用户名: 密码: 验证码:
辣椒碱降大鼠胆固醇效果及其分子机理的研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
高胆固醇血症是导致动脉粥样硬化及心脑血管疾病主要的危险因素之一,对人们的生命健康构成了严重威胁。因此,控制和降低血中胆固醇水平是防治心脑血管疾病的重要环节。降低胆固醇的功能食品和保健品在控制和改善血脂水平中起到了重要的作用,尤其适用于患者血液中的胆固醇水平略高,但还没有高到足以使用降胆固醇处方药物的情况。
     辣椒碱是存在辣椒中的一类辣味物质,是辣椒主要的活性成分,具有多种生理功能。近年来研究表明,辣椒碱具有促进能量消耗,减少脂肪在体内的聚集,降低血压,保护心血管健康等作用。还有研究表明辣椒碱具有抗氧化活性,能阻止人类LDLs的氧化。这些结果均表明辣椒碱具有降低胆固醇的潜在效果。但是,在辣椒碱降低血浆胆固醇方面的研究较少,其降胆固醇的效果还不明确,尤其是作用机制还不清楚。因此,本研究分别于在体动物实验和离体细胞培养中开展了对辣椒碱降低血浆胆固醇效果及机理的探索。研究的内容分为四个部分,主要研究结果如下:
     1.辣椒碱对喂食高胆固醇饲料雌性大鼠血浆及肝脏胆固醇代谢的影响
     研究不同剂量的辣椒碱喂养不同时间对大鼠血脂和肝脂的影响,探讨辣椒碱对喂食高胆固醇饲料大鼠血浆胆固醇的降低效果。以96只雌性SD大鼠为研究对象,喂食高胆固醇饲料,辣椒碱的灌胃剂量选取每日0mg kg-1·bw、4mg kg-1·bw、8mg kg-1·bw和12mg kg-1·bw,试验期分为4周、8周和12周。
     结果表明:与空白组相比,每日喂食4mg kg-1·bw辣椒碱8周才能显著降低大鼠血浆中Non-HDL-C、肝脏中TC含量和TG/HDL-C的比值;喂食12周后才能显著降低大鼠血浆和肝脏中的胆固醇。而喂食8mg kg-1·bw和12mg kg-1·bw辣椒碱4周就能显著降低血浆中Non-HDL-C和肝脏中TC含量;喂食8周就能显著调节大鼠血浆和肝脏胆固醇含量,降低大鼠的致动脉硬化指数。另外,各剂量的辣椒碱喂食4周就能显著增加大鼠小肠内容物中总胆汁酸含量,但只有喂食12mg kg-1·bw辣椒碱才能显著增加大鼠粪便中总胆汁酸和中性固醇含量。说明辣椒碱喂食辣椒碱对大鼠体重、血脂和肝脂的降低作用存在剂量效应和时间效应。
     2.辣椒碱对卵巢切除大鼠胆固醇代谢及机理的研究
     人们在日常生活中主要通过食入辣椒摄取辣椒碱。本节主要研究了辣椒中的其它化学成分对辣椒碱降胆固醇效果的影响,以及辣椒碱和全辣椒降低机体胆固醇的作用机理。将32只雌性SD大鼠随机分为两组,24只进行双侧卵巢切除手术,8只进行伪切除手术(Sham-CON)。恢复一周后,24只双侧卵巢切除大鼠按体质量随机分成3组,每组8只,分别为卵巢切除空白组(OVX-CON)、卵巢切除辣椒碱组(OVX-CAP)和卵巢切除朝天椒组(OVX-RP)。Sham-CON组和OVX-CON组喂食高胆固醇饲料;OVX-CAP喂食添加了0.01%辣椒碱的高胆固醇饲料;OVX-RP畏食添加了2%朝天椒粉末的高胆固醇饲料(与OVX-CAP含相同量的辣椒碱)。
     结果表明:卵巢切除术能显著增加卵巢切除大鼠血浆中TG和TC,尤其是LDL-C浓度增加最明显;另外,卵巢切除大鼠肝脏中甘油三酯和胆固醇的积聚也显著增加。然而,在饲料中添加辣椒碱和朝天椒能通过降低血浆TC、LDL-C和TG含量,很好的改善卵巢切除大鼠血浆中的脂蛋白水平;并能降低卵巢切除大鼠肝脏中胆固醇和甘油三酯的浓度;阻止脂滴在卵巢切除大鼠肝脏中的积聚。这些数据表明,辣椒碱和朝天椒能阻止雌激素缺乏和高胆固醇饲料引发的高脂血症。辣椒碱和朝天椒的摄入对肝脏中HMG-CoA还原酶、回肠中IBABP和ASBT的蛋白及mRNA的表达没有显著性影响,但能显著上调卵巢切除大鼠肝脏中CYP7A1和TRPV1蛋白及mRNA的表达,并且能增加小肠内容和粪便中总胆汁酸的含量,增加粪便中中性固醇的含量。辣椒碱和朝天椒降低机体胆固醇的可能机制是:促进肝脏中胆固醇合成胆汁酸,并增加粪便中总胆汁酸和中性固醇的排泄。全辣椒降胆固醇的效果优于辣椒碱。
     3.膳食纤维对辣椒碱生理功效的协调作用
     辣椒中含有丰富的纤维素,为探讨纤维素对辣椒碱降低胆固醇效果中的协调作用,研究了辣椒碱与纤维素对大鼠血脂、肝脂的降低效果,及肠道发酵环境的影响。以32只双侧卵巢切除SD大鼠为研究对象,大鼠分为空白组(CON):喂食高胆固醇饲料;高辣椒碱组(HCAP):喂食添加0.01%的辣椒碱的高胆固醇饲料;纤维素组(DF):喂食添加5%的纤维素的高胆固醇饲料;纤维素+辣椒碱组(DF+LCAP):喂食添加5%的纤维素+0.005%的辣椒碱的高胆固醇饲料。
     结果表明:饲料中添加DF+LCAP能显著降低卵巢切除大鼠体重增加量、血脂和肝脂水平,增加粪便胆汁酸和中性固醇的分泌;其对大鼠胆固醇降低效果优于HCAP。另外,0.01%的辣椒碱能显著增加大鼠盲肠内容物的pH值和游离氨含量,并能显著增加有害微生物大肠杆菌和肠球菌的数量,减少有益微生物乳酸杆菌和双歧杆菌的数量。而DF+LCAP能显著增加大鼠盲肠内容物中短链脂肪酸含量和有益微生物数量,降低盲肠内容物pH值和游离氨含量。说明纤维素和辣椒碱在卵巢切除大鼠胆固醇代谢中具有协同作用,纤维素能降低辣椒碱的食用剂量及其对肠道健康潜在的损伤。
     4.辣椒素受体在辣椒碱降胆固醇中的调节作用
     肝脏是胆固醇代谢的主要器官。为探讨辣椒素受体TRPV1在辣椒碱影响机体胆固醇代谢环节中的作用,选用人肝L02细胞作为研究对象,以TRPV1激动剂(辣椒素)及其特异性拮抗剂(辣椒卓平)作为干预手段,研究了0、10nmol/L、100nmol/L、1μmol/L和10μmol/L辣椒素对人肝L02细胞中胆固醇及胆固醇代谢相关基因表达的影响。
     结果表明:辣椒素处理48h可呈剂量依赖性的降低人肝L02细胞和培养基中的总胆固醇,增加培养基中的总胆汁酸含量,其中1μmol/L和10μmol/L的辣椒素效果较好。同时,10nmol/L和100nmol/L的辣椒素对HMG-CoA还原酶的表达无显著影响;而1μmol/L和10μmol/L的辣椒素能显著下调HMG-CoA还原酶的表达。各辣椒素剂量均能显著上调肝脏CYP7A1和TRPV1的蛋白和mRNA表达。
     在辣椒卓平阻断TRPV1的实验中发现,1μmol/L的辣椒素可显著上调CYP7A1的表达,抑制HMG-CoA还原酶的表达;应用TRPV1受体拮据剂辣椒卓平则明显阻断辣椒素的作用。说明辣椒素降低人肝细胞中胆固醇可能的机制是:低剂量的辣椒素主要通过促进胆固醇转化为胆汁酸;中、高剂量的辣椒素不仅促进胆固醇转化为胆汁酸,还能减少肝脏中胆固醇的合成。辣椒素可能是通过激活辣椒素受体TRPV1调节胆固醇代谢的相关基因。
Hypercholesterolemia is the main risk factor of atherosclerosis and coronary heart disease, which threaten life and health of human being severely. Therefore, control and decrease of blood cholesterol level is important for preventing the development of coronary heart disease. The cholesterol-lowering functional foods and nutraceuticals are possible alternative therapies for lowering plasma total cholesterol, especially for patients, whose blood cholesterol level is marginally high but not high enough to warrant the prescription of cholesterol-lowering medication.
     Capsaicinoids refer to a group of pungent compounds and the main active components of chili peppers. They are the focus of numerous studies because of their extensive biological and physiological properties. Recently, some studies reported that capsaicinoids can promote energy metabolism and suppress the accumulation of body fat, prevent hypertension and improve cardiovascular function. In addition, capsaicinoids possess antioxidant activities that can prevent the oxidation of human LDL. These data suggest that capsaicinoids exhibit cholesterol-lowering effects. However, very little information is available on the effect of administration of capsaicinoids on different aspects of cholesterol metabolism in Vivo and Viro. What's more, the mechanisms by which capsaicinoids affect cholesterol homeostasis have not been completely clarified yet. The present study aims to investigate the influence of capsaicinoids on the change in cholesterol metabolism and its mechanism. Four parts of work were conducted and the corresponding results are as following:
     1. The effect of capsaicinoids on plasma and hepatic lipids in female rats fed with high cholesterol diet
     This study investigated the doses effect and time effect of capsaicinoids on plasma lipid and hepatic lipid in the rats. Female Sprague-Dawley rats were fed with high-cholesterol diet and orally administered0mg kg-1·bw,4mg kg-1·bw,8mg kg-1·bw and12mg kg-1·bw capsaicinoids daily for4weeks,8weeks and12weeks.
