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Decreased Paraoxonase-2 Expression in Human Carotids During the Progression of Atherosclerosis

Authors :
Maria Donata Di Taranto
Giuliana Fortunato
Maria D'Armiento
Cristina Mazzaccara
Francesco Salvatore
Lucia Sacchetti
Luca del Guercio
Francesco Paolo D'Armiento
Umberto Bracale
Porcellini M
Giancarlo Bracale
F Carbone
Alberto Morgante
Fortunato, Giuliana
Di Taranto, Maria Donata
Bracale, Umberto Marcello
Del Guercio, Luca
Carbone, Francesca
Mazzaccara, Cristina
Morgante, A.
D'Armiento, Francesco Paolo
D'Armiento, Maria
Porcellini, Massimo
Sacchetti, Lucia
Bracale, Giancarlo
Salvatore, Francesco
FORTUNATO, G
DI TARANTO, MD
BRACALE, UM
DEL GUERCIO, L
CARBONE, F
MAZZACCARA, C
MORGANTE, A
D'ARMIENTO, FP
D'ARMIENTO, M
PORCELLINI, M
SACCHETTI, L
BRACALE, G
SALVATORE, F
Publication Year :
2008

Abstract

Objective— Many gene products involved in oxidation and inflammation are implicated in the pathogenesis of atherosclerosis. We investigated paraoxonase 2 (PON2), 5-lipoxygenase (5-LO), and 5-LO activating protein (FLAP) expression and malondialdehyde (MDA) levels in carotid lesions to assess their involvement in plaque formation. Methods and Results— We measured gene expression and MDA levels in atherosclerotic plaques from 59 patients undergoing carotid endarterectomy, and in plaque-adjacent tissue from 41/59 patients. Twenty-three fetal carotids and 6 mammary arteries were also investigated. Real-time polymerase chain reaction and immunohistochemistry revealed decreased PON2 expression in plaques versus adjacent regions ( P P P P P P P Conclusions— We demonstrate that PON2 mRNA and protein are decreased in plaques versus plaque-adjacent tissue, mammary arteries, and fetal carotids. Our data indicate that the protective effect of PON2 could fail during atherosclerosis exacerbation; this was confirmed by the increase of MDA levels. The increase of 5-LO and FLAP mRNA expression confirms their role as inflammatory markers associated to atherosclerosis.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....71276919c4f09e6a1d91f556b07a1dba