Skip navigation

DSpace

機構典藏 DSpace 系統致力於保存各式數位資料(如:文字、圖片、PDF)並使其易於取用。

點此認識 DSpace
DSpace logo
English
中文
  • 瀏覽論文
    • 校院系所
    • 出版年
    • 作者
    • 標題
    • 關鍵字
    • 指導教授
  • 搜尋 TDR
  • 授權 Q&A
    • 我的頁面
    • 接受 E-mail 通知
    • 編輯個人資料
  1. NTU Theses and Dissertations Repository
  2. 公共衛生學院
  3. 環境衛生研究所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/54881
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor吳焜裕(Kuen-Yuh Wu)
dc.contributor.authorTai-Ying Longen
dc.contributor.author龍泰穎zh_TW
dc.date.accessioned2021-06-16T03:40:35Z-
dc.date.available2020-03-12
dc.date.copyright2015-03-12
dc.date.issued2015
dc.date.submitted2015-02-13
dc.identifier.citation1. Smith, C., et al., “IARC group 2A Carcinogens” reported in cigarette mainstream smoke. Food and Chemical Toxicology, 2000. 38(4): p. 371-383.
2. Bergmark, E., Hemoglobin adducts of acrylamide and acrylonitrile in laboratory workers, smokers and nonsmokers. Chemical research in toxicology, 1997. 10(1): p. 78-84.
3. Tareke, E., et al., Analysis of acrylamide, a carcinogen formed in heated foodstuffs. Journal of agricultural and food chemistry, 2002. 50(17): p. 4998-5006.
4. Mottram, D.S., B.L. Wedzicha, and A.T. Dodson, Acrylamide is formed in the Maillard reaction. Nature, 2002. 419(6906): p. 448-9.
5. Stadler, R.H., et al., Food chemistry: acrylamide from Maillard reaction products. Nature, 2002. 419(6906): p. 449-450.
6. JECFA, Summary report of the seventy-second meetong of JECFA. 2010, JOINT FAO/WHO EXPERT COMITTEE ON FOOD ADDITIVES: Rome.
7. LoPachin, R., C. Balaban, and J. Ross, Acrylamide axonopathy revisited. Toxicology and applied pharmacology, 2003. 188(3): p. 135-153.
8. Calleman, C., et al., Relationships between biomarkers of exposure and neurological effects in a group of workers exposed to acrylamide. Toxicology and applied pharmacology, 1994. 126(2): p. 361-371.
9. Dearfield, K.L., et al., Acrylamide: a review of its genotoxicity and an assessment of heritable genetic risk. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 1995. 330(1): p. 71-99.
10. Johnson, K.A., et al., Chronic toxicity and oncogenicity study on acrylamide incorporated in the drinking water of Fischer 344 rats. Toxicology and applied pharmacology, 1986. 85(2): p. 154-168.
11. Friedman, M.A., L.H. Dulak, and M.A. Stedham, A lifetime oncogenicity study in rats with acrylamide. Toxicological Sciences, 1995. 27(1): p. 95-105.
12. Mucci, L., et al., Dietary acrylamide and cancer of the large bowel, kidney, and bladder: absence of an association in a population-based study in Sweden. British Journal of Cancer, 2003. 88(1): p. 84-89.
13. Pelucchi, C., et al., Fried potatoes and human cancer. International Journal of Cancer, 2003. 105(4): p. 558-560.
14. IARC, Acrylamide. Monographs on the evaluation of carcinogen risk to humans. Lyon, France. 1994, International Agency for Research on Cancer. p. 389-433.
15. Baum, M., et al., Acrylamide and glycidamide: approach towards risk assessment based on biomarker guided dosimetry of genotoxic/mutagenic effects in human blood, in Chemistry and Safety of Acrylamide in Food. 2005, Springer. p. 77-88.
16. Puppel, N., et al., DNA strand breaking capacity of acrylamide and glycidamide in mammalian cells. Mutation Research/Genetic Toxicology and Environmental Mutagenesis, 2005. 580(1): p. 71-80.
