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Trehangelin A 改善高脂肪饮食引起的代谢临床状况。

Improvement Effects of Trehangelin A on High-Fat Diet Causing Metabolic Clinical Conditions.

机构信息

Department of Microbiology and Immunology, Showa University School of Medicine.

Kitasato Institute for Life Sciences, Kitasato University.

出版信息

Biol Pharm Bull. 2019;42(12):2095-2101. doi: 10.1248/bpb.b19-00668.

Abstract

The purpose of this study is to determine whether or not trehangelin A (THG-A) is effective in treating the metabolic clinical condition caused by a high-fat diet. The body weight, epididymal adipose volume, alanine transaminase (ALT), total-cholesterol (T-CHO), triglycerides (TG), low-density lipoprotein cholesterol (LDL-C) and glucose concentrations in serum increased in mice fed a high-fat diet compared to mice fed a control diet. On the other hand, adiponectin level in serum of mice fed a high-fat diet decreased compared to that of control mice. When mice fed a high-fat diet were intraperitoneally administered THG-A of 20 mg/kg three times per week, the levels of TG and glucose in serum were significantly reduced compared to those fed high-fat without THG-A. Interestingly, the levels of high-density lipoprotein cholesterol (HDL-C) in serum were increased by THG-A administration in both mice fed a control diet and those fed high-fat diet. The decreased level of adiponectin by a high-fat diet was also recovered by THG-A treatment. The liver expression of mRNA from pro-inflammatory cytokines, including interleukin (IL)-6 and tumor necrosis factor (TNF)-α, were significantly increased in mice fed a high-fat diet compared to those fed a control diet. However, the increased IL-6 levels in mice fed a high-fat diet were significantly suppressed by THG-A treatment. Furthermore, the increased expression of TNF-α mRNA or COL1A2 mRNA by a high-fat diets tended to be decreased in mice treated with THG-A. These results show that THG-A treatment attenuates the progression of metabolic clinical conditions, suggesting its potential efficacy against obesity-related metabolic disorders.

摘要

本研究旨在确定 trehangelin A(THG-A)是否可有效治疗高脂肪饮食引起的代谢临床病症。与正常饮食喂养的小鼠相比,高脂肪饮食喂养的小鼠体重、附睾脂肪体积、丙氨酸转氨酶(ALT)、总胆固醇(T-CHO)、甘油三酯(TG)、低密度脂蛋白胆固醇(LDL-C)和血清葡萄糖浓度均增加,而高脂肪饮食喂养的小鼠血清中脂联素水平降低。当给予高脂肪饮食喂养的小鼠每周腹膜内注射 20mg/kg 的 THG-A 三次时,与未给予 THG-A 的高脂肪饮食喂养的小鼠相比,血清 TG 和葡萄糖水平显著降低。有趣的是,THG-A 给药可使正常饮食和高脂肪饮食喂养的小鼠血清中高密度脂蛋白胆固醇(HDL-C)水平升高。高脂肪饮食引起的脂联素水平降低也可通过 THG-A 治疗得到恢复。与正常饮食喂养的小鼠相比,高脂肪饮食喂养的小鼠肝脏中促炎细胞因子(包括白细胞介素(IL)-6 和肿瘤坏死因子(TNF)-α)的 mRNA 表达显著增加。然而,THG-A 治疗可显著抑制高脂肪饮食喂养的小鼠中 IL-6 水平的升高。此外,THG-A 处理可使高脂肪饮食诱导的 TNF-α mRNA 或 COL1A2 mRNA 表达增加趋势降低。这些结果表明 THG-A 治疗可减轻代谢临床病症的进展,提示其对肥胖相关代谢紊乱具有潜在疗效。

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