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Identification of Novel Changes in Human Skeletal Muscle Proteome After Roux-en-Y Gastric Bypass Surgery

The mechanisms of metabolic improvements after Roux-en-Y gastric bypass (RYGB) surgery are not entirely clear. Therefore, the aim of our study was to investigate the role of obesity and RYGB on the human skeletal muscle proteome. Basal muscle biopsies were obtained from seven obese (BMI >40 kg/m(...

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Autores principales: Campbell, Latoya E., Langlais, Paul R., Day, Samantha E., Coletta, Richard L., Benjamin, Tonya R., De Filippis, Elena Anna, Madura, James A., Mandarino, Lawrence J., Roust, Lori R., Coletta, Dawn K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5001187/
https://www.ncbi.nlm.nih.gov/pubmed/27207528
http://dx.doi.org/10.2337/db16-0004
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author Campbell, Latoya E.
Langlais, Paul R.
Day, Samantha E.
Coletta, Richard L.
Benjamin, Tonya R.
De Filippis, Elena Anna
Madura, James A.
Mandarino, Lawrence J.
Roust, Lori R.
Coletta, Dawn K.
author_facet Campbell, Latoya E.
Langlais, Paul R.
Day, Samantha E.
Coletta, Richard L.
Benjamin, Tonya R.
De Filippis, Elena Anna
Madura, James A.
Mandarino, Lawrence J.
Roust, Lori R.
Coletta, Dawn K.
author_sort Campbell, Latoya E.
collection PubMed
description The mechanisms of metabolic improvements after Roux-en-Y gastric bypass (RYGB) surgery are not entirely clear. Therefore, the aim of our study was to investigate the role of obesity and RYGB on the human skeletal muscle proteome. Basal muscle biopsies were obtained from seven obese (BMI >40 kg/m(2)) female subjects (45.1 ± 3.6 years) pre- and 3 months post-RYGB, and euglycemic-hyperinsulinemic clamps were used to assess insulin sensitivity. Four age-matched (48.5 ± 4.7 years) lean (BMI <25 kg/m(2)) females served as control subjects. We performed quantitative mass spectrometry and microarray analyses on protein and RNA isolated from the muscle biopsies. Significant improvements in fasting plasma glucose (104.2 ± 7.8 vs. 86.7 ± 3.1 mg/dL) and BMI (42.1 ± 2.2 vs. 35.3 ± 1.8 kg/m(2)) were demonstrated in the pre- versus post-RYGB, both P < 0.05. Proteomic analysis identified 2,877 quantifiable proteins. Of these, 395 proteins were significantly altered in obesity before surgery, and 280 proteins differed significantly post-RYGB. Post-RYGB, 49 proteins were returned to normal levels after surgery. KEGG pathway analysis revealed a decreased abundance in ribosomal and oxidative phosphorylation proteins in obesity, and a normalization of ribosomal proteins post-RYGB. The transcriptomic data confirmed the normalization of the ribosomal proteins. Our results provide evidence that obesity and RYGB have a dynamic effect on the skeletal muscle proteome.
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spelling pubmed-50011872017-09-01 Identification of Novel Changes in Human Skeletal Muscle Proteome After Roux-en-Y Gastric Bypass Surgery Campbell, Latoya E. Langlais, Paul R. Day, Samantha E. Coletta, Richard L. Benjamin, Tonya R. De Filippis, Elena Anna Madura, James A. Mandarino, Lawrence J. Roust, Lori R. Coletta, Dawn K. Diabetes Pathophysiology The mechanisms of metabolic improvements after Roux-en-Y gastric bypass (RYGB) surgery are not entirely clear. Therefore, the aim of our study was to investigate the role of obesity and RYGB on the human skeletal muscle proteome. Basal muscle biopsies were obtained from seven obese (BMI >40 kg/m(2)) female subjects (45.1 ± 3.6 years) pre- and 3 months post-RYGB, and euglycemic-hyperinsulinemic clamps were used to assess insulin sensitivity. Four age-matched (48.5 ± 4.7 years) lean (BMI <25 kg/m(2)) females served as control subjects. We performed quantitative mass spectrometry and microarray analyses on protein and RNA isolated from the muscle biopsies. Significant improvements in fasting plasma glucose (104.2 ± 7.8 vs. 86.7 ± 3.1 mg/dL) and BMI (42.1 ± 2.2 vs. 35.3 ± 1.8 kg/m(2)) were demonstrated in the pre- versus post-RYGB, both P < 0.05. Proteomic analysis identified 2,877 quantifiable proteins. Of these, 395 proteins were significantly altered in obesity before surgery, and 280 proteins differed significantly post-RYGB. Post-RYGB, 49 proteins were returned to normal levels after surgery. KEGG pathway analysis revealed a decreased abundance in ribosomal and oxidative phosphorylation proteins in obesity, and a normalization of ribosomal proteins post-RYGB. The transcriptomic data confirmed the normalization of the ribosomal proteins. Our results provide evidence that obesity and RYGB have a dynamic effect on the skeletal muscle proteome. American Diabetes Association 2016-09 2016-05-10 /pmc/articles/PMC5001187/ /pubmed/27207528 http://dx.doi.org/10.2337/db16-0004 Text en © 2016 by the American Diabetes Association. http://diabetesjournals.org/site/licenseReaders may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. More information is available at http://diabetesjournals.org/site/license.
spellingShingle Pathophysiology
Campbell, Latoya E.
Langlais, Paul R.
Day, Samantha E.
Coletta, Richard L.
Benjamin, Tonya R.
De Filippis, Elena Anna
Madura, James A.
Mandarino, Lawrence J.
Roust, Lori R.
Coletta, Dawn K.
Identification of Novel Changes in Human Skeletal Muscle Proteome After Roux-en-Y Gastric Bypass Surgery
title Identification of Novel Changes in Human Skeletal Muscle Proteome After Roux-en-Y Gastric Bypass Surgery
title_full Identification of Novel Changes in Human Skeletal Muscle Proteome After Roux-en-Y Gastric Bypass Surgery
title_fullStr Identification of Novel Changes in Human Skeletal Muscle Proteome After Roux-en-Y Gastric Bypass Surgery
title_full_unstemmed Identification of Novel Changes in Human Skeletal Muscle Proteome After Roux-en-Y Gastric Bypass Surgery
title_short Identification of Novel Changes in Human Skeletal Muscle Proteome After Roux-en-Y Gastric Bypass Surgery
title_sort identification of novel changes in human skeletal muscle proteome after roux-en-y gastric bypass surgery
topic Pathophysiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5001187/
https://www.ncbi.nlm.nih.gov/pubmed/27207528
http://dx.doi.org/10.2337/db16-0004
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