Department of Orthodontics and Pediatric Dentistry, Faculty of Dentistry, Chiang Mai University, Chiang Mai, 50200, Thailand.
Department of Oral Biology and Diagnostic Sciences, Faculty of Dentistry, Chiang Mai University, Chiang Mai, 50200, Thailand.
Eur J Nutr. 2019 Oct;58(7):2801-2810. doi: 10.1007/s00394-018-1829-4. Epub 2018 Sep 24.
PURPOSE: Chronic high-fat diet (HFD) consumption results in gut dysbiosis, systemic inflammation, obese-insulin resistance, and osteoporosis of the jawbones. The probiotics, prebiotics or synbiotics alleviated gut dysbiosis and the metabolic disturbance in HFD-induced obesity. However, the effects on jawbone properties have not been investigated. This study aimed to investigate the effects of probiotic Lactobacillus paracasei HII01, prebiotic xylooligosaccharide (XOS), and synbiotics on the jawbone properties along with metabolic parameters, gut and systemic inflammation in HFD-fed rats. METHODS: Forty-eight male Wistar rats were fed with either a HFD or normal diet for 12 weeks. Rats in each group were subdivided into four subgroups to be treated with either vehicle, probiotics, prebiotics, or synbiotics for the additional 12 weeks. Blood samples, gut, bone marrows, and jawbones were collected to determine metabolic parameters, inflammation, and bone properties. RESULTS: The HFD-fed rats developed obese-insulin resistance, as indicated by increased body weight, dyslipidemia and decreased insulin sensitivity. Serum lipopolysaccharide levels and interleukin-6 mRNA expression in the ileum and bone marrows were elevated. Altered bone metabolism and the impaired jawbone properties were evident as indicated by decreased bone mineral density with increased trabecular separation. Reduced ultimate load and stiffness were observed in HFD-fed rats. Treatments with probiotics, prebiotics or synbiotics in HFD-fed rats improved metabolic parameters and reduced inflammation. However, no alterations in jawbone properties were found in all treatments. CONCLUSION: The osteoporosis of the jawbone occurred in obese-insulin resistance, and treatments with probiotics, prebiotics and synbiotics were not sufficient to improve the jawbone properties.
目的:慢性高脂肪饮食(HFD)的摄入会导致肠道菌群失调、全身炎症、肥胖型胰岛素抵抗和颌骨骨质疏松。益生菌、益生元和合生剂可缓解 HFD 诱导的肥胖中的肠道菌群失调和代谢紊乱。然而,它们对颌骨特性的影响尚未得到研究。本研究旨在探讨益生菌副干酪乳杆菌 HII01、益生元木寡糖(XOS)和合生剂对 HFD 喂养大鼠颌骨特性以及代谢参数、肠道和全身炎症的影响。
方法:将 48 只雄性 Wistar 大鼠分别用 HFD 或正常饮食喂养 12 周。每组大鼠再分为 4 个亚组,分别用载体、益生菌、益生元和合生剂处理 12 周。收集血液样本、肠道、骨髓和颌骨,以确定代谢参数、炎症和骨特性。
结果:HFD 喂养的大鼠出现肥胖型胰岛素抵抗,表现为体重增加、血脂异常和胰岛素敏感性降低。血清脂多糖水平和回肠及骨髓中白细胞介素-6mRNA 表达升高。骨代谢改变和颌骨特性受损明显,表现为骨密度降低,骨小梁分离增加。HFD 喂养大鼠的最大载荷和刚度降低。HFD 喂养大鼠用益生菌、益生元和合生剂治疗可改善代谢参数和降低炎症,但所有治疗均未改善颌骨特性。
结论:肥胖型胰岛素抵抗可导致颌骨骨质疏松,用益生菌、益生元和合生剂治疗不足以改善颌骨特性。
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