     The results demonstrated that the plasma Non-HDL-C, TG/HDL-C, and hepatic cholesterol were significantly decreased after treating the rats with4mg kg-1·bw capsaicinoids for8weeks, the plasma lipids and hepatic lipids were remarkably decreased after12weeks, compare with control group. However, the plasma Non-HDL-C and hepatic cholesterol were significantly decreased administrated with8mg kg-1·bw or12mg kg-1·bw capsaicinoids only for4weeks, and effective cholesterol-lowering actions were exhibited after8weeks. What'more, the total bile acid levels in small intestinal contents were significantly increased by treated with each dose of capsaicinoids after4weeks. While only12mg kg-1·bw capsaicinoids could elevate the amount of total bile acid and sterol in feces. In conclusion, the hypocholesterolemic effect of capsaicinoids exhibited dose effect and time effect.
     2. The influence of capsaicinoids on the change in cholesterol metabolism associated with estrogen deficiency in ovariectomized rats
     People ingest capsaicin mainly through eating chili in daily life. This study investigated the effect and mechanism of action of capsaicinoids and red pepper on cholesterol metabolism in ovariectomized (OVX) rats. Female Sprague-Dawley rats were subjected to sham operation or ovariectomy. After recovery,24OVX rats were randomly divided into three dietary groups consisting of8rats each using a randomized block design. The sham group (sham-CON) and OVX control group (OVX-CON) were fed with high-cholesterol diets, whereas the capsaicinoids group (OVX-CAP) fed with high-cholesterol plus0.01%capsaicinoids diets, and the red pepper group (OVX-RP) fed with high-cholesterol plus2%red pepper powder diets for3weeks.
     The results demonstrated that the plasma triacylglycerol and cholesterol concentrations, particularly the LDL-C level, were significantly increased, and triacylglycerol and cholesterol accumulations in the liver were elevated in the OVX rats. However, supplementation of capsaicinoids in diet can favorably modify the plasma lipoprotein profile by decreasing plasma TC, LDL-C, and TG, and reducing the concentrations of hepatic cholesterol and triacylglycerol in OVX rats. The hepatic fat-droplet accumulation was ameliorated by the capsaicinoids-supplemented diet in the OVX-CAP group. These data suggest that capsaicinoids can prevent ovarian hormone deficiency induced hypercholesterolemia. Western blot and real-time PCR analyses revealed that capsaicinoids and red pepper significantly enhanced the expressions of hepatic CYP7A1and TRPV1but did not affect the expression of HMG-CoA reductase, IBABP and ASBT in the OVX rats. In conclusion, Capsaicinoids have cholesterol-lowering effects in OVX rats. The hypocholesterolemic activity of capsaicinoids is caused by the stimulating conversion of cholesterol to bile acids by up-regulation of CYP7A1expression and the increase in fecal total bile acid excretion. Red pepper had a greater efficacy in producing beneficial anti-hyperlipidemic effects in the cholesterol-fed OVX rats.
     3. The synergistic effect of capsaicinoids and dietary fiber in regulation of cholesterol homeostasis
     This study investigated the synergistic effect of capsaicinoids and dietary fiber on cholesterol metabolism in ovariectomized rats. Female Sprague-Dawley rats were performed to ovariectomy. After recovery,32OVX rats were randomly divided into four dietary groups consisting of8rats each using a randomized block design. The OVX control group (CON) was fed with high-cholesterol diets, the dietary fiber group (DF) was fed with high-cholesterol plus5%fiber diets, the high capsaicinoids group (HCAP) was fed with high-cholesterol plus0.01%capsaicinoids diets, and the capsaicinoids+dietary fiber group (DF+LCAP) was fed with high-cholesterol plus5%fiber and0.005%capsaicinoids diets for4weeks.
     The results demonstrated that body weight gain, plasma lipids and hepatic lipids levels were significantly decreased, while the amount of total bile acid and sterol in feces were dramatically increased in DF+LCAP group rats. What' more, the concentration of free ammonia and pH of cecal content were significantly increased in HCAP group rats. The0.01%dose of capsaicinoids could promote the growth of Escherichia coli and Enterococcus, and inhibit Bifidobacterium and Lacticacidbacteria in cecal content. However, the administration of5%dietary fiber+0.05%capsaicinoids remarkable increased the concentration of SCFA and the amount of Bifidobacterium and Lacticacidbacteria, and decreased the pH and free ammonia of cecal content in the OVX rats. In conclusion, the combination of dietary fiber and capsaicinoids work synergistically in regulating the homeostasis of cholesterol in OVX rats. In addition, dietary fiber also modifies the injury caused by0.01%capsaicinoids.
     4. Regulating mechanism of TRPV1on cholesterol metabolism in human hepatocyte
     Liver is the main organ for endogenous cholesterol synthesis. This study investigated the interaction of administrated0,10nmol/L,100nmol/L,1μmol/L and10μmol/L capsaicin with the mRNA and protein expressions of key receptors and enzymes involved in cholesterol metabolism in human hepatocyte L02. We also used the TRPV1 antagonist capsazepine to explore the involvement and hypocholesterolemic mechanism of TRPV1.
     The results demonstrated that after treating the human hepatocyte L02with capsaicin48h, the concentration of cholesterol in cell and medium were decreased, while the total bile acid in medium was significantly increased compared with the control group as the dose of capsaicin increased. The1μmol/L and10μmol/L capsaicin have the best effect on the cholesterol-lowering action. In addition, Western blot and real-time PCR analyses revealed that10nmol/L and100nmol/L capsaicin had no effect on the protein and mRNA expression of HMG-CoA reductase, while the1μmol/L and10μmol/L cpacaicin could significantly enhance its expression. The protein and mRNA expression of CYP7A1and TRPV1were dramatically elevated as the capsaicin dose increased.
     The blockage of TRPV1was obtained by antagonist of TRPV1named capsazepin. In the human hepatocyte L02, the protein and mRNA levels of CYP7A1were up-regulated while the levels of HMG-CoA reducatase were down-regulated by1μmol/L capsaicin, but not in the presence of capsazepine. In conclusion, the cholesterol-lowering effect low dose of of capsaicin in human hepatocyte L02ascribed to stimulating conversion of cholesterol to bile acid. The1μmol/L and10μmol/L capsaicin inhibited the endogenous cholesterol synthesis and promoted cholesterol metabolism. Activation of TRPV1by capsaicin could modulate the expressions of genes involved in cholesterol metabolisms.
引文
[1]LUO X-J, PENG J, LI Y-J. Recent advances in the study on capsaicinoids and capsinoids [J]. European Journal of Pharmacology,2011,650(1):1-7.
    [2]DE LOURDES REYES-ESCOGIDO M, GONZALEZ-MONDRAGON E G, VAZQUEZ-TZOMPANTZI E. Chemical and Pharmacological Aspects of Capsaicin [J]. Molecules, 2011,16(2):1253-1270.
    [3]唐胜球,董小英.辣椒素研究及其应用[J].江西饲料,2003,1:13-16.
    [4]缪武,刘志敏.辣椒素类物质代谢生理研究进展[J].辣椒杂志,2005,1:1-4.
    [5]聂乾忠,夏延斌,曾晓楠等.辣椒素的代谢途径及生理功能的研究进展[J].食品与机械,2008.2:141-145.
    [6]KNOPP R H. Drug treatment of lipid disorders [J]. N Engl J Med,1999,341(7):498-511.
    [7]SRINIVASAN M R, CHANDRASEKHARA N. comparative influence of vanillin and capsaicin on liver and blood-lipids in the rat [J]. Indian Journal of Medical Research Section B-Biomedical Research Other Than Infectious Diseases,1992,96:133-135.
    [8]MANJUNATHA H, SRINIVASAN K. Hypolipidemic and antioxidant effects of dietary curcumin and capsaicin in induced hypercholesterolemic rats [J]. Lipids,2007,42(12):1133-1142.
    [9]WONG G Y, GAVVA N R. Therapeutic potential of vanilloid receptor TRPV1 agonists and antagonists as analgesics:Recent advances and setbacks [J]. Brain Research Reviews,2009,60(1): 267-277.
    [10]SANCHO R, LUCENA C, MACHO A, et al. Immunosuppressive activity of capsaicinoids: capsiate derived from sweet peppers inhibits NF-kappa B activation and is a potent antiinflammatory compound in vivole [J]. European Journal of Immunology,2002,32(6):1753-1763.
    [11]萨仁高娃,胡文忠,姜爱丽.辣椒营养保健功能及辣椒食品的研究进展[J].食品工业科技,2012,15:371-375.
    [12]郝新忠.辣椒素激活TRPV1预防高盐膳食小鼠高血压的机制研究[D];第三军医大学2011.
    [13]杨大春.激活TRPV1改善血管功能和预防高血压的机制研究[D];第三军医大学,2009.
    [14]KAWADA T, WATANABE T, TAKAISHI T, et al. Capsaicin-induced beta-adrenergic action on energy metabolism in rats:influence of capsaicin on oxygen consumption, the respiratory quotient, and substrate utilization [J]. Proceedings of the Society for Experimental Biology and Medicine, 1986,183(2):250-256.
