999 to 2018
$4.6M
NIDDK NIH HHS DK053903NIDDK NIH HHS R01 DK053903NIGMS NIH HHS U54 GM104940
6 · The paper itself

Abstract

Rats offered 30% sucrose solution in addition to chow and water become leptin resistant therefore we investigated the effect of sucrose solution consumption on leptin signaling. In Experiment 1 rats were resistant to 3rd ventricle injections of1.5 μg leptin after 36 days of sucrose and western blot indicated that resistance was associated with increased basal levels of signal transducer and activator of transcription 3 phosphorylation (pSTAT3). In Experiment 2 rats were resistant to a peripheral injection of 2mg leptin/kg after 26 days of sucrose. Immunohistochemistry indicated that increased basal pSTAT3 was limited to the medial and lateral arcuate nucleus of the hypothalamus. Increased availability of glucose and fructose can stimulate the hexosamine biosynthetic pathway (HBP) which O-GlcNAc-modifies proteins. This has the potential to change protein bioactivity. We tested whether this pathway could account for the leptin resistance. There was no increase in the expression of HBP enzymes in tissues from sucrose rats in Experiment 1, however, direct activation of the HBP with a 3h intravenous infusion of 30 μmol/kg/min glucosamine significantly increased hypothalamic pSTAT3. Although sucrose consumption and activation of the HBP both increase hypothalamic pSTAT3 experiments described here did not provide evidence of a direct link between sucrose consumption, HBP activity and leptin resistance. Unexpectedly, we found that the HBP enzyme glutamine fructose-6-phosphate amidotransferase (GFAT) in liver and O-GlcNAcase in hypothalamus were increased 30min after leptin injection in leptin responsive animals, implying a complex interaction between activity of the HBP and leptin responsiveness.

Indexed as

AcetylglucosamineAnimalsBiosynthetic PathwaysBlood GlucoseCentral Nervous System AgentsDietary SucroseEatingGlucosamineGlutamine-Fructose-6-Phosphate Transaminase (Isomerizing)HexosaminesHypothalamusInsulinLeptinLiverMaleN-AcetylglucosaminyltransferasesAcetylglucosamineBlood GlucoseCentral Nervous System AgentsDietary SucroseGlucosamineGlutamine-Fructose-6-Phosphate Transaminase (Isomerizing)HexosaminesInsulinLeptinN-AcetylglucosaminyltransferasesStat3 protein, ratSTAT3 Transcription FactorUDP-N-acetylglucosamine-peptide beta-N-acetylglucosaminyltransferaseGFATGlucosamineHexosamine biosynthetic pathwayHypothalamic pSTAT3OGT

Identifiers

PMID25446204
PMCPMC4400807
OpenAlexW2037204375

What OpenQuestion holds

Textmetadata
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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.