A chronic increase of corticosterone age-dependently reduces systemic DNA damage from oxidation in rats

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A chronic increase of corticosterone age-dependently reduces systemic DNA damage from oxidation in rats. / Jorgensen, Anders; Kalliokoski, Otto; Forsberg, Kristin; Breitenstein, Katrine; Weimann, Allan; Henriksen, Trine; Hau, Jann; Wörtwein, Gitta; Poulsen, Henrik Enghusen; Jorgensen, Martin Balslev.

In: Free Radical Biology & Medicine, Vol. 104, 03.2017, p. 64-74.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Jorgensen, A, Kalliokoski, O, Forsberg, K, Breitenstein, K, Weimann, A, Henriksen, T, Hau, J, Wörtwein, G, Poulsen, HE & Jorgensen, MB 2017, 'A chronic increase of corticosterone age-dependently reduces systemic DNA damage from oxidation in rats', Free Radical Biology & Medicine, vol. 104, pp. 64-74. https://doi.org/10.1016/j.freeradbiomed.2017.01.013

APA

Jorgensen, A., Kalliokoski, O., Forsberg, K., Breitenstein, K., Weimann, A., Henriksen, T., ... Jorgensen, M. B. (2017). A chronic increase of corticosterone age-dependently reduces systemic DNA damage from oxidation in rats. Free Radical Biology & Medicine, 104, 64-74. https://doi.org/10.1016/j.freeradbiomed.2017.01.013

Vancouver

Jorgensen A, Kalliokoski O, Forsberg K, Breitenstein K, Weimann A, Henriksen T et al. A chronic increase of corticosterone age-dependently reduces systemic DNA damage from oxidation in rats. Free Radical Biology & Medicine. 2017 Mar;104:64-74. https://doi.org/10.1016/j.freeradbiomed.2017.01.013

Author

Jorgensen, Anders ; Kalliokoski, Otto ; Forsberg, Kristin ; Breitenstein, Katrine ; Weimann, Allan ; Henriksen, Trine ; Hau, Jann ; Wörtwein, Gitta ; Poulsen, Henrik Enghusen ; Jorgensen, Martin Balslev. / A chronic increase of corticosterone age-dependently reduces systemic DNA damage from oxidation in rats. In: Free Radical Biology & Medicine. 2017 ; Vol. 104. pp. 64-74.

Bibtex

@article{bc51617cbbce49debae6b0e7d96d5b98,
title = "A chronic increase of corticosterone age-dependently reduces systemic DNA damage from oxidation in rats",
abstract = "Stress and depression are associated with an acceleration of brain and bodily aging; effects which have been attributed to chronic elevations of glucocorticoids. We tested the hypothesis that a three week administration of stress-associated levels of corticosterone (CORT, the principal rodent glucocorticoid) would increase systemic and CNS DNA and RNA damage from oxidation; a phenomenon known to be centrally involved in the aging process. We also hypothesized that older individuals would be more sensitive to this effect and that the chronic CORT administration would exacerbate age-related memory decline. Young and old male Sprague-Dawley rats were non-invasively administered CORT by voluntary ingestion of nut paste containing either CORT (25mg/kg) or vehicle for a total of 22 days. CORT increased the 24h urinary excretion of the hormone to the levels previously observed after experimental psychological stress and caused a downregulation of the glucocorticoid receptor in the CA1 area of the hippocampus. Contrary to our hypothesis, 24h excretion of 8-oxodG/8-oxoGuo (markers of DNA/RNA damage from oxidation) was reduced in CORT-treated young animals, whereas old animals showed no significant differences. In old animals, CORT caused a borderline significant reduction of RNA oxidation in CNS, which was paralleled by a normalization of performance in an object location memory test. To our knowledge, this is the first demonstration that chronic stress-associated levels of CORT can reduce nucleic acid damage from oxidation. These findings contradict the notion of elevated CORT as a mediator of the accelerated aging observed in stress and depression.",
author = "Anders Jorgensen and Otto Kalliokoski and Kristin Forsberg and Katrine Breitenstein and Allan Weimann and Trine Henriksen and Jann Hau and Gitta W{\"o}rtwein and Poulsen, {Henrik Enghusen} and Jorgensen, {Martin Balslev}",
note = "Copyright {\circledC} 2017 Elsevier Inc. All rights reserved.",
year = "2017",
month = "3",
doi = "10.1016/j.freeradbiomed.2017.01.013",
language = "English",
volume = "104",
pages = "64--74",
journal = "Free Radical Biology & Medicine",
issn = "0891-5849",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - A chronic increase of corticosterone age-dependently reduces systemic DNA damage from oxidation in rats

