Saturation diving alters folate status and biomarkers of DNA damage and repair.

Exposure to oxygen-rich environments can lead to oxidative damage, increased body iron stores, and changes in status of some vitamins, including folate. Assessing the type of oxidative damage in these environments and determining its relationships with changes in folate status are important for defi...

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Main Authors: Sara R Zwart, J Milburn Jessup, Jiuping Ji, Scott M Smith
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3274529?pdf=render
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spelling doaj-742d0a95ce244640b20820212e7666ea2020-11-25T02:51:44ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0172e3105810.1371/journal.pone.0031058Saturation diving alters folate status and biomarkers of DNA damage and repair.Sara R ZwartJ Milburn JessupJiuping JiScott M SmithExposure to oxygen-rich environments can lead to oxidative damage, increased body iron stores, and changes in status of some vitamins, including folate. Assessing the type of oxidative damage in these environments and determining its relationships with changes in folate status are important for defining nutrient requirements and designing countermeasures to mitigate these effects. Responses of humans to oxidative stressors were examined in participants undergoing a saturation dive in an environment with increased partial pressure of oxygen, a NASA Extreme Environment Mission Operations mission. Six participants completed a 13-d saturation dive in a habitat 19 m below the ocean surface near Key Largo, FL. Fasting blood samples were collected before, twice during, and twice after the dive and analyzed for biochemical markers of iron status, oxidative damage, and vitamin status. Body iron stores and ferritin increased during the dive (P<0.001), with a concomitant decrease in RBC folate (P<0.001) and superoxide dismutase activity (P<0.001). Folate status was correlated with serum ferritin (Pearson r = -0.34, P<0.05). Peripheral blood mononuclear cell poly(ADP-ribose) increased during the dive and the increase was significant by the end of the dive (P<0.001); γ-H2AX did not change during the mission. Together, the data provide evidence that when body iron stores were elevated in a hyperoxic environment, a DNA damage repair response occurred in peripheral blood mononuclear cells, but double-stranded DNA damage did not. In addition, folate status decreases quickly in this environment, and this study provides evidence that folate requirements may be greater when body iron stores and DNA damage repair responses are elevated.http://europepmc.org/articles/PMC3274529?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Sara R Zwart
J Milburn Jessup
Jiuping Ji
Scott M Smith
spellingShingle Sara R Zwart
J Milburn Jessup
Jiuping Ji
Scott M Smith
Saturation diving alters folate status and biomarkers of DNA damage and repair.
PLoS ONE
author_facet Sara R Zwart
J Milburn Jessup
Jiuping Ji
Scott M Smith
author_sort Sara R Zwart
title Saturation diving alters folate status and biomarkers of DNA damage and repair.
title_short Saturation diving alters folate status and biomarkers of DNA damage and repair.
title_full Saturation diving alters folate status and biomarkers of DNA damage and repair.
title_fullStr Saturation diving alters folate status and biomarkers of DNA damage and repair.
title_full_unstemmed Saturation diving alters folate status and biomarkers of DNA damage and repair.
title_sort saturation diving alters folate status and biomarkers of dna damage and repair.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Exposure to oxygen-rich environments can lead to oxidative damage, increased body iron stores, and changes in status of some vitamins, including folate. Assessing the type of oxidative damage in these environments and determining its relationships with changes in folate status are important for defining nutrient requirements and designing countermeasures to mitigate these effects. Responses of humans to oxidative stressors were examined in participants undergoing a saturation dive in an environment with increased partial pressure of oxygen, a NASA Extreme Environment Mission Operations mission. Six participants completed a 13-d saturation dive in a habitat 19 m below the ocean surface near Key Largo, FL. Fasting blood samples were collected before, twice during, and twice after the dive and analyzed for biochemical markers of iron status, oxidative damage, and vitamin status. Body iron stores and ferritin increased during the dive (P<0.001), with a concomitant decrease in RBC folate (P<0.001) and superoxide dismutase activity (P<0.001). Folate status was correlated with serum ferritin (Pearson r = -0.34, P<0.05). Peripheral blood mononuclear cell poly(ADP-ribose) increased during the dive and the increase was significant by the end of the dive (P<0.001); γ-H2AX did not change during the mission. Together, the data provide evidence that when body iron stores were elevated in a hyperoxic environment, a DNA damage repair response occurred in peripheral blood mononuclear cells, but double-stranded DNA damage did not. In addition, folate status decreases quickly in this environment, and this study provides evidence that folate requirements may be greater when body iron stores and DNA damage repair responses are elevated.
url http://europepmc.org/articles/PMC3274529?pdf=render
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