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柚皮素

維基百科,自由的百科全書
柚皮素
IUPAC名
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one
別名 Naringetol; Salipurol; Salipurpol; 4',5,7-Trihydroxyflavanone
識別
CAS號 480-41-1  checkY
PubChem 439246
ChemSpider 388383
SMILES
 
  • O=C2c3c(O[C@H](c1ccc(O)cc1)C2)cc(O)cc3O
ChEBI 50202
DrugBank DB03467
性質
化學式 C15H12O5
摩爾質量 272.25 g·mol−1
熔點 251 °C(524 K)
溶解性 475 mg/L [1]
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。

柚皮素是一種無味,顏色由白色至淡黃的黃烷酮,是一種類黃酮。它是葡萄柚中的主要黃烷酮,[2]並存在於多種水果與草藥中。 [3]

結構

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柚皮素具有黃烷酮的骨架結構,其4',5和7位碳原子處有三個羥基。柚皮素可以單體存在,亦有糖苷形式即柚皮苷,其具有加入的二糖新橙皮糖與7位碳原子連接而成。

像大多數黃烷酮一樣,柚皮素在碳2上有一個手性中心,儘管光學純度是可變的。 [3] [4] S(-)-柚皮素的外消旋已顯示相當快地發生。 [5]

來源和生物利用度

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柚皮素及其糖苷存在於多種草藥水果中,包括葡萄柚[6]佛手柑[7]酸橙[8]酸櫻桃[9]西紅柿[10] [11]可可[12] [11] [12]希臘牛至[13]水薄荷[14]以及豆類[15]柚皮素與柚皮苷的比例因來源而異,對映體比例也是如此。 [4]

柚皮苷-7-葡萄糖苷形式的生物利用度似乎低於聚乙二醇形式。[16]

服用葡萄柚汁後,柚皮素血漿濃度比服用橙汁更高。 [17]在葡萄柚中還發現了相關的化合物山柰酚,其羥基緊挨著酮基

柚皮素可以從煮熟的番茄醬中吸收。 每10克番茄醬中含有253毫克柚皮素。 [18]

生物合成與代謝

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它衍生自丙二醯基CoA4-香豆醯基CoA 。後者衍生自苯丙氨酸。將所得丁烯酮通過作用於查耳酮合成酶,得到查耳酮。查爾酮隨後經歷閉環,生成柚皮素。 [19]

柚皮素-8-二甲基烯丙基轉移酶使用二甲基烯丙基二磷酸和(−)- (2S)-柚皮素以產生二磷酸和8-戊基柚皮素雅致小克銀漢霉Cunninghamella elegans)是一種哺乳動物新陳代謝的真菌模型生物,它可用於研究柚皮素的硫酸化[20]

潛在的生物學影響

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抗菌,抗真菌和抗病毒

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柚皮素對表皮葡萄球菌,金黃色葡萄球菌枯草芽孢桿菌黃球菌大腸桿菌具有抗菌作用。 [21]進一步的研究增加了對乳酸乳球菌[22]嗜酸乳桿菌內氏放線菌口腔普雷沃菌[22]嗜酸乳桿菌黑色素丙酸桿菌牙齦卟啉單胞菌[23]以及白色念珠菌熱帶克柔念珠菌等抗菌藥物的證據。 [24]儘管沒有證明柚皮苷對微生物的脲酶活性有任何抑制作用,但有證據證明其對幽門螺桿菌具有抗菌作用。 [25]

柚皮素可以減少體外培養的HCV感染的肝細胞病毒的產生。這可能繼發於柚皮素抑制極低密度脂蛋白分泌的作用。 [26]柚皮苷的抗病毒作用目前正在臨床研究中。 [27]關於脊髓灰質炎病毒HSV-1HSV-2的抗病毒作用的報道也已經發表,儘管病毒的複製並未受到抑制。 [28] [29]

抗炎

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儘管有柚皮苷抗炎活性的證據, [30]但已觀察到柚皮苷的抗炎活性很差或根本不存在。 [31] [32]

抗氧化劑

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柚皮素已被證明具有顯著的抗氧化性能。 [33] [34]在體外和動物研究中已證明它可以減少DNA的氧化損傷。 [35] [36]

