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Does nifedipine suppress atherogenesis in WHHL rabbits?

作者信息

Van Niekerk J L, Hendriks T, De Boer H H, Van 't Laar A

出版信息

Atherosclerosis. 1984 Oct;53(1):91-8. doi: 10.1016/0021-9150(84)90109-6.

DOI:10.1016/0021-9150(84)90109-6
PMID:6497947
Abstract

The effects of the calcium antagonist, nifedipine, on atherogenesis were investigated in WHHL rabbits, a unique animal model for human familial hypercholesterolemia. Nifedipine, in a daily dose of 40 mg, was fed orally to 9 rabbits over a period of 26 weeks, resulting in serum concentrations of between 740 and 1370 ng/ml. Rabbits were killed at an age of 40 weeks and atherosclerotic plaque formation in various aortic segments was quantified. Atherosclerosis was most pronounced in the aortic arch and the thoracic aorta, plaques covering, respectively, 59 +/- 17% and 17 +/- 9% of total vessel area. These results are similar to those observed in a control group, which received the same diet and no nifedipine and displayed lesions on 62 +/- 19% and 21 +/- 13% of total area of aortic arch and thoracic aorta, respectively. Although variations in plaque area between WHHL rabbits are large and thus preclude the observation of small effects, the efficacy of nifedipine as an anti-atherogenic agent in rabbits with hereditary hypercholesterolemia appears questionable.

摘要

相似文献

1
Does nifedipine suppress atherogenesis in WHHL rabbits?
Atherosclerosis. 1984 Oct;53(1):91-8. doi: 10.1016/0021-9150(84)90109-6.
2
Nifedipine reduces atherogenesis in cholesterol-fed heterozygous WHHL rabbits.
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3
No effect of nifedipine on atherogenesis in cholesterol-fed rabbits.
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Effects of partial ileal bypass on the progression of atherosclerotic lesions in WHHL rabbits.部分回肠旁路术对WHHL兔动脉粥样硬化病变进展的影响。
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引用本文的文献

1
Roles of the WHHL rabbit in translational research on hypercholesterolemia and cardiovascular diseases.WHHL兔在高胆固醇血症和心血管疾病转化研究中的作用。
J Biomed Biotechnol. 2011;2011:406473. doi: 10.1155/2011/406473. Epub 2011 Apr 19.
2
Nifedipine increases cholesteryl ester hydrolytic activity in lipid-laden rabbit arterial smooth muscle cells. A possible mechanism for its antiatherogenic effect.硝苯地平可增加富含脂质的兔动脉平滑肌细胞中的胆固醇酯水解活性。这可能是其抗动脉粥样硬化作用的一种机制。
J Clin Invest. 1985 May;75(5):1554-8. doi: 10.1172/JCI111860.
3
International nifedipine trial on antiatherosclerotic therapy (INTACT).
国际硝苯地平抗动脉粥样硬化治疗试验(INTACT)
Cardiovasc Drugs Ther. 1987;1(1):71-9. doi: 10.1007/BF02125836.
4
Suppression of rat carotid lesion development by the calcium channel blocker PN 200-110.钙通道阻滞剂PN 200 - 110对大鼠颈动脉病变发展的抑制作用
Am J Pathol. 1986 Jul;124(1):88-93.
5
Retardation of development and progression of coronary atherosclerosis: a new indication for calcium antagonists?延缓冠状动脉粥样硬化的发展和进程:钙拮抗剂的新适应证?
Eur J Clin Pharmacol. 1990;39 Suppl 1:S17-23.
6
Quantitative analysis of antiatherosclerotic effect of nifedipine in cholesterol-fed rabbits.
Cardiovasc Drugs Ther. 1990 Aug;4 Suppl 5:1021-6. doi: 10.1007/BF02018311.
7
Watanabe heritable hyperlipidemic rabbits. Familial hypercholesterolemia.渡边遗传性高脂血症兔。家族性高胆固醇血症。
Am J Pathol. 1992 Mar;140(3):749-53.
8
ACE-inhibitors and atherosclerosis.
Eur J Epidemiol. 1992 May;8 Suppl 1:129-33. doi: 10.1007/BF00145364.