    [15]KAWADA T, HAGIHARA K I, IWAI K. Effects of capsaicin on lipid-metabolism in rats fed a high-fat diet [J]. Journal of Nutrition,1986,116(7):1272-1278.
    [16]YOSHIOKA M, ST-PIERRE S, SUZUKI M, et al. Effects of red pepper added to high-fat and high-carbohydrate meals on energy metabolism and substrate utilization in Japanese women [J]. British Journal of Nutrition,1998,80(6):503-510.
    [17]LEE M-S, KIM C-T, KIM I-H, et al. Effects of Capsaicin on Lipid Catabolism in 3T3-L1 Adipocytes [J]. Phytotherapy Research,2011,25(6):93593-9.
    [18]袁泉.辣椒素对大鼠营养性肥胖防治作用的研究[D];中南大学,2011.
    [19]MACHO A, LUCENA C, SANCHO R, et al. Non-pungent capsaicinoids from sweet pepper-Synthesis and evaluation of the chemopreventive and anticancer potential [J]. European Journal of Nutrition,2003,42(1):2-9.
    [20]陈世化.辣椒素类物质抑菌作用的研究与评价[D];湖南农业大学,2008.
    [21]MATERSKA M, PERUCKA I. Antioxidant activity of the main phenolic compounds isolated from hot pepper fruit (Capsicum annuum L.) [J]. Journal of Agricultural and Food Chemistry,2005, 53(5):1750-1756.
    [22]MANJUNATHA H M H, SRINIVASAN K S K. Hypolipidemic and antioxidant effects of curcumin and capsaicin in high-fat-fed rats [J]. Canadian journal of physiology and pharmacology, 2007,85(6):588-596.
    [23]罗永祥.辣椒素对乙醇诱导大鼠胃粘膜损伤的保护作用[D];泸州医学院,2011.
    [24]傅志贤,张惠斌,黄文龙.香草酸受体调节剂[J].药学进展,2005,29(9):409-416.
    [25]FRAENKEL L, BOGARDUS S T, CONCATO J, et al. Treatment options in knee osteoarthritis-The patient's perspective [J]. Archives of Internal Medicine,2004,164(12):1299-1304.
    [26]MAIHOFNER C, SCHMELZ M, FORSTER C, et al. Neural activation during experimental allodynia:a functional magnetic resonance imaging study [J]. European Journal of Neuroscience, 2004,19(12):3211-3218.
    [27]ALVAREZ N A. Tolerability of treatments for postherpetic neuralgia [J]. Drug safety:an international journal of medical toxicology and drug experience,2005,28(8):742-746.
    [28]AVELLAN N L, KEMPPAINEN P, TERVAHARTIALA T, et al. Capsaicin-induced local elevations in collagenase-2 (matrix metalloproteinase-8) levels in human gingival crevice fluid [J]. Journal of Periodontal Research,2006,41(1):33-38.
    [29]RAPOPORT A M, BIGAL M E, TEPPER S J, et al. Intranasal medications for the treatment of migraine and cluster headache [J]. Cns Drugs,2004,18(10):671-685.
    [30]AHMED M, BJURHOLM A, SRINIVASAN G R, et al. Capsaicin effects on substance P and CGRP in rat adjuvant arthritis [J]. Regulatory Peptides,1995,55(1):85-102.
    [31]LEE M R, SHUMACK S. Prurigo nodularis:a review [J]. The Australasian journal of dermatology,2005,46(4):211-218.
    [32]ZHUKOVA E M. Role of capsaicin-sensitive neurons in the regulation of structural organization of the thymus [J]. Bulletin of Experimental Biology and Medicine,2005,140(2): 249-252.
    [33]KNOTKOVA H, PAPPAGALLO M, SZALLASI A. Capsaicin (TRPV1 Agonist) therapy for pain relief:farewell or revival? [J]. The Clinical journal of pain,2008,24(2):142-154.
    [34]OH S H, KIM Y S, LIM S C, et al. Dihydrocapsaicin (DHC), a saturated structural analog of capsaicin, induces autophagy in human cancer cells in a catalase-regulated manner [J]. Autophagy, 2008,4(8):1009-1019.
    [35]THOENNISSEN N H, O'KELLY J, LU D, et al. Capsaicin causes cell-cycle arrest and apoptosis in ER-positive and -negative breast cancer cells by modulating the EGFR/HER-2 pathway [J]. Oncogene,2010,29(2):285-296.
    [36]YANG Z-H, WANG X-H, WANG H-P, et al. Capsaicin Mediates Cell Death in Bladder Cancer T24 Cells Through Reactive Oxygen Species Production and Mitochondrial Depolarization [J]. Urology,2010,75(3):735-741.
    [37]ITO K, NAKAZATO T, YAMATO K, et al. Induction of Apoptosis in Leukemic Cells by Homovanillic Acid Derivative, Capsaicin, through Oxidative Stress Implication of Phosphorylation of p53 at Ser-15 Residue by Reactive Oxygen Species [J]. Cancer Research,2004,64(3):1071-1078.
    [38]MAITY R, SHARMA J, JANA N R. Capsaicin Induces Apoptosis Through Ubiquitin-Proteasome System Dysfunction [J]. Journal of Cellular Biochemistry,2010,109(5): 933-942.
    [39]KANG J Y, ALEXANDER B, BARKER F, et al. The effect of chilli ingestion on gastrointestinal mucosal proliferation and azoxymethane-induced cancer in the rat [J]. Journal of gastroenterology and hepatology,1992,7(2):194-198.
    [40]廖新明,李兴红,陈志芬.辣椒素对人结肠癌SW-480生长及Bcl-2/Bax表达的影响[J].实用医院临床杂志,2007,4(4):39-41.
    [41]KIM C S, PARK W H, PARK J Y, et al. Capsaicin, a spicy component of hot pepper, induces apoptosis by activation of the peroxisome proliferator-activated receptor gamma in HT-29 human colon cancer cells [J]. Journal of Medicinal Food,2004,7(3):267-273.
    [42]JOHNSON W. Final report on the safety assessment of capsicum annuum extract, capsicum annuum fruit extract, capsicum annuum resin, capsicum annuum fruit powder, capsicum frutescens fruit, capsicum frutescens fruit extract, capsicum frutescens resin, and capsaicin [J]. International Journal of Toxicology,2007,26:101-106.
    [43]CUI J Y, HIMMSHAGEN J. Long-term decrease in body fat and in brown adipose tissue in capsaicin-desensitized rats [J]. American Journal of Physiology,1992,262(4):568-573.
    [44]JOO J I, KIM D H, CHOI J-W, et al. Proteomic Analysis for Antiobesity Potential of Capsaicin on White Adipose Tissue in Rats Fed with a High Fat Diet [J]. Journal of Proteome Research,2010, 9(6):2977-2987.
    [45]LEUNG F W. Capsaicin-sensitive intestinal mucosal afferent mechanism and body fat distribution [J]. Life Sciences,2008,83(2):1-5.
    [46]张莉莉.辣椒素及其受体TRPV1预防肥胖的机制研究[D];第三军医大学,2006.
    [47]HARADA N, OKAJIMA K. Effects of Capsaicin and Isoflavone on Blood Pressure and Serum Levels of Insulin-Like Growth Factor-I in Normotensive and Hypertensive Volunteers with Alopecia [J]. Bioscience Biotechnology and Biochemistry,2009,73(6):1456-1459.
    [48]朱翔,匡希斌.降钙素基因相关肽与高血压的研究现状[J].心血管病学进展,2004,25(2): 105-107.
    [49]VAISHNAVA P, WANG D H. Capsaicin sensitive-sensory nerves and blood pressure regulation [J]. Current Medicinal Chemistry-Cardiovascular & Hematological Agents,2003,1(2):1771-1788.
    [50]KEMPAIAH R K, SRINIVASAN K. Influence of dietary spices on the fluidity of erythrocytes in hypercholesterolaemic rats [J]. British Journal of Nutrition,2005,93(1):81-91.
    [51]朱振宇.激活瞬时受体电位香草醛亚家族1改善高脂介导的血管功能异常的机制研究[D];第三军医大学,2012.
    [52]徐兴森.激活PRPV1预防动脉粥样硬化及脑卒中的机制研究[D];第三军医大学,2012.
    [53]PENG J, LU R, DENG H W, et al. Involvement of alpha-calcitonin gene-related peptide in monophosphoryl lipid A-induced delayed preconditioning in rat hearts [J]. European Journal of Pharmacology,2002,436(2):89-96.
    [54]PENG J, LU R, XIAO L, et al. Involvement Of a-Calcitonin Gene-Related Peptide In Heat Stress-Induced Delayed Preconditioning In Rat Hearts [J]. Clinical and experimental pharmacology and physiology,2002,29(7):569-574.
    [55]ADAMS M J, AHUJA K D K, GERAGHTY D P. Effect of capsaicin and dihydrocapsaicin on in vitro blood coagulation and platelet aggregation [J]. Thrombosis Research,2009,124(6):721-723.
    [56]HOGABOAM C M, WALLACE J L. Inhibition of platelet aggregation by capsaicin-an effect unrelated to actions on sensory afferent neurons [J]. European Journal of Pharmacology,1991, 202(1):129-131.
    [57]HARPER A G S, BROWNLOW S L, SAGE S O. A role for TRPV1 in agonist-evoked activation of human platelets [J]. Journal of Thrombosis and Haemostasis,2009,7(2):330-338.
    [58]王锋,谭兴和,张礼红等.辣椒的生理功能及开发利用[J].中国食物与营养,2006,6:9-17.
    [59]顾洛,闫长栋,杜军等.辣椒素敏感传入神经和NO中介大鼠胃扩张引起的胃酸分泌和胃粘膜血流量变化[J].中国应用生理学杂志,2003,19(2):193-196.