抗腫瘤

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研究指出,柚皮素在乳腺癌胃癌肝癌宮頸癌胰腺癌結腸組織癌細胞中以及白血病細胞中都可誘導細胞毒性[37]柚皮素抑制人類乳腺癌生長的機制已被證實,在此基礎上提出了兩種柚皮素抗癌的假說。[38][39] 第一種假說是柚皮素抑制芳香化酶,從而減少了腫瘤生長。 [40]第二種假說提出與雌激素受體的互作是其調節腫瘤生長的原因。 [41]柚皮苷的新衍生物多藥耐藥英語multiple drug resistance的癌症具有活性。 [42]

補充閱讀

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參考文獻

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  1. ^ Naringenin. ChemIDplus. (原始內容存檔於2015-12-20). 
  2. ^ Bioavailability of the flavanone naringenin and its glycosides in rats (PDF). Am. J. Physiol. Gastrointest. Liver Physiol. December 2000, 279 (6): G1148–54 [2020-09-29]. PMID 11093936. doi:10.1152/ajpgi.2000.279.6.G1148. (原始內容存檔 (PDF)於2020-11-07). 
  3. ^ 3.0 3.1 Yáñez, Jaime A.; Andrews, Preston K.; Davies, Neal M. Methods of analysis and separation of chiral flavonoids. Journal of Chromatography B. 2007-04-01, 848 (2): 159–181. PMID 17113835. doi:10.1016/j.jchromb.2006.10.052. 
  4. ^ 4.0 4.1 Yáñez, Jaime A.; Remsberg, Connie M.; Miranda, Nicole D.; Vega-Villa, Karina R.; Andrews, Preston K.; Davies, Neal M. Pharmacokinetics of selected chiral flavonoids: hesperetin, naringenin and eriodictyol in rats and their content in fruit juices. Biopharmaceutics & Drug Disposition. 2008-01-01, 29 (2): 63–82. ISSN 1099-081X. PMID 18058792. doi:10.1002/bdd.588 (英語). 
  5. ^ Krause, M.; Galensa, R. Analysis of enantiomeric flavanones in plant extracts by high-performance liquid chromatography on a cellulose triacetate based chiral stationary phase. Chromatographia. 1991-07-01, 32 (1–2): 69–72. ISSN 0009-5893. doi:10.1007/BF02262470 (英語). 
  6. ^ Ho, Ping C; Saville, Dorothy J; Coville, Peter F; Wanwimolruk, Sompon. Content of CYP3A4 inhibitors, naringin, naringenin and bergapten in grapefruit and grapefruit juice products. Pharmaceutica Acta Helvetiae. 2000-04-01, 74 (4): 379–385. PMID 10812937. doi:10.1016/S0031-6865(99)00062-X. 
  7. ^ Gattuso, Giuseppe; Barreca, Davide; Gargiulli, Claudia; Leuzzi, Ugo; Caristi, Corrado. Flavonoid Composition of Citrus Juices. Molecules. 2007-08-03, 12 (8): 1641–1673. PMC 6149096可免費查閱. PMID 17960080. doi:10.3390/12081641 (英語). 
  8. ^ Gel-Moreto, Nuria; Streich, René; Galensa, Rudolf. Chiral separation of diastereomeric flavanone-7-O-glycosides in citrus by capillary electrophoresis. Electrophoresis. 2003-08-01, 24 (15): 2716–2722. ISSN 0173-0835. PMID 12900888. doi:10.1002/elps.200305486. 
  9. ^ Wang, H.; Nair, M. G.; Strasburg, G. M.; Booren, A. M.; Gray, J. I. Antioxidant polyphenols from tart cherries (Prunus cerasus). Journal of Agricultural and Food Chemistry. 1999-03-01, 47 (3): 840–844. ISSN 0021-8561. PMID 10552377. doi:10.1021/jf980936f. 
  10. ^ Minoggio, M.; Bramati, L.; Simonetti, P.; Gardana, C.; Iemoli, L.; Santangelo, E.; Mauri, P. L.; Spigno, P.; Soressi, G. P. Polyphenol pattern and antioxidant activity of different tomato lines and cultivars. Annals of Nutrition & Metabolism. 2003-01-01, 47 (2): 64–69. ISSN 0250-6807. PMID 12652057. doi:10.1159/000069277. 
  11. ^ 11.0 11.1 Vallverdú-Queralt, A; Odriozola-Serrano, I; Oms-Oliu, G; Lamuela-Raventós, RM; Elez-Martínez, P; Martín-Belloso, O. Changes in the polyphenol profile of tomato juices processed by pulsed electric fields. J Agric Food Chem. 2012, 60 (38): 9667–9672. PMID 22957841. doi:10.1021/jf302791k. 
