跳到主要內容

臺灣博碩士論文加值系統

(216.73.216.106) 您好!臺灣時間:2026/04/04 22:39
字體大小: 字級放大   字級縮小   預設字形  
回查詢結果 :::

詳目顯示

我願授權國圖
: 
twitterline
研究生:張值維
研究生(外文):Chih-Wei Chang
論文名稱:市售草本複合補充品對於高血脂症倉鼠之血脂質、血糖指標及發炎反應的影響
論文名稱(外文):Effects of a Commercial Herbal Complex Supplement on Lipid Profiles, Glycaemic markers, and Inflammation in Hyperlipidaemic Hamsters
指導教授:許美智許美智引用關係
指導教授(外文):Mei-Chich Hsu
學位類別:碩士
校院名稱:高雄醫學大學
系所名稱:運動醫學系碩士班
學門:醫藥衛生學門
學類:復健醫學學類
論文種類:學術論文
論文出版年:2015
畢業學年度:103
語文別:中文
論文頁數:62
中文關鍵詞:膽固醇劑量相關胰島素阻抗性細胞激素
外文關鍵詞:CholesterolDose-dependentInsulin resistanceCytokine
相關次數:
  • 被引用被引用:0
  • 點閱點閱:397
  • 評分評分:
  • 下載下載:0
  • 收藏至我的研究室書目清單書目收藏:0
背景:血脂異常會嚴重地威脅到我們的健康且造成龐大的醫療支出,除了服用藥物,如何預防或尋求整合性療法是目前的研究趨勢,例如補充常見的植物萃取物。目的:使用一個適當的動物模組-黃金敘利亞倉鼠,探討一草本複合補充品 (含有可可、咖啡、綠茶、及山竹,CCGG) 對於調節血脂、血糖指標及促發炎細胞激素之作用。方法:40隻雄性倉鼠隨機分作五組:(1) 正常飲食控制組、(2) 高膽固醇飲食組、(3) 高膽固醇飲食並管餵1倍之CCGG (311 mg/kg/d)、(4) 高膽固醇飲食並管餵2倍之CCGG (622 mg/kg/d)、(5) 高膽固醇飲食並管餵5倍之CCGG (1555 mg/kg/d),在實驗結束後蒐集血清、組織、糞便檢體以便陸續分析。結果:經過六週的實驗,發現CCGG補充劑可顯著地減少血清與肝臟脂肪含量,且有劑量相關之效應。此外,介入後亦增加糞便脂肪量的排出。再者,與血脂異常有關聯的胰島素平衡之指標與促發炎細胞激素之濃度皆有得到明顯地改善。此外,藉由監測血清生化指標與觀察主要臟器之切片,結果發現補充CCGG 6週後並未有毒性產生。結論:CCGG補充品的介入可改善高血脂、胰島素阻抗性、脂肪肝、及發炎反應。

Background: Dyslipidaemia severely threatens health and is associated with exorbitant medical &;#8232;expenses. Instead of taking medicine, integrative therapy by plant extract is the current research trend. Purpose: To understand the synergic beneficial effects of a herbal complex supplement (comprising cocoa, coffee, green tea, and garcinia; CCGG) on regulating lipid profiles, glycaemic markers, and related proinflammatory cytokines by using an appropriate animal model, the golden Syrian hamster. Methods: A total of 40 male hamsters were randomly assigned to five groups: (1) vehicle control, (2) high-cholesterol diet control, (3) high-cholesterol diet of 311 mg/kg/d of CCGG, (4) high-cholesterol diet of 622 mg/kg/d of CCGG, and (5) high-cholesterol diet of 1555 mg/kg/d of CCGG. At the end of an experiment, blood, tissue and faecal samples were collected for further analysis.&;#8232;Results: After 6 wk of treatment, CCGG supplementation significantly reduced serum and hepatic lipid levels with dose-dependent effects. In addition, an increase in excretion of faecal lipids was observed after supplementation. Furthermore, the homeostasis model assessment of insulin resistance index and serum proinflammatory cytokine levels involved in dyslipidaemia was markedly improved. In addition, by monitoring biochemical parameters as well as histopathology of major tissues, no toxic results were observed after 6-week consuming CCGG. Conclusion: Dietary CCGG supplementation may exert potential effects on ameliorating hyperlipidaemia, insulin resistance, liver steatosis, and inflammation.

