Effects of Roux-en-Y gastric bypass on circulating follistatin, activin A, and peripheral ActRIIB signaling in humans with obesity and type 2 diabetes
Autor: | Kirstine N. Bojsen-Møller, Sten Madsbad, Tang Cam Phung Pham, Jørgen F. P. Wojtaszewski, Erik A. Richter, Lykke Sylow |
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Rok vydání: | 2020 |
Předmět: |
Blood Glucose
Male Follistatin Time Factors endocrine system diseases Endocrinology Diabetes and Metabolism Activin Receptors Type II Biopsy Medicine (miscellaneous) Adipose tissue Type 2 diabetes 0302 clinical medicine 030212 general & internal medicine Inhibin-beta Subunits Nutrition and Dietetics biology Muscles Middle Aged Roux-en-Y anastomosis Activins Obesity Morbid medicine.anatomical_structure Adipose Tissue Female Signal transduction hormones hormone substitutes and hormone antagonists Signal Transduction Adult endocrine system medicine.medical_specialty Gastric Bypass 030209 endocrinology & metabolism Glycemic Control 03 medical and health sciences Downregulation and upregulation Internal medicine medicine Humans business.industry nutritional and metabolic diseases Skeletal muscle medicine.disease Obesity Endocrinology Glucose Diabetes Mellitus Type 2 biology.protein business human activities Follow-Up Studies |
Zdroj: | International journal of obesity (2005). 45(2) |
ISSN: | 1476-5497 |
Popis: | Roux-en-Y gastric bypass (RYGB) surgery is a therapeutic intervention for morbid obesity and type 2 diabetes (T2D) that improves metabolic regulation. Follistatin (Fst) could be implicated in improved glycemia as it is highly regulated by RYGB. However, it is unknown if metabolic status, such as T2D, alters the Fst response to RYGB. In addition, the effect of RYGB on the Fst target, activin A, is unknown in individuals with obesity and T2D, but is needed to interpret the functional effects of altering Fst. Finally, whether Fst-regulated intracellular signaling contributes to beneficial effects of RYGB is undetermined. Circulating Fst and activin A were measured before, 1 week, and 1 year after RYGB surgery in a total of 20 individuals with obesity, 10 with normoglycemia (NGT) and 10 with preoperative T2D. Intracellular signaling downstream of the Activin receptor type IIB (ActRIIB) signaling pathway was analyzed in skeletal muscle and adipose tissue. The doubling in circulating Fst observed in subjects with NGT 1-week and 1-year post surgery was absent in T2D. After 1 week, RYGB reduced activin A by 27% (p |
Databáze: | OpenAIRE |
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