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高脂饮食诱导的肥胖会刺激小鼠骨骼破骨细胞中的酮体利用。

High-fat diet-induced obesity stimulates ketone body utilization in osteoclasts of the mouse bone.

作者信息

Yamasaki Masahiro, Hasegawa Shinya, Imai Masahiko, Takahashi Noriko, Fukui Tetsuya

机构信息

Department of Health Chemistry, Hoshi University, Shinagawa-ku, Tokyo 142-8501, Japan.

Department of Health Chemistry, Hoshi University, Shinagawa-ku, Tokyo 142-8501, Japan.

出版信息

Biochem Biophys Res Commun. 2016 Apr 29;473(2):654-61. doi: 10.1016/j.bbrc.2016.03.115. Epub 2016 Mar 25.

DOI:10.1016/j.bbrc.2016.03.115
PMID:27021680
Abstract

Previous studies have shown that high-fat diet (HFD)-induced obesity increases the acetoacetyl-CoA synthetase (AACS) gene expression in lipogenic tissue. To investigate the effect of obesity on the AACS gene in other tissues, we examined the alteration of AACS mRNA levels in HFD-fed mice. In situ hybridization revealed that AACS was observed in several regions of the embryo, including the backbone region (especially in the somite), and in the epiphysis of the adult femur. AACS mRNA expression in the adult femur was higher in HFD-fed mice than in normal-diet fed mice, but this increase was not observed in high sucrose diet (HSD)-induced obese mice. In addition, HFD-specific increases were observed in the 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGCR) and interleukin (IL)-6 genes. Moreover, we detected higher AACS mRNA expression in the differentiated osteoclast cells (RAW 264), and found that AACS mRNA expression was significantly up-regulated by IL-6 treatment only in osteoclasts. These results indicate the novel function of the ketone body in bone metabolism. Because the abnormal activation of osteoclasts by IL-6 induces bone resorption, our data suggest that AACS and ketone bodies are important factors in the relationship between obesity and osteoporosis.

摘要

先前的研究表明,高脂饮食(HFD)诱导的肥胖会增加脂肪生成组织中乙酰乙酰辅酶A合成酶(AACS)基因的表达。为了研究肥胖对其他组织中AACS基因的影响,我们检测了高脂饮食喂养小鼠中AACS mRNA水平的变化。原位杂交显示,在胚胎的几个区域观察到AACS,包括脊柱区域(特别是在体节中)以及成年股骨的骨骺。高脂饮食喂养小鼠成年股骨中的AACS mRNA表达高于正常饮食喂养的小鼠,但在高蔗糖饮食(HSD)诱导的肥胖小鼠中未观察到这种增加。此外,在3-羟基-3-甲基戊二酰辅酶A还原酶(HMGCR)和白细胞介素(IL)-6基因中观察到了高脂饮食特异性的增加。此外,我们在分化的破骨细胞(RAW 264)中检测到较高的AACS mRNA表达,并发现仅在破骨细胞中,IL-6处理可显著上调AACS mRNA表达。这些结果表明了酮体在骨代谢中的新功能。由于IL-6异常激活破骨细胞会诱导骨吸收,我们的数据表明AACS和酮体是肥胖与骨质疏松症关系中的重要因素。

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