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Transcriptomic changes in pancreatic islets, adipose and liver after Roux-en-Y gastric bypass in a diet-induced obese rat model.
- Source :
-
Peptides [Peptides] 2021 Feb; Vol. 136, pp. 170467. Date of Electronic Publication: 2020 Nov 27. - Publication Year :
- 2021
-
Abstract
- Roux-en-Y gastric bypass (RYGB) is the most efficient intervention in morbid obesity and promotes metabolic improvements in several peripheral tissues. However, the underlying molecular mechanisms are still poorly understood. To further understand the effects of RYGB on peripheral tissues transcriptomes, we determined transcriptome signatures in pancreatic islets, adipose and liver tissue from diet-induced obese (DIO) rats model following RYGB. Whereas RYGB led to discrete gene expression changes in pancreatic islets, substantial transcriptome changes were observed in metabolic and immune signaling pathways in adipose tissue and the liver, indicating major gene adaptive responses in fat-storing tissues. Compared to RYGB DIO rats, peripheral tissue transcriptome signatures were markedly different in caloric restricted weight matching DIO rats, implying that caloric restriction paradigms do not reflect transcriptomic regulations of RYGB induced weight loss. The present gene expression study may serve as a basis for further investigations into molecular regulatory effects in peripheral tissues following RYGB-induced weight loss.<br /> (Copyright © 2020 Elsevier Inc. All rights reserved.)
- Subjects :
- Adipose Tissue metabolism
Animals
Diet, High-Fat adverse effects
Disease Models, Animal
Gastric Bypass
Humans
Islets of Langerhans metabolism
Islets of Langerhans pathology
Islets of Langerhans surgery
Liver pathology
Male
Obesity etiology
Obesity pathology
Obesity surgery
Obesity, Morbid metabolism
Obesity, Morbid pathology
Obesity, Morbid surgery
Rats
Rats, Sprague-Dawley
Weight Loss genetics
Insulin Resistance genetics
Liver metabolism
Obesity genetics
Obesity, Morbid genetics
Transcriptome genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1873-5169
- Volume :
- 136
- Database :
- MEDLINE
- Journal :
- Peptides
- Publication Type :
- Academic Journal
- Accession number :
- 33253774
- Full Text :
- https://doi.org/10.1016/j.peptides.2020.170467