  12. ^ 12.0 12.1 Sánchez-Rabaneda, Ferran; Jáuregui, Olga; Casals, Isidre; Andrés-Lacueva, Cristina; Izquierdo-Pulido, Maria; Lamuela-Raventós, Rosa M. Liquid chromatographic/electrospray ionization tandem mass spectrometric study of the phenolic composition of cocoa (Theobroma cacao). Journal of Mass Spectrometry. 2003-01-01, 38 (1): 35–42. Bibcode:2003JMSp...38...35S. ISSN 1076-5174. PMID 12526004. doi:10.1002/jms.395. 
  13. ^ Exarchou, Vassiliki; Godejohann, Markus; van Beek, Teris A.; Gerothanassis, Ioannis P.; Vervoort, Jacques. LC-UV-Solid-Phase Extraction-NMR-MS Combined with a Cryogenic Flow Probe and Its Application to the Identification of Compounds Present in Greek Oregano. Analytical Chemistry. 2003-11-01, 75 (22): 6288–6294. ISSN 0003-2700. PMID 14616013. doi:10.1021/ac0347819. 
  14. ^ Olsen, Helle T.; Stafford, Gary I.; van Staden, Johannes; Christensen, Søren B.; Jäger, Anna K. Isolation of the MAO-inhibitor naringenin from Mentha aquatica L.. Journal of Ethnopharmacology. 2008-05-22, 117 (3): 500–502. PMID 18372132. doi:10.1016/j.jep.2008.02.015. 
  15. ^ Hungria, M.; Johnston, A. W.; Phillips, D. A. Effects of flavonoids released naturally from bean (Phaseolus vulgaris) on nodD-regulated gene transcription in Rhizobium leguminosarum bv. phaseoli. Molecular Plant-Microbe Interactions. 1992-05-01, 5 (3): 199–203. ISSN 0894-0282. PMID 1421508. doi:10.1094/mpmi-5-199. 
  16. ^ Interactions of the flavonoid naringenin in the gastrointestinal tract and the influence of glycosylation. Biochem. Biophys. Res. Commun. November 1999, 265 (2): 410–5. PMID 10558881. doi:10.1006/bbrc.1999.1695. 
  17. ^ Plasma kinetics and urinary excretion of the flavanones naringenin and hesperetin in humans after ingestion of orange juice and grapefruit juice. J. Nutr. February 2001, 131 (2): 235–41. PMID 11160539. doi:10.1093/jn/131.2.235. 
  18. ^ Naringenin from cooked tomato paste is bioavailable in men. J. Nutr. November 2002, 132 (11): 3349–52. PMID 12421849. doi:10.1093/jn/132.11.3349. 
  19. ^ Wang, Chuanhong; Zhi, Shuang; Liu, Changying; Xu, Fengxiang; Zhao, Aichun; Wang, Xiling; Ren, Yanhong; Li, Zhengang; Yu, Maode. Characterization of Stilbene Synthase Genes in Mulberry (Morus atropurpurea) and Metabolic Engineering for the Production of Resveratrol in Escherichia coli. Journal of Agricultural and Food Chemistry. 2017, 65 (8): 1659–1668. PMID 28168876. doi:10.1021/acs.jafc.6b05212. 
  20. ^ Ibrahim AR. Sulfation of naringenin by Cunninghamella elegans. Phytochemistry. January 2000, 53 (2): 209–12. PMID 10680173. doi:10.1016/S0031-9422(99)00487-2. 
  21. ^ Rauha, Jussi-Pekka; Remes, Susanna; Heinonen, Marina; Hopia, Anu; Kähkönen, Marja; Kujala, Tytti; Pihlaja, Kalevi; Vuorela, Heikki; Vuorela, Pia. Antimicrobial effects of Finnish plant extracts containing flavonoids and other phenolic compounds. International Journal of Food Microbiology. 2000-05-25, 56 (1): 3–12. PMID 10857921. doi:10.1016/S0168-1605(00)00218-X. 