AU - Jorgensen, Anders

AU - Kalliokoski, Otto

AU - Forsberg, Kristin

AU - Breitenstein, Katrine

AU - Weimann, Allan

AU - Henriksen, Trine

AU - Hau, Jann

AU - Wörtwein, Gitta

AU - Poulsen, Henrik Enghusen

AU - Jorgensen, Martin Balslev

N1 - Copyright © 2017 Elsevier Inc. All rights reserved.

PY - 2017/3

Y1 - 2017/3

N2 - Stress and depression are associated with an acceleration of brain and bodily aging; effects which have been attributed to chronic elevations of glucocorticoids. We tested the hypothesis that a three week administration of stress-associated levels of corticosterone (CORT, the principal rodent glucocorticoid) would increase systemic and CNS DNA and RNA damage from oxidation; a phenomenon known to be centrally involved in the aging process. We also hypothesized that older individuals would be more sensitive to this effect and that the chronic CORT administration would exacerbate age-related memory decline. Young and old male Sprague-Dawley rats were non-invasively administered CORT by voluntary ingestion of nut paste containing either CORT (25mg/kg) or vehicle for a total of 22 days. CORT increased the 24h urinary excretion of the hormone to the levels previously observed after experimental psychological stress and caused a downregulation of the glucocorticoid receptor in the CA1 area of the hippocampus. Contrary to our hypothesis, 24h excretion of 8-oxodG/8-oxoGuo (markers of DNA/RNA damage from oxidation) was reduced in CORT-treated young animals, whereas old animals showed no significant differences. In old animals, CORT caused a borderline significant reduction of RNA oxidation in CNS, which was paralleled by a normalization of performance in an object location memory test. To our knowledge, this is the first demonstration that chronic stress-associated levels of CORT can reduce nucleic acid damage from oxidation. These findings contradict the notion of elevated CORT as a mediator of the accelerated aging observed in stress and depression.

AB - Stress and depression are associated with an acceleration of brain and bodily aging; effects which have been attributed to chronic elevations of glucocorticoids. We tested the hypothesis that a three week administration of stress-associated levels of corticosterone (CORT, the principal rodent glucocorticoid) would increase systemic and CNS DNA and RNA damage from oxidation; a phenomenon known to be centrally involved in the aging process. We also hypothesized that older individuals would be more sensitive to this effect and that the chronic CORT administration would exacerbate age-related memory decline. Young and old male Sprague-Dawley rats were non-invasively administered CORT by voluntary ingestion of nut paste containing either CORT (25mg/kg) or vehicle for a total of 22 days. CORT increased the 24h urinary excretion of the hormone to the levels previously observed after experimental psychological stress and caused a downregulation of the glucocorticoid receptor in the CA1 area of the hippocampus. Contrary to our hypothesis, 24h excretion of 8-oxodG/8-oxoGuo (markers of DNA/RNA damage from oxidation) was reduced in CORT-treated young animals, whereas old animals showed no significant differences. In old animals, CORT caused a borderline significant reduction of RNA oxidation in CNS, which was paralleled by a normalization of performance in an object location memory test. To our knowledge, this is the first demonstration that chronic stress-associated levels of CORT can reduce nucleic acid damage from oxidation. These findings contradict the notion of elevated CORT as a mediator of the accelerated aging observed in stress and depression.

U2 - 10.1016/j.freeradbiomed.2017.01.013

DO - 10.1016/j.freeradbiomed.2017.01.013

M3 - Journal article

C2 - 28069523

VL - 104

SP - 64

EP - 74

JO - Free Radical Biology & Medicine

JF - Free Radical Biology & Medicine

SN - 0891-5849

ER -

ID: 172637743