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Arteriovenous Blood Metabolomics: A Readout of Intra-Tissue Metabostasis

The human circulatory system consists of arterial blood that delivers nutrients to tissues, and venous blood that removes the metabolic by-products. Although it is well established that arterial blood generally has higher concentrations of glucose and oxygen relative to venous blood, a comprehensive...

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Autores principales: Ivanisevic, Julijana, Elias, Darlene, Deguchi, Hiroshi, Averell, Patricia M., Kurczy, Michael, Johnson, Caroline H., Tautenhahn, Ralf, Zhu, Zhengjiang, Watrous, Jeramie, Jain, Mohit, Griffin, John, Patti, Gary J., Siuzdak, Gary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4525490/
https://www.ncbi.nlm.nih.gov/pubmed/26244428
http://dx.doi.org/10.1038/srep12757
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author Ivanisevic, Julijana
Elias, Darlene
Deguchi, Hiroshi
Averell, Patricia M.
Kurczy, Michael
Johnson, Caroline H.
Tautenhahn, Ralf
Zhu, Zhengjiang
Watrous, Jeramie
Jain, Mohit
Griffin, John
Patti, Gary J.
Siuzdak, Gary
author_facet Ivanisevic, Julijana
Elias, Darlene
Deguchi, Hiroshi
Averell, Patricia M.
Kurczy, Michael
Johnson, Caroline H.
Tautenhahn, Ralf
Zhu, Zhengjiang
Watrous, Jeramie
Jain, Mohit
Griffin, John
Patti, Gary J.
Siuzdak, Gary
author_sort Ivanisevic, Julijana
collection PubMed
description The human circulatory system consists of arterial blood that delivers nutrients to tissues, and venous blood that removes the metabolic by-products. Although it is well established that arterial blood generally has higher concentrations of glucose and oxygen relative to venous blood, a comprehensive biochemical characterization of arteriovenous differences has not yet been reported. Here we apply cutting-edge, mass spectrometry-based metabolomic technologies to provide a global characterization of metabolites that vary in concentration between the arterial and venous blood of human patients. Global profiling of paired arterial and venous plasma from 20 healthy individuals, followed up by targeted analysis made it possible to measure subtle (<2 fold), yet highly statistically significant and physiologically important differences in water soluble human plasma metabolome. While we detected changes in lactic acid, alanine, glutamine, and glutamate as expected from skeletal muscle activity, a number of unanticipated metabolites were also determined to be significantly altered including Krebs cycle intermediates, amino acids that have not been previously implicated in transport, and a few oxidized fatty acids. This study provides the most comprehensive assessment of metabolic changes in the blood during circulation to date and suggests that such profiling approach may offer new insights into organ homeostasis and organ specific pathology.
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spelling pubmed-45254902015-08-06 Arteriovenous Blood Metabolomics: A Readout of Intra-Tissue Metabostasis Ivanisevic, Julijana Elias, Darlene Deguchi, Hiroshi Averell, Patricia M. Kurczy, Michael Johnson, Caroline H. Tautenhahn, Ralf Zhu, Zhengjiang Watrous, Jeramie Jain, Mohit Griffin, John Patti, Gary J. Siuzdak, Gary Sci Rep Article The human circulatory system consists of arterial blood that delivers nutrients to tissues, and venous blood that removes the metabolic by-products. Although it is well established that arterial blood generally has higher concentrations of glucose and oxygen relative to venous blood, a comprehensive biochemical characterization of arteriovenous differences has not yet been reported. Here we apply cutting-edge, mass spectrometry-based metabolomic technologies to provide a global characterization of metabolites that vary in concentration between the arterial and venous blood of human patients. Global profiling of paired arterial and venous plasma from 20 healthy individuals, followed up by targeted analysis made it possible to measure subtle (<2 fold), yet highly statistically significant and physiologically important differences in water soluble human plasma metabolome. While we detected changes in lactic acid, alanine, glutamine, and glutamate as expected from skeletal muscle activity, a number of unanticipated metabolites were also determined to be significantly altered including Krebs cycle intermediates, amino acids that have not been previously implicated in transport, and a few oxidized fatty acids. This study provides the most comprehensive assessment of metabolic changes in the blood during circulation to date and suggests that such profiling approach may offer new insights into organ homeostasis and organ specific pathology. Nature Publishing Group 2015-08-05 /pmc/articles/PMC4525490/ /pubmed/26244428 http://dx.doi.org/10.1038/srep12757 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Ivanisevic, Julijana
Elias, Darlene
Deguchi, Hiroshi
Averell, Patricia M.
Kurczy, Michael
Johnson, Caroline H.
Tautenhahn, Ralf
Zhu, Zhengjiang
Watrous, Jeramie
Jain, Mohit
Griffin, John
Patti, Gary J.
Siuzdak, Gary
Arteriovenous Blood Metabolomics: A Readout of Intra-Tissue Metabostasis
title Arteriovenous Blood Metabolomics: A Readout of Intra-Tissue Metabostasis
title_full Arteriovenous Blood Metabolomics: A Readout of Intra-Tissue Metabostasis
title_fullStr Arteriovenous Blood Metabolomics: A Readout of Intra-Tissue Metabostasis
title_full_unstemmed Arteriovenous Blood Metabolomics: A Readout of Intra-Tissue Metabostasis
title_short Arteriovenous Blood Metabolomics: A Readout of Intra-Tissue Metabostasis
title_sort arteriovenous blood metabolomics: a readout of intra-tissue metabostasis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4525490/
https://www.ncbi.nlm.nih.gov/pubmed/26244428
http://dx.doi.org/10.1038/srep12757
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