第一章 緒論 1
第一節 研究背景 1
第二節 研究目的 3
第二章 文獻回顧 4
第一節 血脂異常的分類與定義 4
第二節 血脂異常的生理生化機轉 7
第三節 血脂異常常見的膳食補充劑之使用與治療方式 10
第四節 血脂異常伴隨的發炎反應 15
第五節 補充劑的介紹 17
第六節 動物模式的介紹 22
第三章 材料與方法 23
第一節 飲食及化學材料 23
第二節 實驗動物及處理 25
第三節 血清檢體之生化分析 28
第四節 肝臟脂肪含量 29
第五節 糞便中脂肪含量 29
第六節 臟器組織病理 30
第七節 統計分析 30
第四章 結果與討論 31
第一節 CCGG對體重、臟器重量以及飲食攝取之影響 31
第二節 CCGG對血脂之影響 31
第三節 CCGG對血糖與胰島素阻抗之影響 32
第四節 CCGG對血清促發炎細胞激素之影響 32
第五節 CCGG補充對血清生化指標之影響 33
第六節 CCGG補充對肝臟及糞便脂質含量之影響 33
第七節 CCGG補充對組織切片之影響 34
第五章 討論 35
第一節 CCGG對倉鼠脂肪、醣類指標及重量之影響 35
第二節 CCGG對發炎反應之影響 37
第三節 CCGG之劑量比較 39
第六章 結論 41
參考文獻 42

Fried SK, Bunkin DA, Greenberg AS. Omental and subcutaneous adipose tissues of obese subjects release interleukin-6: depot difference and regulation by glucocorticoid. The Journal of clinical endocrinology and metabolism. 1998;83(3):847-50. doi:10.1210/jcem.83.3.4660.
2.Samad F, Yamamoto K, Pandey M, Loskutoff DJ. Elevated expression of transforming growth factor-beta in adipose tissue from obese mice. Molecular medicine. 1997;3(1):37-48.
3.衛生福利部. 2014. Retrieved from http://www.mohw.gov.tw/cht/DOS/Statistic.aspx?f_list_no=312&;fod_list_no=1601
4.Luo XY, Li NN, Liang YR. Effects of Ilex latifolia and Camellia sinensis on cholesterol and circulating immune complexes in rats fed with a high-cholesterol diet. Phytotherapy research : PTR. 2013;27(1):62-5. doi:10.1002/ptr.4693.
5.Li RW, Douglas TD, Maiyoh GK, Adeli K, Theriault AG. Green tea leaf extract improves lipid and glucose homeostasis in a fructose-fed insulin-resistant hamster model. Journal of ethnopharmacology. 2006;104(1-2):24-31. doi:10.1016/j.jep.2005.08.045.
6.Lin YL, Chang YY, Yang DJ, Tzang BS, Chen YC. Beneficial effects of noni (Morinda citrifolia L.) juice on livers of high-fat dietary hamsters. Food chemistry. 2013;140(1-2):31-8. doi:10.1016/j.foodchem.2013.02.035.
7.Jung UJ, Park YB, Kim SR, Choi MS. Supplementation of persimmon leaf ameliorates hyperglycemia, dyslipidemia and hepatic fat accumulation in type 2 diabetic mice. PloS one. 2012;7(11):e49030. doi:10.1371/journal.pone.0049030.
8.Jan Wollgast, Anklam E. Polyphenols in chocolate: is there a contribution to human health? Food Research International. 2000;33(6):449-59.
