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C57BL/6J小鼠从成年早期到中年期与年龄相关的行为变化。

Age-related changes in behavior in C57BL/6J mice from young adulthood to middle age.

作者信息

Shoji Hirotaka, Takao Keizo, Hattori Satoko, Miyakawa Tsuyoshi

机构信息

Division of Systems Medical Science, Institute for Comprehensive Medical Science, Fujita Health University, 1-98 Dengakugakubo, Kutsukake-cho, Toyoake, Aichi, 470-1192, Japan.

Japan Science and Technology Agency, Core Research for Evolutional Science and Technology, 4-1-8 Honcho, Kawaguchi, Saitama, 332-0012, Japan.

出版信息

Mol Brain. 2016 Jan 28;9:11. doi: 10.1186/s13041-016-0191-9.

Abstract

BACKGROUND

Aging is considered to be associated with progressive changes in the brain and its associated sensory, motor, and cognitive functions. A large number of studies comparing young and aged animals have reported differences in various behaviors between age-cohorts, indicating behavioral dysfunctions related to aging. However, relatively little is known about behavioral changes from young adulthood to middle age, and the effect of age on behavior during the early stages of life remains to be understood. In order to investigate age-related changes in the behaviors of mice from young adulthood to middle age, we performed a large-scale analysis of the behavioral data obtained from our behavioral test battery involving 1739 C57BL/6J wild-type mice at 2-12 months of age.

RESULTS

Significant behavioral differences between age groups (2-3-, 4-5-, 6-7-, and 8-12-month-old groups) were found in all the behavioral tests, including the light/dark transition, open field, elevated plus maze, rotarod, social interaction, prepulse inhibition, Porsolt forced swim, tail suspension, Barnes maze, and fear conditioning tests, except for the hot plate test. Compared with the 2-3-month-old group, the 4-5- and 6-7-month-old groups exhibited decreased locomotor activity to novel environments, motor function, acoustic startle response, social behavior, and depression-related behavior, increased prepulse inhibition, and deficits in spatial and cued fear memory. For most behaviors, the 8-12-month-old group showed similar but more pronounced changes in most of these behaviors compared with the younger age groups. Older groups exhibited increased anxiety-like behavior in the light/dark transition test whereas those groups showed seemingly decreased anxiety-like behavior measured by the elevated plus maze test.

CONCLUSIONS

The large-scale analysis of behavioral data from our battery of behavioral tests indicated age-related changes in a wide range of behaviors from young adulthood to middle age in C57BL/6J mice, though these results might have been influenced by possible confounding factors such as the time of day at testing and prior test experience. Our results also indicate that relatively narrow age differences can produce significant behavioral differences during adulthood in mice. These findings provide an insight into our understanding of the neurobiological processes underlying brain function and behavior that are subject to age-related changes in early to middle life. The findings also indicate that age is one of the critical factors to be carefully considered when designing behavioral tests and interpreting behavioral differences that might be induced by experimental manipulations.

摘要

背景

衰老被认为与大脑及其相关的感觉、运动和认知功能的渐进性变化有关。大量比较年轻和老年动物的研究报告了不同年龄组之间在各种行为上的差异,表明存在与衰老相关的行为功能障碍。然而,对于从青年期到中年期的行为变化了解相对较少,并且年龄对生命早期行为的影响仍有待明确。为了研究从青年期到中年期小鼠行为的年龄相关变化,我们对从我们的行为测试组中获得的行为数据进行了大规模分析,该测试组涉及1739只2至12月龄的C57BL/6J野生型小鼠。

结果

在所有行为测试中,包括明暗转换、旷场、高架十字迷宫、转棒、社交互动、前脉冲抑制、波索尔特强迫游泳、悬尾、巴恩斯迷宫和恐惧条件测试(热板测试除外),均发现不同年龄组(2 - 3月龄、4 - 5月龄、6 - 7月龄和8 - 12月龄组)之间存在显著的行为差异。与2 - 3月龄组相比,4 - 5月龄和6 - 7月龄组对新环境的运动活动、运动功能、听觉惊吓反应、社交行为和抑郁相关行为减少,前脉冲抑制增加,空间和线索恐惧记忆存在缺陷。对于大多数行为,8 - 12月龄组与较年轻年龄组相比,在大多数这些行为上表现出相似但更明显的变化。在明暗转换测试中,较年长组表现出焦虑样行为增加,而在高架十字迷宫测试中,这些组表现出看似减少的焦虑样行为。

结论

我们行为测试组的行为数据大规模分析表明,C57BL/6J小鼠从青年期到中年期在广泛行为上存在年龄相关变化,尽管这些结果可能受到诸如测试时间和先前测试经验等可能的混杂因素影响。我们的结果还表明,相对较小的年龄差异在小鼠成年期可产生显著的行为差异。这些发现为我们理解大脑功能和行为背后的神经生物学过程提供了见解,这些过程在生命早期到中期会发生与年龄相关的变化。这些发现还表明,在设计行为测试和解释可能由实验操作引起的行为差异时,年龄是需要仔细考虑的关键因素之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7b4/4730600/468e2d7eb6e5/13041_2016_191_Fig1_HTML.jpg

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