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Catecholamine receptor polymorphisms affect decision-making in C. elegans.儿茶酚胺受体多态性影响秀丽隐杆线虫的决策。
Nature. 2011 Apr 21;472(7343):313-8. doi: 10.1038/nature09821. Epub 2011 Mar 16.
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Dietary restriction: standing up for sirtuins.饮食限制:为沉默调节蛋白挺身而出。
Science. 2010 Aug 27;329(5995):1012-3; author reply 1013-4. doi: 10.1126/science.329.5995.1012.
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Behavioral profiles of three C57BL/6 substrains.三种C57BL/6亚系的行为特征。
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The impact of dietary energy intake on cognitive aging.膳食能量摄入对认知老化的影响。
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Dietary restriction affects lifespan but not cognitive aging in Drosophila melanogaster.饮食限制影响寿命但不影响黑腹果蝇的认知衰老。
Aging Cell. 2010 Jun;9(3):327-35. doi: 10.1111/j.1474-9726.2010.00560.x. Epub 2010 Feb 12.
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Behavioral changes in aging female C57BL/6 mice.衰老雌性 C57BL/6 小鼠的行为变化。
Neurobiol Aging. 2011 Oct;32(10):1868-80. doi: 10.1016/j.neurobiolaging.2009.11.003. Epub 2009 Dec 14.
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Metabolic reprogramming, caloric restriction and aging.代谢重编程、热量限制与衰老。
Trends Endocrinol Metab. 2010 Mar;21(3):134-41. doi: 10.1016/j.tem.2009.11.005. Epub 2009 Dec 7.
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Genetic differences among C57BL/6 substrains.C57BL/6亚系之间的遗传差异。
Exp Anim. 2009 Apr;58(2):141-9. doi: 10.1538/expanim.58.141.
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Behavioral differences among C57BL/6 substrains: implications for transgenic and knockout studies.C57BL/6亚系之间的行为差异:对转基因和基因敲除研究的启示。
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10
How long will my mouse live? Machine learning approaches for prediction of mouse life span.我的小鼠能活多久?预测小鼠寿命的机器学习方法。
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成年雄性C57BL/6J小鼠在整个寿命周期中的行为变化及饮食限制的影响。

Changes in behaviors of male C57BL/6J mice across adult life span and effects of dietary restriction.

作者信息

Fahlström Andreas, Zeberg Hugo, Ulfhake Brun

机构信息

Experimental Neurogerontology, Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.

出版信息

Age (Dordr). 2012 Dec;34(6):1435-52. doi: 10.1007/s11357-011-9320-7. Epub 2011 Oct 12.

DOI:10.1007/s11357-011-9320-7
PMID:21989972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3528371/
Abstract

Behavioral analysis is a high-end read-out of aging impact on an organism, and here, we have analyzed behaviors in 4-, 22-, and 28-month-old male C57BL/6J with a broad range of tests. For comparison, a group of 28-month-old males maintained on dietary restriction (DR) was included. The most conspicuous alteration was the decline in exploration activity with advancing age. Aging also affected other behaviors such as motor skill acquisition and grip strength, in contrast to latency to thermal stimuli and visual placement which were unchanged. Object recognition tests revealed intact working memory at 28 months while memory recollection was impaired already at 22 months. Comparison with female C57BL/6J (Fahlström et al., Neurobiol Aging 32:1868-1880, 2011) revealed that alterations in aged males and females are similar and that several of the behavioral indices correlate with age in both sexes. Moreover, we examined if behavioral indices in 22-month-old males could predict remaining life span as suggested in the study by Ingram and Reynolds (Exp Aging Res 12(3):155-162, 1986) and found that exploratory activity and motor skills accounted for up to 65% of the variance. Consistent with that a high level of exploratory activity and preserved motor capacity indicated a long post-test survival, 28-month-old males maintained on DR were more successful in such tests than ad libitum fed age-matched males. In summary, aged C57BL/6J males are marked by a reduced exploratory activity, an alteration that DR impedes. In light of recently published data, we discuss if a diminishing drive to explore may associate with aging-related impairment of central aminergic pathways.

摘要

行为分析是对衰老对生物体影响的一种高端解读,在此,我们通过一系列广泛的测试分析了4个月、22个月和28个月大的雄性C57BL/6J小鼠的行为。为作比较,纳入了一组维持饮食限制(DR)的28个月大的雄性小鼠。最明显的变化是随着年龄增长探索活动减少。衰老还影响了其他行为,如运动技能习得和握力,而热刺激潜伏期和视觉定位则未改变。物体识别测试显示,28个月大时工作记忆完好,而记忆回忆在22个月大时就已受损。与雌性C57BL/6J小鼠(Fahlström等人,《神经生物学衰老》32:1868 - 1880,2011年)的比较表明,老年雄性和雌性的变化相似,且一些行为指标在两性中均与年龄相关。此外,我们按照英格拉姆和雷诺兹(《实验衰老研究》12(3):155 - 162,1986年)研究中的建议,检验了22个月大雄性小鼠的行为指标是否能预测剩余寿命,发现探索活动和运动技能占方差的比例高达65%。与高水平的探索活动和保留的运动能力表明测试后生存期较长一致,维持饮食限制的28个月大雄性小鼠在此类测试中比自由进食的年龄匹配雄性小鼠更成功。总之,老年C57BL/6J雄性小鼠的特点是探索活动减少,而饮食限制可阻碍这种变化。根据最近发表的数据,我们讨论探索驱动力的减弱是否可能与衰老相关的中枢胺能通路损伤有关。