Source:http://linkedlifedata.com/resource/pubmed/id/19226207
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2009-3-11
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pubmed:abstractText |
Lysophosphatidylcholine (LPC) is a lysolipid, acting as a potent cellular mediator of various biological processes. The purpose of this study was to define the role of LPC as a possible causative factor of disrupted redox balance in aged aorta from rats. In this study, we found elevated serum LPC levels in 24-month-old rats that were correlated with the age-related increase in cytosolic phospholipase A(2) (PLA(2)) activity. We also found that aortas from old rats showed increased 5-lipoxygenase (5-LO) activity. With the LPC-treated endothelial cells (YPEN-1 cells), we observed a rapid generation of reactive species, leading to enhanced oxidative stress. Our further investigations using specific 5-LO inhibitors led to the identification of a 5-LO pathway as the reactive species production source in the LPC-treated cells. Additional validation of this 5-LO pathway was made by the detection of increased leukotriene B4 generation in the LPC-treated cells. These in vitro data supported findings of increased expression and activation of aortic 5-LO in old rats by LPC. Together, our data strongly suggested that LPC caused the enhancement of oxidative stress in aged aorta through reactive species generation by an activated 5-LO pathway. LPC may well be an important contributor to age-related oxidative stress in aging aorta.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Arachidonate 5-Lipoxygenase,
http://linkedlifedata.com/resource/pubmed/chemical/Group IV Phospholipases A2,
http://linkedlifedata.com/resource/pubmed/chemical/Lysophosphatidylcholines,
http://linkedlifedata.com/resource/pubmed/chemical/Reactive Oxygen Species
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1549-1684
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
12
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
15-24
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pubmed:meshHeading |
pubmed-meshheading:19226207-Aging,
pubmed-meshheading:19226207-Animals,
pubmed-meshheading:19226207-Aorta,
pubmed-meshheading:19226207-Arachidonate 5-Lipoxygenase,
pubmed-meshheading:19226207-Cells, Cultured,
pubmed-meshheading:19226207-Endothelial Cells,
pubmed-meshheading:19226207-Group IV Phospholipases A2,
pubmed-meshheading:19226207-Lysophosphatidylcholines,
pubmed-meshheading:19226207-Male,
pubmed-meshheading:19226207-Oxidative Stress,
pubmed-meshheading:19226207-Rats,
pubmed-meshheading:19226207-Rats, Inbred F344,
pubmed-meshheading:19226207-Reactive Oxygen Species,
pubmed-meshheading:19226207-Signal Transduction,
pubmed-meshheading:19226207-Specific Pathogen-Free Organisms
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pubmed:year |
2009
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pubmed:articleTitle |
Lysophosphatidylcholine enhances oxidative stress via the 5-lipoxygenase pathway in rat aorta during aging.
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pubmed:affiliation |
College of Pharmacy, Aging Tissue Bank, Busan, South Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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