  22. ^ 22.0 22.1 Mandalari, G.; Bennett, R. N.; Bisignano, G.; Trombetta, D.; Saija, A.; Faulds, C. B.; Gasson, M. J.; Narbad, A. Antimicrobial activity of flavonoids extracted from bergamot (Citrus bergamia Risso) peel, a byproduct of the essential oil industry. Journal of Applied Microbiology. 2007-12-01, 103 (6): 2056–2064. ISSN 1364-5072. PMID 18045389. doi:10.1111/j.1365-2672.2007.03456.x. 
  23. ^ Koru, Ozgur; Toksoy, Fulya; Acikel, Cengiz Han; Tunca, Yasar Meric; Baysallar, Mehmet; Uskudar Guclu, Aylin; Akca, Eralp; Ozkok Tuylu, Asli; Sorkun, Kadriye. In vitro antimicrobial activity of propolis samples from different geographical origins against certain oral pathogens. Anaerobe. 2007-06-01, 13 (3–4): 140–145. ISSN 1075-9964. PMID 17475517. doi:10.1016/j.anaerobe.2007.02.001. 
  24. ^ Uzel, Ataç; Sorkun, Kadri˙ye; Önçağ, Özant; Çoğulu, Dilşah; Gençay, Ömür; Sali˙h, Beki˙r. Chemical compositions and antimicrobial activities of four different Anatolian propolis samples. Microbiological Research. 2005-04-25, 160 (2): 189–195. PMID 15881836. doi:10.1016/j.micres.2005.01.002. 
  25. ^ Bae, Eun-Ah; Han, Myung; Kim, Dong-Hyun. In vitroAnti-Helicobacter pylori Activity of Some Flavonoids and Their Metabolites. Planta Medica. 1999, 65 (5): 442–443. PMID 10454900. doi:10.1055/s-2006-960805. 
  26. ^ Apolipoprotein B-dependent hepatitis C virus secretion is inhibited by the grapefruit flavonoid naringenin. Hepatology. May 2008, 47 (5): 1437–45. PMC 4500072可免費查閱. PMID 18393287. doi:10.1002/hep.22197. 
  27. ^ A Pilot Study of the Grapefruit Flavonoid Naringenin for HCV Infection - Full Text View - ClinicalTrials.gov. clinicaltrials.gov. (原始內容存檔於2010-10-01). 
  28. ^ Mucsi, I.; Prágai, B. M. Inhibition of virus multiplication and alteration of cyclic AMP level in cell cultures by flavonoids. Experientia. 1985-07-01, 41 (7): 930–931. ISSN 0014-4754. PMID 2989000. doi:10.1007/BF01970018 (英語). 
  29. ^ Lyu, Su-Yun; Rhim, Jee-Young; Park, Won-Bong. Antiherpetic activities of flavonoids against herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2)in vitro. Archives of Pharmacal Research. 2005-11-01, 28 (11): 1293–1301. ISSN 0253-6269. PMID 16350858. doi:10.1007/BF02978215 (英語). 
  30. ^ Kawaguchi, K.; Kikuchi, S.; Hasunuma, R.; Maruyama, H.; Ryll, R.; Kumazawa, Y. Suppression of Infection-Induced Endotoxin Shock in Mice by aCitrusFlavanone Naringin. Planta Medica. 2004, 70 (1): 17–22. PMID 14765287. doi:10.1055/s-2004-815449. 
  31. ^ Gutiérrez-Venegas, Gloria; Kawasaki-Cárdenas, Perla; Rita Arroyo-Cruz, Santa; Maldonado-Frías, Silvia. Luteolin inhibits lipopolysaccharide actions on human gingival fibroblasts. European Journal of Pharmacology. 2006-07-10, 541 (1–2): 95–105. PMID 16762341. doi:10.1016/j.ejphar.2006.03.069. 
  32. ^ Olszanecki, R.; Gebska, A.; Kozlovski, V. I.; Gryglewski, R. J. Flavonoids and nitric oxide synthase. Journal of Physiology and Pharmacology. 2002-12-01, 53 (4 Pt 1): 571–584. ISSN 0867-5910. PMID 12512693. 
  33. ^ Gorinstein, Shela; Leontowicz, Hanna; Leontowicz, Maria; Krzeminski, Ryszard; Gralak, Mikolaj; Delgado-Licon, Efren; Martinez Ayala, Alma Leticia; Katrich, Elena; Trakhtenberg, Simon. Changes in Plasma Lipid and Antioxidant Activity in Rats as a Result of Naringin and Red Grapefruit Supplementation. Journal of Agricultural and Food Chemistry. 2005-04-01, 53 (8): 3223–3228. ISSN 0021-8561. PMID 15826081. doi:10.1021/jf058014h. 
