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Hydrogen sulphide-induced hypometabolism in human-sized porcine kidneys

BACKGROUND: Since the start of organ transplantation, hypothermia-forced hypometabolism has been the cornerstone in organ preservation. Cold preservation showed to protect against ischemia, although post-transplant injury still occurs and further improvement in preservation techniques is needed. We...

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Autores principales: Maassen, Hanno, Hendriks, Koen D. W., Venema, Leonie H., Henning, Rob H., Hofker, Sijbrand H., van Goor, Harry, Leuvenink, Henri G. D., Coester, Annemieke M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6863563/
https://www.ncbi.nlm.nih.gov/pubmed/31743376
http://dx.doi.org/10.1371/journal.pone.0225152
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author Maassen, Hanno
Hendriks, Koen D. W.
Venema, Leonie H.
Henning, Rob H.
Hofker, Sijbrand H.
van Goor, Harry
Leuvenink, Henri G. D.
Coester, Annemieke M.
author_facet Maassen, Hanno
Hendriks, Koen D. W.
Venema, Leonie H.
Henning, Rob H.
Hofker, Sijbrand H.
van Goor, Harry
Leuvenink, Henri G. D.
Coester, Annemieke M.
author_sort Maassen, Hanno
collection PubMed
description BACKGROUND: Since the start of organ transplantation, hypothermia-forced hypometabolism has been the cornerstone in organ preservation. Cold preservation showed to protect against ischemia, although post-transplant injury still occurs and further improvement in preservation techniques is needed. We hypothesize that hydrogen sulphide can be used as such a new preservation method, by inducing a reversible hypometabolic state in human sized kidneys during normothermic machine perfusion. METHODS: Porcine kidneys were connected to an ex-vivo isolated, oxygen supplemented, normothermic blood perfusion set-up. Experimental kidneys (n = 5) received a 85mg NaHS infusion of 100 ppm and were compared to controls (n = 5). As a reflection of the cellular metabolism, oxygen consumption, mitochondrial activity and tissue ATP levels were measured. Kidney function was assessed by creatinine clearance and fractional excretion of sodium. To rule out potential structural and functional deterioration, kidneys were studied for biochemical markers and histology. RESULTS: Hydrogen sulphide strongly decreased oxygen consumption by 61%, which was associated with a marked decrease in mitochondrial activity/function, without directly affecting ATP levels. Renal biological markers, renal function and histology did not change after hydrogen sulphide treatment. CONCLUSION: In conclusion, we showed that hydrogen sulphide can induce a controllable hypometabolic state in a human sized organ, without damaging the organ itself and could thereby be a promising therapeutic alternative for cold preservation under normothermic conditions in renal transplantation.
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spelling pubmed-68635632019-12-07 Hydrogen sulphide-induced hypometabolism in human-sized porcine kidneys Maassen, Hanno Hendriks, Koen D. W. Venema, Leonie H. Henning, Rob H. Hofker, Sijbrand H. van Goor, Harry Leuvenink, Henri G. D. Coester, Annemieke M. PLoS One Research Article BACKGROUND: Since the start of organ transplantation, hypothermia-forced hypometabolism has been the cornerstone in organ preservation. Cold preservation showed to protect against ischemia, although post-transplant injury still occurs and further improvement in preservation techniques is needed. We hypothesize that hydrogen sulphide can be used as such a new preservation method, by inducing a reversible hypometabolic state in human sized kidneys during normothermic machine perfusion. METHODS: Porcine kidneys were connected to an ex-vivo isolated, oxygen supplemented, normothermic blood perfusion set-up. Experimental kidneys (n = 5) received a 85mg NaHS infusion of 100 ppm and were compared to controls (n = 5). As a reflection of the cellular metabolism, oxygen consumption, mitochondrial activity and tissue ATP levels were measured. Kidney function was assessed by creatinine clearance and fractional excretion of sodium. To rule out potential structural and functional deterioration, kidneys were studied for biochemical markers and histology. RESULTS: Hydrogen sulphide strongly decreased oxygen consumption by 61%, which was associated with a marked decrease in mitochondrial activity/function, without directly affecting ATP levels. Renal biological markers, renal function and histology did not change after hydrogen sulphide treatment. CONCLUSION: In conclusion, we showed that hydrogen sulphide can induce a controllable hypometabolic state in a human sized organ, without damaging the organ itself and could thereby be a promising therapeutic alternative for cold preservation under normothermic conditions in renal transplantation. Public Library of Science 2019-11-19 /pmc/articles/PMC6863563/ /pubmed/31743376 http://dx.doi.org/10.1371/journal.pone.0225152 Text en © 2019 Maassen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Maassen, Hanno
Hendriks, Koen D. W.
Venema, Leonie H.
Henning, Rob H.
Hofker, Sijbrand H.
van Goor, Harry
Leuvenink, Henri G. D.
Coester, Annemieke M.
Hydrogen sulphide-induced hypometabolism in human-sized porcine kidneys
title Hydrogen sulphide-induced hypometabolism in human-sized porcine kidneys
title_full Hydrogen sulphide-induced hypometabolism in human-sized porcine kidneys
title_fullStr Hydrogen sulphide-induced hypometabolism in human-sized porcine kidneys
title_full_unstemmed Hydrogen sulphide-induced hypometabolism in human-sized porcine kidneys
title_short Hydrogen sulphide-induced hypometabolism in human-sized porcine kidneys
title_sort hydrogen sulphide-induced hypometabolism in human-sized porcine kidneys
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6863563/
https://www.ncbi.nlm.nih.gov/pubmed/31743376
http://dx.doi.org/10.1371/journal.pone.0225152
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