9.Celik T, Iyisoy A, Amasyali B. The effects of coffee intake on coronary heart disease: ongoing controversy. International journal of cardiology. 2010;144(1):118. doi:10.1016/j.ijcard.2008.12.112.
10.Sae-tan S, Grove KA, Lambert JD. Weight control and prevention of metabolic syndrome by green tea. Pharmacological research : the official journal of the Italian Pharmacological Society. 2011;64(2):146-54. doi:10.1016/j.phrs.2010.12.013.
11.Pedraza-Chaverri J, Cardenas-Rodriguez N, Orozco-Ibarra M, Perez-Rojas JM. Medicinal properties of mangosteen (Garcinia mangostana). Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2008;46(10):3227-39. doi:10.1016/j.fct.2008.07.024.
12.Gu Y, Yu S, Lambert JD. Dietary cocoa ameliorates obesity-related inflammation in high fat-fed mice. European journal of nutrition. 2014;53(1):149-58. doi:10.1007/s00394-013-0510-1.
13.Jia L, Liu X, Bai YY, Li SH, Sun K, He C et al. Short-term effect of cocoa product consumption on lipid profile: a meta-analysis of randomized controlled trials. The American journal of clinical nutrition. 2010;92(1):218-25. doi:10.3945/ajcn.2009.28202.
14.Kim A, Chiu A, Barone MK, Avino D, Wang F, Coleman CI et al. Green tea catechins decrease total and low-density lipoprotein cholesterol: a systematic review and meta-analysis. Journal of the American Dietetic Association. 2011;111(11):1720-9. doi:10.1016/j.jada.2011.08.009.
15.Zheng XX, Xu YL, Li SH, Liu XX, Hui R, Huang XH. Green tea intake lowers fasting serum total and LDL cholesterol in adults: a meta-analysis of 14 randomized controlled trials. The American journal of clinical nutrition. 2011;94(2):601-10. doi:10.3945/ajcn.110.010926.
16.Adiputro DL, Widodo MA, Romdoni R, Sargowo D. Extract of mangosteen increases high density lipoprotein levels in rats fed high lipid. Universa Medicina. 2013;32(1):37-43.
17.Udani JK, Singh BB, Barrett ML, Singh VJ. Evaluation of Mangosteen juice blend on biomarkers of inflammation in obese subjects: a pilot, dose finding study. Nutrition journal. 2009;8:48. doi:10.1186/1475-2891-8-48.
18.Nistor A, Bulla A, Filip DA, Radu A. The hyperlipidemic hamster as a model of experimental atherosclerosis. Atherosclerosis. 1987;68(1-2):159-73.
19.Dillard A, Matthan NR, Lichtenstein AH. Use of hamster as a model to study diet-induced atherosclerosis. Nutrition &; metabolism. 2010;7:89. doi:10.1186/1743-7075-7-89.
20.Zhang X, Wu C, Wu H, Sheng L, Su Y, Zhang X et al. Anti-hyperlipidemic effects and potential mechanisms of action of the caffeoylquinic acid-rich Pandanus tectorius fruit extract in hamsters fed a high fat-diet. PloS one. 2013;8(4):e61922. doi:10.1371/journal.pone.0061922.
21.Caimari A, del Bas JM, Crescenti A, Arola L. Low doses of grape seed procyanidins reduce adiposity and improve the plasma lipid profile in hamsters. International journal of obesity. 2013;37(4):576-83. doi:10.1038/ijo.2012.75.
22.Yeh TS, Chan KH, Hsu MC, Liu JF. Supplementation with soybean peptides, taurine, Pueraria isoflavone, and ginseng saponin complex improves endurance exercise capacity in humans. Journal of medicinal food. 2011;14(3):219-25. doi:10.1089/jmf.2010.1096.
23.European Association for Cardiovascular Prevention &; Rehabilitation, Reiner Z, Catapano AL, De Backer G, Graham I, Taskinen MR et al. ESC/EAS Guidelines for the management of dyslipidaemias: the Task Force for the management of dyslipidaemias of the European Society of Cardiology (ESC) and the European Atherosclerosis Society (EAS). European heart journal. 2011;32(14):1769-818. doi:10.1093/eurheartj/ehr158.
