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Genistein Supplementation Inhibits Atherosclerosis with Stabilization of the Lesions in Hypercholesterolemic Rabbits

The effect of genistein on aortic atherosclerosis was studied by immunohistochemistry with RAM-11 and HHF-35 antibodies and western blotting for matrix metalloproteinase-3 (MMP-3) in New Zealand White rabbits. After provocation of atherosclerosis with hyperlipidemic diet, the rabbits were divided as...

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Detalles Bibliográficos
Autores principales: Lee, Choong-Sik, Kwon, Su-Jin, Na, Sun-Young, Lim, Seung-Pyung, Lee, Jung-Hee
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816326/
https://www.ncbi.nlm.nih.gov/pubmed/15483339
http://dx.doi.org/10.3346/jkms.2004.19.5.656
Descripción
Sumario:The effect of genistein on aortic atherosclerosis was studied by immunohistochemistry with RAM-11 and HHF-35 antibodies and western blotting for matrix metalloproteinase-3 (MMP-3) in New Zealand White rabbits. After provocation of atherosclerosis with hyperlipidemic diet, the rabbits were divided as hyperlipidemic diet group (HD), normal diet group (ND) and hyperlipidemic plus genistein diet group (HD+genistein) for 4 and half months. The average cross sectional area of atherosclerotic lesion was 0.269 mm(2) after provocation. The lesion was progressed by continuous hyperlipidemic diet (10.06 mm(2)) but was increased mildly by genistein (0.997 mm(2)), and decreased by normal diet (0.228 mm(2)). The ratio of macrophages to smooth muscle cells in the lesion was not changed by genistein supplementmentation. The western blotting showed reduction of MMP-3 expression in HD+genistein and ND groups than HD group. The inhibition of atherogenesis by genistein was might be due to improve the endothelial dysfunction rather than direct action on macrophages and/or smooth muscle cells in the lesion, since endothelial dysfunction by lipid peroxidation was the main atherogenic factor in the hypercholesterolemicrabbits. The genistein supplementmentation also suggests that it helps the stabilization of the atherosclerotic lesion by inhibition of MMP-3 expression.