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本文引用的文献

1
Adipokines as regulators of muscle metabolism and insulin sensitivity.脂肪因子作为肌肉代谢和胰岛素敏感性的调节因子。
Appl Physiol Nutr Metab. 2009 Jun;34(3):396-402. doi: 10.1139/H09-037.
2
Peroxisome proliferator-activated receptor-alpha (PPARalpha): at the crossroads of obesity, diabetes and cardiovascular disease.过氧化物酶体增殖物激活受体α(PPARα):处于肥胖、糖尿病和心血管疾病的交叉点。
Atherosclerosis. 2009 Jul;205(1):1-8. doi: 10.1016/j.atherosclerosis.2009.03.008. Epub 2009 Mar 20.
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The road from obesity to type 2 diabetes.从肥胖到2型糖尿病之路。
Angiology. 2008 Apr-May;59(2 Suppl):39S-43S. doi: 10.1177/0003319708318583. Epub 2008 May 27.
4
Is weight loss beneficial for reduction of morbidity and mortality? What is the controversy about?体重减轻对降低发病率和死亡率有益吗?争议点是什么?
Diabetes Care. 2008 Feb;31 Suppl 2:S278-83. doi: 10.2337/dc08-s268.
5
Targeted disruption of AdipoR1 and AdipoR2 causes abrogation of adiponectin binding and metabolic actions.对脂联素受体1(AdipoR1)和脂联素受体2(AdipoR2)的靶向破坏会导致脂联素结合及代谢作用的丧失。
Nat Med. 2007 Mar;13(3):332-9. doi: 10.1038/nm1557. Epub 2007 Feb 1.
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Epidemiology, trends, and morbidities of obesity and the metabolic syndrome.肥胖症及代谢综合征的流行病学、趋势和发病率
Endocrine. 2006 Feb;29(1):109-17. doi: 10.1385/ENDO:29:1:109.
7
Multinutrient supplement containing ephedra and caffeine causes weight loss and improves metabolic risk factors in obese women: a randomized controlled trial.含有麻黄和咖啡因的多种营养素补充剂可导致肥胖女性体重减轻并改善代谢风险因素:一项随机对照试验。
Int J Obes (Lond). 2006 Oct;30(10):1545-56. doi: 10.1038/sj.ijo.0803283. Epub 2006 Mar 21.
8
The high-fat diet-fed mouse: a model for studying mechanisms and treatment of impaired glucose tolerance and type 2 diabetes.高脂饮食喂养的小鼠:一种用于研究糖耐量受损和2型糖尿病机制及治疗方法的模型。
Diabetes. 2004 Dec;53 Suppl 3:S215-9. doi: 10.2337/diabetes.53.suppl_3.s215.
9
Adipokines: inflammation and the pleiotropic role of white adipose tissue.脂肪因子:炎症与白色脂肪组织的多效性作用
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Ephedra in perspective--a current review.麻黄的现状综述
Phytother Res. 2003 Aug;17(7):703-12. doi: 10.1002/ptr.1337.

膳食麻黄对高脂饮食喂养小鼠肥胖和葡萄糖不耐受的有益作用。

Beneficial effect of dietary Ephedra sinica on obesity and glucose intolerance in high-fat diet-fed mice.

作者信息

Song Moon-Koo, Um Jae-Young, Jang Hyeung-Jin, Lee Byung-Cheol

机构信息

Departments of Internal Medicine.

出版信息

Exp Ther Med. 2012 Apr;3(4):707-712. doi: 10.3892/etm.2012.462. Epub 2012 Jan 30.

DOI:10.3892/etm.2012.462
PMID:22969956
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3438832/
Abstract

Obesity is a major contributor to both glucose intolerance and metabolic syndrome. In this study, we investigated the anti-obesity and anti-hyperglycemic effects of Ephedra sinica on high-fat diet-fed mice. Male ICR mice were divided into four groups; the normal group, the obese and diabetic control group treated with a high-fat diet, the positive control group treated with a high-fat diet containing acarbose, and the experimental group treated with a high-fat diet containing Ephedra sinica. The effects of Ephedra sinica on obesity and glucose intolerance were measured by an oral glucose tolerance test (OGTT), plasma biochemistry, body and epididymal fat weight; the expression of adiponectin, peroxisome-proliferator-activated receptor α (PPAR-α), tumor necrosis factor α (TNF-α) and leptin was also determined. Ephedra sinica reduced weight gain and epididymal fat accumulation, improved glucose intolerance on the OGTT, decreased triglycerides and increased high-density lipoprotein cholesterol compared to the controls. Moreover, it reduced weight gain and fasting glucose levels and improved HDL-cholesterol levels more than acarbose. Gene expression analysis revealed that Ephedra sinica upregulated the expression of adiponectin and PPAR-α, and downregulated the expression of TNF-α. From these results, we suggest that Ephedra sinica may reduce obesity and hyperglycemia by increasing PPAR-α and adiponectin and reducing TNF-α, and that it may have the potential to be used clinically as an ingredient in food or drugs effective in obesity-related glucose intolerance treatments.

摘要

肥胖是导致葡萄糖不耐受和代谢综合征的主要因素。在本研究中,我们调查了麻黄对高脂饮食喂养小鼠的抗肥胖和降血糖作用。雄性ICR小鼠分为四组:正常组、高脂饮食处理的肥胖和糖尿病对照组、含阿卡波糖的高脂饮食处理的阳性对照组以及含麻黄的高脂饮食处理的实验组。通过口服葡萄糖耐量试验(OGTT)、血浆生化指标、体重和附睾脂肪重量来测定麻黄对肥胖和葡萄糖不耐受的影响;还测定了脂联素、过氧化物酶体增殖物激活受体α(PPAR-α)、肿瘤坏死因子α(TNF-α)和瘦素的表达。与对照组相比,麻黄减少了体重增加和附睾脂肪堆积,改善了OGTT上的葡萄糖不耐受,降低了甘油三酯并增加了高密度脂蛋白胆固醇。此外,与阿卡波糖相比,它在减轻体重增加和空腹血糖水平以及改善高密度脂蛋白胆固醇水平方面效果更显著。基因表达分析表明,麻黄上调了脂联素和PPAR-α的表达,并下调了TNF-α的表达。从这些结果来看,我们认为麻黄可能通过增加PPAR-α和脂联素以及减少TNF-α来减轻肥胖和高血糖,并且它有可能在临床上作为食品或药物中的一种成分用于治疗与肥胖相关的葡萄糖不耐受。