24.National Institutes of Health. Third Report of the Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III). 2004.
25.行政院衛生署國民健康局. 高血脂肪治手冊 國人血脂異常診療及預防指引. 2003.
26.王文憲. 生物化學要論. 合記圖書出版社; 1995.
27.Wellen KE, Hotamisligil GS. Inflammation, stress, and diabetes. The Journal of clinical investigation. 2005;115(5):1111-9. doi:10.1172/JCI25102.
28.Judith A. Berliner P, Mohamad Navab P, Alan M. Fogelman M, Joy S. Frank P, Linda L. Demer M, PhD; , Peter A. Edwards P et al. Atherosclerosis: Basic Mechanisms. Circulation. 1995(91):2488-96.
29.Hegsted DM. Serum-cholesterol response to dietary cholesterol: a re-evaluation. The American journal of clinical nutrition. 1986;44(2):299-305.
30.Lin DS, Connor WE. The long term effects of dietary cholesterol upon the plasma lipids, lipoproteins, cholesterol absorption, and the sterol balance in man: the demonstration of feedback inhibition of cholesterol biosynthesis and increased bile acid excretion. Journal of lipid research. 1980;21(8):1042-52.
31.Wells B, DiPiro J, Schwinghammer T, DiPiro C. Pharmacotherapy Handbook. 8th ed. The McGraw-Hill Compamies, Inc; 2012.
32.Health WK. UpToDate. 2014.
33.Calder PC. Mechanisms of action of (n-3) fatty acids. The Journal of nutrition. 2012;142(3):592S-9S. doi:10.3945/jn.111.155259.
34.Esteve E, Ricart W, Fernandez-Real JM. Dyslipidemia and inflammation: an evolutionary conserved mechanism. Clinical nutrition. 2005;24(1):16-31. doi:10.1016/j.clnu.2004.08.004.
35.Cinti S, Mitchell G, Barbatelli G, Murano I, Ceresi E, Faloia E et al. Adipocyte death defines macrophage localization and function in adipose tissue of obese mice and humans. Journal of lipid research. 2005;46(11):2347-55. doi:10.1194/jlr.M500294-JLR200.
36.Johnston TP, Li Y, Jamal AS, Stechschulte DJ, Dileepan KN. Poloxamer 407-induced atherosclerosis in mice appears to be due to lipid derangements and not due to its direct effects on endothelial cells and macrophages. Mediators of inflammation. 2003;12(3):147-55. doi:10.1080/0962935031000134860.
37.Deanfield J, Donald A, Ferri C, Giannattasio C, Halcox J, Halligan S et al. Endothelial function and dysfunction. Part I: Methodological issues for assessment in the different vascular beds: a statement by the Working Group on Endothelin and Endothelial Factors of the European Society of Hypertension. Journal of hypertension. 2005;23(1):7-17.
38.Coppack SW. Pro-inflammatory cytokines and adipose tissue. The Proceedings of the Nutrition Society. 2001;60(3):349-56.
39.Moller DE. Potential role of TNF-alpha in the pathogenesis of insulin resistance and type 2 diabetes. Trends in endocrinology and metabolism: TEM. 2000;11(6):212-7.
40.Weisberg SP, McCann D, Desai M, Rosenbaum M, Leibel RL, Ferrante AW, Jr. Obesity is associated with macrophage accumulation in adipose tissue. The Journal of clinical investigation. 2003;112(12):1796-808. doi:10.1172/JCI19246.
41.Hotamisligil GS, Arner P, Caro JF, Atkinson RL, Spiegelman BM. Increased adipose tissue expression of tumor necrosis factor-alpha in human obesity and insulin resistance. The Journal of clinical investigation. 1995;95(5):2409-15. doi:10.1172/JCI117936.
