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韩国红参提取物可预防小鼠糖皮质激素诱导性骨质疏松口腔模型中的骨质流失。

Korean red ginseng extract prevents bone loss in an oral model of glucocorticoid induced osteoporosis in mice.

作者信息

Chargo Nicholas J, Kang Ho Jun, Das Subhashari, Jin Yining, Rockwell Cheryl, Cho Jae Youl, McCabe Laura R, Parameswaran Narayanan

机构信息

Department of Physiology, Michigan State University, East Lansing, MI, United States.

College of Osteopathic Medicine, Michigan State University, East Lansing, MI, United States.

出版信息

Front Pharmacol. 2024 Mar 12;15:1268134. doi: 10.3389/fphar.2024.1268134. eCollection 2024.

Abstract

The gut microbiota and barrier function play important roles in bone health. We previously demonstrated that chronic glucocorticoid (GC)-induced bone loss in mice is associated with significant shifts in gut microbiota composition and impaired gut barrier function. Korean Red Ginseng (KRG, Meyer, Araliaceae) extract has been shown to prevent glucocorticoid-induced osteoporosis (GIO) in a subcutaneous pellet model in mice, but its effect on gut microbiota and barrier function in this context is not known. The overall goal of this study was to test the effect of KRG extract in a clinically relevant, oral model of GIO and further investigate its role in modulating the gut-bone axis. Growing male mice (CD-1, 8 weeks) were treated with 75 μg/mL corticosterone (∼9 mg/kg/day) or 0.4% ethanol vehicle in the drinking water for 4 weeks. During this 4-week period, mice were treated daily with 500 mg/kg/day KRG extract dissolved in sterile water or an equal amount of sterile water via oral gastric gavage. After 4 weeks of treatment, we assessed bone volume, microbiota composition, gut barrier integrity, and immune cells in the bone marrow (BM) and mesenteric lymph nodes (MLNs). 4 weeks of oral GC treatment caused significant distal femur trabecular bone loss, and this was associated with changes in gut microbiota composition, impaired gut barrier function and altered immune cell composition. Importantly, KRG extract prevented distal femur trabecular bone loss and caused significant alterations in gut microbiota composition but had only modest effects on gut barrier function and immune cell populations. Taken together, these results demonstrate that KRG extract significantly modulates the gut microbiota-bone axis and prevents glucocorticoid-induced bone loss in mice.

摘要

肠道微生物群和屏障功能在骨骼健康中发挥着重要作用。我们之前证明,小鼠慢性糖皮质激素(GC)诱导的骨质流失与肠道微生物群组成的显著变化以及肠道屏障功能受损有关。韩国红参(KRG,五加科人参属)提取物已被证明在小鼠皮下植入模型中可预防糖皮质激素诱导的骨质疏松症(GIO),但其在这种情况下对肠道微生物群和屏障功能的影响尚不清楚。本研究的总体目标是在临床相关的GIO口服模型中测试KRG提取物的效果,并进一步研究其在调节肠骨轴中的作用。将生长中的雄性小鼠(CD-1,8周龄)用75μg/mL皮质酮(约9mg/kg/天)或饮用水中的0.4%乙醇载体处理4周。在这4周期间,通过口服胃管饲法,每天给小鼠灌胃500mg/kg/天溶解在无菌水中的KRG提取物或等量的无菌水。治疗4周后,我们评估了骨体积、微生物群组成、肠道屏障完整性以及骨髓(BM)和肠系膜淋巴结(MLN)中的免疫细胞。口服GC治疗4周导致显著的股骨远端小梁骨丢失,这与肠道微生物群组成的变化、肠道屏障功能受损以及免疫细胞组成改变有关。重要的是,KRG提取物预防了股骨远端小梁骨丢失,并导致肠道微生物群组成发生显著改变,但对肠道屏障功能和免疫细胞群体的影响较小。综上所述,这些结果表明,KRG提取物显著调节肠道微生物群-骨轴,并预防小鼠糖皮质激素诱导的骨质流失。

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