Hsieh Ching-Hua, Rau Cheng-Shyuan, Wu Shao-Chun, Yang Johnson Chia-Shen, Wu Yi-Chan, Lu Tsu-Hsiang, Tzeng Siou-Ling, Wu Chia-Jung, Lin Chia-Wei
Department of Plastic and Reconstructive Surgery, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, No. 123, Ta-Pei Road, Niao-Song District, Kaohsiung City, 833, Taiwan.
Department of Neurosurgery, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, No. 123, Ta-Pei Road, Niao-Song District, Kaohsiung City, 833, Taiwan.
BMC Genomics. 2015 Sep 16;16(1):699. doi: 10.1186/s12864-015-1896-3.
To examine the circulating microRNA (miRNA) expression profile in a mouse model of diet-induced obesity (DIO) with subsequent weight reduction achieved via low-fat diet (LFD) feeding.
Eighteen C57BL/6NCrl male mice were divided into three subgroups: (1) control, mice were fed a standard AIN-76A (fat: 11.5 kcal %) diet for 12 weeks; (2) DIO, mice were fed a 58 kcal % high-fat diet (HFD) for 12 weeks; and (3) DIO + LFD, mice were fed a HFD for 8 weeks to induce obesity and then switched to a 10.5 kcal % LFD for 4 weeks. A switch to LFD feeding led to decreases in body weight, adiposity, and blood glucose levels in DIO mice. Microarray analysis of miRNA using The Mouse & Rat miRNA OneArray® v4 system revealed significant alterations in the expression of miRNAs in DIO and DIO + LFD mice. Notably, 23 circulating miRNAs (mmu-miR-16, mmu-let-7i, mmu-miR-26a, mmu-miR-17, mmu-miR-107, mmu-miR-195, mmu-miR-20a, mmu-miR-25, mmu-miR-15b, mmu-miR-15a, mmu-let-7b, mmu-let-7a, mmu-let-7c, mmu-miR-103, mmu-let-7f, mmu-miR-106a, mmu-miR-106b, mmu-miR-93, mmu-miR-23b, mmu-miR-21, mmu-miR-30b, mmu-miR-221, and mmu-miR-19b) were significantly downregulated in DIO mice but upregulated in DIO + LFD mice. Target prediction and function annotation of associated genes revealed that these genes were predominantly involved in metabolic, insulin signaling, and adipocytokine signaling pathways that directly link the pathophysiological changes associated with obesity and weight reduction.
These results imply that obesity-related reductions in the expression of circulating miRNAs could be reversed through changes in metabolism associated with weight reduction achieved through LFD feeding.
研究饮食诱导肥胖(DIO)小鼠模型中循环微小RNA(miRNA)的表达谱,以及随后通过低脂饮食(LFD)喂养实现体重减轻后的表达谱变化。
18只C57BL/6NCrl雄性小鼠被分为三个亚组:(1)对照组,小鼠喂食标准AIN-76A(脂肪:11.5千卡%)饮食12周;(2)DIO组,小鼠喂食58千卡%的高脂饮食(HFD)12周;(3)DIO+LFD组,小鼠先喂食HFD 8周以诱导肥胖,然后改为10.5千卡%的LFD喂养4周。改为LFD喂养导致DIO小鼠的体重、肥胖程度和血糖水平下降。使用小鼠和大鼠miRNA OneArray® v4系统对miRNA进行微阵列分析,发现DIO和DIO+LFD小鼠中miRNA的表达有显著变化。值得注意的是,23种循环miRNA(mmu-miR-16、mmu-let-7i、mmu-miR-26a、mmu-miR-17、mmu-miR-107、mmu-miR-195、mmu-miR-20a、mmu-miR-25、mmu-miR-15b、mmu-miR-15a、mmu-let-7b、mmu-let-7a、mmu-let-7c、mmu-miR-103、mmu-let-7f、mmu-miR-106a、mmu-miR-106b、mmu-miR-93、mmu-miR-23b、mmu-miR-21、mmu-miR-30b、mmu-miR-221和mmu-miR-19b)在DIO小鼠中显著下调,但在DIO+LFD小鼠中上调。相关基因的靶标预测和功能注释表明,这些基因主要参与代谢、胰岛素信号传导和脂肪细胞因子信号传导途径,这些途径直接与肥胖和体重减轻相关的病理生理变化相关。
这些结果表明,与肥胖相关的循环miRNA表达降低可通过LFD喂养实现体重减轻所伴随的代谢变化而逆转。