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Comparison of area under the curve in various models of diabetic rats receiving chronic medication

INTRODUCTION: The oral glucose tolerance test (OGTT) is widely used as a diagnostic tool for impaired glucose tolerance (IGT) in clinical settings and animal experiments. The area under the curve (AUC) is then developed to quantify the total increase in blood glucose during the OGTT. Similarly, atte...

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Autores principales: Liu, Keng-Fan, Niu, Chiang-Shan, Tsai, Jen-Chieh, Yang, Chao-Lin, Peng, Wen-Huang, Niu, Ho-Shan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9266878/
https://www.ncbi.nlm.nih.gov/pubmed/35832712
http://dx.doi.org/10.5114/aoms.2019.91471
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author Liu, Keng-Fan
Niu, Chiang-Shan
Tsai, Jen-Chieh
Yang, Chao-Lin
Peng, Wen-Huang
Niu, Ho-Shan
author_facet Liu, Keng-Fan
Niu, Chiang-Shan
Tsai, Jen-Chieh
Yang, Chao-Lin
Peng, Wen-Huang
Niu, Ho-Shan
author_sort Liu, Keng-Fan
collection PubMed
description INTRODUCTION: The oral glucose tolerance test (OGTT) is widely used as a diagnostic tool for impaired glucose tolerance (IGT) in clinical settings and animal experiments. The area under the curve (AUC) is then developed to quantify the total increase in blood glucose during the OGTT. Similarly, attenuation of the increased AUC indicates the improvement of IGT in animals. Variations in fasting plasma glucose between individuals stimulate the development of incremental area under the curve (iAUC). However, the iAUC determined from subtracting the baseline value of fasting plasma glucose (similar to ΔAUC) has been challenged as problematic without evidence. MATERIAL AND METHODS: We developed four different diabetic animal models. In each model, rats were treated with metformin, dapagliflozin, and insulin respectively for 1 week. OGTTs were performed after 7 days of the drug treatment. The acute blood glucose changes induced by one-time treatment of drugs were also compared. RESULTS: After a daily application of each drug at an effective dose for 7 days, results indicated potency in the following order: insulin > dapagliflozin > metformin. This was determined by calculation using the AUC in all diabetic models. However, the order changed when using the calculation with iAUC. Additionally, signals were changed before the OGTT in each model that received repeated treatment of each drug. Notably, drug potency was shown to be the same in OGTT calculated from iAUC and AUC in diabetic rats receiving acute treatment. CONCLUSIONS: iAUC seems unsuitable for application in cases where subjects are receiving chronic medication(s).
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spelling pubmed-92668782022-07-12 Comparison of area under the curve in various models of diabetic rats receiving chronic medication Liu, Keng-Fan Niu, Chiang-Shan Tsai, Jen-Chieh Yang, Chao-Lin Peng, Wen-Huang Niu, Ho-Shan Arch Med Sci Experimental Research INTRODUCTION: The oral glucose tolerance test (OGTT) is widely used as a diagnostic tool for impaired glucose tolerance (IGT) in clinical settings and animal experiments. The area under the curve (AUC) is then developed to quantify the total increase in blood glucose during the OGTT. Similarly, attenuation of the increased AUC indicates the improvement of IGT in animals. Variations in fasting plasma glucose between individuals stimulate the development of incremental area under the curve (iAUC). However, the iAUC determined from subtracting the baseline value of fasting plasma glucose (similar to ΔAUC) has been challenged as problematic without evidence. MATERIAL AND METHODS: We developed four different diabetic animal models. In each model, rats were treated with metformin, dapagliflozin, and insulin respectively for 1 week. OGTTs were performed after 7 days of the drug treatment. The acute blood glucose changes induced by one-time treatment of drugs were also compared. RESULTS: After a daily application of each drug at an effective dose for 7 days, results indicated potency in the following order: insulin > dapagliflozin > metformin. This was determined by calculation using the AUC in all diabetic models. However, the order changed when using the calculation with iAUC. Additionally, signals were changed before the OGTT in each model that received repeated treatment of each drug. Notably, drug potency was shown to be the same in OGTT calculated from iAUC and AUC in diabetic rats receiving acute treatment. CONCLUSIONS: iAUC seems unsuitable for application in cases where subjects are receiving chronic medication(s). Termedia Publishing House 2020-01-07 /pmc/articles/PMC9266878/ /pubmed/35832712 http://dx.doi.org/10.5114/aoms.2019.91471 Text en Copyright: © 2019 Termedia & Banach https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Experimental Research
Liu, Keng-Fan
Niu, Chiang-Shan
Tsai, Jen-Chieh
Yang, Chao-Lin
Peng, Wen-Huang
Niu, Ho-Shan
Comparison of area under the curve in various models of diabetic rats receiving chronic medication
title Comparison of area under the curve in various models of diabetic rats receiving chronic medication
title_full Comparison of area under the curve in various models of diabetic rats receiving chronic medication
title_fullStr Comparison of area under the curve in various models of diabetic rats receiving chronic medication
title_full_unstemmed Comparison of area under the curve in various models of diabetic rats receiving chronic medication
title_short Comparison of area under the curve in various models of diabetic rats receiving chronic medication
title_sort comparison of area under the curve in various models of diabetic rats receiving chronic medication
topic Experimental Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9266878/
https://www.ncbi.nlm.nih.gov/pubmed/35832712
http://dx.doi.org/10.5114/aoms.2019.91471
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