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不影响血清胆固醇水平升高的药物对兔钙化纤维脂肪斑块形成的抑制作用。噻吩化合物的作用。

Suppression of calcific fibrous-fatty plaque formation in rabbits by agents not affecting elevated serum cholesterol levels. The effect of thiophene compounds.

作者信息

Chan C T, Wells H, Kramsch D M

出版信息

Circ Res. 1978 Jul;43(1):115-25. doi: 10.1161/01.res.43.1.115.

DOI:10.1161/01.res.43.1.115
PMID:657453
Abstract

We tested the suppressive effect of antihypercalcemic-hyperphosphatemic agents on atherogenesis. We studied five groups of rabbits for 8 weeks, one control group and four groups on a fibrogenic atherogenic diet. One group received the atherogenic diet alone, and the remaining three atherogenic groups were treated simultaneously with 2-thiophenecarboxylic acid (ThCA), 5-methyl-2-thiophenecarboxylic acid (5-CH3-ThCA), and 5-bromo-2-thiophenecarboxaldehyde (5-Br-ThCA). Rabbits receiving the atherogenic diet alone developed: (1) elevations of serum cholesterol, calcium, and phosphorus; (2) massive fibrous-fatty aortic plaques with excessive accumulation of aortic collagen, elastin, and lipids; (3) marked deposition of calcium and phosphorus in both aortic tissue and elastin; and (4) severe lipid infiltration of the liver. Treatment with all three drugs normalized the elevated serum calcium but not the cholesterol levels, and effectively inhibited all aspects of the atherosclerotic process as determined morphologically and biochemically. The order of effectiveness was: 5-CH3-ThCa greater than 5-Br-ThCA greater than ThCA. No bone resorption occurred in the treated groups. The normalizing effects of the thiophene compounds on serum phosphorus levels were not significant at the dosages used.

摘要

我们测试了抗高钙血症-高磷血症药物对动脉粥样硬化形成的抑制作用。我们将五组兔子研究了8周,一组为对照组,四组给予致纤维化动脉粥样硬化饮食。一组仅接受致动脉粥样硬化饮食,其余三组致动脉粥样硬化组同时用2-噻吩羧酸(ThCA)、5-甲基-2-噻吩羧酸(5-CH3-ThCA)和5-溴-2-噻吩甲醛(5-Br-ThCA)进行治疗。仅接受致动脉粥样硬化饮食的兔子出现了:(1)血清胆固醇、钙和磷升高;(2)大量纤维脂肪性主动脉斑块,伴有主动脉胶原蛋白、弹性蛋白和脂质过度积聚;(3)钙和磷在主动脉组织和弹性蛋白中均有明显沉积;(4)肝脏严重脂质浸润。用这三种药物治疗均使升高的血清钙恢复正常,但未使胆固醇水平恢复正常,并有效抑制了动脉粥样硬化过程的各个方面,这在形态学和生物化学上均得到了证实。有效性顺序为:5-CH3-ThCa>5-Br-ThCA>ThCA。治疗组未发生骨吸收。所用剂量下,噻吩化合物对血清磷水平的正常化作用不显著。

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Suppression of calcific fibrous-fatty plaque formation in rabbits by agents not affecting elevated serum cholesterol levels. The effect of thiophene compounds.不影响血清胆固醇水平升高的药物对兔钙化纤维脂肪斑块形成的抑制作用。噻吩化合物的作用。
Circ Res. 1978 Jul;43(1):115-25. doi: 10.1161/01.res.43.1.115.
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[Thickening of the aortic wall in experimental cholesterol arteriosclerosis].
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引用本文的文献

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Investigation of gender heterogeneity in the associations of serum phosphorus with incident coronary artery disease and all-cause mortality.血清磷与冠心病发病及全因死亡率关联中的性别异质性研究。
Am J Epidemiol. 2009 Jan 1;169(1):67-77. doi: 10.1093/aje/kwn285. Epub 2008 Nov 2.
2
Supersensitivity of atherosclerotic rabbit aorta to ergonovine. Mediation by a serotonergic mechanism.动脉粥样硬化兔主动脉对麦角新碱的超敏反应。由5-羟色胺能机制介导。
J Clin Invest. 1980 Aug;66(2):306-13. doi: 10.1172/JCI109858.
3
Suppression of experimental atherosclerosis by the Ca++-antagonist lanthanum. Possible role of calcium in atherogenesis.
钙离子拮抗剂镧对实验性动脉粥样硬化的抑制作用。钙在动脉粥样硬化发生中的可能作用。
J Clin Invest. 1980 May;65(5):967-81. doi: 10.1172/JCI109783.
4
Suppression of atherogenesis in cholesterol-fed rabbit treated with nifedipine.硝苯地平治疗对喂食胆固醇的兔子动脉粥样硬化形成的抑制作用
J Clin Invest. 1981 Nov;68(5):1366-9. doi: 10.1172/jci110384.
5
Effects of vasoactive stimuli on coronary vascular resistance in isolated perfused rabbit hearts: no vasospastic response to ergonovine with or without atherogenic diet.
Basic Res Cardiol. 1983 Jul-Aug;78(4):415-22. doi: 10.1007/BF02070165.
6
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.
7
Effects of diltiazem on suppression and regression of experimental atherosclerosis.地尔硫䓬对实验性动脉粥样硬化的抑制和消退作用。
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8
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.
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Cardiovasc Drugs Ther. 1987;1(1):65-9. doi: 10.1007/BF02125835.
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Nifedipine and experimental cardioprotection.硝苯地平与实验性心脏保护作用
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