42.Tsigos C, Kyrou I, Chala E, Tsapogas P, Stavridis JC, Raptis SA et al. Circulating tumor necrosis factor alpha concentrations are higher in abdominal versus peripheral obesity. Metabolism: clinical and experimental. 1999;48(10):1332-5.
43.Charriere G, Cousin B, Arnaud E, Andre M, Bacou F, Penicaud L et al. Preadipocyte conversion to macrophage. Evidence of plasticity. The Journal of biological chemistry. 2003;278(11):9850-5. doi:10.1074/jbc.M210811200.
44.Bastard JP, Jardel C, Bruckert E, Blondy P, Capeau J, Laville M et al. Elevated levels of interleukin 6 are reduced in serum and subcutaneous adipose tissue of obese women after weight loss. The Journal of clinical endocrinology and metabolism. 2000;85(9):3338-42. doi:10.1210/jcem.85.9.6839.
45.Andujar I, Recio MC, Giner RM, Rios JL. Cocoa polyphenols and their potential benefits for human health. Oxidative medicine and cellular longevity. 2012;2012:906252. doi:10.1155/2012/906252.
46.Yasuda A, Natsume M, Osakabe N, Kawahata K, Koga J. Cacao polyphenols influence the regulation of apolipoprotein in HepG2 and Caco2 cells. Journal of agricultural and food chemistry. 2011;59(4):1470-6. doi:10.1021/jf103820b.
47.Ramiro E, Franch A, Castellote C, Perez-Cano F, Permanyer J, Izquierdo-Pulido M et al. Flavonoids from Theobroma cacao down-regulate inflammatory mediators. Journal of agricultural and food chemistry. 2005;53(22):8506-11. doi:10.1021/jf0511042.
48.Butt MS, Sultan MT. Coffee and its consumption: benefits and risks. Critical reviews in food science and nutrition. 2011;51(4):363-73. doi:10.1080/10408390903586412.
49.Cornelis MC, El-Sohemy A. Coffee, caffeine, and coronary heart disease. Current opinion in lipidology. 2007;18(1):13-9. doi:10.1097/MOL.0b013e3280127b04.
50.Lopez-Garcia E, van Dam RM, Li TY, Rodriguez-Artalejo F, Hu FB. The relationship of coffee consumption with mortality. Annals of internal medicine. 2008;148(12):904-14.
51.Yamashita K, Yatsuya H, Muramatsu T, Toyoshima H, Murohara T, Tamakoshi K. Association of coffee consumption with serum adiponectin, leptin, inflammation and metabolic markers in Japanese workers: a cross-sectional study. Nutrition &; diabetes. 2012;2:e33. doi:10.1038/nutd.2012.6.
52.Cai L, Ma D, Zhang Y, Liu Z, Wang P. The effect of coffee consumption on serum lipids: a meta-analysis of randomized controlled trials. European journal of clinical nutrition. 2012;66(8):872-7. doi:10.1038/ejcn.2012.68.
53.Franco R, Onatibia-Astibia A, Martinez-Pinilla E. Health benefits of methylxanthines in cacao and chocolate. Nutrients. 2013;5(10):4159-73. doi:10.3390/nu5104159.
54.Inoue H, Kobayashi-Hattori K, Horiuchi Y, Oishi Y, Arai S, Takita T. Regulation of the body fat percentage in developmental-stage rats by methylxanthine derivatives in a high-fat diet. Bioscience, biotechnology, and biochemistry. 2006;70(5):1134-9. doi:10.1271/bbb.70.1134.
55.Panchal SK, Wong WY, Kauter K, Ward LC, Brown L. Caffeine attenuates metabolic syndrome in diet-induced obese rats. Nutrition. 2012;28(10):1055-62. doi:10.1016/j.nut.2012.02.013.
56.Tipoe GL, Leung TM, Hung MW, Fung ML. Green tea polyphenols as an anti-oxidant and anti-inflammatory agent for cardiovascular protection. Cardiovascular &; hematological disorders drug targets. 2007;7(2):135-44.
