Zarins C K, Glagov S, Vesselinovitch D, Wissler R W
Department of Surgery, University of Chicago, IL 60637.
J Vasc Surg. 1990 Sep;12(3):246-56.
To determine whether aneurysms form in experimental diet-induced atherosclerosis, we reviewed our experience with cynomolgus monkeys (n = 268) and rhesus monkeys (n = 175) fed an atherogenic diet for various lengths of time. Many animals in long-term experiments were fed "regression" diets and cholestyramine to lower cholesterol levels after lesions were established. No aneurysms were found in animals on normal diet. There were no aneurysms in 252 animals fed an atherogenic diet with or without regression for 12 months or less. However, aneurysms formed in 13% of cynomolgus monkeys (4 of 31) and 1% (1 of 107) rhesus monkeys on an atherogenic regimen for 16 to 24 months. Four of the five animals with aneurysms were on a regression diet and cholestyramine for 4 to 12 months. The fifth was fed the atherogenic diet for 20 months without subsequent regression. Aneurysms were prominent and involved the thoracic and abdominal aorta, innominate artery, carotid arteries, iliac and femoral arteries, and formed in areas most involved with plaque formation in both species. Histologic evidence was found of thinning of the media and atrophy with loss of normal architecture. The higher incidence of aneurysms in cynomolgus monkeys was associated with greater media destruction than was noted in the rhesus. These data support the thesis that aneurysm formation is a manifestation of atherosclerosis. In primate atherosclerosis, aneurysms form only after prolonged exposure to the atherogenic regimen, even in the presence of declining serum cholesterol levels. Matrix fibers in plaques may provide structural support to the aortic wall where there is underlying atrophy of the media. With time or declining serum cholesterol levels or both, plaques may atrophy leaving an aortic wall too thin to support increasing mural tension, leading to aneurysmal enlargement.
为了确定实验性饮食诱导的动脉粥样硬化中是否会形成动脉瘤,我们回顾了我们对食蟹猴(n = 268)和恒河猴(n = 175)喂食致动脉粥样硬化饮食不同时长的经验。在长期实验中,许多动物在病变形成后被喂食“回归”饮食并使用消胆胺以降低胆固醇水平。正常饮食的动物未发现动脉瘤。252只喂食致动脉粥样硬化饮食(无论是否进行回归饮食)12个月及以内的动物未出现动脉瘤。然而,在16至24个月的致动脉粥样硬化方案下,13%的食蟹猴(31只中的4只)和1%的恒河猴(107只中的1只)形成了动脉瘤。五只患有动脉瘤的动物中有四只在4至12个月内接受回归饮食并使用消胆胺。第五只动物喂食致动脉粥样硬化饮食20个月,随后未进行回归饮食。动脉瘤很明显,累及胸主动脉和腹主动脉、无名动脉、颈动脉、髂动脉和股动脉,并且在两个物种中均形成于斑块形成最严重的区域。组织学证据显示中膜变薄和萎缩,正常结构丧失。食蟹猴中动脉瘤的发生率较高与比恒河猴更严重的中膜破坏有关。这些数据支持动脉瘤形成是动脉粥样硬化表现的论点。在灵长类动物动脉粥样硬化中,动脉瘤仅在长期暴露于致动脉粥样硬化方案后形成,即使血清胆固醇水平下降。斑块中的基质纤维可能为中膜存在潜在萎缩的主动脉壁提供结构支撑。随着时间推移或血清胆固醇水平下降或两者兼而有之,斑块可能萎缩,使主动脉壁变得过薄而无法承受不断增加的壁张力,从而导致动脉瘤扩大。