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 |
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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. We propose that age-related alterations of MPO, dityrosine, and VCAM were modulated by CR through its anti-inflammatory action.</description><identifier>ISSN: 1071-5762</identifier><identifier>EISSN: 1029-2470</identifier><identifier>DOI: 10.1080/10715760500053461</identifier><identifier>PMID: 15788232</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>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</subject><ispartof>Free radical research, 2005-03, Vol.39 (3), p.283-289</ispartof><rights>2005 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c404t-5a335d49d1ae06a1aa948dd5ba465fe8b876a1cfd97118a3a0128085b6dcac8b3</citedby><cites>FETCH-LOGICAL-c404t-5a335d49d1ae06a1aa948dd5ba465fe8b876a1cfd97118a3a0128085b6dcac8b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/10715760500053461$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/10715760500053461$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,780,784,27922,27923,59645,60434,61219,61400</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15788232$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gen Son, Tae</creatorcontrib><creatorcontrib>Zou, Yani</creatorcontrib><creatorcontrib>Pal Yu, Byung</creatorcontrib><creatorcontrib>Lee, Jaewon</creatorcontrib><creatorcontrib>Young Chung, Hae</creatorcontrib><title>Aging effect on myeloperoxidase in rat kidney and its modulation by calorie restriction</title><title>Free radical research</title><addtitle>Free Radic Res</addtitle><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.</description><subject>aging</subject><subject>Aging - drug effects</subject><subject>Aging - physiology</subject><subject>Animals</subject><subject>Caloric Restriction</subject><subject>calorie restriction</subject><subject>Diet</subject><subject>dityrosine</subject><subject>Energy Intake</subject><subject>inflammation</subject><subject>Inflammation - enzymology</subject><subject>Inflammation - etiology</subject><subject>Kidney - drug effects</subject><subject>Kidney - enzymology</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Male</subject><subject>Myeloperoxidase</subject><subject>Oxidation-Reduction</subject><subject>Oxidative Stress</subject><subject>Peroxidase - metabolism</subject><subject>Rats</subject><subject>Rats, Inbred F344</subject><subject>Tyrosine - analogs & derivatives</subject><subject>Tyrosine - metabolism</subject><subject>vascular cell adhesion molecule</subject><subject>Vascular Cell Adhesion Molecule-1 - metabolism</subject><issn>1071-5762</issn><issn>1029-2470</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LHTEUhoNUqtX-ADclq-6mTWaSSQa7EekXCN0oLsOZ5IzGziTXZAY7_95c7gWRgqsTDs_znvAScsbZF840-8qZ4lK1TDLGZCNafkCOOau7qhaKvdu-Fa8KUB-RDzk_MMYbIdV7clQsreumPia3F3c-3FEcBrQzjYFOK45xgyn-8w4yUh9ogpn-9S7gSiE46udMp-iWEWZfhH6lFsaYPNKEeU7ebten5HCAMePH_TwhNz--X1_-qq7-_Px9eXFVWcHEXEloGulE5zgga4EDdEI7J3sQrRxQ91qVrR1cpzjX0ADjtWZa9q2zYHXfnJDPu9xNio9LuW8mny2OIwSMSzatkkIL1RWQ70CbYs4JB7NJfoK0Gs7Mtk3zX5vF-bQPX_oJ3Yuxr68A33aAD0NMEzzFNDozw1r6GBIE67Np3so_f6XfI4zzvYWE5iEuKZTi3vjdM33ilac</recordid><startdate>200503</startdate><enddate>200503</enddate><creator>Gen Son, Tae</creator><creator>Zou, Yani</creator><creator>Pal Yu, Byung</creator><creator>Lee, Jaewon</creator><creator>Young Chung, Hae</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200503</creationdate><title>Aging effect on myeloperoxidase in rat kidney and its modulation by calorie restriction</title><author>Gen Son, Tae ; Zou, Yani ; Pal Yu, Byung ; Lee, Jaewon ; Young Chung, Hae</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-5a335d49d1ae06a1aa948dd5ba465fe8b876a1cfd97118a3a0128085b6dcac8b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>aging</topic><topic>Aging - drug effects</topic><topic>Aging - physiology</topic><topic>Animals</topic><topic>Caloric Restriction</topic><topic>calorie restriction</topic><topic>Diet</topic><topic>dityrosine</topic><topic>Energy Intake</topic><topic>inflammation</topic><topic>Inflammation - enzymology</topic><topic>Inflammation - etiology</topic><topic>Kidney - drug effects</topic><topic>Kidney - enzymology</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Male</topic><topic>Myeloperoxidase</topic><topic>Oxidation-Reduction</topic><topic>Oxidative Stress</topic><topic>Peroxidase - metabolism</topic><topic>Rats</topic><topic>Rats, Inbred F344</topic><topic>Tyrosine - analogs & 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. 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.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>15788232</pmid><doi>10.1080/10715760500053461</doi><tpages>7</tpages></addata></record> |
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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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