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Benefits of quercetin on metabolic and inflammatory biomarkers in high fat diet induced obesity: A dose response study.

机译:槲皮素对高脂饮食诱导的肥胖患者代谢和炎症生物标志物的益处:一项剂量反应研究。

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摘要

Obesity is a chronic low-grade inflammatory disease that can lead to a variety of health complications including coronary heart disease, type 2 diabetes, hypertension, degenerative diseases and a wide array of cancers. For this reason, dietary supplements with anti-inflammatory properties have been the focal point of many recent studies on diet-induced obesity. Quercetin, a polyphenolic compound found in many fruits and vegetables, is of interest due to its low toxicity and its wide range of bioactivity. While multiple studies have revealed the anti-inflammatory capabilities of quercetin in different mouse models, quercetin's effects on metabolic and inflammatory biomarkers in a high fat diet induced obesity model have not yet been well established. We examined the effects of three different doses (0.02%, 0.2% & 2%) of quercetin on obesity markers, macrophage populations, and inflammatory mediators in a mouse model of high fat diet induced obesity. Our high fat diet treatment was 16 weeks and based on the American Standard Diet that contains approximately 40% of calories from fat (12% saturated, 28% unsaturated). The results show that the 0.02% and 2% doses of quercetin reduced total body weight, fat mass, and mesenteric fat weight, while all three quercetin doses reduced the mRNA gene expression of the macrophage marker EMR1 as well as the pro-inflammatory M1 macrophage marker CD11c in the epididymal adipose tissue. This was consistent with a general decrease in the gene expression of inflammatory mediators (MCP-1, TNF-alpha, and TLR-4). This data confirm the ability of quercetin to reduce metabolic and inflammatory biomarkers in a high fat diet induced obesity model. These findings may lead to the development of a safe and effective dose of a natural dietary supplement that has protective anti-inflammatory effects against the visceral adipose tissue inflammation associated with obesity.
机译:肥胖症是一种慢性低度炎症性疾病,可导致多种健康并发症,包括冠心病,2型糖尿病,高血压,变性疾病和多种癌症。由于这个原因,具有抗炎特性的膳食补充剂已成为饮食诱导肥胖的许多最新研究的焦点。槲皮素是一种在许多水果和蔬菜中发现的多酚化合物,由于其低毒性和广泛的生物活性而备受关注。尽管多项研究揭示了槲皮素在不同小鼠模型中的抗炎能力,但在高脂饮食诱导的肥胖模型中,槲皮素对代谢和炎性生物标志物的作用尚未得到很好的证实。我们检查了三种不同剂量的槲皮素(0.02%,0.2%和2%)对高脂饮食诱导的肥胖小鼠模型中肥胖标志物,巨噬细胞种群和炎性介质的影响。我们的高脂饮食疗程为16周,基于美国标准饮食,其中包含约40%的脂肪卡路里(12%饱和,28%不饱和)。结果表明,0.02%和2%的槲皮素可降低总体重,脂肪量和肠系膜脂肪重量,而所有三种槲皮素均可降低巨噬细胞标记物EMR1和促炎性M1巨噬细胞的mRNA基因表达。附睾脂肪组织中的标志物CD11c。这与炎症介质(MCP-1,TNF-α和TLR-4)的基因表达普遍下降相一致。该数据证实了槲皮素在高脂饮食诱导的肥胖症模型中减少代谢和炎症生物标志物的能力。这些发现可能导致开发出安全有效剂量的天然膳食补充剂,其具有针对与肥胖症相关的内脏脂肪组织炎症的保护性抗炎作用。

著录项

  • 作者单位

    University of South Carolina.;

  • 授予单位 University of South Carolina.;
  • 学科 Biology Molecular.;Health Sciences Pharmacology.
  • 学位 M.S.
  • 年度 2012
  • 页码 63 p.
  • 总页数 63
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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