    [60]HOLZER P, PAINSIPP E, SCHULIGOI R. Differential effects of intragastric acid and capsaicin on gastric emptying and afferent input to the rat spinal cord and brainstem [J]. Bmc Neuroscience, 2005,6:1-9.
    [61]PENG J, LI Y-J. The vanilloid receptor TRPV1:Role in cardiovascular and gastrointestinal protection [J]. European Journal of Pharmacology,2010,627(3):1-7.
    [62]SATYANARAYANA M N. Capsaicin and gastric ulcers [J]. Critical reviews in food science and nutrition,2006,46(4):275-328.
    [63]TENG C H, KANG J Y, WEE A, et al. Protective action of capsaicin and chilli on haemorrhagic shock-induced gastric mucosal injury in the rat [J]. Journal of gastroenterology and hepatology, 2008,13(10):1007-1014.
    [64]WANG L, HU C P, DENG P Y, et al. The protective effects of rutaecarpine on gastric mucosa injury in rats [J]. Planta Medica,2005,71(5):416-419.
    [65]NISHIHARA K, NOZAWA Y, NAKANO M, et al. Sensitizing effects of lafutidine on CGRP-containing afferent nerves in the rat stomach [J]. British Journal of Pharmacology,2002, 135(6):1487-1494.
    [66]MOZSIK G, SZOLCSANYI J, DOEMOETOER A. Capsaicin research as a new tool to approach of the human gastrointestinal physiology, pathology and pharmacology [J]. Inflammopharmacology,2007,15(6):232-245.
    [67]ZHANG L L, LIU D Y, MA L Q, et al. Activation of transient receptor potential vanilloid type-1 channel prevents adipogenesis and obesity [J]. Circulation Research,2007,100(7): 1063-1070.
    [68]MONSEREENUSORN Y. Subchronic Toxicity Studies of Capsaicin and Capsicum in Rats [J]. Res Commun Chem Path,1983,41(1):95-110.
    [69]NEGULESCO J A, YOUNG R M, KI P. Capsaicin lowers plasma cholesterol and triglycerides of lagomorphs [J]. Artery,1985,12(5):301-311.
    [70]NEGULESCO J A, NOEL S A, NEWMAN H A I, et al. Effects of pure capsaicinoids (capsaicin and dihydrocapsaicin) on plasma lipid and lipoprotein concentrations of turkey poults [J]. Atherosclerosis,1987,64(3):85-90.
    [71]聂乾忠,夏延斌,曾晓楠等.辣椒素类物质对高脂血症大鼠血脂的影响[J].食品与机械,2010.1:77-80.
    [72]SRINIVASAN K, PLATEL K, RAO M V L. Hypotriglyceridemic effect of dietary vanillin in experimental rats [J]. European Food Research and Technology,2008,228(1):103-108.
    [73]THOMAS YEUNG C H, YANG L, HUANG Y, et al. Dietary conjugated linoleic acid mixture affects the activity of intestinal acyl coenzyme A:cholesterol acyltransferase in hamsters [J]. The British journal of nutrition,2000,84(6):935-941.
    [74]CHUNG M J, PARK K W, KIM K H, et al. Asian plantain (Plantago asiatica) essential oils suppress 3-hydroxy-3-methylglutaryl-co-enzyme A reductase expression in vitro and in vivo and show hypocholesterolaemic properties in mice [J]. British Journal of Nutrition,2008,99(1):67-75.
    [75]TAKAHASHI Y, KONISHI T. Tofu (Soybean Curd) Lowers Serum Lipid Levels and Modulates Hepatic Gene Expression Involved in Lipogenesis Primarily through Its Protein, Not Isoflavone, Component in Rats [J]. Journal of Agricultural and Food Chemistry,2011,59(16): 8976-8984.
    [76]胡叶碧.改性玉米皮膳食纤维的酶法制备及其降血脂机理研究[D];江南大学,2008.
    [77]GRUNDY S M. Absorption and metabolism of dietary-cholesterol [J]. Annual Review of Nutrition,1983,3:71-96.
    [78]KATO M, OGAWA H, KISHIDA T, et al. The mechanism of the cholesterol-lowering effect of water-insoluble fish protein in ovariectomised rats [J]. British Journal of Nutrition,2009,102(6): 816-824.
    [79]HOFMANN A F. The enterohepatic circulation of bile acids in mammals:form and functions [J]. Frontiers in Bioscience,2009,14(2):2584-2598.
    [80]LANDRIER J F, GROBER J, ZAGHINI I, et al. Regulation of the ileal bile acid-binding protein gene:An approach to determine its physiological function(s) [J]. Molecular and Cellular Biochemistry,2002,239(2):149-155.
    [81]KISHIDA T, ISHIKAWA H, TSUKAOKA M, et al. Increase of bile acids synthesis and excretion caused by taurine administration prevents the ovariectomy-induced increase in cholesterol concentrations in the serum low-density lipoprotein fraction of Wistar rats [J]. Journal of Nutritional Biochemistry,2003,14(1):7-16.
    [82]JIA L, BETTERS J L, YU L. Niemann-Pick Cl-Like 1 (NPC1L1) Protein in Intestinal and Hepatic Cholesterol Transport [M]//JULIUS D, CLAPHAM D E. Annual Review of Physiology, 2011,73(6):239-259.
    [83]CHEN Z-Y, JIAO R, MA K Y. Cholesterol-lowering nutraceuticals and functional foods [J]. Journal of Agricultural and Food Chemistry,2008,56(19):8761-8773.
    [84]GRUNDY S M, METZGER A L. Physiological method for estimation of hepatic secretion of biliary lipids in man [J]. Gastroenterology,1972,62(6):1200-1206.
    [85]ATZEL A, WETTERAU J R. Mechanism of microsomal triglyceride transfer protein catalyzed lipid transport [J]. Biochemistry,1993,32(39):10444-10450.
    [86]DAVIS H R, ZHU L J, HOOS L M, et al. Niemann-Pick Cl like 1 (NPC1L1) is the intestinal phytosterol and cholesterol transporter and a key modulator of whole-body cholesterol homeostasis [J]. Journal of Biological Chemistry,2004,279(32):33586-33592.
    [87]BERGE K E, TIAN H, GRAF G A, et al. Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters [J]. Science,2000,290(5497):1771-1775.
    [88]LEE M H, LU K, HAZARD S, et al. Identification of a gene, ABCG5, important in the regulation of dietary cholesterol absorption [J]. Nature Genetics,2001,27(1):79-83.
    [89]LEE R G, SHAH R, SAWYER J K, et al. ACAT2 contributes cholesteryl esters to newly secreted VLDL, whereas LCAT adds cholesteryl ester to LDL in mice [J]. Journal of Lipid Research, 2005,46(6):1205-1212.
    [90]LARGIS E E, WANG C H, DEVRIES V G, et al. CL 277,082:a novel inhibitor of ACAT-catalyzed cholesterol esterification and cholesterol absorption [J]. Journal of Lipid Research, 1989,30(5):681-690.
    [91]REPA J J, BUHMAN K K, FARESE R V, et al. ACAT2 deficiency limits cholesterol absorption in the cholesterol-fed mouse:Impact on hepatic cholesterol homeostasis [J]. Hepatology,2004,40(5): 1088-1097.
    [92]NAMMI S, KIM M S, GAVANDE N S, et al. Regulation of Low-Density Lipoprotein Receptor and 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Expression by Zingiber officinale in the Liver of High-Fat Diet-Fed Rats [J]. Basic & Clinical Pharmacology & Toxicology,2010,106(5): 389-395.
    [93]KOVANEN P T, BILHEIMER D W, GOLDSTEIN J L, et al. Regulatory role for hepatic low density lipoprotein receptors in vivo in the dog [J]. Proceedings of the National Academy of Sciences of the United States of America-Biological Sciences,1981,78(2):1194-1198.
    [94]SHIN S-K, HA T-Y, MCGREGOR R A, et al. Long-term curcumin administration protects against atherosclerosis via hepatic regulation of lipoprotein cholesterol metabolism [J]. Molecular Nutrition & Food Research,2011,55(12):1829-1840.
    [95]HASIMUN P, SUKANDAR E Y, ADNYANAI K, et al. Synergistic Effect of Curcuminoid and S-methyl Cysteine in Regulation of Cholesterol Homeostasis [J]. International Journal of Pharmacology,2011,7(2):268-272.
    [96]GUAN L, CHUNG H Y, SU Y, et al. Hypocholesterolemic activity of onion is mediated by enhancing excretion of fecal sterols in hamsters [J]. Food & Function,2010,1(1):84-89.
    [97]VIDYASHANKAR S, SAMBAIAH K, SRINIVASAN K. Dietary garlic and onion reduce the incidence of atherogenic diet-induced cholesterol gallstones in experimental mice [J]. British Journal of Nutrition,2009,101(11):1621-1629.
    [98]VIDYASHANKAR S, SAMBAIAH K, SRINIVASAN K. Regression of preestablished cholesterol gallstones by dietary garlic and onion in experimental mice [J]. Metabolism-Clinical and Experimental,2010,59(10):1402-1412.
    [99]汪俊军,张春妮.胆固醇酯转运蛋白基因变异与血脂和动脉粥样硬化性心血管病的关系[J].医学研究生学报,2007,20(1):76-79.
    [100]黄竹颖,郭红卫.胆固醇酯转运蛋白基因缺陷与动脉粥样硬化关系研究进展[J].卫生研究,2005,34(6):765-767.
