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Time-Dependent Molecular Responses Differ between Gastric Bypass and Dieting but Are Conserved Across Species
- Source :
- Cell Metabolism. 28:310-323.e6
- Publication Year :
- 2018
- Publisher :
- Elsevier BV, 2018.
-
Abstract
- The effectiveness of Roux-en-Y gastric bypass (RYGB) against obesity and its comorbidities has generated excitement about developing new, less invasive treatments that use the same molecular mechanisms. Although controversial, RYGB-induced improvement of metabolic function may not depend entirely upon weight loss. To elucidate the differences between RYGB and dieting, we studied several individual organ molecular responses and generated an integrative, interorgan view of organismal physiology. We also compared murine and human molecular signatures. We show that, although dieting and RYGB can bring about the same degree of weight loss, post-RYGB physiology is very different. RYGB induces distinct, organ-specific adaptations in a temporal pattern that is characterized by energetically demanding processes, which may be coordinated by HIF1a activation and the systemic repression of growth hormone receptor signaling. Many of these responses are conserved in rodents and humans and may contribute to the remarkable ability of surgery to induce and sustain metabolic improvement.
- Subjects :
- Male
0301 basic medicine
Diet, Reducing
Physiology
Adipose Tissue, White
Gastric bypass
Circadian clock
Gastric Bypass
Mice, Obese
030209 endocrinology & metabolism
Growth hormone receptor
Biology
Bioinformatics
Article
Time
Mice
03 medical and health sciences
0302 clinical medicine
Weight loss
Intestine, Small
Weight Loss
medicine
Animals
Humans
Muscle, Skeletal
Molecular Biology
Psychological repression
Metabolic function
nutritional and metabolic diseases
Anastomosis, Roux-en-Y
Cell Biology
Middle Aged
Hypoxia-Inducible Factor 1, alpha Subunit
medicine.disease
Obesity
Obesity, Morbid
Mice, Inbred C57BL
030104 developmental biology
Liver
Female
medicine.symptom
Transcriptome
Dieting
Subjects
Details
- ISSN :
- 15504131
- Volume :
- 28
- Database :
- OpenAIRE
- Journal :
- Cell Metabolism
- Accession number :
- edsair.doi.dedup.....0d343744c40a4e4c09966bf49f5edb7c
- Full Text :
- https://doi.org/10.1016/j.cmet.2018.06.004