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蒙莫朗西酸樱桃可预防雌性 C57BL/6 小鼠的与年龄相关的骨质流失,并表现出一些合成代谢作用。

Montmorency tart cherry protects against age-related bone loss in female C57BL/6 mice and demonstrates some anabolic effects.

机构信息

HS 420, Department of Nutritional Sciences, Oklahoma State University, Stillwater, OK, 74078, USA.

出版信息

Eur J Nutr. 2019 Dec;58(8):3035-3046. doi: 10.1007/s00394-018-1848-1. Epub 2018 Oct 30.

Abstract

PURPOSE

Age-related bone loss is a consequence of endocrine and immune changes that disrupt bone remodeling. Functional foods (e.g., tart cherries) with antioxidant, anti-inflammatory and prebiotic activity can potentially counter this age-related phenomenon. The aim of this study was to determine if Montmorency tart cherry protects against early age-related bone loss and the culpable alterations in bone metabolism.

METHODS

Female, 5-month-old, C57BL/6 mice were assigned to baseline or treatment groups: AIN-93M diet supplemented with 0, 1, 5, or 10% tart cherry for 90 days. Bone mineral density (BMD) and trabecular and cortical bone microarchitecture were assessed. Treatment effects on bone metabolism and regulators of bone formation, resorption and mineralization were determined.

RESULTS

Mice consuming the 5% and 10% doses had higher vertebral and tibial BMD (p < 0.05) compared to controls. The age-related decrease in trabecular bone volume (BV/TV) of the distal femur was prevented with these doses. Vertebral trabecular BV/TV and cortical bone thickness of the femur mid-diaphysis were greater (p < 0.05) in the groups receiving the 5% and 10% cherry than the control diet. Notably, these improvements were significantly greater than the baseline controls, consistent with an anabolic response. Although no differences in systemic biomarkers of bone formation or resorption were detected at 90 days, local increases in Phex and decreases in Ppar-γ suggest a bone environment that supports increased mineralization.

CONCLUSIONS

These findings demonstrate that cherry supplementation (5% and 10%) improves BMD and some indices of trabecular and cortical bone microarchitecture; these effects are likely attributed to increased bone mineralization.

摘要

目的

与年龄相关的骨质流失是内分泌和免疫变化破坏骨重塑的结果。具有抗氧化、抗炎和益生元活性的功能性食品(如酸樱桃)可能有助于对抗这种与年龄相关的现象。本研究旨在确定蒙莫朗西酸樱桃是否能预防与年龄相关的早期骨质流失和骨代谢的改变。

方法

将 5 月龄雌性 C57BL/6 小鼠分为基线或治疗组:AIN-93M 饮食补充 0、1、5 或 10%的酸樱桃,共 90 天。评估骨密度(BMD)和小梁及皮质骨微结构。测定治疗对骨代谢和骨形成、吸收和矿化调节剂的影响。

结果

与对照组相比,摄入 5%和 10%剂量的小鼠的椎体和胫骨 BMD 更高(p<0.05)。这些剂量可预防远端股骨小梁骨体积(BV/TV)随年龄的下降。5%和 10%樱桃组的椎体小梁 BV/TV 和股骨中段皮质骨厚度大于对照组(p<0.05)。值得注意的是,这些改善明显大于基线对照组,与合成代谢反应一致。尽管在 90 天时未检测到骨形成或吸收的系统生物标志物的差异,但 Phex 的增加和 Ppar-γ的减少表明骨环境支持矿化增加。

结论

这些发现表明,樱桃补充(5%和 10%)可提高 BMD 和小梁及皮质骨微结构的一些指数;这些作用可能归因于骨矿化增加。

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