    [101]NICOLOSI R J, WILSON T A. The anti-atherogenic effect of dietary soybean protein concentrate in hamsters [J]. Nutrition Research,1997,17(9):1457-1467.
    [102]MIYAZAKI A, KOGA T. Pravastatin sodium, an inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase, decreases serum total cholesterol in Japanese White rabbits by two different mechanisms [J]. Atherosclerosis,2002,162(2):299-306.
    [103]REILLY C A, EHLHARDT W J, JACKSON D A, et al. Metabolism of capsaicin by cytochrome P450 produces novel dehydrogenated metabolites and decreases cytotoxicity to lung and liver cells [J]. Chemical Research in Toxicology,2003,16(3):336-349.
    [104]REILLY C A, YOST G S. Metabolism of capsaicinoids by P450 enzymes:A review of recent findings on reaction mechanisms, bio-activation, and detoxification processes [J]. Drug Metabolism Reviews,2006,38(4):685-706.
    [105]SRINIVASAN K. Spices as influencers of body metabolism:an overview of three decades of research [J]. Food Research International,2005,38(1):77-86.
    [106]MILLER C H, ZHANG Z, HAMILTON S M, et al. Effects of capsaicin on liver microsomal metabolism of the tobacco-specific nitrosamine NNK [J]. Cancer Lett,1993,75(1):45-52.
    [107]SRINIVASAN M, SATYANARAYANA M. Influence of capsaicin, curcumin and ferulic acid in rats fed high fat diets [J]. Journal of Biosciences,1987,12(2):143-152.
    [108]SEO K-I, CHOI M-S, JUNG U J, et al. Effect of curcumin supplementation on blood glucose, plasma insulin, and glucose homeostasis related enzyme activities in diabetic db/db mice [J]. Molecular Nutrition & Food Research,2008,52(9):995-1004.
    [109]CHANG C J, TZENG T-F, LIOU S-S, et al. Regulation of lipid disorders by ethanol extracts from Zingiber zerumbet in high-fat diet-induced rats [J]. Food Chemistry,2012,132(1):460-467.
    [110]KIM M, KIM Y. Hypocholesterolemic effects of curcumin via up-regulation of cholesterol 7a-hydroxylase in rats fed a high fat diet [J]. Nutrition Research and Practice,2010,4(3):191-195.
    [111]SRINIVASAN K, SAMBAIAH K. The effect of spices on cholesterol 7 alpha-hydroxylase activity and on serum and hepatic cholesterol levels in the rat [J]. International Journal for Vitamin and Nutrition Research,1991,61(4):364-369.
    [112]ABDEL SALAM O M E, HEKAL O A, EL-SHENAWY S M. Effect of capsaicin on bile secretion in the rat [J]. Pharmacology,2005,73(3):121-128.
    [113]NALINI N, MANJU V, MENON V. Effect of spices on lipid metabolism in 1, 2-dimethylhydrazine-induced rat colon carcinogenesis [J]. Journal of Medicinal Food,2006,9(2): 237-245.
    [114]SAMBAIAH K, SATYANARAYANA M N, RAO M V L. Effect of red pepper (chillies) and capsaicin on fat absorption and liver fat in rats [J]. Nutrition Reports International,1978,18(5): 521-529.
    [115]HUSSAIN M S, CHANDRASEKHARA N. curcumin and capsaicin on cholesterol gallstone induction in hamsters and mice [J]. Nutrition Research,1993,13(3):349-357.
    [116]HUSSAIN M S, CHANDRASEKHARA N. Effect of curcumin and capsaicin on the regression of preestablished cholesterol gallstones in mice [J]. Nutrition Research,1994,14(10): 1561-1574.
    [117]IWAI K, KAWADA T, WATANABE T. Effects of capsaicin on lipid metabolism in rats fed a high fat diet [J]. Appetite,1986,7(3):268-271.
    [118]LEJEUNE M, KOVACS E M R, WESTERTERP-PLANTENGA M S. Effect of capsaicin on substrate oxidation and weight maintenance after modest body-weight loss in human subjects [J]. British Journal of Nutrition,2003,90(3):651-659.
    [119]INOUE N, MATSUNAGA Y, SATOH H, et al. Enhanced energy expenditure and fat oxidation in humans with. high BMI scores by the ingestion of novel and non-pungent capsaicin analogues (capsinoids) [J]. Bioscience Biotechnology and Biochemistry,2007,71(2):380-389.
    [120]YANG D C, MA S T, MA L Q, et al. Activation of TRPV1 inhibits angiotensin Ⅱ induced vasoconstriction in mice [J]. International Journal of Cardiology,2009,137:97-102.
    [121]TANI Y, FUJIOKA T, SUMIOKA M, et al. Effects of capsinoid on serum and liver lipids in hyperlipidemic rats [J]. Journal of Nutritional Science and Vitaminology,2004,50(5):351-355.
    [122]李辉,刘德平.胆固醇吸收蛋白——降脂治疗的新靶点[J].中国心血管杂志,2008,4:311-314.
    [123]SHNEIDER B L, DAWSON P A, CHRISTIE D M, et al. Cloning and molecular characterization of the ontogeny of a rat ileal sodium-dependent bile-acid transporter [J]. Journal of Clinical Investigation,1995,95(2):745-754.
    [124]陈敏,张陆勇,严明.辣椒素受体研究进展[J].中国临床药理学与治疗学,2006,2:126-130.
    [125]SURI A, SZALLASI A. The emerging role of TRPV1 in diabetes and obesity [J]. Trends in Pharmacological Sciences,2008,29(1):29-36.
    [126]SZALLASI A, APPENDINO G. Vanilloid receptor TRPV1 antagonists as the next generation of painkillers. Are we putting the cart before the horse[J]. ChemInform,2004,35(33):1-6.
    [127]FLOCKERZI V. An introduction on TRP channels [M]FLOCKERZI V, NILIUS B. Handbook of Experimental Pharmacology.2007:1-19.
    [128]RYCHKOV G Y, BARRITT G J. Expression and Function of TRP Channels in Liver Cells [M]ISLAM M S. Transient Receptor Potential Channels.2011:667-686.
    [129]TOTH B I, GECZY T, GRIGER Z, et al. Transient Receptor Potential Vanilloid-1 Signaling as a Regulator of Human Sebocyte Biology [J]. Journal of Investigative Dermatology,2009,129(2): 329-339.
    [130]MOTTER A L, AHERN G P. TRPV1-null mice are protected from diet-induced obesity [J]. Febs Letters,2008,582(15):2257-2262.
    [131]MA S T, ZHANG L L, YANG D C, et al. Dietary capsaicin upregulates uncoupling protein 2/3 expression in visceral adipose tissue and enhances acetylcholine-induced hypotensive effect in mice [J]. Progress in Nutrition,2010,12(1):19-23.
    [1]DAVIS C B, MARKEY C E, BUSCH M A, et al. Determination of capsaicinoids in habanero peppers by chemometric analysis of UV spectral data [J]. Journal of Agricultural and Food Chemistry,2007,55(15):5925-5933.
    [2]MUELLER-SEITZ E, HIEPLER C, PETZ M. Chili Pepper Fruits:Content and Pattern of Capsaicinoids in Single Fruits of Different Ages [J]. Journal of Agricultural and Food Chemistry, 2008,56(24):12114-12121.
    [3]LUO X J, PENG J, LI Y J. Recent advances in the study on capsaicinoids and capsinoids [J]. European Journal of Pharmacology,2011,650(1):1-7.
    [4]SAMBAIAH K, SATYANARAYANA M N, RAO M V L. Effect of red pepper (chillies) and capsaicin on fat absorption and liver fat in rats [J]. Nutrition Reports International,1978,18(5): 521-529.
    [5]KIM H, TUROWSKI M, ANDERSON W H K, et al. Supplementation of Hydroxypropyl Methylcellulose into Yeast Leavened All-Whole Grain Barley Bread Potentiates Cholesterol-Lowering Effect [J]. Journal of Agricultural and Food Chemistry,2011,59(14): 7672-7678.
    [6]MANJUNATHA H M H, SRINIVASAN K S K. Hypolipidemic and antioxidant effects of curcumin and capsaicin in high-fat-fed rats [J]. Canadian journal of physiology and pharmacology, 2007,85(6):588-596.
    [7]LEE S O. Studies on the influence of diets and lipotropic substances upon the various organs and metabolic changes in rabbits on long-term feeding with red pepper [J]. The Korean journal of internal medicine,1963,41:471-481.
    [8]KAWADA T, WATANABE T, TAKAISHI T, et al. Capsaicin-induced beta-adrenergic action on energy metabolism in rats:influence of capsaicin on oxygen consumption, the respiratory quotient, and substrate utilization [J]. Proceedings of the Society for Experimental Biology and Medicine, 1986,183(2):250-256.
    [9]KAWADA T, HAGIHARA K I, IWAI K. Effects of capsaicin on lipid-metabolism in rats fed a high-fat diet [J]. Journal of Nutrition,1986,116(7):1272-1278.
    [10]KIM Y. Reduction of Body Weight by Capsaicin is Associated with Inhibition of Glycerol-3-Phosphate Dehydrogenase Activity and Stimulation of Uncoupling Protein 2 mRNA Expression in Diet-induced Obese Rats [J]. Journal of Food Science and Nutrition,2011,16(3): 210-216.
    [11]YOSHIOKA M, ST-PIERRE S, SUZUKI M, et al. Effects of red pepper added to high-fat and high-carbohydrate meals on energy metabolism and substrate utilization in Japanese women [J]. British Journal of Nutrition,1998,80(6):503-510.
    [12]杨大春.激活TRPV1改善血管功能和预防高血压的机制研究[D];第三军医大学,2009.