17. Thielen, S., et al., Genotoxicity of glycidamide in comparison to (±)‐anti‐benzo [a] pyrene‐7, 8‐dihydrodiol‐9, 10‐epoxide and α‐acetoxy‐N‐nitroso‐diethanolamine in human blood and in mammalian V79‐cells. Molecular nutrition & food research, 2006. 50(4‐5): p. 430-436.
18. Sumner, S.C., et al., Role of cytochrome P450 2E1 in the metabolism of acrylamide and acrylonitrile in mice. Chemical research in toxicology, 1999. 12(11): p. 1110-1116.
19. Doerge, D.R., et al., DNA adducts derived from administration of acrylamide and glycidamide to mice and rats. Mutation Research/Genetic Toxicology and Environmental Mutagenesis, 2005. 580(1): p. 131-141.
20. Gamboa da Costa, G., et al., DNA adduct formation from acrylamide via conversion to glycidamide in adult and neonatal mice. Chemical research in toxicology, 2003. 16(10): p. 1328-1337.
21. Maniere, I., et al., DNA damage and DNA adduct formation in rat tissues following oral administration of acrylamide. Mutation Research/Genetic Toxicology and Environmental Mutagenesis, 2005. 580(1): p. 119-129.
22. Sumner, S.C., J.P. MacNeela, and T.R. Fennell, Characterization and quantitation of urinary metabolites of [1, 2, 3-13C] acrylamide in rats and mice using carbon-13 nuclear magnetic resonance spectroscopy. Chemical research in toxicology, 1992. 5(1): p. 81-89.
23. Dixit, R., et al., Interaction of acrylamide with bovine serum albumin. Environmental research, 1986. 40(2): p. 365-371.
24. Tong, G.C., W.K. Cornwell, and G.E. Means, Reactions of acrylamide with glutathione and serum albumin. Toxicology letters, 2004. 147(2): p. 127-131.
25. Fuhr, U., et al., Toxicokinetics of acrylamide in humans after ingestion of a defined dose in a test meal to improve risk assessment for acrylamide carcinogenicity. Cancer Epidemiology Biomarkers & Prevention, 2006. 15(2): p. 266-271.
26. Boettcher, M.I., et al., Excretion of mercapturic acids of acrylamide and glycidamide in human urine after single oral administration of deuterium-labelled acrylamide. Archives of toxicology, 2006. 80(2): p. 55-61.
27. Berger, F.I., et al., Biological effects of acrylamide after daily ingestion of various foods in comparison to water: a study in rats. Molecular nutrition & food research, 2011. 55(3): p. 387-399.
28. Watzek, N., et al., N 7-Glycidamide-Guanine DNA Adduct Formation by Orally Ingested Acrylamide in Rats: A Dose–Response Study Encompassing Human Diet-Related Exposure Levels. Chemical research in toxicology, 2012. 25(2): p. 381-390.
29. Watzek, N., et al., Toxicokinetics of acrylamide in primary rat hepatocytes: coupling to glutathione is faster than conversion to glycidamide. Archives of toxicology, 2013. 87(8): p. 1545-1556.
30. Kurebayashi, H. and Y. Ohno, Metabolism of acrylamide to glycidamide and their cytotoxicity in isolated rat hepatocytes: protective effects of GSH precursors. Archives of toxicology, 2006. 80(12): p. 820-828.
31. Luo, Y.-S., In vivo Monitoring Metabolite profiles of Acrylamide, in Institute of Occupational Medicine and Industrial Hygiene. 2012, National Taiwan University: Taipei, Taiwan.
32. Probst, R.J., et al., Gender differences in the blood volume of conscious Sprague-Dawley rats. Journal of the American Association for Laboratory Animal Science: JAALAS, 2006. 45(2): p. 49.
33. Doerge, D.R., et al., Toxicokinetics of acrylamide and glycidamide in Fischer 344 rats. Toxicology and applied pharmacology, 2005. 208(3): p. 199-209.
34. Hales, B.F. and A.H. Neims, A sex difference in hepatic glutathione S-transferase B and the effect of hypophysectomy. Biochem. j, 1976. 160: p. 223-229.
