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A reappraisal of xanthine dehydrogenase and oxidase in hypoxic reperfusion injury: the role of NADH as an electron donor

A reappraisal of xanthine dehydrogenase and oxidase in hypoxic reperfusion injury: the role of NADH as an electron donor
A reappraisal of xanthine dehydrogenase and oxidase in hypoxic reperfusion injury: the role of NADH as an electron donor
Xanthine oxidase (XO) is conventionally known as a generator of reactive oxygen species (ROS) which contribute to hypoxic-reperfusion injury in tissues. However, this role for human XO is disputed due to its distinctive lack of activity towards xanthine, and the failure of allopurinol to suppress reperfusion injury. In this paper, we have employed native gel electrophoresis together with activity staining to investigate the role human xanthine dehydrogenase (XD) and XO in hypoxic reperfusion injury. This approach has provided information which cannot be obtained by conventional spectrophotometric assays. We found that both XD and XO of human umbilical vein endothelial cells (HUVECs) and lymphoblastic leukaemic cells (CEMs) catalysed ROS generation by oxidising NADH, but not hypoxanthine. The conversion of XD to XO was observed in both HUVECs and CEMs in response to hypoxia, although the level of conversion varied. Purified human milk XD generated ROS more efficiently in the presence of NADH than in the presence of hypoxanthine. This NADH oxidising activity was blocked by the FAD site inhibitor, diphenyleneiodonium (DPI), but was not suppressible by the molybdenum site inhibitor, allopurinol. However, in the presence of both DPI and allopwinol the activities of XD/XO were completely blocked with either NADH or hypoxanthine as substrates. We conclude that both human XD and XO can oxidise NADH to generate ROS. Therefore, the conversion of XD to XO is not necessary for post-ischaemic ROS generation. The hypoxic-reperfusion injury hypothesis should be reappraised to take into account the important role played by XD and XO in oxidising NADH to yield ROS.
xanthine dehydrogenase, xanthine oxidase, NADH oxidase, reperfusion injury, reactive oxygen species, hypoxia
1071-5762
151-164
Zhang, Zhi
ec64de99-9d5b-429c-90d1-f10609f56803
Blake, David R.
f9527a3a-b4f0-4ffa-a3cc-16c634c5e41b
Stevens, Cliff R.
bcefc445-6fa7-4a48-b6e3-6ba597342d2f
Kanczler, Janos M.
eb8db9ff-a038-475f-9030-48eef2b0559c
Winyard, Paul G.
ad5c2a93-c433-49f3-b69f-6c6b00ea5a6c
Symons, Martyn C.
627d351b-f737-45be-b656-e88f22920a3c
Benboubetra, Mustapha
80a8db1b-a11c-4e41-a965-1103265a8860
Harrison, Roger
345f8121-fe3b-4246-ad8e-2f3cd93f6971
Zhang, Zhi
ec64de99-9d5b-429c-90d1-f10609f56803
Blake, David R.
f9527a3a-b4f0-4ffa-a3cc-16c634c5e41b
Stevens, Cliff R.
bcefc445-6fa7-4a48-b6e3-6ba597342d2f
Kanczler, Janos M.
eb8db9ff-a038-475f-9030-48eef2b0559c
Winyard, Paul G.
ad5c2a93-c433-49f3-b69f-6c6b00ea5a6c
Symons, Martyn C.
627d351b-f737-45be-b656-e88f22920a3c
Benboubetra, Mustapha
80a8db1b-a11c-4e41-a965-1103265a8860
Harrison, Roger
345f8121-fe3b-4246-ad8e-2f3cd93f6971

Zhang, Zhi, Blake, David R., Stevens, Cliff R., Kanczler, Janos M., Winyard, Paul G., Symons, Martyn C., Benboubetra, Mustapha and Harrison, Roger (1998) A reappraisal of xanthine dehydrogenase and oxidase in hypoxic reperfusion injury: the role of NADH as an electron donor. Free Radical Research, 28 (2), 151-164. (PMID:9645392)

Record type: Article

Abstract

Xanthine oxidase (XO) is conventionally known as a generator of reactive oxygen species (ROS) which contribute to hypoxic-reperfusion injury in tissues. However, this role for human XO is disputed due to its distinctive lack of activity towards xanthine, and the failure of allopurinol to suppress reperfusion injury. In this paper, we have employed native gel electrophoresis together with activity staining to investigate the role human xanthine dehydrogenase (XD) and XO in hypoxic reperfusion injury. This approach has provided information which cannot be obtained by conventional spectrophotometric assays. We found that both XD and XO of human umbilical vein endothelial cells (HUVECs) and lymphoblastic leukaemic cells (CEMs) catalysed ROS generation by oxidising NADH, but not hypoxanthine. The conversion of XD to XO was observed in both HUVECs and CEMs in response to hypoxia, although the level of conversion varied. Purified human milk XD generated ROS more efficiently in the presence of NADH than in the presence of hypoxanthine. This NADH oxidising activity was blocked by the FAD site inhibitor, diphenyleneiodonium (DPI), but was not suppressible by the molybdenum site inhibitor, allopurinol. However, in the presence of both DPI and allopwinol the activities of XD/XO were completely blocked with either NADH or hypoxanthine as substrates. We conclude that both human XD and XO can oxidise NADH to generate ROS. Therefore, the conversion of XD to XO is not necessary for post-ischaemic ROS generation. The hypoxic-reperfusion injury hypothesis should be reappraised to take into account the important role played by XD and XO in oxidising NADH to yield ROS.

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More information

Published date: February 1998
Keywords: xanthine dehydrogenase, xanthine oxidase, NADH oxidase, reperfusion injury, reactive oxygen species, hypoxia

Identifiers

Local EPrints ID: 177295
URI: http://eprints.soton.ac.uk/id/eprint/177295
ISSN: 1071-5762
PURE UUID: a67ae748-25d3-4ac8-a81a-1faf7bd82e85
ORCID for Janos M. Kanczler: ORCID iD orcid.org/0000-0001-7249-0414

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Date deposited: 16 Mar 2011 14:05
Last modified: 09 Jan 2022 03:19

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Contributors

Author: Zhi Zhang
Author: David R. Blake
Author: Cliff R. Stevens
Author: Janos M. Kanczler ORCID iD
Author: Paul G. Winyard
Author: Martyn C. Symons
Author: Mustapha Benboubetra
Author: Roger Harrison

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