    [13]郝新忠.辣椒素激活TRPV1预防高盐膳食小鼠高血压的机制研究[D];第三军医大学,2011.
    [14]MATERSKA M, PERUCKA I. Antioxidant activity of the main phenolic compounds isolated from hot pepper fruit (Capsicum annuum L.) [J]. Journal of Agricultural and Food Chemistry,2005, 53(5):1750-1756.
    [15]DIAZ M N, FREI B, VITA J A, et al. Mechanisms of disease-Antioxidants and atherosclerotic heart disease [J]. New England Journal of Medicine,1997,337(6):408-416.
    [16]KEMPAIAH R K, MANJUNATHA H, SRINIVASAN K. Protective effect of dietary capsaicin on induced oxidation of low-density lipoprotein in rats [J]. Molecular and Cellular Biochemistry, 2005,275(1-2):7-13.
    [17]郑龙辉.辣椒素对体内胆固醇代谢机理的研究[D];西南大学,2012.
    [18]21266-2007 G T辣椒及辣椒制品中辣椒素类物质测定及辣度表示方法[S].2007.
    [19]Hidehiko Y, Hideki M, Ken N, et al. Dietary taurine enhances cholesterol degradation and reduces serum and liver cholesterol concentrations in rats fed a high-cholesterol diet [J]. The Journal of Nutrition,1999,129(9):1705-1712.
    [20]Afrose S, Hossain M, Maki T, et al. Karaya root saponin exerts a hypocholesterolemic response in tats fed a high-cholesterol diet [J]. Nutrition Reseatch,2009,29(5):350-354.
    [21]LIU X, OGAWA H, KISHIDA T, et al. The effect of high-amylose cornstarch on lipid metabolism in OVX rats is affected by fructose feeding [J]. Journal of Nutritional Biochemistry, 2010,21(2):89-97.
    [22]FOLCH J, LEES M, SLOANE-STANLEY G. A simple method for the isolation and purification of total lipids from animal tissues [J]. J biol Chem,1957,226(1):497-509.
    [23]KATO M, OGAWA H, KISHIDA T, et al. The mechanism of the cholesterol-lowering effect of water-insoluble fish protein in ovariectomised rats [J]. British Journal of Nutrition,2009,102(6): 816-824.
    [24]王静,李素君,刘宗林等.辣椒素衍生物对大鼠血脂影响的研究[J].食品科学,2008,29(06):395-398.
    [25]袁泉.辣椒素对大鼠营养性肥胖防治作用的研究[D];中南大学,2011.
    [26]ZHANG L L, LIU D Y, MA L Q, et al. Activation of transient receptor potential vanilloid type-1 channel prevents adipogenesis and obesity [J]. Circulation Research,2007,100(7): 1063-1070.
    [27]REIHNER E, RUDLING M, STAHLBERG D, et al. Influence of pravastatin, a specific inhibitor of HMG-CoA reductase, on hepatic metabolism of cholesterol [J]. New England Journal of Medicine,1990,323(4):224-228.
    [28]MIYAZAKI A, KOGA T. Pravastatin sodium, an inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase, decreases serum total cholesterol in Japanese White rabbits by two different mechanisms [J]. Atherosclerosis,2002,162(2):299-306.
    [29]MANJUNATHA H, SRINIVASAN K. Hypolipidemic and antioxidant effects of dietary curcumin and capsaicin in induced hypercholesterolemic rats [J]. Lipids,2007,42(12):1133-1142.
    [30]MONSEREENUSORN Y. Subchronic toxicity studies of capsaicin and capsicum in rats [J]. Res Commun Chem Path,1983,41(1):95-99.
    [31]NEGULESCO J A, NOEL S A, NEWMAN H A I, et al. Effects of pure capsaicinoids (capsaicin and dihydrocapsaicin) on plasma lipid and lipoprotein concentrations of turkey poults [J]. Atherosclerosis,1987,64(2-3):85-90.
    [32]SRINIVASAN M, SATYANARAYANA M. Influence of capsaicin, curcumin and ferulic acid in rats fed high fat diets [J]. Journal of Biosciences,1987,12(2):143-152.
    [33]KAWADA T, SUZUKI T, TAKAHASHI M, et al. Gastrointestinal absorption and metabolism of capsaicin and dihydrocapsaicin in rats [J]. Toxicology and Applied Pharmacology,1984,72(3): 449-456.
    [34]MONSEREENUSORN Y. In vitro intestinal absorption of capsaicin [J]. Toxicology and Applied Pharmacology,1980,53(1):134-139.
    [35]NALINI N, MANJU V, MENON V. Effect of spices on lipid metabolism in 1, 2-dimethylhydrazine-induced rat colon carcinogenesis [J]. Journal of Medicinal Food,2006,9(2): 237-245.
    [1]BRUSCHI F, MESCHIA M, SOMA M, et al. Lipoprotein(a) and other lipids after oophorectomy and estrogen replacement therapy [J]. Obstetrics and Gynecology,1996,88(6): 950-954.
    [2]FUKAMI K, KOIKE K, HIROTA K, et al. Perimenopausal changes in serum lipids and lipoproteins:A 7-year longitudinal study [J]. Maturitas,1995,22(3):193-197.
    [3]GRODSTEIN F, STAMPFER M J, MANSON J E, et al. Postmenopausal estrogen and progestin use and the risk of cardiovascular disease [J]. New England Journal of Medicine,1996, 335(7):453-461.
    [4]JUDD H L, MELDRUM D R, DEFTOS L J, et al. Estrogen replacement therapy:indications and complications [J]. Annals of Internal Medicine,1983,98(2):195-205.
    [5]HENDERSON B E, ROSS R K, PIKE M C. Hormonal chemoprevention of cancer in women [J]. Science,1993,259(5095):633-638.
    [6]21266-2007 G T.辣椒及辣椒制品中辣椒素类物质测定及辣度表示方法[S].2007.
    [7]梅福荣.0.3%戊巴比妥钠用于大鼠麻醉的方法[J].实验动物科学与管理,2003,20(003):44-45.
    [8]KISHIDA T, ISHIKAWA H, TSUKAOKA M, et al. Increase of bile acids synthesis and excretion caused by taurine administration prevents the ovariectomy-induced increase in cholesterol concentrations in the serum low-density lipoprotein fraction of Wistar rats [J]. Journal of Nutritional Biochemistry,2003,14(1):7-16.
    [9]LIU X, SAWAUCHIH, OGAWA H, et al. Retrograded tapioca starch prevents ovarian hormone deficiency-induced hypercholesterolemia [J]. Journal of Nutritional Science and Vitaminology,2006, 52(2):134-141.
    [10]VANLENTEN B J, MELCHIOR G W, ROHEIM P S. Lipoprotein metabolism in the ovariectomized rat [J]. Journal of Lipid Research,1983,24(11):1475-1484.
    [11]张磊,刘雄,陈宗道.辣椒素降血脂作用及其机制的研究进展[C].管产学研助推食品安全重庆高峰论坛.中国重庆,2011:463-467.
    [12]CHEN Z-Y, MA K Y, LIANG Y, et al. Role and classification of cholesterol-lowering functional foods [J]. Journal of Functional Foods,2011,3(2):61-69.
    [13]SRINIVASAN K. Dietary spices as beneficial modulators of lipid profile in conditions of metabolic disorders and diseases [J]. Food & Function,2013:1-9
    [14]MIYAZAKI A, KOGA T. Pravastatin sodium, an inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase, decreases serum total cholesterol in Japanese White rabbits by two different mechanisms [J]. Atherosclerosis,2002,162(2):299-306.
    [15]MARIA MARTIN-NAVARRO C, LORENZO-MORALES J, MACHIN R P, et al. Inhibition of 3-Hydroxy-3-Methylglutaryl-Coenzyme A Reductase and Application of Statins as a Novel Effective Therapeutic Approach against Acanthamoeba Infections [J]. Antimicrobial Agents and Chemotherapy,2013,57(1):375-381.
    [16]STORMO C, KRINGEN M K, GRIMHOLT R M, et al. A novel 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) splice variant with an alternative exon 1 potentially encoding an extended N-terminus [J]. Bmc Molecular Biology,2012,13:134-141.
    [17]CHOI H-J, CHUNG M J, HAM S-S. Antiobese and hypocholesterolaemic effects of an Adenophora triphylla extract in HepG2 cells and high fat diet-induced obese mice [J]. Food Chemistry,2010,119(2):437-444.
    [18]JONES P J H. Regulation of cholesterol biosynthesis by diet in humans [J]. American Journal of Clinical Nutrition,1997,66(2):438-446.
    [19]SRINIVASAN K. Spices as influencers of body metabolism:an overview of three decades of research [J]. Food Research International,2005,38(1):77-86.
    [20]CAO Y, BEI W, HU Y, et al. Hypocholesterolemia of Rhizoma Coptidis alkaloids is related to the bile acid by up-regulated CYP7A1 in hyperlipidemic rats [J]. Phytomedicine,2012,19(8-9): 686-692.
    [21]SHIN S-K, HA T-Y, MCGREGOR R A, et al. Long-term curcumin administration protects against atherosclerosis via hepatic regulation of lipoprotein cholesterol metabolism [J]. Molecular Nutrition & Food Research,2011,55(12):1829-1840.
    [22]HASIMUN P, SUKANDAR E Y, ADNYANAI K, et al. Synergistic Effect of Curcuminoid and S-methyl Cysteine in Regulation of Cholesterol Homeostasis [J]. International Journal of Pharmacology,2011,7(2):268-272.
    [23]CHEN Z-Y, JIAO R, MA K Y. Cholesterol-lowering nutraceuticals and functional foods [J]. Journal of Agricultural and Food Chemistry,2008,56(19):8761-8773.
