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Ophthalmic acid as a read-out for hepatic glutathione metabolism in humans

BACKGROUND AND AIM: Animal studies indicated that systemic ophthalmic acid (OPH) is a biomarker for hepatic glutathione (GSH) homeostasis, an important determinant of liver function. We aimed to clarify whether OPH levels can be used as a read-out for hepatic GSH homeostasis after paracetamol (APAP)...

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Autores principales: Kim MC van, Mierlo, Dello, Simon AWG, de Jong, Mechteld C, van Eijk, Hans MH, de Kok, Theo M, Briedé, Jacob J, Schaap, Frank G, Damink, Steven WM Olde, Dejong, Cornelius HC
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Whioce Publishing Pte. Ltd. 2018
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412618/
https://www.ncbi.nlm.nih.gov/pubmed/30873484
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author Kim MC van, Mierlo
Dello, Simon AWG
de Jong, Mechteld C
van Eijk, Hans MH
de Kok, Theo M
Briedé, Jacob J
Schaap, Frank G
Damink, Steven WM Olde
Dejong, Cornelius HC
author_facet Kim MC van, Mierlo
Dello, Simon AWG
de Jong, Mechteld C
van Eijk, Hans MH
de Kok, Theo M
Briedé, Jacob J
Schaap, Frank G
Damink, Steven WM Olde
Dejong, Cornelius HC
author_sort Kim MC van, Mierlo
collection PubMed
description BACKGROUND AND AIM: Animal studies indicated that systemic ophthalmic acid (OPH) is a biomarker for hepatic glutathione (GSH) homeostasis, an important determinant of liver function. We aimed to clarify whether OPH levels can be used as a read-out for hepatic GSH homeostasis after paracetamol (APAP) challenges during pylorus-preserving pancreaticoduodenectomy (PPPD) or partial hepatectomy (PH). METHODS: Nineteen patients undergoing PPPD (n=7, control group) or PH (n=12) were included. APAP (1000 mg) was administered intravenously before resection (first challenge), and six and twelve hours later, with sequential blood sampling during this period. Arterial, hepatic and portal venous blood samples and liver biopsies were taken on three occasions during the first APAP challenge. Plasma and hepatic OPH and GSH levels were quantified, and venous-arterial differences were calculated to study hepatic release. RESULTS: Systemic GSH levels decreased during the course of the APAP challenge in both surgical groups, without notable change in OPH levels. Hepatic GSH and OPH content was not affected within ˜3 hours after administration of the first APAP dose in patients undergoing PPPD or PH. In this period, net release of OPH by the liver was observed only in patients undergoing PPPD. CONCLUSION: The drop in circulating GSH levels following APAP administrations, did not result in an increase in plasma OPH in both patients with an intact liver and in those undergoing liver resection. Hepatic content of GSH and OPH was not affected during the first APAP dose. It is uncertain whether hepatic GSH homeostasis was sufficiently challenged in the present study. RELEVANCE FOR PATIENTS: In the present study, plasma OPH seemed not useful as a marker for GSH depletion because APAP administration during liver surgery did not lead to (immediate) GSH depletion or increased OPH levels. Based on stable levels of hepatic GSH, OPH and thiyl radicals during surgery, standard APAP administration seems to be safe in a postoperative care program with regards to GSH homeostasis in this specific population. However, no general statements can be made on the basis of the current experiment, since GSH homeostasis and susceptibility to xenobiotic toxicity are influenced by several metabolic and genetic factors.
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spelling pubmed-64126182019-03-14 Ophthalmic acid as a read-out for hepatic glutathione metabolism in humans Kim MC van, Mierlo Dello, Simon AWG de Jong, Mechteld C van Eijk, Hans MH de Kok, Theo M Briedé, Jacob J Schaap, Frank G Damink, Steven WM Olde Dejong, Cornelius HC J Clin Transl Res Special Issue Article BACKGROUND AND AIM: Animal studies indicated that systemic ophthalmic acid (OPH) is a biomarker for hepatic glutathione (GSH) homeostasis, an important determinant of liver function. We aimed to clarify whether OPH levels can be used as a read-out for hepatic GSH homeostasis after paracetamol (APAP) challenges during pylorus-preserving pancreaticoduodenectomy (PPPD) or partial hepatectomy (PH). METHODS: Nineteen patients undergoing PPPD (n=7, control group) or PH (n=12) were included. APAP (1000 mg) was administered intravenously before resection (first challenge), and six and twelve hours later, with sequential blood sampling during this period. Arterial, hepatic and portal venous blood samples and liver biopsies were taken on three occasions during the first APAP challenge. Plasma and hepatic OPH and GSH levels were quantified, and venous-arterial differences were calculated to study hepatic release. RESULTS: Systemic GSH levels decreased during the course of the APAP challenge in both surgical groups, without notable change in OPH levels. Hepatic GSH and OPH content was not affected within ˜3 hours after administration of the first APAP dose in patients undergoing PPPD or PH. In this period, net release of OPH by the liver was observed only in patients undergoing PPPD. CONCLUSION: The drop in circulating GSH levels following APAP administrations, did not result in an increase in plasma OPH in both patients with an intact liver and in those undergoing liver resection. Hepatic content of GSH and OPH was not affected during the first APAP dose. It is uncertain whether hepatic GSH homeostasis was sufficiently challenged in the present study. RELEVANCE FOR PATIENTS: In the present study, plasma OPH seemed not useful as a marker for GSH depletion because APAP administration during liver surgery did not lead to (immediate) GSH depletion or increased OPH levels. Based on stable levels of hepatic GSH, OPH and thiyl radicals during surgery, standard APAP administration seems to be safe in a postoperative care program with regards to GSH homeostasis in this specific population. However, no general statements can be made on the basis of the current experiment, since GSH homeostasis and susceptibility to xenobiotic toxicity are influenced by several metabolic and genetic factors. Whioce Publishing Pte. Ltd. 2018-03-25 /pmc/articles/PMC6412618/ /pubmed/30873484 Text en Copyright © 2015, Whioce Publishing Pte. Ltd. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. This work is licensed under a Creative Commons Attribution 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Special Issue Article
Kim MC van, Mierlo
Dello, Simon AWG
de Jong, Mechteld C
van Eijk, Hans MH
de Kok, Theo M
Briedé, Jacob J
Schaap, Frank G
Damink, Steven WM Olde
Dejong, Cornelius HC
Ophthalmic acid as a read-out for hepatic glutathione metabolism in humans
title Ophthalmic acid as a read-out for hepatic glutathione metabolism in humans
title_full Ophthalmic acid as a read-out for hepatic glutathione metabolism in humans
title_fullStr Ophthalmic acid as a read-out for hepatic glutathione metabolism in humans
title_full_unstemmed Ophthalmic acid as a read-out for hepatic glutathione metabolism in humans
title_short Ophthalmic acid as a read-out for hepatic glutathione metabolism in humans
title_sort ophthalmic acid as a read-out for hepatic glutathione metabolism in humans
topic Special Issue Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412618/
https://www.ncbi.nlm.nih.gov/pubmed/30873484
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