57.Serisier S, Leray V, Poudroux W, Magot T, Ouguerram K, Nguyen P. Effects of green tea on insulin sensitivity, lipid profile and expression of PPARalpha and PPARgamma and their target genes in obese dogs. The British journal of nutrition. 2008;99(6):1208-16. doi:10.1017/S0007114507862386.
58.Koo SI, Noh SK. Green tea as inhibitor of the intestinal absorption of lipids: potential mechanism for its lipid-lowering effect. The Journal of nutritional biochemistry. 2007;18(3):179-83. doi:10.1016/j.jnutbio.2006.12.005.
59.Bumrungpert A, Kalpravidh RW, Chitchumroonchokchai C, Chuang CC, West T, Kennedy A et al. Xanthones from mangosteen prevent lipopolysaccharide-mediated inflammation and insulin resistance in primary cultures of human adipocytes. The Journal of nutrition. 2009;139(6):1185-91. doi:10.3945/jn.109.106617.
60.Matsuura N, Gamo K, Miyachi H, Iinuma M, Kawada T, Takahashi N et al. gamma-Mangostin from Garcinia mangostana pericarps as a dual agonist that activates Both PPARalpha and PPARdelta. Bioscience, biotechnology, and biochemistry. 2013;77(12):2430-5. doi:10.1271/bbb.130541.
61.Gajda AM, Pellizzon MA, Ricci MR, Ulman EA. Diet-Induced Metabolic Syndrome in Rodent Models. animal LAB NEWS. 2007.
62.Fernandez ML, Wilson TA, Conde K, Vergara-Jimenez M, Nicolosi RJ. Hamsters and guinea pigs differ in their plasma lipoprotein cholesterol distribution when fed diets varying in animal protein, soluble fiber, or cholesterol content. The Journal of nutrition. 1999;129(7):1323-32.
63.Pai-Wen Wu H-YL, Yu-Chi Cheng, Su-Hsiang Tseng, Shu-Chu Su and Lih-Ching Chiueh. Determination of Catechins in Tea Drinks by High Performance Liquid Chromatography. Annual Report of Food and Drug Research. 2011(2):90-6.
64.Syamsudin F, Lestari Rahayu. HPLC analysis and pharmacokinetic study of mangostin after orally administration in rats. International Journal of Pharma and Bio Sciences. 2010;1(1):1-7.
65.Haffner SM, Miettinen H, Stern MP. The homeostasis model in the San Antonio Heart Study. Diabetes care. 1997;20(7):1087-92.
66.Khan N, Monagas M, Andres-Lacueva C, Casas R, Urpi-Sarda M, Lamuela-Raventos RM et al. Regular consumption of cocoa powder with milk increases HDL cholesterol and reduces oxidized LDL levels in subjects at high-risk of cardiovascular disease. Nutrition, metabolism, and cardiovascular diseases : NMCD. 2012;22(12):1046-53. doi:10.1016/j.numecd.2011.02.001.
67.Panchal SK, Poudyal H, Waanders J, Brown L. Coffee extract attenuates changes in cardiovascular and hepatic structure and function without decreasing obesity in high-carbohydrate, high-fat diet-fed male rats. The Journal of nutrition. 2012;142(4):690-7. doi:10.3945/jn.111.153577.
68.Murase T, Yokoi Y, Misawa K, Ominami H, Suzuki Y, Shibuya Y et al. Coffee polyphenols modulate whole-body substrate oxidation and suppress postprandial hyperglycaemia, hyperinsulinaemia and hyperlipidaemia. The British journal of nutrition. 2012;107(12):1757-65. doi:10.1017/S0007114511005083.
69.Abdul-Ghani MA, Tripathy D, DeFronzo RA. Contributions of beta-cell dysfunction and insulin resistance to the pathogenesis of impaired glucose tolerance and impaired fasting glucose. Diabetes care. 2006;29(5):1130-9. doi:10.2337/diacare.2951130.
