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Vitamin D Insufficiency Reduces Grip Strength Grip Endurance and Increases Frailty in Aged C57Bl/6J Mice

机译:维生素D功能不全降低握力握持耐久性增加了老年C57BL / 6J小鼠的脆弱性

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摘要

Low 25-OH serum vitamin D (VitD) is pervasive in older adults and linked to functional decline and progression of frailty. We have previously shown that chronic VitD insufficiency in “middle-aged” mice results in impaired anaerobic exercise capacity, decreased lean mass, and increased adiposity. Here, we examine if VitD insufficiency results in similar deficits and greater frailty progression in old-aged (24 to 28 months of age) mice. Similar to what we report in younger mice, older mice exhibit a rapid and sustained response in serum 25-OH VitD levels to differential supplementation, including insufficient (125 IU/kg chow), sufficient (1000 IU/kg chow), and hypersufficient (8000 IU/kg chow) groups. During the 4-month time course, mice were assessed for body composition (DEXA), physical performance, and frailty using a Fried physical phenotype-based assessment tool. The 125 IU mice exhibited worse grip strength (p = 0.002) and inverted grip hang time (p = 0.003) at endpoint and the 8000 IU mice transiently displayed greater rotarod performance after 3 months (p = 0.012), yet other aspects including treadmill performance and gait speed were unaffected. However, 125 and 1000 IU mice exhibited greater frailty compared to baseline (p = 0.001 and p = 0.038, respectively), whereas 8000 IU mice did not (p = 0.341). These data indicate targeting higher serum 25-OH vitamin D levels may attenuate frailty progression during aging.
机译:低25-OH血清维生素D(VITD)在老年人普遍存在,与功能下降和脆弱的进展相关联。我们以前表明,“中年”小鼠的慢性VitD不足导致厌氧运动能力受损,减少瘦肿块,肥厚增加。在这里,我们检查Vitd不足是否导致类似的缺陷和旧老年(年龄24至28个月)小鼠的更大的脆弱进展。类似于我们在年轻小鼠中报告的内容,较旧的小鼠在血清25-OH VITD水平中表现出快速且持续的响应,以差异补充,包括不足(125 IU / kg Chow),足够的(1000 IU / kg Chow)和高度( 8000 iu / kg chow)组。在4个月的时间过程中,使用油炸物理表型的评估工具评估对小鼠的身体成分(DEXA),物理性能和脆弱。 125 IU小鼠在终点上表现出较差的握力(P = 0.002)和倒置抓地悬挂时间(P = 0.003),3个月后,8000IU小鼠瞬时显示旋转旋转性能(P = 0.012),其他方面包括跑步机表现步态速度不受影响。然而,与基线相比,125和1000 IU小鼠表现出更大的脆弱(P = 0.001和P = 0.038),而8000只IU小鼠没有(P = 0.341)。这些数据表明靶向更高的血清25-OH维生素D水平可以在老化期间衰减脆弱的进展。

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