Aging effect on myeloperoxidase in rat kidney and its modulation by calorie restriction

Myeloperoxidase (MPO), a heme protein existing in neutrophil and monocyte, is implicated in various stages of inflammatory conditions with the production of a variety of potent oxidants. To investigate the extent of the involvement of MPO in aging, we measured MPO activities in kidney of rats at dif...

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Veröffentlicht in:Free radical research 2005-03, Vol.39 (3), p.283-289
Hauptverfasser: Gen Son, Tae, Zou, Yani, Pal Yu, Byung, Lee, Jaewon, Young Chung, Hae
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Zou, Yani
Pal Yu, Byung
Lee, Jaewon
Young Chung, Hae
description Myeloperoxidase (MPO), a heme protein existing in neutrophil and monocyte, is implicated in various stages of inflammatory conditions with the production of a variety of potent oxidants. To investigate the extent of the involvement of MPO in aging, we measured MPO activities in kidney of rats at different ages maintained with an ad libitum (AL) or a calorie restriction (CR) dietary regimen. Results showed that the MPO activities increased during aging in AL rats, but were significantly attenuated by CR. This result was consistent with altered protein level of MPO during aging. In addition, we were able to detect dityrosine that is a stable end MPO-oxidation product. The amount of dityrosine increased in old AL, but not in old CR rats. To examine the source responsible for increased MPO activity during aging for leukocyte recruitment and infiltration, the levels of vascular cell adhesion molecule (VCAM-1) protein were measured. The level of VCAM-1 showed age-dependent increase in AL rats, which was correlated with higher activity of MPO in old AL rats. Furthermore, we have found that LPS-induced inflammation increased the activity and protein levels of MPO, and VCAM-1 expression in young rat kidneys. These findings suggest that increased MPO activity with aging may related to increased recruitment of inflammatory cells, contributing to protein oxidation accumulation in the aging process. We propose that age-related alterations of MPO, dityrosine, and VCAM were modulated by CR through its anti-inflammatory action.
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To investigate the extent of the involvement of MPO in aging, we measured MPO activities in kidney of rats at different ages maintained with an ad libitum (AL) or a calorie restriction (CR) dietary regimen. Results showed that the MPO activities increased during aging in AL rats, but were significantly attenuated by CR. This result was consistent with altered protein level of MPO during aging. In addition, we were able to detect dityrosine that is a stable end MPO-oxidation product. The amount of dityrosine increased in old AL, but not in old CR rats. To examine the source responsible for increased MPO activity during aging for leukocyte recruitment and infiltration, the levels of vascular cell adhesion molecule (VCAM-1) protein were measured. The level of VCAM-1 showed age-dependent increase in AL rats, which was correlated with higher activity of MPO in old AL rats. Furthermore, we have found that LPS-induced inflammation increased the activity and protein levels of MPO, and VCAM-1 expression in young rat kidneys. These findings suggest that increased MPO activity with aging may related to increased recruitment of inflammatory cells, contributing to protein oxidation accumulation in the aging process. 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derivatives</topic><topic>Tyrosine - metabolism</topic><topic>vascular cell adhesion molecule</topic><topic>Vascular Cell Adhesion Molecule-1 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gen Son, Tae</creatorcontrib><creatorcontrib>Zou, Yani</creatorcontrib><creatorcontrib>Pal Yu, Byung</creatorcontrib><creatorcontrib>Lee, Jaewon</creatorcontrib><creatorcontrib>Young Chung, Hae</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Free radical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gen Son, Tae</au><au>Zou, Yani</au><au>Pal Yu, Byung</au><au>Lee, Jaewon</au><au>Young Chung, Hae</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aging effect on myeloperoxidase in rat kidney and its modulation by calorie restriction</atitle><jtitle>Free radical research</jtitle><addtitle>Free Radic Res</addtitle><date>2005-03</date><risdate>2005</risdate><volume>39</volume><issue>3</issue><spage>283</spage><epage>289</epage><pages>283-289</pages><issn>1071-5762</issn><eissn>1029-2470</eissn><abstract>Myeloperoxidase (MPO), a heme protein existing in neutrophil and monocyte, is implicated in various stages of inflammatory conditions with the production of a variety of potent oxidants. 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source MEDLINE; Taylor & Francis:Master (3349 titles)
subjects aging
Aging - drug effects
Aging - physiology
Animals
Caloric Restriction
calorie restriction
Diet
dityrosine
Energy Intake
inflammation
Inflammation - enzymology
Inflammation - etiology
Kidney - drug effects
Kidney - enzymology
Lipopolysaccharides - pharmacology
Male
Myeloperoxidase
Oxidation-Reduction
Oxidative Stress
Peroxidase - metabolism
Rats
Rats, Inbred F344
Tyrosine - analogs & derivatives
Tyrosine - metabolism
vascular cell adhesion molecule
Vascular Cell Adhesion Molecule-1 - metabolism
title Aging effect on myeloperoxidase in rat kidney and its modulation by calorie restriction
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