Thermoneutral housing has limited effects on social isolation-induced bone loss in male C57BL/6J mice.

IF 3.4 Q2 ENDOCRINOLOGY & METABOLISM
JBMR Plus Pub Date : 2025-05-11 eCollection Date: 2025-07-01 DOI:10.1093/jbmrpl/ziaf088
Rebecca V Mountain, Rebecca L Peters, Audrie L Langlais, Julia Patrizia Stohn, Christine W Lary, Katherine J Motyl
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引用次数: 0

Abstract

Social isolation stress has numerous known negative health effects, including increased risk for cardiovascular disease, dementia, as well as overall mortality. The impacts of social isolation on skeletal health, however, have not been thoroughly investigated. We previously found that 4 wk of social isolation through single housing led to a significant reduction in trabecular and cortical bone in male, but not female, mice. One possible explanation for these changes in male mice is thermal stress due to sub-thermoneutral housing and sex differences in thermal physiology. Single housing at room temperature (~20 to 25 °C)-below the thermoneutral range of mice (~26 to 34 °C)-may lead to cold stress, which has known negative effects on bone. Therefore, the aim of this study was to test the hypothesis that housing mice near thermoneutrality, thereby ameliorating cold-stress, will prevent social isolation-induced bone loss in male C57BL/6J mice. 16-wk-old mice were randomized into social isolation (1 mouse/cage) or grouped housing (4 mice/cage) at either room temperature (~23 °C) or in a warm temperature incubator (~28 °C) for 4 wk (N = 8/group). As seen in our previous studies, isolated mice at room temperature had significantly reduced bone parameters, including femoral bone volume fraction (-35% BV/TV), bone mineral density (-27% BMD), and cortical thickness (-12%). Contrary to our hypothesis, these negative effects on bone were not fully ameliorated by thermoneutral housing. There was no significant effect of housing or temperature on serum turnover markers. Social isolation increased glucocorticoid-related gene expression in bone and Ucp1 and Pdk4 expression in BAT across temperatures, while thermoneutral housing increased percent lipid area and decreased Ucp1 and Pdk4 expression in BAT across housing conditions. Overall, our data suggest thermal stress from single housing cannot fully explain social isolation-induced bone loss and provide a key insight into the mechanism mediating the effects of isolation on skeletal health.

热中性住房对社会隔离引起的雄性C57BL/6J小鼠骨质流失的影响有限。
社会孤立压力对健康有许多已知的负面影响,包括心血管疾病、痴呆和总体死亡率的风险增加。然而,社会孤立对骨骼健康的影响尚未得到彻底调查。我们之前发现,通过单一住房进行4周的社会隔离会导致雄性小鼠的小梁和皮质骨显著减少,而雌性小鼠则没有。对于雄性小鼠的这些变化,一个可能的解释是由于亚热中性的住房和热生理上的性别差异造成的热应激。在室温(~20至25°C)下的单一住房-低于小鼠的热中性范围(~26至34°C)-可能导致冷应激,这对骨骼有已知的负面影响。因此,本研究的目的是验证一种假设,即在接近热中性的环境中饲养小鼠,从而改善冷应激,可以防止社会隔离导致的雄性C57BL/6J小鼠骨质流失。16周龄小鼠随机分为社会隔离(1只/笼)或分组饲养(4只/笼),在室温(~23°C)或恒温培养箱(~28°C)中饲养4周(N = 8只/组)。如我们之前的研究所见,室温下离体小鼠的骨参数显著降低,包括股骨骨体积分数(-35% BV/TV)、骨矿物质密度(-27% BMD)和皮质厚度(-12%)。与我们的假设相反,这些对骨骼的负面影响并没有被热中性外壳完全改善。饲养环境和温度对血清周转指标无显著影响。社会隔离增加了骨中糖皮质激素相关基因的表达以及BAT中Ucp1和Pdk4的表达,而热中性住房增加了BAT中脂质面积的百分比,降低了BAT中Ucp1和Pdk4的表达。总的来说,我们的数据表明,来自单一住房的热应力不能完全解释社会隔离引起的骨质流失,并为隔离对骨骼健康影响的中介机制提供了关键见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JBMR Plus
JBMR Plus Medicine-Orthopedics and Sports Medicine
CiteScore
5.80
自引率
2.60%
发文量
103
审稿时长
8 weeks
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