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The pattern of plasma BCAA concentration and liver Bckdha gene expression in GK rats during T2D progression

BACKGROUND: This study was conducted to measure the concentration of branched chain amino acid (BCAA) in different species and detect the expression pattern of the liver Bckdha gene in Goto‐Kakizaki (GK) rats during type 2 diabetes (T2D) progression. METHODS: We measured the concentration of BCAA in...

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Autores principales: Zhang, Wenlu, Wu, Yu'e, Fan, Wei, Chen, Hongmei, Du, Hongli, Rao, Junhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6388062/
https://www.ncbi.nlm.nih.gov/pubmed/30891580
http://dx.doi.org/10.1002/ame2.12038
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author Zhang, Wenlu
Wu, Yu'e
Fan, Wei
Chen, Hongmei
Du, Hongli
Rao, Junhua
author_facet Zhang, Wenlu
Wu, Yu'e
Fan, Wei
Chen, Hongmei
Du, Hongli
Rao, Junhua
author_sort Zhang, Wenlu
collection PubMed
description BACKGROUND: This study was conducted to measure the concentration of branched chain amino acid (BCAA) in different species and detect the expression pattern of the liver Bckdha gene in Goto‐Kakizaki (GK) rats during type 2 diabetes (T2D) progression. METHODS: We measured the concentration of BCAA in GK rats, induced T2D cynomolgus monkeys and T2D humans by liquid chromatography tandem mass spectrometry, and used real‐time quantitative PCR to analyze the gene expression of Bckdha and Bckdk, which encode the rate‐limiting enzymes in catabolism of, respectively, branched chain amino acids and branched chain α‐keto acid dehydrogenase kinase. RESULTS: In this study, we showed that GK rat BCAA concentrations were significantly reduced at 4 and 8 weeks (P < 0.05 and P < 0.01, respectively), while the expression of Bckdha in GK rat liver was increased at 4 and 8 weeks (1.62‐fold and 1.93‐fold, respectively). The BCAA concentrations were significantly reduced in diet‐induced T2D cynomolgus monkeys (P < 0.01), but significantly increased in T2D humans (P < 0.001). CONCLUSIONS: Our results showed that BCAA concentrations changed at different times and by different amounts in different species and during different periods of T2D progress, and the significant changes of BCAA concentration in the three species indicated that BCAA might participate in the progress of T2D. The results suggested that the increased expression of Bckdha in GK rat liver might partially explain the reduced plasma BCAA concentration at 4 and 8 weeks. Further studies are required to investigate the exact mechanism of BCAA changes in non‐obese T2D.
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spelling pubmed-63880622019-03-19 The pattern of plasma BCAA concentration and liver Bckdha gene expression in GK rats during T2D progression Zhang, Wenlu Wu, Yu'e Fan, Wei Chen, Hongmei Du, Hongli Rao, Junhua Animal Model Exp Med Original Articles BACKGROUND: This study was conducted to measure the concentration of branched chain amino acid (BCAA) in different species and detect the expression pattern of the liver Bckdha gene in Goto‐Kakizaki (GK) rats during type 2 diabetes (T2D) progression. METHODS: We measured the concentration of BCAA in GK rats, induced T2D cynomolgus monkeys and T2D humans by liquid chromatography tandem mass spectrometry, and used real‐time quantitative PCR to analyze the gene expression of Bckdha and Bckdk, which encode the rate‐limiting enzymes in catabolism of, respectively, branched chain amino acids and branched chain α‐keto acid dehydrogenase kinase. RESULTS: In this study, we showed that GK rat BCAA concentrations were significantly reduced at 4 and 8 weeks (P < 0.05 and P < 0.01, respectively), while the expression of Bckdha in GK rat liver was increased at 4 and 8 weeks (1.62‐fold and 1.93‐fold, respectively). The BCAA concentrations were significantly reduced in diet‐induced T2D cynomolgus monkeys (P < 0.01), but significantly increased in T2D humans (P < 0.001). CONCLUSIONS: Our results showed that BCAA concentrations changed at different times and by different amounts in different species and during different periods of T2D progress, and the significant changes of BCAA concentration in the three species indicated that BCAA might participate in the progress of T2D. The results suggested that the increased expression of Bckdha in GK rat liver might partially explain the reduced plasma BCAA concentration at 4 and 8 weeks. Further studies are required to investigate the exact mechanism of BCAA changes in non‐obese T2D. John Wiley and Sons Inc. 2018-11-13 /pmc/articles/PMC6388062/ /pubmed/30891580 http://dx.doi.org/10.1002/ame2.12038 Text en © 2018 The Authors. Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Zhang, Wenlu
Wu, Yu'e
Fan, Wei
Chen, Hongmei
Du, Hongli
Rao, Junhua
The pattern of plasma BCAA concentration and liver Bckdha gene expression in GK rats during T2D progression
title The pattern of plasma BCAA concentration and liver Bckdha gene expression in GK rats during T2D progression
title_full The pattern of plasma BCAA concentration and liver Bckdha gene expression in GK rats during T2D progression
title_fullStr The pattern of plasma BCAA concentration and liver Bckdha gene expression in GK rats during T2D progression
title_full_unstemmed The pattern of plasma BCAA concentration and liver Bckdha gene expression in GK rats during T2D progression
title_short The pattern of plasma BCAA concentration and liver Bckdha gene expression in GK rats during T2D progression
title_sort pattern of plasma bcaa concentration and liver bckdha gene expression in gk rats during t2d progression
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6388062/
https://www.ncbi.nlm.nih.gov/pubmed/30891580
http://dx.doi.org/10.1002/ame2.12038
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