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罗伊氏乳杆菌治疗可预防绝经后去卵巢小鼠模型的骨质流失。

Probiotic L. reuteri treatment prevents bone loss in a menopausal ovariectomized mouse model.

机构信息

Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, Michigan, 48824.

出版信息

J Cell Physiol. 2014 Nov;229(11):1822-30. doi: 10.1002/jcp.24636.

Abstract

Estrogen deficiency is a major risk factor for osteoporosis that is associated with bone inflammation and resorption. Half of women over the age of 50 will experience an osteoporosis related fracture in their lifetime, thus novel therapies are needed to combat post-menopausal bone loss. Recent studies suggest an important role for gut-bone signaling pathways and the microbiota in regulating bone health. Given that the bacterium Lactobacillus reuteri ATCC PTA 6475 (L. reuteri) secretes beneficial immunomodulatory factors, we examined if this candidate probiotic could reduce bone loss associated with estrogen deficiency in an ovariectomized (Ovx) mouse menopausal model. Strikingly, L. reuteri treatment significantly protected Ovx mice from bone loss. Osteoclast bone resorption markers and activators (Trap5 and RANKL) as well as osteoclastogenesis are significantly decreased in L. reuteri-treated mice. Consistent with this, L. reuteri suppressed Ovx-induced increases in bone marrow CD4+ T-lymphocytes (which promote osteoclastogenesis) and directly suppressed osteoclastogenesis in vitro. We also identified that L. reuteri treatment modifies microbial communities in the Ovx mouse gut. Together, our studies demonstrate that L. reuteri treatment suppresses bone resorption and loss associated with estrogen deficiency. Thus, L. reuteri treatment may be a straightforward and cost-effective approach to reduce post-menopausal bone loss.

摘要

雌激素缺乏是骨质疏松症的一个主要危险因素,与骨炎症和吸收有关。超过 50 岁的女性中有一半在其一生中会经历一次与骨质疏松症相关的骨折,因此需要新的疗法来对抗绝经后骨丢失。最近的研究表明,肠道-骨骼信号通路和微生物群在调节骨骼健康方面起着重要作用。鉴于细菌乳杆菌 ATCC PTA 6475(L. reuteri)分泌有益的免疫调节因子,我们研究了这种候选益生菌是否可以减少去卵巢(Ovx)小鼠绝经模型中与雌激素缺乏相关的骨丢失。令人惊讶的是,L. reuteri 治疗显著保护 Ovx 小鼠免受骨丢失。L. reuteri 治疗的小鼠破骨细胞骨吸收标志物和激活剂(Trap5 和 RANKL)以及破骨细胞生成明显减少。与此一致,L. reuteri 抑制 Ovx 诱导的骨髓 CD4+T 淋巴细胞增加(促进破骨细胞生成),并直接在体外抑制破骨细胞生成。我们还发现,L. reuteri 治疗改变了 Ovx 小鼠肠道中的微生物群落。总之,我们的研究表明,L. reuteri 治疗可抑制与雌激素缺乏相关的骨吸收和丢失。因此,L. reuteri 治疗可能是一种简单有效的方法,可减少绝经后骨丢失。

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