Kang Ho Jun, Chargo Nicholas, Chennupati Soumya, Neugebauer Kerri, Cho Jae Youl, Quinn Robert, McCabe Laura R, Parameswaran Narayanan
Department of Physiology, Michigan State University, East Lansing, MI, USA.
Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, MI, USA.
J Ginseng Res. 2023 Mar;47(2):265-273. doi: 10.1016/j.jgr.2022.08.006. Epub 2022 Aug 31.
The intestinal microbiota is an important regulator of bone health. In previous studies we have shown that intestinal microbiota dysbiosis, induced by treatment with broad spectrum antibiotics (ABX) followed by natural repopulation, results in gut barrier dysfunction and bone loss. We have also shown that treatment with probiotics or a gut barrier enhancer can inhibit dysbiosis-induced bone loss. The overall goal of this project was to test the effect of Korean Red Ginseng (KRG) extract on bone and gut health using antibiotics (ABX) dysbiosis-induced bone loss model in mice.
Adult male mice (Balb/C, 12-week old) were administered broad spectrum antibiotics (ampicillin and neomycin) for 2 weeks followed by 4 weeks of natural repopulation. During this 4-week period, mice were treated with vehicle (water) or KRG extract. Other controls included mice that did not receive either antibiotics or KRG extract and mice that received only KRG extract. At the end of the experiments, we assessed various parameters to assess bone, microbiota and intestinal permeability.
Consistent with our previous results, post-ABX- dysbiosis led to significant bone loss. Importantly, this was associated with a decrease in gut microbiota alpha diversity and an increase in intestinal permeability. All these effects including bone loss were prevented by KRG extract treatment. Furthermore, our studies identified multiple genera including and as well as to be potentially linked to the effect of KRG extract on gut-bone axis.
Together, our results demonstrate that KRG extract regulates the gut-bone axis and is effective at preventing dysbiosis-induced bone loss in mice.
肠道微生物群是骨骼健康的重要调节因子。在先前的研究中,我们已经表明,用广谱抗生素(ABX)治疗后自然再定殖所诱导的肠道微生物群失调会导致肠道屏障功能障碍和骨质流失。我们还表明,用益生菌或肠道屏障增强剂治疗可以抑制失调诱导的骨质流失。本项目的总体目标是使用抗生素(ABX)失调诱导的小鼠骨质流失模型来测试韩国红参(KRG)提取物对骨骼和肠道健康的影响。
成年雄性小鼠(Balb/C,12周龄)接受广谱抗生素(氨苄青霉素和新霉素)治疗2周,随后进行4周的自然再定殖。在这4周期间,小鼠接受载体(水)或KRG提取物治疗。其他对照组包括未接受抗生素或KRG提取物的小鼠以及仅接受KRG提取物的小鼠。在实验结束时,我们评估了各种参数以评估骨骼、微生物群和肠道通透性。
与我们之前的结果一致,ABX后失调导致显著的骨质流失。重要的是,这与肠道微生物群α多样性的降低和肠道通透性的增加有关。KRG提取物治疗可预防所有这些影响,包括骨质流失。此外,我们的研究确定了多个属,包括[具体属名缺失]以及[具体属名缺失]可能与KRG提取物对肠骨轴的影响有关。
总之,我们的结果表明,KRG提取物调节肠骨轴,并且在预防小鼠失调诱导的骨质流失方面有效。