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首页> 外文期刊>Chemico-biological interactions >Bardoxolone methyl prevents fat deposition and inflammation in the visceral fat of mice fed a high-fat diet
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Bardoxolone methyl prevents fat deposition and inflammation in the visceral fat of mice fed a high-fat diet

机译:喂食高脂饮食的老鼠,Bardoxolonemethyl可以防止脂肪沉积和内脏脂肪发炎

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Key features of diet-induced obesity are visceral fat deposition, macrophage infiltration and inflammation that can lead to metabolic disorders. This study examined the effects of bardoxolone methyl (BARD) in preventing obesity and inflammation in the visceral fat of mice fed high-fat diet. Male C57BL/6J mice were fed a high-fat diet (HFD), a low-fat diet (LFD, i.e., lab chow diet) or a high-fat diet supplemented with BARD (HFD/BARD) for 21 weeks. BARD at a dosage of 10 mg/kg body weight was administered orally in drinking water. Histology, immunohistochemistry and Western blot were used for the analysis of epididymal adipose tissue. Morphological results demonstrated that HFD fed mice treated with BARD had smaller adipocytes and fewer macrophages present in epididymal adipose tissue than the HFD group. Furthermore, BARD administration reduced the inflammatory profile in this tissue by increasing the expression of nuclear factor of kappa-light-polypeptide gene enhancer in B-cells inhibitor, alpha (I kappa B-alpha) protein and decreasing the protein expression of tumour necrosis factor alpha (TNF-alpha). BARD also prevented oxidative stress reflected by a reduction in stress activated proteins, including signal transducer and activator of transcription 3 (STAT3), protein kinase B (Akt), extracellular-signal-regulated kinase (ERK) and c-Jun N-terminal kinase (JNK). BARD administration activated the sympathetic nervous system in epididymal adipose tissue assessed by the increased synthesis of tyrosine hydroxylase (TH) and uncoupling protein 2 (UCP2). The expression of inflammatory and sympathetic nervous system proteins in BARD mice fed a HFD was equivalent to that of the LFD control mice, indicating the anti-inflammatory and anti-obesity properties of this drug. In conclusion, the oral administration of BARD in HFD mice prevented fat deposition, inflammation and oxidative stress, and improved sympathetic activity in visceral fat. This study suggests a potential therapeutic role of BARD in preventing the development of obesity. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
机译:饮食引起的肥胖症的主要特征是内脏脂肪沉积,巨噬细胞浸润和炎症,可导致代谢异常。这项研究检查了Bardoxolone甲基(BARD)在预防高脂饮食小鼠的内脏脂肪肥胖和炎症中的作用。给雄性C57BL / 6J小鼠喂食高脂饮食(HFD),低脂饮食(LFD,即实验室食物)或补充BARD的高脂饮食(HFD / BARD),持续21周。在饮用水中口服施用体重为10 mg / kg体重的BARD。组织学,免疫组织化学和蛋白质印迹法用于附睾脂肪组织的分析。形态学结果表明,与HFD组相比,接受BARD处理的HFD喂养小鼠的附睾脂肪组织中脂肪细胞更少,巨噬细胞更少。此外,BARD给药通过增加B细胞抑制剂α(I kappa B-alpha)蛋白中kappa-轻多肽基因增强子的核因子的表达并降低肿瘤坏死因子的蛋白表达,从而减少了该组织的炎性反应。 α(TNF-α)。 BARD还防止了应激激活蛋白的减少所反映的氧化应激,包括信号转导和转录激活因子3(STAT3),蛋白激酶B(Akt),细胞外信号调节激酶(ERK)和c-Jun N端激酶(JNK)。 BARD给药通过酪氨酸羟化酶(TH)和解偶联蛋白2(UCP2)的合成增加来评估附睾脂肪组织中的交感神经系统。用HFD喂养的BARD小鼠中炎症和交感神经系统蛋白的表达与LFD对照小鼠中的表达相同,表明该药物具有抗炎和抗肥胖特性。总之,在HFD小鼠中口服BARD可以防止脂肪沉积,炎症和氧化应激,并改善内脏脂肪的交感活性。这项研究表明,BARD在预防肥胖症发展中具有潜在的治疗作用。 (C)2015 Elsevier Ireland Ltd.保留所有权利。

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