Effects of Spermidine and p-Cresol on Polymorphonuclear Cell Apoptosis and Function

Polymorphonuclear leukocytes (PMNs) from chronic kidney disease (CKD) patients display accelerated apoptosis and dysfunction, which may predispose CKD patients to infections. In this study, we investigated the effect of spermidine and p‐cresol on apoptosis and function on PMN from healthy subjects....

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Published inArtificial organs Vol. 35; no. 2; pp. E27 - E32
Main Authors de Carvalho Jr, Jose Tarcisio G., Dalboni, Maria A., Watanabe, Renato, Peres, Alines T., Goes, Miguel A., Manfredi, Silvia R., Canziani, Maria E., Cendoroglo, Gabriel S., Guimarães-Souza, Nadia, Batista, Marcelo C., Cendoroglo, Miguel
Format Journal Article
LanguageEnglish
Published Malden, USA Blackwell Publishing Inc 01.02.2011
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ISSN0160-564X
1525-1594
1525-1594
DOI10.1111/j.1525-1594.2010.01116.x

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Summary:Polymorphonuclear leukocytes (PMNs) from chronic kidney disease (CKD) patients display accelerated apoptosis and dysfunction, which may predispose CKD patients to infections. In this study, we investigated the effect of spermidine and p‐cresol on apoptosis and function on PMN from healthy subjects. We measured the effect of spermidine and p‐cresol on apoptosis, ROS production unstimulated and stimulated (S. aureus and PMA) and expression of CD95, caspase 3, and CD11b on PMN. After incubation with p‐cresol and spermidine, we did not observe any changes in apoptosis, viability or expression of caspase 3 and CD95 in PMN from healthy subjects. PMN incubated for 10 minutes with spermidine demonstrated a significant reduction in spontaneous, S. aureus and PMA‐stimulated ROS production. p‐cresol induced a decrease in PMA‐stimulated ROS production. Spermidine and p‐cresol also induced a decrease in the expression of CD11b on PMN. Spermidine and p‐cresol decreased the expression of CD11b and oxidative burst of PMN from healthy subjects and had no effect on PMN apoptosis and viability.
Bibliography:ark:/67375/WNG-H47WQ760-J
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ArticleID:AOR1116
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0160-564X
1525-1594
1525-1594
DOI:10.1111/j.1525-1594.2010.01116.x