    [24]VLAHCEVIC Z R, PANDAK W M, STRAVITZ R T. Regulation of bile acid biosynthesis [J]. Gastroenterology Clinics of North America,1999,28(1):1-9.
    [25]HOFMANN A F. The enterohepatic circulation of bile acids in mammals:form and functions [J]. Frontiers in Bioscience,2009,14:2584-2598.
    [26]LANDRIER J F, GROBER J, ZAGHINI I, et al. Regulation of the ileal bile acid-binding protein gene:An approach to determine its physiological function(s) [J]. Molecular and Cellular Biochemistry,2002,239(1-2):149-155.
    [27]MAKISHIMA M, OKAMOTO A Y, REPA J J, et al. Identification of a nuclear receptor for bile acids [J]. Science,1999,284(5418):1362-1365.
    [28]SHNEIDER B L, DAWSON P A, CHRISTIE D M, et al. Cloning and molecular characterization of the ontogeny of a rat ileal sodium-dependent bile-acid transporter [J]. Journal of Clinical Investigation,1995,95(2):745-754.
    [29]LIANG Y T, TIAN X Y, CHEN J N, et al. Capsaicinoids lower plasma cholesterol and improve endothelial function in hamsters [J]. European Journal of Nutrition,2012,1-10.
    [30]SRINIVASAN K, SAMBAIAH K. The effect of spices on cholesterol 7 alpha-hydroxylase activity and on serum and hepatic cholesterol levels in the rat [J]. International Journal for Vitamin and Nutrition Research,1991,61(4):364-369.
    [31]毛奇琦,孙旭.核受体在胆汁酸和胆固醇代谢中的作用[J].国际消化病杂志,2008,28(003):243-245.
    [32]SURI A, SZALLASI A. The emerging role of TRPV1 in diabetes and obesity [J]. Trends in Pharmacological Sciences,2008,29(1):29-36.
    [33]ZHANG L L, LIU D Y, MA L Q, et al. Activation of transient receptor potential vanilloid type-1 channel prevents adipogenesis and obesity [J]. Circulation Research,2007,100(7): 1063-1070.
    [34]LEUNG F W. Capsaicin-sensitive intestinal mucosal afferent mechanism and body fat distribution [J]. Life Sciences,2008,83(1-2):1-5.
    [35]DONNERER J, AMANN R, SCHULIGOI R, et al. Absorption and metabolism of capsaicinoids following intragastric administration in rats [J]. Naunyn-Schmiedebergs Archives of Pharmacology,1990,342(3):357-361.
    [36]REILLY C A, EHLHARDT W J, JACKSON D A, et al. Metabolism of capsaicin by cytochrome P450 produces novel dehydrogenated metabolites and decreases cytotoxicity to lung and liver cells [J]. Chemical Research in Toxicology,2003,16(3):336-349.
    [37]MA L, ZHONG J, ZHAO Z, et al. Activation of TRPV1 reduces vascular lipid accumulation and attenuates atherosclerosis [J]. Cardiovascular Research,2011,92(3):504-513.
    [38]YANG D C, MA S T, MA L Q, et al. Activation of TRPV1 inhibits angiotensin II induced vasoconstriction in mice [J]. International Journal of Cardiology,2009,137:S97-S102.
    [39]MA S T, ZHANG L L, YANG D C, et al. Dietary capsaicin upregulates uncoupling protein 2/3 expression in visceral adipose tissue and enhances acetylcholine-induced hypotensive effect in mice [J]. Progress in Nutrition,2010,12(1):19-23.
    [40]马丽群.激活瞬时受体电位香草醛亚家族1抗动脉粥样硬化机制研究[D];第三军医大学,2010.
    [41]徐兴森.激活TRPV1预防动脉粥样硬化及脑卒中的机制研究[D];第三军医大学,2012.
    [42]NEGULESCO J A, NOEL S A, NEWMAN H A I, et al. Effects of pure capsaicinoids (capsaicin and dihydrocapsaicin) on plasma lipid and lipoprotein concentrations of turkey poults [J]. Atherosclerosis,1987,64(2-3):85-90.
    [43]MCRAE M P. The efficacy of vitamin C supplementation on reducing total serum cholesterol in human subjects:a review and analysis of 51 experimental trials [J]. Journal of chiropractic medicine, 2006,5(1):2-12.
    [44]MCRAE M P. Vitamin C supplementation lowers serum low-density lipoprotein cholesterol and triglycerides:a meta-analysis of 13 randomized controlled trials [J]. Journal of chiropractic medicine, 2008,7(2):48-58.
    [45]胡叶碧.改性玉米皮膳食纤维的酶法制备及其降血脂机理研究[D];江南大学,2008.
    [46]吴洪斌,王永刚,郑刚等.膳食纤维生理功能研究进展[J].中国酿造,2012,240(03):13-16.
    [47]DONGOWSKI G. Interactions between dietary fibre-rich preparations and glycoconjugated bile acids in vitro [J]. Food Chemistry,2007,104(1):390-397.
    [48]SRINIVASAN K. Role of spices beyond food flavoring:Nutraceuticals with multiple health effects [J]. Food Reviews International,2005,21(2):167-188.
    [49]CHOI J-H. Effect of Red Pepper Seeds Powder on Lipid Composition in Rats Fed High-Fat·High-Cholesterol Diets [J]. Journal of Food Science and Nutrition,2010,15(3):184-188.
    [50]NATALI F, SICULELLA L, SALVATI S, et al. Oleic acid is a potent inhibitor of fatty acid and cholesterol synthesis in C6 glioma cells [J]. Journal of Lipid Research,2007,48(9):1966-1975.
    [1]Opinion of the Scientific Committee on Food on Capsaicin. European Commission Health & Consumer Protection Directorate-General [J]. SCF/CS/FLAV/FLAVOUR/8 ADD1 Final.2002, 28-35.
    [2]苏昕峰,文红丽,刘雄.辣椒素对胃肠道健康的影响[J].食品工业科技,2011,6:443-446.
    [3]李明泽,苏昕峰,彭林等.辣椒素剂量对大鼠肠道发酵产物的影响[J].食品科学,2013,1-6.
    [4]任文瑾,吕娇,苏昕峰等.辣椒素对肠道菌体外发酵的影响[J].食品工业科技,2013,1-7.
    [5]KISSELL L, BEAN M. AACC [American Association of Cereal Chemists] Technical Committee report:development of a method for angel food cake [J]. Cereal Foods World,1978,23: 1256-1259.
    [6]曾霞娟,刘家鹏,严梅娣等.膳食纤维对胃肠道作用的研究进展[J].微量元素与健康研究,2011,121(01):52-59.
    [7]蒋与刚,张茂玉.膳食纤维与结肠癌[J].现代预防医学,1993,2:119-128.
    [8]蔺新英.膳食纤维与肿瘤关系的研究进展[C].山东营养学会营养与疾病学术研讨会,中国山东济南,2006.
    [9]王子花,申瑞玲,李文全.膳食纤维降血糖作用研究进展[J].粮食与油脂,2006,7:42-44.
    [10]章瑜.膳食纤维对Ⅱ型糖尿病大鼠的血糖影响及机理研究[D];南昌大学,2011.
    [11]麦紫欣,关东华,林敏霞等.膳食纤维降血脂作用及其机制的研究进展[J].广东微量元素科学,2011,198(18):11-16.
    [12]胡叶碧.改性玉米皮膳食纤维的酶法制备及其降血脂机理研究[D];江南大学,2008.
    [13]LOPEZ-CARRILLO L, CAMARGO M C, SCHNEIDER B G, et al. Capsaicin consumption, Helicobacter pylori CagA status and IL1B-31C T genotypes:A host and environment interaction in gastric cancer [J]. Food and Chemical Toxicology,2012,50(6):2118-2122.
    [14]吴洪斌,王永刚,郑刚等.膳食纤维生理功能研究进展[J].中国酿造,2012,240(03):13-16.
    [15]刘成梅,李资玲,梁瑞红等.膳食纤维的生理功能与应用现状[J].食品研究与开发,2006,1:122-125.
    [16]连晓蔚.肠道菌群利用几种膳食纤维体外发酵产短链脂肪酸的研究[D];暨南大学,2011.
    [17]ZHOU K, XIA W, ZHANG C, et al. In vitro binding of bile acids and triglycerides by selected chitosan preparations and their physico-chemical properties [J]. Lwt-Food Science and Technology, 2006,39(10):1087-1092.
    [18]DONGOWSKI G. Interactions between dietary fibre-rich preparations and glycoconjugated bile acids in vitro [J]. Food Chemistry,2007,104(1):390-397.
    [19]陆红佳,郑龙辉,刘雄.超声波辅助酶结合碱法提取薯渣纤维素的工艺研究[J].食品工业科技,2012,1(6):10-16.
    [20]FOLCH J, LEES M, SLOANE-STANLEY G. A simple method for the isolation and purification of total lipids from animal tissues [J]. Journal of biology Chemistry,1957,226(1):497-509.
    [21]LIU X, OGAWA H, KISHIDA T, et al. The effect of high-amylose cornstarch on lipid metabolism in OVX rats is affected by fructose feeding [J]. Journal of Nutritional Biochemistry, 2010,21(2):89-97.
    [22]张磊,冯媛媛,刘雄等.薛荔籽果胶对去势雌性大鼠矿物质吸收的影响[J].食品科学,2012,33(07):132-137.
    [23]李明泽,苏听峰,彭林等.辣椒素剂量对大鼠肠道发酵产物的影响[J].食品科学,2013,1-7.