35. Staffas, L., et al., Further characterization of hormonal regulation of glutathione transferase in rat liver and adrenal glands. Sex differences and demonstration that growth hormone regulates the hepatic levels. Biochem. J, 1992. 286: p. 65-72.
36. Barber, D., et al., Metabolism, toxicokinetics and hemoglobin adduct formation in rats following subacute and subchronic acrylamide dosing. Neurotoxicology, 2001. 22(3): p. 341-353.
37. Sumner, S.C., et al., Acrylamide: a comparison of metabolism and hemoglobin adducts in rodents following dermal, intraperitoneal, oral, or inhalation exposure. Toxicological Sciences, 2003. 75(2): p. 260-270.
38. Fennell, T.R., et al., Kinetics of elimination of urinary metabolites of acrylamide in humans. Toxicological Sciences, 2006. 93(2): p. 256-267.
39. Doerge, D.R., et al., Toxicokinetics of acrylamide and glycidamide in B6C3F< sub> 1</sub> mice. Toxicology and applied pharmacology, 2005. 202(3): p. 258-267.
40. Twaddle, N.C., et al., Determination of acrylamide and glycidamide serum toxicokinetics in B6C3F< sub> 1</sub> mice using LC–ES/MS/MS. Cancer letters, 2004. 207(1): p. 9-17.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/54881-
dc.description.abstract丙烯醯胺(Acrylamide)為廣泛應用的工業用化合物。近年來發現丙烯醯胺普遍存在於高溫油炸食品中,因而在食品安全議題上受到重視。過去研究指出,丙烯醯胺的潛在致癌性主要來自於中間代謝物環氧丙醯胺(glycidamide),而丙烯醯胺與環氧丙醯胺可以與體內廣泛分布的谷胱甘肽(glutathione, GSH)結合而降低其毒性。本研究的目的在於建立固相萃取前處理法與電灑離子化搭配液相層析串聯質譜儀分析方法,以此方法去分析Sprague-Dawley大鼠血液樣本中經由Phase-II reactions的三種丙烯醯胺-谷胱甘肽加合物(GSH conjugates),分別為AAGSH、GA2GSH和GA3GSH,藉由WinNonlin模型軟體分析此三種加合物來了解其毒物動力學資料,其數據可用來提供研究物種間代謝機制差異,以評估丙烯醯胺對於人體的致癌性。本研究經由腹腔注射法,分別給予雄性、雌性大鼠0.1 mg/kg-wt、1.0 mg/kg-wt及5.0 mg/kg-wt的丙烯醯胺。本研究在低劑量0.1 mg/kg-wt下沒有偵測出GA2GSH,除此之外皆有測到AAGSH、GA2GSH和GA3GSH。曲線下面積(AUC, Area under the curve)、代謝速率常數(keli)以及半衰期(T1/2)等毒物動力學參數經由Win-Nonlin模型軟體計算出來。AAGSH、GA2GSH和GA3GSH曲線下面積(AUC)相對於AA給藥劑量的比率分別為0.97-1.78 %、0.03-0.07%和0.17-0.25%。∑ [GAGSH/AAGSH] 比率為0.13-0.18。從GA3GSH曲線下面積大於GA2GSH曲線下面積來看,可以證實谷胱甘肽與環氧丙烯胺上較少取代基的碳容易產生鑑結。本研究的動力學數據除了進一步了解丙烯醯胺的代謝機制外,能夠對於致癌性風險評估上有所幫助。zh_TW
dc.description.abstractAcrylamide (AA) is a widely-used industrial chemical. For the past few years, AA was found in high-temperature fried food, so the food safety has been concerned. According to previous researches, the potential carcinogensis of AA mainly come from its metabolite: glycidamide (GA), which can be reacted with glutathione and further decreased the toxicity. The study is aimed to develop a solid phase extraction (SPE) pretreatment with LC-ESI-MS/MS method. With this analytical method, we can quantify the GSH conjugates (AAGSH, GA2GSH, and GA3GSH) through Phase-II reactions in the blood of Sprague-Dawley rats. The male/female Sprague-Dawley rats were treated with AA of 0.1 mg/kg-wt, 1.0 mg/kg-wt, and 5.0 mg/kg-wt by intraperitoneal injection, respectively (N=5). The toxicokinetic parameters including AUC0-∞, elimination rate constant (keli), and half life (T1/2) were calculated by Win-Nonlin modeling software. Although the concentration of GA2GSH were not detected from the SD rat dosed 0.1 mg/kg-wt AA, Molar percentage for AAGSH, GA2GSH, and GA3GSH of dosing AA accounted for 0.97-1.78 %, 0.03-0.07 %, and 0.17-0.25 %, respectively. Overall, ratio of ∑GAGSH/AAGSH amount excreted were 013-0.18.Based on AUC0-∞, glycidamide were preferred to conjugate with glutathione as GA3GSH than GA2GSH because of attacking least substituted carbon on GA.
