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Effects of glucose and meal ingestion on incretin secretion in Japanese subjects with normal glucose tolerance

Aims/Introduction:  Gastric inhibitory polypeptide (GIP) and glucagon‐like peptide‐1 (GLP‐1) are the major incretins; their secretion after various nutrient loads are well‐evaluated in Caucasians. However, little is known of the relationship between incretin secretion and differing nutritional loadi...

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Autores principales: Yamane, Shunsuke, Harada, Norio, Hamasaki, Akihiro, Muraoka, Atsushi, Joo, Erina, Suzuki, Kazuyo, Nasteska, Daniela, Tanaka, Daisuke, Ogura, Masahito, Harashima, Shin‐ichi, Inagaki, Nobuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4014936/
https://www.ncbi.nlm.nih.gov/pubmed/24843549
http://dx.doi.org/10.1111/j.2040-1124.2011.00143.x
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author Yamane, Shunsuke
Harada, Norio
Hamasaki, Akihiro
Muraoka, Atsushi
Joo, Erina
Suzuki, Kazuyo
Nasteska, Daniela
Tanaka, Daisuke
Ogura, Masahito
Harashima, Shin‐ichi
Inagaki, Nobuya
author_facet Yamane, Shunsuke
Harada, Norio
Hamasaki, Akihiro
Muraoka, Atsushi
Joo, Erina
Suzuki, Kazuyo
Nasteska, Daniela
Tanaka, Daisuke
Ogura, Masahito
Harashima, Shin‐ichi
Inagaki, Nobuya
author_sort Yamane, Shunsuke
collection PubMed
description Aims/Introduction:  Gastric inhibitory polypeptide (GIP) and glucagon‐like peptide‐1 (GLP‐1) are the major incretins; their secretion after various nutrient loads are well‐evaluated in Caucasians. However, little is known of the relationship between incretin secretion and differing nutritional loading in Japanese subjects. In the present study, we evaluated GIP and GLP‐1 secretion in Japanese subjects with normal glucose tolerance (NGT) after glucose loading (75 g glucose and 17 g glucose) and meal ingestion. Materials and Methods:  A total of 10 Japanese NGT subjects participated in 75 g oral glucose tolerance test (OGTT), 17 g OGTT and meal tolerance test (MTT). Plasma glucose (PG), serum insulin (IRI), serum C‐peptide (CPR), plasma total GIP, and plasma total GLP‐1 levels during OGTT and MTT were determined. Results:  Area under the curve (AUC)‐GIP was increased in proportion to the amount of glucose, and was highest in MTT, showing that GIP secretion is also stimulated by nutrients other than glucose, such as lipid. In contrast, although the larger glucose load tended to induce a larger GLP‐1 release, AUC‐GLP‐1 was not significantly different among the three loading tests (75 g OGTT, 17 g OGTT, MTT) irrespective of the kind or amount of nutrition load. Conclusions:  Our results suggest that nutritional composition might have a greater effect on GIP secretion than that on GLP‐1 secretion in Japanese NGT subjects. (J Diabetes Invest, doi: 10.1111/j.2040‐1124.2011.00143.x, 2012)
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spelling pubmed-40149362014-05-19 Effects of glucose and meal ingestion on incretin secretion in Japanese subjects with normal glucose tolerance Yamane, Shunsuke Harada, Norio Hamasaki, Akihiro Muraoka, Atsushi Joo, Erina Suzuki, Kazuyo Nasteska, Daniela Tanaka, Daisuke Ogura, Masahito Harashima, Shin‐ichi Inagaki, Nobuya J Diabetes Investig Articles Aims/Introduction:  Gastric inhibitory polypeptide (GIP) and glucagon‐like peptide‐1 (GLP‐1) are the major incretins; their secretion after various nutrient loads are well‐evaluated in Caucasians. However, little is known of the relationship between incretin secretion and differing nutritional loading in Japanese subjects. In the present study, we evaluated GIP and GLP‐1 secretion in Japanese subjects with normal glucose tolerance (NGT) after glucose loading (75 g glucose and 17 g glucose) and meal ingestion. Materials and Methods:  A total of 10 Japanese NGT subjects participated in 75 g oral glucose tolerance test (OGTT), 17 g OGTT and meal tolerance test (MTT). Plasma glucose (PG), serum insulin (IRI), serum C‐peptide (CPR), plasma total GIP, and plasma total GLP‐1 levels during OGTT and MTT were determined. Results:  Area under the curve (AUC)‐GIP was increased in proportion to the amount of glucose, and was highest in MTT, showing that GIP secretion is also stimulated by nutrients other than glucose, such as lipid. In contrast, although the larger glucose load tended to induce a larger GLP‐1 release, AUC‐GLP‐1 was not significantly different among the three loading tests (75 g OGTT, 17 g OGTT, MTT) irrespective of the kind or amount of nutrition load. Conclusions:  Our results suggest that nutritional composition might have a greater effect on GIP secretion than that on GLP‐1 secretion in Japanese NGT subjects. (J Diabetes Invest, doi: 10.1111/j.2040‐1124.2011.00143.x, 2012) Blackwell Publishing Ltd 2011-07-04 2012-02-20 /pmc/articles/PMC4014936/ /pubmed/24843549 http://dx.doi.org/10.1111/j.2040-1124.2011.00143.x Text en © 2011 Asian Association for the Study of Diabetes and Blackwell Publishing Asia Pty Ltd
spellingShingle Articles
Yamane, Shunsuke
Harada, Norio
Hamasaki, Akihiro
Muraoka, Atsushi
Joo, Erina
Suzuki, Kazuyo
Nasteska, Daniela
Tanaka, Daisuke
Ogura, Masahito
Harashima, Shin‐ichi
Inagaki, Nobuya
Effects of glucose and meal ingestion on incretin secretion in Japanese subjects with normal glucose tolerance
title Effects of glucose and meal ingestion on incretin secretion in Japanese subjects with normal glucose tolerance
title_full Effects of glucose and meal ingestion on incretin secretion in Japanese subjects with normal glucose tolerance
title_fullStr Effects of glucose and meal ingestion on incretin secretion in Japanese subjects with normal glucose tolerance
title_full_unstemmed Effects of glucose and meal ingestion on incretin secretion in Japanese subjects with normal glucose tolerance
title_short Effects of glucose and meal ingestion on incretin secretion in Japanese subjects with normal glucose tolerance
title_sort effects of glucose and meal ingestion on incretin secretion in japanese subjects with normal glucose tolerance
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4014936/
https://www.ncbi.nlm.nih.gov/pubmed/24843549
http://dx.doi.org/10.1111/j.2040-1124.2011.00143.x
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