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肠道菌群对菊花提取物的代谢作用 被引量:19

Metabolism of Chrysanthemum morifolium extracts in intestinal flora
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摘要 目的观察和比较人、大鼠、B eag le犬及家兔肠道菌群对菊花提取物(Chry santhem um m orif olium ex tracts,CM E)的代谢作用。方法采用人、大鼠、B eag le犬及家兔的新鲜粪便37℃厌氧培养,经醋酸乙酯提取后采用RP-HPLC及LC-M S方法对代谢成分进行分离和定性、定量分析。结果CM E容易被肠道菌群代谢,0.5 h后样本中能检测出较高浓度代谢物;经LC-M S检测,主要的代谢物为木犀草素和芹菜素;随着代谢时间的延长,两者均出现降解代谢的现象,24 h后几乎检测不到这两种代谢物;且人、大鼠和B eag le犬肠道菌群对CM E的代谢较快,而家兔肠道菌群对CM E的代谢过程比较平缓。结论在离体条件下,CM E可以被人、大鼠、B eag le犬及家兔的肠道菌群代谢,主要的代谢物为木犀草素和芹菜素。 Objective To study and compare the metabolism of Chrysanthemum morifolium extracts (CME) in vitro intestinal flora from human, rat, Beagle dog, and rabbit. Methods Intestinal flora of human, rat, Beagle dog, and rabbit and CME were anaerobically cultured at 37℃ in vitro. After being extracted by acetic ether, the main metabolites of CME were separated and quantified by HPLC. Results In vitro, CME was easily metabolized by the intestinal flora and the main metabolites in incubation medium were determined in high concentration after 0.5 h. By LC-MS, luteolin and apigenin were identified, respectively; both metabolites were degraded with prolongation of incubation time and the concentrations of luteolin and apigenin were low after 24 h; moreover, CME was quickly metabolized by human, rat, Beagle dog intestinal flora, and gently by rabbit intesinal flora. Conclusion In vitro, CME is easily metabolized by intestinal flora human, rat, Beagle dog, and rabbit and the main metabolites are luteolin and apigenin.
出处 《中草药》 CAS CSCD 北大核心 2006年第7期1001-1004,共4页 Chinese Traditional and Herbal Drugs
基金 浙江省自然科学基金(Y204379) 浙江省中药现代化专项资助(G20050066)
关键词 菊花提取物 木犀草素 芹菜素 肠道菌群代谢 高效液相色谱 Chrysanthemum morifolium Ramat. extracts (CME) luteolin apigenin intestinal flora metabolism HPLC
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  • 1戴敏,刘青云,李道中,刘丽.菊花解热、降压作用的物质基础研究[J].中药材,2001,24(7):505-506. 被引量:74
  • 2胡春,丁霄霖.菊花提取物对人红细胞膜的保护作用研究[J].食品科学,1996,17(2):7-12. 被引量:24
  • 3汪民海.安徽产三种菊花总黄酮量的比色测定[J].基层中药杂志,1997,11(2):37-38. 被引量:24
  • 4江苏新医学院.中药大辞典(下册)[M].上海:上海人民出版社,1997.1496.
  • 5.中国药典2000年版[S]:一部[M].,2000.253~254.
  • 6江苏新医学学院,中药大辞典.下,1997年
  • 7Shekher A, Singh M. Role of Eicosanoid inhibition of ischemia reperfusion injury: intact and isolated rat heart studies[J]. Methods Find Exp Clin Pharmacol, 1997, 19(4): 223-239.
  • 8Post JM, Gelband CH, Hume JR. [Ca2+]i inhibition of K+ channels in canine pulmonary artery. Novel mechanism for hypoxia-induced membrane depolarization[J]. Circ Res, 1995, 77(1): 131-139.
  • 9Zhuang J, Zhou Z. Protective effects of intermittent hypoxia adaptation on myocardium and its mechanism[J]. Biol Signals Recept, 1999, 8(4-5): 316-322.
  • 10Okabe E, Odajima C, Taga R, et al. The effect of oxygen free radicals on calcium permeability and calcium loading at steady state in cardiac sarcoplasmic reticulum[J]. Mol Pharmacol, 1988, 34(3): 388-394.

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