Marsillach_2011_Eur.J.Clin.Invest_41_308

Reference

Title : Immunohistochemical analysis of paraoxonases-1 and 3 in human atheromatous plaques - Marsillach_2011_Eur.J.Clin.Invest_41_308
Author(s) : Marsillach J , Camps J , Beltran-Debon R , Rull A , Aragones G , Maestre-Martinez C , Sabench F , Hernandez M , Castillo DD , Joven J , Mackness MI , Mackness B
Ref : European Journal of Clinical Investigation , 41 :308 , 2011
Abstract : BACKGROUND: The paraoxonase (PON) enzyme family comprising PON1, PON2 and PON3 are antioxidant enzymes that degrade bioactive oxidised lipids and are thus antiatherogenic. MATERIALS AND
METHODS: We investigated the localisation of the PON proteins during the development of atherosclerosis by immunohistochemical analysis.
RESULTS: In normal aortas, PON1 and PON3 were localised to smooth muscle cells (SMC) and endothelial cells. PON3 staining was stronger than that of PON1. During atherosclerosis development, SMC staining for PON1 and PON3 was greatly reduced, while macrophage staining for both proteins increased with PON1 predominating. Macrophage staining for PON1 and PON3 was significantly and positively related to the amount of aortic inflammation (both P<0.001).
CONCLUSIONS: Our data add support to the growing body of evidence for a cellular protective effect of PON1 and PON3 against the proinflammatory/proatherosclerotic effects of lipid peroxidation.
ESTHER : Marsillach_2011_Eur.J.Clin.Invest_41_308
PubMedSearch : Marsillach_2011_Eur.J.Clin.Invest_41_308
PubMedID: 20964682

Related information

Citations formats

Marsillach J, Camps J, Beltran-Debon R, Rull A, Aragones G, Maestre-Martinez C, Sabench F, Hernandez M, Castillo DD, Joven J, Mackness MI, Mackness B (2011)
Immunohistochemical analysis of paraoxonases-1 and 3 in human atheromatous plaques
European Journal of Clinical Investigation 41 :308

Marsillach J, Camps J, Beltran-Debon R, Rull A, Aragones G, Maestre-Martinez C, Sabench F, Hernandez M, Castillo DD, Joven J, Mackness MI, Mackness B (2011)
European Journal of Clinical Investigation 41 :308