Kaplan J R, Adams M R, Clarkson T B, Manuck S B, Shively C A
Department of Comparative Medicine, Bowman Gray School of Medicine, Winston Salem, NC 27157-1040.
Lab Anim Sci. 1991 Aug;41(4):334-43.
We review the use of socially housed cynomolgus monkeys (Macaca fascicularis) in biomedical research with emphasis on studies of atherosclerosis, particularly in the two specific domains of atherosclerosis investigation for which nonhuman primates are especially well-suited as animal models: gender differences and psychosocial influences. We found that the presence of normal ovarian function prevented exacerbation of diet-induced coronary artery atherosclerosis in female monkeys. However, any manipulation or condition which impaired ovarian function tended to diminish or abolish this "female" protection. Among group-housed female monkeys, low social status was accompanied by ovarian dysfunction and, not surprisingly, by exacerbated coronary artery atherosclerosis as well. Surgical menopause (ovariectomy) also induced exacerbation of coronary atherosclerosis in monkeys, a situation which was prevented by estrogen replacement therapy. Conversely, pregnancy (a hyperestrogenic state) resulted in markedly diminished atherosclerosis. A somewhat different pattern of atherogenesis emerged among socially-housed males. Here, socially dominant animals developed exacerbated coronary artery atherosclerosis, but only under conditions of social stress (viz., disruption caused by periodic reorganization of social group membership). We hypothesized that exposure to repeated group reorganizations provoked activation of the sympathetic nervous system among dominant animals; in turn, the hemodynamic and metabolic concomitants of sympathetic activation may have damaged the coronary arteries of these monkeys, potentiating atherogenesis. To test this hypothesis, males were housed in unstable social groupings, with half of the monkeys administered a beta-adrenergic blocking agent (to attenuate heart rate and blood pressure responses to stress). The beta-blocker inhibited atherosclerosis, but only among those animals behaviorally predisposed to develop exacerbated lesions (i.e. dominant monkeys). These results support the view that monkeys are suitable research models of atherosclerosis, a disease that affects millions of humans.
我们回顾了圈养食蟹猴(猕猴)在生物医学研究中的应用,重点是动脉粥样硬化的研究,特别是在动脉粥样硬化研究的两个特定领域,即非人灵长类动物作为动物模型特别合适的领域:性别差异和社会心理影响。我们发现,正常卵巢功能的存在可防止雌性猴子因饮食诱导的冠状动脉粥样硬化加重。然而,任何损害卵巢功能的操作或状况往往会削弱或消除这种“雌性”保护作用。在群居的雌性猴子中,社会地位低下伴随着卵巢功能障碍,不出所料,也伴随着冠状动脉粥样硬化的加重。手术绝经(卵巢切除术)也会导致猴子冠状动脉粥样硬化加重,而雌激素替代疗法可预防这种情况。相反,怀孕(高雌激素状态)会使动脉粥样硬化明显减轻。在群居的雄性猴子中出现了一种略有不同的动脉粥样硬化发生模式。在这里,处于社会优势地位的动物会出现冠状动脉粥样硬化加重的情况,但仅在社会压力条件下(即由于社会群体成员定期重新组织导致的干扰)。我们假设,反复接触群体重新组织会引发优势动物交感神经系统的激活;反过来,交感神经激活所伴随的血液动力学和代谢变化可能损害了这些猴子的冠状动脉,从而促进了动脉粥样硬化的发生。为了验证这一假设,将雄性猴子饲养在不稳定的社会群体中,一半的猴子给予β-肾上腺素能阻滞剂(以减弱心率和血压对应激的反应)。β-阻滞剂抑制了动脉粥样硬化,但仅在那些行为上易患病变加重的动物(即优势猴子)中有效。这些结果支持了这样一种观点,即猴子是动脉粥样硬化的合适研究模型,这种疾病影响着数百万人。