70.Yamauchi R, Kobayashi M, Matsuda Y, Ojika M, Shigeoka S, Yamamoto Y et al. Coffee and caffeine ameliorate hyperglycemia, fatty liver, and inflammatory adipocytokine expression in spontaneously diabetic KK-Ay mice. Journal of agricultural and food chemistry. 2010;58(9):5597-603. doi:10.1021/jf904062c.
71.Heber D, Zhang Y, Yang J, Ma JE, Henning SM, Li Z. Green tea, black tea, and oolong tea polyphenols reduce visceral fat and inflammation in mice fed high-fat, high-sucrose obesogenic diets. The Journal of nutrition. 2014;144(9):1385-93. doi:10.3945/jn.114.191007.
72.Kumar B, Gupta SK, Nag TC, Srivastava S, Saxena R. Green tea prevents hyperglycemia-induced retinal oxidative stress and inflammation in streptozotocin-induced diabetic rats. Ophthalmic research. 2012;47(2):103-8. doi:10.1159/000330051.
73.Liu SH, Lee LT, Hu NY, Huange KK, Shih YC, Munekazu I et al. Effects of alpha-mangostin on the expression of anti-inflammatory genes in U937 cells. Chinese medicine. 2012;7(1):19. doi:10.1186/1749-8546-7-19.
74.Sampath PD, Vijayaragavan K. Ameliorative prospective of alpha-mangostin, a xanthone derivative from Garcinia mangostana against beta-adrenergic cathecolamine-induced myocardial toxicity and anomalous cardiac TNF-alpha and COX-2 expressions in rats. Experimental and toxicologic pathology : official journal of the Gesellschaft fur Toxikologische Pathologie. 2008;60(4-5):357-64. doi:10.1016/j.etp.2008.02.006.
75.Lee S, Kwak HB. Role of adiponectin in metabolic and cardiovascular disease. Journal of exercise rehabilitation. 2014;10(2):54-9. doi:10.12965/jer.140100.
76.Hotta K, Funahashi T, Arita Y, Takahashi M, Matsuda M, Okamoto Y et al. Plasma concentrations of a novel, adipose-specific protein, adiponectin, in type 2 diabetic patients. Arteriosclerosis, thrombosis, and vascular biology. 2000;20(6):1595-9.
77.Shen CL, Cao JJ, Dagda RY, Chanjaplammootil S, Lu C, Chyu MC et al. Green tea polyphenols benefits body composition and improves bone quality in long-term high-fat diet-induced obese rats. Nutrition research. 2012;32(6):448-57. doi:10.1016/j.nutres.2012.05.001.
78.Larsson SC. Coffee, tea, and cocoa and risk of stroke. Stroke; a journal of cerebral circulation. 2014;45(1):309-14. doi:10.1161/STROKEAHA.113.003131.
79.Soare A, Weiss EP, Holloszy JO, Fontana L. Multiple dietary supplements do not affect metabolic and cardio-vascular health. Aging. 2014;6(2):149-57.
80.Ormsbee MJ, Rawal SR, Baur DA, Kinsey AW, Elam ML, Spicer MT et al. The effects of a multi-ingredient dietary supplement on body composition, adipokines, blood lipids, and metabolic health in overweight and obese men and women: a randomized controlled trial. Journal of the International Society of Sports Nutrition. 2014;11:37. doi:10.1186/1550-2783-11-37.
81.Wong RH, Garg ML, Wood LG, Howe PR. Antihypertensive potential of combined extracts of olive leaf, green coffee bean and beetroot: a randomized, double-blind, placebo-controlled crossover trial. Nutrients. 2014;6(11):4881-94. doi:10.3390/nu6114881.
82.Reagan-Shaw S, Nihal M, Ahmad N. Dose translation from animal to human studies revisited. FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 2008;22(3):659-61. doi:10.1096/fj.07-9574LSF.

QRCODE
 
 
 
 
 
                                                                                                                                                                                                                                                                                                                                                                                                               
第一頁 上一頁 下一頁 最後一頁 top
無相關期刊