Gastric bypass surgery in lean adolescent mice prevents diet-induced obesity later in life.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
27 05 2019
Historique:
received: 13 12 2018
accepted: 15 05 2019
entrez: 29 5 2019
pubmed: 28 5 2019
medline: 21 10 2020
Statut: epublish

Résumé

Gastric bypass surgery is the most effective treatment and is often the only option for subjects with severe obesity. However, investigation of critical molecular mechanisms involved has been hindered by confounding of specific effects of surgery and side effects associated with acute surgical trauma. Here, we dissociate the two components by carrying out surgery in the lean state and testing its effectiveness to prevent diet-induced obesity later in life. Body weight and composition of female mice with RYGB performed at 6 weeks of age were not significantly different from sham-operated and age-matched non-surgical mice at the time of high-fat diet exposure 12 weeks after surgery. These female mice were completely protected from high-fat diet-induced obesity and accompanying metabolic impairments for up to 50 weeks. Similar effects were seen in male mice subjected to RYGB at 5-6 weeks, although growth was slightly inhibited and protection from diet-induced obesity was less complete. The findings confirm that RYGB does not indiscriminately lower body weight but specifically prevents excessive diet-induced obesity and ensuing metabolic impairments. This prevention of obesity model should be crucial for identifying the molecular mechanisms underlying gastric bypass surgery.

Identifiants

pubmed: 31133715
doi: 10.1038/s41598-019-44344-7
pii: 10.1038/s41598-019-44344-7
pmc: PMC6536499
doi:

Substances chimiques

Blood Glucose 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

7881

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK092587
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK081563
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK072476
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK105032
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK047348
Pays : United States

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Auteurs

Michael B Mumphrey (MB)

Neurobiology of Nutrition & Metabolism Department, Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LA, USA.

Zheng Hao (Z)

Neurobiology of Nutrition & Metabolism Department, Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LA, USA.

R Leigh Townsend (R)

Neurobiology of Nutrition & Metabolism Department, Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LA, USA.

Emily Qualls-Creekmore (E)

Neurobiology of Nutrition & Metabolism Department, Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LA, USA.

Sangho Yu (S)

Neurobiology of Nutrition & Metabolism Department, Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LA, USA.

Thomas A Lutz (TA)

Institute of Veterinary Physiology, Vetsuisse Faculty, University of Zürich, Zürich, Switzerland.

Heike Münzberg (H)

Neurobiology of Nutrition & Metabolism Department, Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LA, USA.

Christopher D Morrison (CD)

Neurobiology of Nutrition & Metabolism Department, Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LA, USA.

Hans-Rudolf Berthoud (HR)

Neurobiology of Nutrition & Metabolism Department, Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LA, USA. berthohr@pbrc.edu.

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Classifications MeSH