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A Newly Developed Method-Based Xanthine Oxidoreductase Activities in Various Human Liver Diseases

Studies evaluating xanthine oxidoreductase (XOR) activities in comprehensive liver diseases are scarce, and different etiologies have previously been combined in groups for comparison. To accurately evaluate XOR activities in liver diseases, the plasma XOR activities in etiology-based comprehensive...

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Autores principales: Sato, Ken, Naganuma, Atsushi, Nagashima, Tamon, Arai, Yosuke, Mikami, Yuka, Nakajima, Yuka, Kanayama, Yuki, Murakami, Tatsuma, Uehara, Sanae, Uehara, Daisuke, Yamazaki, Yuichi, Murase, Takayo, Nakamura, Takashi, Uraoka, Toshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216503/
https://www.ncbi.nlm.nih.gov/pubmed/37239117
http://dx.doi.org/10.3390/biomedicines11051445
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author Sato, Ken
Naganuma, Atsushi
Nagashima, Tamon
Arai, Yosuke
Mikami, Yuka
Nakajima, Yuka
Kanayama, Yuki
Murakami, Tatsuma
Uehara, Sanae
Uehara, Daisuke
Yamazaki, Yuichi
Murase, Takayo
Nakamura, Takashi
Uraoka, Toshio
author_facet Sato, Ken
Naganuma, Atsushi
Nagashima, Tamon
Arai, Yosuke
Mikami, Yuka
Nakajima, Yuka
Kanayama, Yuki
Murakami, Tatsuma
Uehara, Sanae
Uehara, Daisuke
Yamazaki, Yuichi
Murase, Takayo
Nakamura, Takashi
Uraoka, Toshio
author_sort Sato, Ken
collection PubMed
description Studies evaluating xanthine oxidoreductase (XOR) activities in comprehensive liver diseases are scarce, and different etiologies have previously been combined in groups for comparison. To accurately evaluate XOR activities in liver diseases, the plasma XOR activities in etiology-based comprehensive liver diseases were measured using a novel, sensitive, and accurate assay that is a combination of liquid chromatography and triple quadrupole mass spectrometry to detect [(13)C(2), (15)N(2)]uric acid using [(13)C(2), (15)N(2)]xanthine as a substrate. We also mainly evaluated the association between the plasma XOR activities and parameters of liver tests, purine metabolism-associated markers, oxidative stress markers, and an inflammation marker. In total, 329 patients and 32 controls were enrolled in our study. Plasma XOR activities were generally increased in liver diseases, especially in the active phase, such as in patients with hepatitis C virus RNA positivity, those with abnormal alanine transaminase (ALT) levels in autoimmune liver diseases, and uncured hepatocellular carcinoma patients. Plasma XOR activities were numerically highest in patients with acute hepatitis B. Plasma XOR activities were closely correlated with parameters of liver tests, especially serum ALT levels, regardless of etiology and plasma xanthine levels. Our results indicated that plasma XOR activity might reflect the active phase in various liver diseases.
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spelling pubmed-102165032023-05-27 A Newly Developed Method-Based Xanthine Oxidoreductase Activities in Various Human Liver Diseases Sato, Ken Naganuma, Atsushi Nagashima, Tamon Arai, Yosuke Mikami, Yuka Nakajima, Yuka Kanayama, Yuki Murakami, Tatsuma Uehara, Sanae Uehara, Daisuke Yamazaki, Yuichi Murase, Takayo Nakamura, Takashi Uraoka, Toshio Biomedicines Article Studies evaluating xanthine oxidoreductase (XOR) activities in comprehensive liver diseases are scarce, and different etiologies have previously been combined in groups for comparison. To accurately evaluate XOR activities in liver diseases, the plasma XOR activities in etiology-based comprehensive liver diseases were measured using a novel, sensitive, and accurate assay that is a combination of liquid chromatography and triple quadrupole mass spectrometry to detect [(13)C(2), (15)N(2)]uric acid using [(13)C(2), (15)N(2)]xanthine as a substrate. We also mainly evaluated the association between the plasma XOR activities and parameters of liver tests, purine metabolism-associated markers, oxidative stress markers, and an inflammation marker. In total, 329 patients and 32 controls were enrolled in our study. Plasma XOR activities were generally increased in liver diseases, especially in the active phase, such as in patients with hepatitis C virus RNA positivity, those with abnormal alanine transaminase (ALT) levels in autoimmune liver diseases, and uncured hepatocellular carcinoma patients. Plasma XOR activities were numerically highest in patients with acute hepatitis B. Plasma XOR activities were closely correlated with parameters of liver tests, especially serum ALT levels, regardless of etiology and plasma xanthine levels. Our results indicated that plasma XOR activity might reflect the active phase in various liver diseases. MDPI 2023-05-14 /pmc/articles/PMC10216503/ /pubmed/37239117 http://dx.doi.org/10.3390/biomedicines11051445 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sato, Ken
Naganuma, Atsushi
Nagashima, Tamon
Arai, Yosuke
Mikami, Yuka
Nakajima, Yuka
Kanayama, Yuki
Murakami, Tatsuma
Uehara, Sanae
Uehara, Daisuke
Yamazaki, Yuichi
Murase, Takayo
Nakamura, Takashi
Uraoka, Toshio
A Newly Developed Method-Based Xanthine Oxidoreductase Activities in Various Human Liver Diseases
title A Newly Developed Method-Based Xanthine Oxidoreductase Activities in Various Human Liver Diseases
title_full A Newly Developed Method-Based Xanthine Oxidoreductase Activities in Various Human Liver Diseases
title_fullStr A Newly Developed Method-Based Xanthine Oxidoreductase Activities in Various Human Liver Diseases
title_full_unstemmed A Newly Developed Method-Based Xanthine Oxidoreductase Activities in Various Human Liver Diseases
title_short A Newly Developed Method-Based Xanthine Oxidoreductase Activities in Various Human Liver Diseases
title_sort newly developed method-based xanthine oxidoreductase activities in various human liver diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216503/
https://www.ncbi.nlm.nih.gov/pubmed/37239117
http://dx.doi.org/10.3390/biomedicines11051445
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