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Elicited Soybean (Glycine max L.) Extract Improves Regulatory T Cell Activity in High Fat-Fructose Diet Mice

机译:引发的大豆(甘氨酸Max L.)提取物改善了高脂肪果糖饮食小鼠中的调节性T细胞活性

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Obesity is a metabolic disorder characterized by the central distribution of abdominal fat, hyperglycemia, hyperlipidemia, and hypertension. A high-fat diet can lead to overnutrition and directly trigger inflammation in adipose tissue. Regulatory T cells (Tregs) are essential negative regulators of inflammation. Soybean (Glycine max L.) has a variety of beneficial health. It contains isoflavones, particularly daidzein and genistein which can be transformed using microbial and physical stimuli to enhance bioactivity. The aim of this study was to analyze the effect of elicited soybean extract (ESE) on Treg activity in high fat-fructose (HFFD) mice. Twenty-eight femaleBalb/C mice were divided into seven groups: normal diet (ND) only, ND + ESE 104 mg/kg BW, HFFD only, HFFD + Simvastatin 2.8 mg/kg, HFFD + ESE 78 mg/kg BW, HFFD + ESE 104 mg/kg BW, and HFFD + ESE 130 mg/kg BW. The high fat-fructose diet was given over a period of 20 weeks, and ESE was administered orally per day after 20 weeks for four weeks. At week 24, the animals were sacrificed and the spleen was collected. Tregs were labeled as CD4~+CD25~+CD62L~+ and the relative Treg number was measured using flow cytometry. The HFFD treatment significantly decreased Treg number (p < 0.05) compared to a normal diet. The ESE treatment in HFFD mice could improve Treg numbers compared to HFFD mice. Our results suggest that ESE has potential to be used as a supplement to suppress chronic inflammation via increased Treg number.
机译:肥胖是一种代谢障碍,其特征是腹部脂肪,高血糖,高脂血症和高血压的中心分布。高脂饮食可以导致过度持续,直接引发脂肪组织中的炎症。调节性T细胞(Tregs)是炎症的必要负调节因子。大豆(Glycine Max L.)具有各种各样的有益健康。它含有异黄酮,特别是Daidzein和Genistein,可以使用微生物和物理刺激来改变生物活性。本研究的目的是分析引发大豆提取物(ESE)对高脂肪果糖(HFFD)小鼠Treg活性的影响。将二十八只女性巴布/副小鼠分为七组:正常饮食(ND)仅,ND + ESE 104 Mg / kg BW,HFFD仅限HFFD + Simvastatin 2.8 Mg / kg,HFFD + ESE 78 Mg / kg BW,HFFD + ESE 104 mg / kg BW,以及HFFD + ESE 130 mg / kg BW。高脂肪果糖饮食在20周内给出,ESE在20周后口服给药四周。在第24周,处死动物并收集脾脏。将Tregs标记为CD4〜+ CD25〜+ CD62L〜+,并且使用流式细胞术测量相对Treg数。与正常饮食相比,HFFD治疗显着降低了Treg编号(P <0.05)。与HFFD小鼠相比,HFFD小鼠中的ESE治疗可以改善Treg数。我们的研究结果表明,ESE有可能用作补充剂,以通过增加的Treg数量抑制慢性炎症。

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