Aberg G, Ferrer P
Department of Pharmacology, Squibb Institute for Medical Research, Bristol-Myers Squibb Company, Princeton, New Jersey 08543-4000.
J Cardiovasc Pharmacol. 1990;15 Suppl 5:S65-72.
A study was performed to investigate if oral dosing of captopril could influence the development of atherosclerosis in cholesterol-fed cynomolgus monkeys. Twenty-four monkeys were divided into four groups: (a) a control group given a normal monkey diet and placebo medication; (b) a high cholesterol group given a high cholesterol diet and placebo medication; (c) a low-dose captopril group given the cholesterol diet and 25 mg/kg of captopril twice daily; and (d) a high-dose captopril group given the cholesterol diet and 50 mg/kg of captopril twice daily. The doses of captopril used in this study did not change the levels of total serum cholesterol, high-density lipoprotein (HDL), or triglycerides. The total cholesterol/HDL ratio was also unaffected by captopril. The animals were killed after 6 months of treatment. The progression of atherosclerosis was assessed by gross pathology, histopathology, and biochemical methods. The results showed a significantly reduced progression of arterial lesions in monkeys given captopril; the effects of captopril were most evident in the coronary arteries, which were practically free from atherosclerosis in captopril-treated animals.
进行了一项研究,以调查口服卡托普利是否会影响高胆固醇喂养的食蟹猴动脉粥样硬化的发展。24只猴子被分为四组:(a) 给予正常猴饮食和安慰剂的对照组;(b) 给予高胆固醇饮食和安慰剂的高胆固醇组;(c) 给予胆固醇饮食且每天两次服用25 mg/kg卡托普利的低剂量卡托普利组;(d) 给予胆固醇饮食且每天两次服用50 mg/kg卡托普利的高剂量卡托普利组。本研究中使用的卡托普利剂量并未改变血清总胆固醇、高密度脂蛋白(HDL)或甘油三酯的水平。总胆固醇/HDL比值也不受卡托普利影响。治疗6个月后处死动物。通过大体病理学、组织病理学和生化方法评估动脉粥样硬化的进展。结果显示,给予卡托普利的猴子动脉病变进展显著减缓;卡托普利的作用在冠状动脉中最为明显,在接受卡托普利治疗的动物中,冠状动脉几乎没有动脉粥样硬化。