Evidence map›Paper›PMID 24456165›Full record

ArticleEndocrinology2014

Administration of saccharin to neonatal mice influences body composition of adult males and reduces body weight of females.

Sebastian D Parlee, Becky R Simon, Erica L Scheller, Emilyn U Alejandro, Brian S Learman, Venkatesh Krishnan, Ernesto Bernal-Mizrachi, Ormond A MacDougald

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Non-nutritive Sweeteners: Weight Loss or Weight Gain?Endocrine, metabolic & immune disorders drug targets · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Saccharin induced liver inflammation in mice by altering the gut microbiota and its metabolic functions.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2017
    Article
  12. Article
  13. Article
  14. 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

8 authors at 2 institutions in 1 country.

Sebastian D ParleeDepartments of Molecular and Integrative Physiology and Internal Medicine (S.D.P., B.R.S., E.L.S., B.S.L., O.A.M.), and Division of Metabolism, Endocrinology and Diabetes (E.U.A., E.B.-M., O.A.M.), School of Medicine, University of Michigan, Ann Arbor, Michigan 48105; and Musculoskeletal Research (V.K.), Lilly Research Laboratories, Indianapolis, Indiana 46285.
Becky R Simon
Erica L Scheller
Emilyn U Alejandro
Brian S Learman
Venkatesh Krishnan
Ernesto Bernal-Mizrachi
Ormond A MacDougald
University of Michigan–Ann Arbor · USEli Lilly (United States) · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Martin G Myers · 2013 to 2026
$24.3M
Pilot and Feasibility (P and F) ProgramP30DK089503 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Karen Eileen Peterson · 2010 to 2026
$20.3M
Tissue Engineering and RegenerationT32DE007057 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID H. KOHN · 1985 to 2026
$17.3M
CELLULAR AND MOLECULAR BIOLOGY AT MICHIGANT32GM007315 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PUTHENVEEDU, MANOJKUMAR A · 1985 to 2021
$12.8M
Statistics and Bioinformatics Core - WangU24DK097153 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BURANT, CHARLES F · 2012 to 2017
$10.1M
TRAINING PROGRAM IN ORGANOGENESIST32HD007505 · NICHD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PASCA DI MAGLIANO, MARINA, SPENCE, JASON · 1997 to 2021
$6.9M
Postdoc Stipend Supplement: Developmental Origins of Metabolic Disorders T32T32DK071212 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID P OLSON, Kanakadurga Singer · 2005 to 2026
$5.4M
AKT/mTOR Signaling and Regulation of Cell Cycle in beta CellsR01DK073716 · NIDDK · WASHINGTON UNIVERSITY · PI BERNAL-MIZRACHI, ERNESTO · 2006 to 2022
$4.6M
Nutrient Signals and Programming of Pancreas DevelopmentR01DK084236 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BERNAL-MIZRACHI, ERNESTO · 2010 to 2018
$2.9M
Role of Sweet Taste Receptors in Adipocyte Differentiation and MetabolismR01DK095705 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MACDOUGALD, ORMOND A · 2012 to 2015
$1.3M
Mechanisms of Developmental Programing of beta-cell Susceptibility to GlucolipotoxicityK01DK103823 · NIDDK · UNIVERSITY OF MINNESOTA · PI ALEJANDRO, EMILYN · 2014 to 2017
$572k
NICHD NIH HHS T32 HD007505NICHD NIH HHS T32-HD007505NIDCR NIH HHS T32 DE007057NIDDK NIH HHS DK097153NIDDK NIH HHS K01 DK103823NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30-DK020572NIDDK NIH HHS P30 DK089503NIDDK NIH HHS P30-DK089503NIDDK NIH HHS R01 DK073716NIDDK NIH HHS R01DK073716NIDDK NIH HHS R01 DK084236NIDDK NIH HHS R01DK084236NIDDK NIH HHS R01 DK095705NIDDK NIH HHS R01DK95705NIDDK NIH HHS T32 DK071212NIDDK NIH HHS T32-DK071212NIDDK NIH HHS U24 DK097153NIGMS NIH HHS T32 GM007315PHS HHS T32-MG007315
6 · The paper itself

Abstract

Nutritional or pharmacological perturbations during perinatal growth can cause persistent effects on the function of white adipose tissue, altering susceptibility to obesity later in life. Previous studies have established that saccharin, a nonnutritive sweetener, inhibits lipolysis in mature adipocytes and stimulates adipogenesis. Thus, the current study tested whether neonatal exposure to saccharin via maternal lactation increased susceptibility of mice to diet-induced obesity. Saccharin decreased body weight of female mice beginning postnatal week 3. Decreased liver weights on week 14 corroborated this diminished body weight. Initially, saccharin also reduced male mouse body weight. By week 5, weights transiently rebounded above controls, and by week 14, male body weights did not differ. Body composition analysis revealed that saccharin increased lean and decreased fat mass of male mice, the latter due to decreased adipocyte size and epididymal, perirenal, and sc adipose weights. A mild improvement in glucose tolerance without a change in insulin sensitivity or secretion aligned with this leaner phenotype. Interestingly, microcomputed tomography analysis indicated that saccharin also increased cortical and trabecular bone mass of male mice and modified cortical bone alone in female mice. A modest increase in circulating testosterone may contribute to the leaner phenotype in male mice. Accordingly, the current study established a developmental period in which saccharin at high concentrations reduces adiposity and increases lean and bone mass in male mice while decreasing generalized growth in female mice.

Indexed as

AdipocytesAdipose TissueAdiposityAnimalsAnimals, NewbornAnthropometryBody CompositionBody WeightBone and BonesBone Marrow CellsFemaleGlucose Tolerance TestInsulinIslets of LangerhansMagnetic Resonance SpectroscopyMaleInsulinNon-Nutritive SweetenersSaccharinTestosterone

Identifiers

PMID24456165
PMCPMC3959603
OpenAlexW2113010033

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.