  34. ^ Yu, Jun; Wang, Limin; Walzem, Rosemary L.; Miller, Edward G.; Pike, Leonard M.; Patil, Bhimanagouda S. Antioxidant Activity of Citrus Limonoids, Flavonoids, and Coumarins. Journal of Agricultural and Food Chemistry. 2005-03-01, 53 (6): 2009–2014. ISSN 0021-8561. PMID 15769128. doi:10.1021/jf0484632. 
  35. ^ Sumit Kumar & Ashu Bhan Tiku. Biochemical and Molecular Mechanisms of Radioprotective Effects of Naringenin, a Phytochemical from Citrus Fruits. J. Agric. Food Chem. 2016, 64 (8): 1676–1685. PMID 26881453. doi:10.1021/acs.jafc.5b05067. 
  36. ^ Chandra Jagetia, Ganesh; Koti Reddy, Tiyyagura; Venkatesha, V. A; Kedlaya, Rajendra. Influence of naringin on ferric iron induced oxidative damage in vitro. Clinica Chimica Acta. 2004-09-01, 347 (1–2): 189–197. PMID 15313158. doi:10.1016/j.cccn.2004.04.022. 
  37. ^ Kanno, Syu-ichi; Tomizawa, Ayako; Hiura, Takako; Osanai, Yuu; Shouji, Ai; Ujibe, Mayuko; Ohtake, Takaharu; Kimura, Katsuhiko; Ishikawa, Masaaki. Inhibitory Effects of Naringenin on Tumor Growth in Human Cancer Cell Lines and Sarcoma S-180-Implanted Mice. Biological and Pharmaceutical Bulletin. 2005-01-01, 28 (3): 527–530. PMID 15744083. doi:10.1248/bpb.28.527. 
  38. ^ So, Felicia V.; Guthrie, Najla; Chambers, Ann F.; Moussa, Madeleine; Carroll, Kenneth K. Inhibition of human breast cancer cell proliferation and delay of mammary tumorigenesis by flavonoids and citrus juices. Nutrition and Cancer. 1996-01-01, 26 (2): 167–181. ISSN 0163-5581. PMID 8875554. doi:10.1080/01635589609514473. 
  39. ^ Hermawan A, Ikawati M, Jenie RI, Khumaira A, Putri H, Nurhayati IP, Angraini SM, Muflikhasari HA. Identification of potential therapeutic target of naringenin in breast cancer stem cells inhibition by bioinformatics and in vitro studies (PDF). Saudi Pharmaceutical Journal. January 2021, 29 (1): 12–26. PMC 7873751可免費查閱. PMID 33603536. doi:10.1016/j.jsps.2020.12.002. (原始內容存檔 (PDF)於2021-10-18). 
  40. ^ van Meeuwen, J. A.; Korthagen, N.; de Jong, P. C.; Piersma, A. H.; van den Berg, M. (Anti)estrogenic effects of phytochemicals on human primary mammary fibroblasts, MCF-7 cells and their co-culture. Toxicology and Applied Pharmacology. 2007-06-15, 221 (3): 372–383. PMID 17482226. doi:10.1016/j.taap.2007.03.016. 
  41. ^ Harmon, Anne W.; Patel, Yashomati M. Naringenin Inhibits Glucose Uptake in MCF-7 Breast Cancer Cells: A Mechanism for Impaired Cellular Proliferation. Breast Cancer Research and Treatment. 2004-05-01, 85 (2): 103–110. ISSN 0167-6806. PMID 15111768. doi:10.1023/B:BREA.0000025397.56192.e2 (英語). 
  42. ^ Ferreira, Ricardo J; Baptista, Rafael; Moreno, Alexis; Madeira, Patricia G; Khonkarn, Ruttiros; Baubichon-Cortay, Hélène; Santos, Daniel JVA dos; Falson, Pierre; Ferreira, Maria-José U. Optimizing the flavanone core toward new selective nitrogen-containing modulators of ABC transporters. Future Medicinal Chemistry. 2018-03-23, 10 (7): 725–741. PMID 29570361. doi:10.4155/fmc-2017-0228 (英語).