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Circulating ANGPTL8/Betatrophin Is Increased in Obesity and Reduced after Exercise Training

OBJECTIVE: ANGPTL8 is a liver and adipose tissue produced protein that regulates the level of triglyceride in plasma as well as glucose homeostasis. This study was designed to evaluate the level of ANGPTL8 in obese and non-obese subjects before and after exercise training. METHODS: A total of 82 non...

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Autores principales: Abu-Farha, Mohamed, Sriraman, Devarajan, Cherian, Preethi, AlKhairi, Irina, Elkum, Naser, Behbehani, Kazem, Abubaker, Jehad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4718617/
https://www.ncbi.nlm.nih.gov/pubmed/26784326
http://dx.doi.org/10.1371/journal.pone.0147367
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author Abu-Farha, Mohamed
Sriraman, Devarajan
Cherian, Preethi
AlKhairi, Irina
Elkum, Naser
Behbehani, Kazem
Abubaker, Jehad
author_facet Abu-Farha, Mohamed
Sriraman, Devarajan
Cherian, Preethi
AlKhairi, Irina
Elkum, Naser
Behbehani, Kazem
Abubaker, Jehad
author_sort Abu-Farha, Mohamed
collection PubMed
description OBJECTIVE: ANGPTL8 is a liver and adipose tissue produced protein that regulates the level of triglyceride in plasma as well as glucose homeostasis. This study was designed to evaluate the level of ANGPTL8 in obese and non-obese subjects before and after exercise training. METHODS: A total of 82 non-obese and 62 adult obese were enrolled in this study. Subjects underwent a three months of exercise training. Both full length and C-terminal 139–198 form of ANGPTL8 were measured by ELISA. RESULTS: Our data show that the full length ANGPTL8 level was increased in obese subjects (1150.04 ± 108.10 pg/mL) compared to non-obese (775.54 ± 46.12) pg/mL (p-Value = 0.002). C-terminal 139–198 form of ANGPTL8 was also increased in obese subjects 0.28 ± 0.04 ng/mL vs 0.20 ± 0.02 ng/mL in non-obese (p-value = 0.058). In obese subjects, the levels of both forms were reduced after three months of exercise training; full length was reduced from 1150.04 ± 108.10 pg/mL to 852.04 ± 51.95 pg/mL (p-Values 0.015) and c-terminal form was reduced from 0.28 ± 0.04 ng/mL to 0.19 ± 0.03 ng/mL (p-Value = 0.058). Interestingly, full length ANGPTL8 was positively associated with fasting blood glucose (FBG) in non-obese (r = 0.317, p-Value = 0.006) and obese subjects (r = 0.346, p-Value = 0.006) C-terminal 139–198 form of ANGPTL8 on the other hand, did not show any correlation in both groups. CONCLUSION: In conclusion, our data demonstrate that ANGPTL8 was increased in obesity and reduced after exercise training supporting the potential therapeutic benefit of reducing ANGPTL8. The various forms of ANGPTL8 associated differently with FBG suggesting that they have different roles in glucose homeostasis.
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spelling pubmed-47186172016-01-30 Circulating ANGPTL8/Betatrophin Is Increased in Obesity and Reduced after Exercise Training Abu-Farha, Mohamed Sriraman, Devarajan Cherian, Preethi AlKhairi, Irina Elkum, Naser Behbehani, Kazem Abubaker, Jehad PLoS One Research Article OBJECTIVE: ANGPTL8 is a liver and adipose tissue produced protein that regulates the level of triglyceride in plasma as well as glucose homeostasis. This study was designed to evaluate the level of ANGPTL8 in obese and non-obese subjects before and after exercise training. METHODS: A total of 82 non-obese and 62 adult obese were enrolled in this study. Subjects underwent a three months of exercise training. Both full length and C-terminal 139–198 form of ANGPTL8 were measured by ELISA. RESULTS: Our data show that the full length ANGPTL8 level was increased in obese subjects (1150.04 ± 108.10 pg/mL) compared to non-obese (775.54 ± 46.12) pg/mL (p-Value = 0.002). C-terminal 139–198 form of ANGPTL8 was also increased in obese subjects 0.28 ± 0.04 ng/mL vs 0.20 ± 0.02 ng/mL in non-obese (p-value = 0.058). In obese subjects, the levels of both forms were reduced after three months of exercise training; full length was reduced from 1150.04 ± 108.10 pg/mL to 852.04 ± 51.95 pg/mL (p-Values 0.015) and c-terminal form was reduced from 0.28 ± 0.04 ng/mL to 0.19 ± 0.03 ng/mL (p-Value = 0.058). Interestingly, full length ANGPTL8 was positively associated with fasting blood glucose (FBG) in non-obese (r = 0.317, p-Value = 0.006) and obese subjects (r = 0.346, p-Value = 0.006) C-terminal 139–198 form of ANGPTL8 on the other hand, did not show any correlation in both groups. CONCLUSION: In conclusion, our data demonstrate that ANGPTL8 was increased in obesity and reduced after exercise training supporting the potential therapeutic benefit of reducing ANGPTL8. The various forms of ANGPTL8 associated differently with FBG suggesting that they have different roles in glucose homeostasis. Public Library of Science 2016-01-19 /pmc/articles/PMC4718617/ /pubmed/26784326 http://dx.doi.org/10.1371/journal.pone.0147367 Text en © 2016 Abu-Farha et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Abu-Farha, Mohamed
Sriraman, Devarajan
Cherian, Preethi
AlKhairi, Irina
Elkum, Naser
Behbehani, Kazem
Abubaker, Jehad
Circulating ANGPTL8/Betatrophin Is Increased in Obesity and Reduced after Exercise Training
title Circulating ANGPTL8/Betatrophin Is Increased in Obesity and Reduced after Exercise Training
title_full Circulating ANGPTL8/Betatrophin Is Increased in Obesity and Reduced after Exercise Training
title_fullStr Circulating ANGPTL8/Betatrophin Is Increased in Obesity and Reduced after Exercise Training
title_full_unstemmed Circulating ANGPTL8/Betatrophin Is Increased in Obesity and Reduced after Exercise Training
title_short Circulating ANGPTL8/Betatrophin Is Increased in Obesity and Reduced after Exercise Training
title_sort circulating angptl8/betatrophin is increased in obesity and reduced after exercise training
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4718617/
https://www.ncbi.nlm.nih.gov/pubmed/26784326
http://dx.doi.org/10.1371/journal.pone.0147367
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