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Proton Nuclear Magnetic Resonance (1H-NMR)-Based Metabolomic Evaluation of Human Renal Allografts from Donations After Circulatory Death

BACKGROUND: Delayed graft function (DGF) is a common complication that impairs allograft function after kidney transplantation. However, the mechanism of DGF remains unclear. Nuclear magnetic resonance (NMR)-based analysis has been widely used in recent times to assess changes in metabolite levels....

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Autores principales: Wang, Zijie, Yang, Haiwei, Zhao, Chunchun, Wei, Jifu, Wang, Junsong, Han, Zhijian, Tao, Jun, Xu, Zhen, Ju, Xiaobin, Tan, Ruoyun, Gu, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5702106/
https://www.ncbi.nlm.nih.gov/pubmed/29149095
http://dx.doi.org/10.12659/MSM.905168
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author Wang, Zijie
Yang, Haiwei
Zhao, Chunchun
Wei, Jifu
Wang, Junsong
Han, Zhijian
Tao, Jun
Xu, Zhen
Ju, Xiaobin
Tan, Ruoyun
Gu, Min
author_facet Wang, Zijie
Yang, Haiwei
Zhao, Chunchun
Wei, Jifu
Wang, Junsong
Han, Zhijian
Tao, Jun
Xu, Zhen
Ju, Xiaobin
Tan, Ruoyun
Gu, Min
author_sort Wang, Zijie
collection PubMed
description BACKGROUND: Delayed graft function (DGF) is a common complication that impairs allograft function after kidney transplantation. However, the mechanism of DGF remains unclear. Nuclear magnetic resonance (NMR)-based analysis has been widely used in recent times to assess changes in metabolite levels. MATERIAL/METHODS: Samples of perfusate from allografts donated after circulatory death were collected prior to transplantation, during static cold storage. (1)H-NMR-based metabolomics combined with the statistical methods, orthogonal partial least-squares discriminant analysis (OPLS-DA), and principle-component analysis (PCA), were employed to test different levels of metabolites between the allografts that exhibited DGF and those that exhibited immediate graft function (IGF). RESULTS: The study population consisted of 36 subjects, 11 with DGF and 25 with IGF. Of the 37 detected and identified metabolites, α-glucose and citrate were significantly elevated in the perfusate of DGF allografts, and taurine and betaine were significantly decreased. CONCLUSIONS: (1)H-NMR analysis of DGF and IGF perfusates revealed some significant differences in their metabolite profiles, which may help explain the mechanisms of kidney ischemia-reperfusion injury and DGF.
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spelling pubmed-57021062017-11-29 Proton Nuclear Magnetic Resonance (1H-NMR)-Based Metabolomic Evaluation of Human Renal Allografts from Donations After Circulatory Death Wang, Zijie Yang, Haiwei Zhao, Chunchun Wei, Jifu Wang, Junsong Han, Zhijian Tao, Jun Xu, Zhen Ju, Xiaobin Tan, Ruoyun Gu, Min Med Sci Monit Clinical Research BACKGROUND: Delayed graft function (DGF) is a common complication that impairs allograft function after kidney transplantation. However, the mechanism of DGF remains unclear. Nuclear magnetic resonance (NMR)-based analysis has been widely used in recent times to assess changes in metabolite levels. MATERIAL/METHODS: Samples of perfusate from allografts donated after circulatory death were collected prior to transplantation, during static cold storage. (1)H-NMR-based metabolomics combined with the statistical methods, orthogonal partial least-squares discriminant analysis (OPLS-DA), and principle-component analysis (PCA), were employed to test different levels of metabolites between the allografts that exhibited DGF and those that exhibited immediate graft function (IGF). RESULTS: The study population consisted of 36 subjects, 11 with DGF and 25 with IGF. Of the 37 detected and identified metabolites, α-glucose and citrate were significantly elevated in the perfusate of DGF allografts, and taurine and betaine were significantly decreased. CONCLUSIONS: (1)H-NMR analysis of DGF and IGF perfusates revealed some significant differences in their metabolite profiles, which may help explain the mechanisms of kidney ischemia-reperfusion injury and DGF. International Scientific Literature, Inc. 2017-11-17 /pmc/articles/PMC5702106/ /pubmed/29149095 http://dx.doi.org/10.12659/MSM.905168 Text en © Med Sci Monit, 2017 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Clinical Research
Wang, Zijie
Yang, Haiwei
Zhao, Chunchun
Wei, Jifu
Wang, Junsong
Han, Zhijian
Tao, Jun
Xu, Zhen
Ju, Xiaobin
Tan, Ruoyun
Gu, Min
Proton Nuclear Magnetic Resonance (1H-NMR)-Based Metabolomic Evaluation of Human Renal Allografts from Donations After Circulatory Death
title Proton Nuclear Magnetic Resonance (1H-NMR)-Based Metabolomic Evaluation of Human Renal Allografts from Donations After Circulatory Death
title_full Proton Nuclear Magnetic Resonance (1H-NMR)-Based Metabolomic Evaluation of Human Renal Allografts from Donations After Circulatory Death
title_fullStr Proton Nuclear Magnetic Resonance (1H-NMR)-Based Metabolomic Evaluation of Human Renal Allografts from Donations After Circulatory Death
title_full_unstemmed Proton Nuclear Magnetic Resonance (1H-NMR)-Based Metabolomic Evaluation of Human Renal Allografts from Donations After Circulatory Death
title_short Proton Nuclear Magnetic Resonance (1H-NMR)-Based Metabolomic Evaluation of Human Renal Allografts from Donations After Circulatory Death
title_sort proton nuclear magnetic resonance (1h-nmr)-based metabolomic evaluation of human renal allografts from donations after circulatory death
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5702106/
https://www.ncbi.nlm.nih.gov/pubmed/29149095
http://dx.doi.org/10.12659/MSM.905168
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