This results could be provided for the species differences of AA metabolism and the risk assessments of its carcinogenicity.
en
dc.description.provenanceMade available in DSpace on 2021-06-16T03:40:35Z (GMT). No. of bitstreams: 1
ntu-104-R00844010-1.pdf: 2349073 bytes, checksum: b9abe375dd584ae607e3471c489420d1 (MD5)
Previous issue date: 2015
en
dc.description.tableofcontentsAcknowledgement i
摘要 ii
ABSTRACT iv
CONTENTS v
LIST OF FIGURES vi
LIST OF TABLES viii
Chapter 1 Introduction 1
1.1 Acrylamide and Glycidamide 1
1.2 Glutathione Conjugates and Mercapturic Acid Conjugates of Acrylamide 2
1.3 Study design 4
1.4 Rationale 4
Chapter 2 Methods and Materials 6
2.1 Reagents 6
2.2 Method Development 7
2.3 Animal Study 13
Chapter 3 Results and Discussions 18
3.1 Method Development 18
3.2 Animal Study 23
Chapter 4 Conclusions and Recommendations 28
References 29
Tables 32
Figures 41
dc.language.isoen
dc.subject毒物動力學zh_TW
dc.subject谷胱甘?zh_TW
dc.subject丙烯醯胺zh_TW
dc.subject固相萃取前處理法zh_TW
dc.subject液相層析-三段四極柱質譜儀zh_TW
dc.subjectAcrylamideen
dc.subjectSolid phase extractionen
dc.subjectLC-MS/MSen
dc.subjectToxicokineticsen
dc.subjectGlutathioneen
dc.title丙烯醯胺、環氧丙醯胺及其谷胱甘肽加合物於Sprague-Dawley大鼠之毒物動力學研究zh_TW
dc.titleToxicokinetics of Acrylamide, Glycidamide, and Their GSH Conjugates in Sprague-Dawley Ratsen
dc.typeThesis
dc.date.schoolyear103-1
dc.description.degree碩士
dc.contributor.coadvisor蔡詩偉
dc.contributor.oralexamcommittee蔡東湖,江素瑛
dc.subject.keyword丙烯醯胺,谷胱甘?,毒物動力學,液相層析-三段四極柱質譜儀,固相萃取前處理法,zh_TW
dc.subject.keywordAcrylamide,Glutathione,Toxicokinetics,LC-MS/MS,Solid phase extraction,en
dc.relation.page60
dc.rights.note有償授權
dc.date.accepted2015-02-13
dc.contributor.author-college公共衛生學院zh_TW
dc.contributor.author-dept環境衛生研究所zh_TW
顯示於系所單位:環境衛生研究所

文件中的檔案:
檔案 大小格式 
ntu-104-1.pdf
  未授權公開取用
2.29 MBAdobe PDF
顯示文件簡單紀錄


系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。

社群連結
聯絡資訊
10617臺北市大安區羅斯福路四段1號
No.1 Sec.4, Roosevelt Rd., Taipei, Taiwan, R.O.C. 106
Tel: (02)33662353
Email: ntuetds@ntu.edu.tw
意見箱
相關連結
館藏目錄
國內圖書館整合查詢 MetaCat
臺大學術典藏 NTU Scholars
臺大圖書館數位典藏館
本站聲明
© NTU Library All Rights Reserved