Restructuring of the male mice peripheral circadian network after bariatric surgery.


Journal

The Journal of endocrinology
ISSN: 1479-6805
Titre abrégé: J Endocrinol
Pays: England
ID NLM: 0375363

Informations de publication

Date de publication:
28 06 2021
Historique:
received: 16 05 2021
accepted: 20 05 2021
pubmed: 21 5 2021
medline: 19 8 2021
entrez: 20 5 2021
Statut: epublish

Résumé

Bariatric surgery is still the most effective long-term weight-loss therapy. Recent data indicate that surgical outcomes may be affected by diurnal food intake patterns. In this study, we aimed to investigate how surgery-induced metabolic adaptations (i.e. weight loss) interact with circadian clock function. For that reason, vertical sleeve gastrectomy (VSG) was performed in obese mice and rhythms in behavior, tissue rhythmicity, and white adipose tissue transcriptome were evaluated. VSG under constant darkness conditions led to a maximum weight loss of 18% compared to a loss of 3% after sham surgery. Post-surgical weight development was characterized by two distinct intervals of catabolic and subsequent anabolic metabolic state. Locomotor activity was not affected. However, VSG significantly increased active phase meal frequency in the anabolic state. No significant effects on clock gene rhythmicity were detected in adrenal and white adipose tissue (WAT) explant cultures. Transcriptome rhythm analyses of subcutaneous WAT revealed a reduction of cycling genes after VSG (sham: 2493 vs VSG: 1013) independent of sustained rhythms in core clock gene expression. This may be a consequence of weight loss-induced morphological reconstruction of WAT that overwrites the direct influence of the local clock machinery on the transcriptome. However, VSG altered rhythmic transcriptional regulation of WAT lipid metabolism pathways. Thus, our data suggest a reorganization of diurnal metabolic rhythms after VSG downstream of the molecular clock machinery.

Identifiants

pubmed: 34014835
doi: 10.1530/JOE-20-0611
pii: JOE-20-0611
doi:
pii:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

67-79

Auteurs

Anne-Marie Neumann (AM)

Institute of Neurobiology, University of Lübeck, Lübeck, Germany.
Center of Brain, Behavior and Metabolism, University of Lübeck, Lübeck, Germany.

Cathleen Geißler (C)

Center of Brain, Behavior and Metabolism, University of Lübeck, Lübeck, Germany.
Institute for Human Genetics, Epigenetics and Metabolism Lab, University of Lübeck, Lübeck, Germany.

Violetta Pilorz (V)

Institute of Neurobiology, University of Lübeck, Lübeck, Germany.
Center of Brain, Behavior and Metabolism, University of Lübeck, Lübeck, Germany.

Iwona Olejniczak (I)

Institute of Neurobiology, University of Lübeck, Lübeck, Germany.
Center of Brain, Behavior and Metabolism, University of Lübeck, Lübeck, Germany.

Alfor G Lewis (AG)

Department of Surgery, University of Michigan, Ann Arbor, Michigan, USA.

Randy J Seeley (RJ)

Department of Surgery, University of Michigan, Ann Arbor, Michigan, USA.

Orr Shomroni (O)

Transcriptome and Genome Analysis Core Unit, University Medical Center Göttingen, Göttingen, Germany.

Gabriela Salinas-Riester (G)

Transcriptome and Genome Analysis Core Unit, University Medical Center Göttingen, Göttingen, Germany.

Henriette Kirchner (H)

Center of Brain, Behavior and Metabolism, University of Lübeck, Lübeck, Germany.
Institute for Human Genetics, Epigenetics and Metabolism Lab, University of Lübeck, Lübeck, Germany.
German Center for Diabetes Research (DZD), Helmholtz Zentrum München, Bayern, Germany.

Henrik Oster (H)

Institute of Neurobiology, University of Lübeck, Lübeck, Germany.
Center of Brain, Behavior and Metabolism, University of Lübeck, Lübeck, Germany.

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Classifications MeSH