    [24]KISHIDA T, NAKAI Y, EBIHARA K. Hydroxypropyl-distarch phosphate from tapioca starch reduces zinc and iron absorption, but not calcium and magnesium absorption, in rats [J]. The Journal of nutrition,2001,131(2):294-300.
    [25]CHANEY A L, MARBACH E P. Modified reagents for determination of urea and ammonia [J]. Clinical chemistry,1962,8(2):130-132.
    [26]中华人民共和国国家标准.GB 11894-89水质总氮的测定[S].国家环境保护局.中国国家标准化管理委员会.2003.
    [27]孙川,刘春霖.膳食纤维:第七大营养素[M].中国民航报.2005.
    [28]CARR T P, WOOD K J, HASSEL C A, et al. Raising intestinal contents viscosity leads to greater excretion of neutral steroids but not bile acids in hamsters and rats [J]. Nutrition Research, 2003,23(1):91-102.
    [29]KRITCHEVSKY D, TEPPER S A. Influence of a fiber mixture on serum and liver lipids and on fecal fat excretion in rats [J]. Nutrition Research,2005,25(5):48548-48549.
    [30]MART N-CARR N N, GO I I, LARRAURI J A, et al. Reduction in serum total and LDL cholesterol concentrations by a dietary fiber and polyphenol-rich grape product in hypercholesterolemic rats [J]. Nutrition Research,1999,19(9):1371-1381.
    [31]SEMBRIES S, DONGOWSKI G, MEHRL NDER K, et al. Dietary fiber-rich colloids from apple pomace extraction juices do not affect food intake and blood serum lipid levels, but enhance fecal excretion of steroids in rats [J]. Journal of Nutritional Biochemistry,2004,15(5):296-302.
    [32]DONGOWSKI G. Interactions between dietary fibre-rich preparations and glycoconjugated bile acids in vitro [J]. Food Chemistry,2007,104(1):390-397.
    [33]KELLEY M J, THOMAS J N, STORY J A. Changes in cholesterol accumulation and steroid-excretion in response to cellulose, alfalfa or oats in cholesterol-fed rats [J]. Nutrition Research,1992,12(4-5):509-518.
    [34]YAMAMOTO Y, TAKAHASHIY, KAWANO M, et al. In vitro digestibility and fermentability of levan and its hypocholesterolemic effects in rats [J]. Journal of Nutritional Biochemistry,1999, 10(1):13-18.
    [35]THONGNGAM M, MCCLEMENTS D J. Isothermal titration calorimetry study of the interactions between chitosan and a bile salt (sodium taurocholate) [J]. Food Hydrocolloids,2005, 19(5):813-819.
    [36]STORY J A, KRITCHEVSKY D. Comparison of binding of various bile-acids and bile-salts invitro by several types of fiber [J]. Journal of Nutrition,1976,106(9):1292-1294.
    [37]唐传核.植物功能性食品[M].化学工业出版社,2004.
    [38]KRITCHEVSKY D, STORY J A. Binding of bile salts in vitro by nonnutritive fiber [J]. The Journal of nutrition,1974,104(4):458-462.
    [1]MIYAZAKI A, KOGA T. Pravastatin sodium, an inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase, decreases serum total cholesterol in Japanese White rabbits by two different mechanisms [J]. Atherosclerosis,2002,162(2):299-306.
    [2]REIHNER E, RUDLING M, STAHLBERG D, et al. Influence of pravastatin, a specific inhibitor of HMG-CoA reductase, on hepatic metabolism of cholesterol [J]. New England Journal of Medicine,1990,323(4):224-228.
    [3]VLAHCEVIC Z R, PANDAK W M, STRAVITZ R T. Regulation of bile acid biosynthesis [J]. Gastroenterology Clinics of North America,1999,28(1):1-7.
    [4]MAKISHIMA M, OKAMOTO A Y, REPA J J, et al. Identification of a nuclear receptor for bile acids [J]. Science,1999,284(5418):1362-1365.
    [5]KOK T, HULZEBOS C V, WOLTERS H, et al. Enterohepatic circulation of bile salts in farnesoid x receptor-deficient mice-Efficient intestinal bile salt absorption in the absence of ileal bile acid-binding protein [J]. Journal of Biological Chemistry,2003,278(43):41930-41937.
    [6]ZHANG L, ZHOU M, FANG G, et al. Hypocholesterolemic effect of capsaicinoids by increased bile acids excretion in ovariectomized rats [J]. Molecular Nutrition & Food Research, 2013,1-9.
    [7]ZHANG L, FANG G, ZHENG L, et al. Hypocholesterolemic effect of capsaicinoids in ovariectomized rats fed cholesterol-free diet was mediated by inhibition of hepatic cholesterol synthesis [J]. Food Funct,2013,1-7.
    [8]FLOCKERZI V. An introduction on TRP channels [M]. FLOCKERZI V, NILIUS B. Handbook of Experimental Pharmacology.2007:1-19.
    [9]郝新忠.辣椒素激活TRPV1预防高盐膳食小鼠高血压的机制研究[D];第三军医大学,2011.
    [10]WONG G Y, GAVVA N R. Therapeutic potential of vanilloid receptor TRPV1 agonists and antagonists as analgesics:Recent advances and setbacks [J]. Brain Research Reviews,2009,60(1): 267-277.
    [11]LUO X-J, PENG J, LI Y-J. Recent advances in the study on capsaicinoids and capsinoids [J]. European Journal of Pharmacology,2011,650(1):1-7.
    [12]YU Q, WANG Y, YU Y, et al. Expression of TRPV1 in rabbits and consuming hot pepper affects its body weight [J]. Molecular Biology Reports,2012,39(7):7583-7589.
    [13]RYCHKOV G Y, BARRITT G J. Expression and Function of TRP Channels in Liver Cells [M]//ISLAM M S. Transient Receptor Potential Channels.2011:667-686.
    [14]SURI A, SZALLASI A. The emerging role of TRPV1 in diabetes and obesity [J]. Trends in Pharmacological Sciences,2008,29(1):29-36.
    [15]田方.辣椒素类似物的生物转化和预防肥胖作用研究[D];河北工业大学,2009.
    [16]袁泉.辣椒素对大鼠营养性肥胖防治作用的研究[D];中南大学,2011.
    [17]杨大春.激活TRPV1改善血管功能和预防高血压的机制研究[D];第三军医大学,2009.
    [18]朱振宇.激活瞬时受体电位香草醛亚家族1改善高脂介导的血管功能异常的机制研究[D];第三军医大学,2012.
    [19]马丽群.激活瞬时受体电位香草醛亚家族1抗动脉粥样硬化机制研究[D];第三军医大学,2010.
    [20]徐兴森.激活TRPV1预防动脉粥样硬化及脑卒中的机制研究[D];第三军医大学,2012.
    [21]LIANG Y T, TIAN X Y, CHEN J N, et al. Capsaicinoids lower plasma cholesterol and improve endothelial function in hamsters [J]. European Journal of Nutrition,2012,1-10.
    [22]TANI Y, FUJIOKA T, SUMIOKA M, et al. Effects of capsinoid on serum and liver lipids in hyperlipidemic rats [J]. Journal of Nutritional Science and Vitaminology,2004,50(5):351-355.
    [23]NEGULESCO J A, NOEL S A, NEWMAN H A I, et al. Effects of pure capsaicinoids (capsaicin and dihydrocapsaicin) on plasma lipid and lipoprotein concentrations of turkey poults [J]. Atherosclerosis,1987,64(2-3):85-90.
    [24]王继,强龙强,李爱琴等.胆汁酸的生理功能及在养殖业上的应用研究进展[J].中国动物保健,2009,1-5.
    [25]KISHIDA T, ISHIKAWA H, TSUKAOKA M, et al. Increase of bile acids synthesis and excretion caused by taurine administration prevents the ovariectomy-induced increase in cholesterol concentrations in the serum low-density lipoprotein fraction of Wistar rats [J]. Journal of Nutritional Biochemistry,2003,14(1):7-16.
    [26]NAMMI S, KIM M S, GAVANDE N S, et al. Regulation of Low-Density Lipoprotein Receptor and 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Expression by Zingiber officinale in the Liver of High-Fat Diet-Fed Rats [J]. Basic & Clinical Pharmacology & Toxicology,2010,106(5): 389-395.
    [27]CHOI H-J, CHUNG M J, HAM S-S. Antiobese and hypocholesterolaemic effects of an Adenophora triphylla extract in HepG2 cells and high fat diet-induced obese mice [J]. Food Chemistry,2010,119(2):437-444.
    [28]姚婕,王继文.低密度脂蛋白受体基因表达调控研究[J].安徽农业科学,2006,34(13):2977-2979.
    [29]KOVANEN P T, BILHEIMER D W, GOLDSTEIN J L, et al. Regulatory role for hepatic low density lipoprotein receptors in vivo in the dog [J]. Proceedings of the National Academy of Sciences of the United States of America-Biological Sciences,1981,78(2):1194-1198.
    [30]SZALLASI A, APPENDINO G. Vanilloid receptor TRPV1 antagonists as the next generation of painkillers. Are we putting the cart before the horse? [J]. ChemInform,2004,35(33):1-5.
    [31]ZHANG L L, LIU D Y, MA L Q, et al. Activation of transient receptor potential vanilloid type-1 channel prevents adipogenesis and obesity [J]. Circulation Research,2007,100(7): 1063-1070.
    [32]MA S T, ZHANG L L, YANG D C, et al. Dietary capsaicin upregulates uncoupling protein 2/3 expression in visceral adipose tissue and enhances acetylcholine-induced hypotensive effect in mice [J]. Progress in Nutrition,2010,12(1):19-23.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700