TY - JOUR
T1 - Anti-Inflammatory Effect of Amlodipine Plus Atorvastatin Treatment on Carotid Atherosclerosis in Zucker Metabolic Syndrome Rats
AU - Zhang, Xuemei
AU - Tian, Fengfeng
AU - Kawai, Hiromi
AU - Kurata, Tomoko
AU - Deguchi, Shoko
AU - Deguchi, Kentaro
AU - Shang, Jingwei
AU - Liu, Ning
AU - Liu, Wentao
AU - Ikeda, Yoshio
AU - Matsuura, Tohru
AU - Kamiya, Tatsushi
AU - Abe, Koji
N1 - Funding Information:
Acknowledgments This study was supported in part by Grant-in-aid for Scientific Research (B) 21390267 and the Ministry of Education, Science, Culture and Sports of Japan, by Grants-in-aid from the Research Committee of CNS Degenerative Diseases (Nakano I), and by grants (Itoyama Y, Imai T, Sobue G, and Mizusawa H) from the Ministry of Health, Labour and Welfare of Japan.
PY - 2012/12
Y1 - 2012/12
N2 - To investigate the effects of amlodipine in combination with atorvastatin on carotid atherosclerotic changes in metabolic syndrome, 8-week-old Zucker fatty rats were treated with vehicle, amlodipine, atorvastatin, or amlodipine in combination with atorvastatin for 28 days. Histological studies of common carotid arteries showed that lipid deposition determined by Sudan III staining was significantly reduced in rats treated with amlodipine or atorvastatin alone and was further reduced by amlodipine in combination with atorvastatin. Immunohistochemical studies of the pro-inflammatory cytokine tumor necrosis factor (TNF)-α, the arterial calcification initiator bone morphogenetic protein (BMP) 2, the angiogenic factor Notch1, and the smooth muscle cell marker α-smooth muscle actin (SMA) showed that the high expression of all four protein in vehicle-treated rats was greatly decreased by amlodipine, atorvastatin, or amlodipine in combination with atorvastatin, in ascending order. Double immunostaining showed marked colocalization of TNF-α with bone morphogenetic protein 2 and Notch1 with α-SMA in the vehicle group, which was greatly reduced by amlodipine plus atorvastatin. These data suggest that combination therapy may be more effective in preventing atherosclerotic processes and subsequent carotid vascular events than administrating amlodipine or atorvastatin alone in metabolic syndrome.
AB - To investigate the effects of amlodipine in combination with atorvastatin on carotid atherosclerotic changes in metabolic syndrome, 8-week-old Zucker fatty rats were treated with vehicle, amlodipine, atorvastatin, or amlodipine in combination with atorvastatin for 28 days. Histological studies of common carotid arteries showed that lipid deposition determined by Sudan III staining was significantly reduced in rats treated with amlodipine or atorvastatin alone and was further reduced by amlodipine in combination with atorvastatin. Immunohistochemical studies of the pro-inflammatory cytokine tumor necrosis factor (TNF)-α, the arterial calcification initiator bone morphogenetic protein (BMP) 2, the angiogenic factor Notch1, and the smooth muscle cell marker α-smooth muscle actin (SMA) showed that the high expression of all four protein in vehicle-treated rats was greatly decreased by amlodipine, atorvastatin, or amlodipine in combination with atorvastatin, in ascending order. Double immunostaining showed marked colocalization of TNF-α with bone morphogenetic protein 2 and Notch1 with α-SMA in the vehicle group, which was greatly reduced by amlodipine plus atorvastatin. These data suggest that combination therapy may be more effective in preventing atherosclerotic processes and subsequent carotid vascular events than administrating amlodipine or atorvastatin alone in metabolic syndrome.
KW - Amlodipine
KW - Atorvastatin
KW - Common carotid artery
KW - Zucker metabolic syndrome rat
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U2 - 10.1007/s12975-012-0198-1
DO - 10.1007/s12975-012-0198-1
M3 - Article
C2 - 24323832
AN - SCOPUS:84869880552
SN - 1868-4483
VL - 3
SP - 435
EP - 441
JO - Translational Stroke Research
JF - Translational Stroke Research
IS - 4
ER -