Post Graduate Program in Health and Development in the Central-West Region of Brazil, Federal University of Mato Grosso do Sul, Campo Grande, MS 79070-900, Brazil.
Institute of Biosciences, Federal University of Mato Grosso do Sul-UFMS, Campo Grande, MS 79070-900, Brazil.
Nutrients. 2020 Nov 10;12(11):3439. doi: 10.3390/nu12113439.
The aim of this study was to evaluate the therapeutic effects of two different doses (250 and 500 mg/kg) of fruit aqueous extract (AE) in high-fat/high-fructose-fed Swiss mice. The food intake, body weight, serum biochemical, oral glucose tolerance test (OGTT), and enzyme-linked immunosorbent assay (ELISA), as well as histological analyses of the liver, pancreatic, and epididymal adipose tissue, were used to determine the biochemical and histological parameters. The chemical profile of the extract was determined by ultra-fast liquid chromatography-diode array detector-tandem mass spectrometry (UFLC-DAD-MS), and quantitative real-time PCR (qRT-PCR) was used to evaluate the gene expressions involved in the lipid and glucose metabolism, such as peroxisome proliferative-activated receptors-γ (PPAR-γ), -α (PPAR-α), fatty acid synthase (FAS), glucose-6-phosphatase (G6P), sterol regulatory binding protein-1c (SREBP-1c), carbohydrate-responsive element-binding protein (ChREBP), and fetuin-A. Seventeen compounds were tentatively identified, including iridoids, noniosides, and the flavonoid rutin. The higher dose of AE (AE 500 mg/kg) was demonstrated to improve the glucose tolerance; however, both doses did not have effects on the other metabolic and histological parameters. AE at 500 mg/kg downregulated the PPAR-γ, SREBP-1c, and fetuin-A mRNA in the liver and upregulated the PPAR-α mRNA in white adipose tissue, suggesting that the hypoglycemic effects could be associated with the expression of genes involved in de novo lipogenesis.
本研究旨在评估两种不同剂量(250 和 500mg/kg)的水果水提物(AE)对高脂肪/高果糖喂养的瑞士小鼠的治疗效果。通过食物摄入量、体重、血清生化、口服葡萄糖耐量试验(OGTT)和酶联免疫吸附试验(ELISA),以及肝、胰腺和附睾脂肪组织的组织学分析,来确定生化和组织学参数。通过超快速液相色谱-二极管阵列检测器-串联质谱法(UFLC-DAD-MS)测定提取物的化学特征,并通过定量实时 PCR(qRT-PCR)评估参与脂质和葡萄糖代谢的基因表达,如过氧化物酶体增殖物激活受体-γ(PPAR-γ)、-α(PPAR-α)、脂肪酸合酶(FAS)、葡萄糖-6-磷酸酶(G6P)、固醇调节元件结合蛋白-1c(SREBP-1c)、碳水化合物反应元件结合蛋白(ChREBP)和胎球蛋白-A。共推测出 17 种化合物,包括环烯醚萜、非环单萜苷和类黄酮芦丁。AE 的高剂量(AE 500mg/kg)被证明可以改善葡萄糖耐量;然而,两种剂量均对其他代谢和组织学参数没有影响。AE 在 500mg/kg 剂量下下调了肝脏中的 PPAR-γ、SREBP-1c 和胎球蛋白-A mRNA,并上调了白色脂肪组织中的 PPAR-α mRNA,这表明其降血糖作用可能与参与从头脂肪生成的基因表达有关。