Experimental Neurogerontology, Department of Neuroscience, Karolinska Institutet, Retzius väg 8, 171 77 Stockholm, Sweden.
Neurobiol Aging. 2011 Oct;32(10):1868-80. doi: 10.1016/j.neurobiolaging.2009.11.003. Epub 2009 Dec 14.
Using a range of tests we have studied alterations in behavior with advancing age in female C57BL/6 (of Jackson origin), the golden standard on which most genetically engineered mice are back-crossed. In parallel, growth and survival data were collected. In a protected environment the 90% and 75% cohort survival age was 20 and 25 months, respectively, and the 50% cohort survival was 32 months. In mice, body weight increases continuously until 15-20 months of age, while in advanced age whole body weight drops. The body mass loss in senescence is associated with emergence of other aged phenotype features such as kyphosis, balding and loss of fur-color. Our behavioral data show that aging modulates certain aspects of basic behavior in a continuous manner, like explorative and locomotor activities. Advanced age associates with an acceleration of behavioral impairments evident in most of the tests used, including motor skill acquisition and memory consolidation. However, certain domains of mouse behavior were well preserved also in advanced age such as thermal noxious threshold and working memory as assessed by an object recognition task. The decreased drive to explore is suggested to be a key factor underlying many aspects of reduced performance including cognitive capacity during aging. Behavioral aging affects genetically closely related individuals housed under strictly standardized conditions differentially (Collier, T.J., Coleman, P.D., 1991. Divergence of biological and chronological aging: evidence from rodent studies. Neurobiol. Aging, 12, 685-693; Ingram, D.K., 1988. Motor performance variability during aging in rodents. Assessment of reliability and validity of individual differences. Ann. N.Y. Acad. Sci., 515, 70-96). Consistent with this a subpopulation of the 28-month-old mice showed an explorative activity similar to young-adult mice and a significantly stronger preference for a novel object than aged mice with a less explorative behavior. Thus, subtle environmental factors and epigenetic modifications may be important modulators of aging.
我们使用一系列测试研究了 C57BL/6(杰克逊起源)雌性小鼠的行为随年龄的变化,该品系是大多数基因工程小鼠的回交标准品。同时,我们收集了生长和存活数据。在受保护的环境中,90%和 75%的群体的存活年龄分别为 20 个月和 25 个月,而 50%的群体的存活年龄为 32 个月。在小鼠中,体重持续增加,直到 15-20 个月大,而在老年时,全身体重下降。衰老过程中的体重减轻与其他老年表型特征的出现有关,如驼背、秃顶和皮毛颜色丧失。我们的行为数据表明,衰老以连续的方式调节某些基本行为,如探索和运动活动。老年与大多数使用的测试中明显的行为损伤加速有关,包括运动技能获得和记忆巩固。然而,在老年时,某些小鼠行为领域也得到了很好的保留,如热伤害阈值和工作记忆,如通过物体识别任务评估。探索动力的降低被认为是衰老过程中许多表现下降的关键因素,包括认知能力。行为衰老以不同的方式影响在严格标准化条件下饲养的遗传上密切相关的个体(Collier, T.J., Coleman, P.D., 1991. 生物和时间老化的分歧:来自啮齿动物研究的证据。神经生物学衰老,12, 685-693; Ingram, D.K., 1988. 衰老过程中啮齿动物的运动表现变异性。个体差异的可靠性和有效性评估。Ann. N.Y. Acad. Sci., 515, 70-96)。与这一结果一致的是,28 个月大的小鼠中的一个亚群表现出类似于年轻成年小鼠的探索活动,并且对新物体的偏好明显强于探索行为较少的老年小鼠。因此,微妙的环境因素和表观遗传修饰可能是衰老的重要调节剂。