• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

五味子木脂素对人肠Caco-2细胞中P-糖蛋白介导的药物外排的影响

Effects of Schisandra lignans on P-glycoprotein-mediated drug efflux in human intestinal Caco-2.

作者信息

Yoo Hye Hyun, Lee Mijin, Lee Min Woo, Lim Sun Young, Shin Jongheon, Kim Dong-Hyun

机构信息

Bioanalysis and Biotransformation Research Center, Korea Institute of Science and Technology, Seoul, Korea.

出版信息

Planta Med. 2007 May;73(5):444-50. doi: 10.1055/s-2007-967178.

DOI:10.1055/s-2007-967178
PMID:17566147
Abstract

Schisandra fruits (Schisandraceae) are often used in traditional medicine and can be taken concomitantly with conventional medicine. In this study, the effects of dibenzocyclooctadiene lignans from Schizandra chinensis on P-gp-mediated efflux were examined to investigate a possible interaction with P-gp substrates. The cellular accumulation of rhodamine-123 in Caco-2 cells was measured with 12 Schisandra lignans. Most compounds resulted in slight or moderate increases of rhodamin-123 cellular uptake, indicating their P-gp inhibitory activity. Among them, deoxyschizandrin exhibited the most potent effect on the accumulation of rhodamine-123. Subsequently, bidirectional transports of digoxin and rhodamine-123 in Caco-2 cells were determined with deoxyschizandrin, the most active compound for the rhodamine-123 assay. In the bidirectional transport study, apical-to-basal (A-to-B) transports of digoxin and rhodamine-123 were increased, whereas basal-to-apical (B-to-A) transports were decreased by deoxyschizandrin in concentration- and time-dependent manners. At 50 microM of deoxyschizandrin, the transport ratios (B-A/A-B) for digoxin and rhodamine-123 were 2.2 and 2.1 compared with the control ratios of 15.2 and 12.2, respectively. These results demonstrated that deoxyschizandrin effectively inhibited the P-gp-mediated efflux in Caco-2 cells, suggesting they could potentially increase the absorption of drugs that can act as a P-gp substrate.

摘要

五味子果实(五味子科)常用于传统医学,并且可以与传统药物同时服用。在本研究中,检测了五味子中双苯并环辛二烯木脂素对P-糖蛋白介导的外排作用,以研究其与P-糖蛋白底物之间可能存在的相互作用。用12种五味子木脂素测定了罗丹明-123在Caco-2细胞中的细胞蓄积量。大多数化合物导致罗丹明-123细胞摄取量略有或中度增加,表明它们具有P-糖蛋白抑制活性。其中,脱氧五味子素对罗丹明-123的蓄积表现出最强的作用。随后,用脱氧五味子素(罗丹明-123测定中活性最强的化合物)测定了地高辛和罗丹明-123在Caco-2细胞中的双向转运。在双向转运研究中,脱氧五味子素以浓度和时间依赖性方式增加了地高辛和罗丹明-123从顶侧向基底(A到B)的转运,而减少了从基底侧向顶侧(B到A)的转运。在50微摩尔的脱氧五味子素作用下,地高辛和罗丹明-123的转运比(B-A/A-B)分别为2.2和2.1,而对照比分别为15.2和12.2。这些结果表明,脱氧五味子素有效地抑制了Caco-2细胞中P-糖蛋白介导的外排,提示它们可能会增加作为P-糖蛋白底物的药物的吸收。

相似文献

1
Effects of Schisandra lignans on P-glycoprotein-mediated drug efflux in human intestinal Caco-2.五味子木脂素对人肠Caco-2细胞中P-糖蛋白介导的药物外排的影响
Planta Med. 2007 May;73(5):444-50. doi: 10.1055/s-2007-967178.
2
Effects of diosmin, a flavonoid glycoside in citrus fruits, on P-glycoprotein-mediated drug efflux in human intestinal Caco-2 cells.柑橘类水果中的黄酮糖苷地奥司明对人肠Caco-2细胞中P-糖蛋白介导的药物外排的影响。
J Agric Food Chem. 2007 Sep 5;55(18):7620-5. doi: 10.1021/jf070893f. Epub 2007 Aug 4.
3
In vitro to in vivo evidence of the inhibitor characteristics of Schisandra lignans toward P-glycoprotein.五味子木脂素对 P 糖蛋白的体外到体内抑制特性的证据。
Phytomedicine. 2013 Aug 15;20(11):1030-8. doi: 10.1016/j.phymed.2013.04.005. Epub 2013 Jun 2.
4
Gomisin A alters substrate interaction and reverses P-glycoprotein-mediated multidrug resistance in HepG2-DR cells.五味子酯甲改变底物相互作用并逆转HepG2-DR细胞中P-糖蛋白介导的多药耐药性。
Biochem Pharmacol. 2006 Sep 28;72(7):824-37. doi: 10.1016/j.bcp.2006.06.036. Epub 2006 Aug 4.
5
Identification of key structural characteristics of Schisandra chinensis lignans involved in P-glycoprotein inhibition.鉴定五味子木脂素类化合物中涉及 P-糖蛋白抑制的关键结构特征。
J Nat Prod. 2014 Oct 24;77(10):2255-63. doi: 10.1021/np500521v. Epub 2014 Oct 10.
6
Schisandrene, a dibenzocyclooctadiene lignan from Schisandra chinensis: structure-antioxidant activity relationships of dibenzocyclooctadiene lignans.五味子烯,一种来自五味子的二苯并环辛二烯木脂素:二苯并环辛二烯木脂素的结构-抗氧化活性关系
J Nat Prod. 2006 Mar;69(3):356-9. doi: 10.1021/np0503707.
7
Schisandrol A from Schisandra chinensis reverses P-glycoprotein-mediated multidrug resistance by affecting Pgp-substrate complexes.五味子中的五味子醇甲通过影响P-糖蛋白-底物复合物逆转P-糖蛋白介导的多药耐药性。
Planta Med. 2007 Mar;73(3):212-20. doi: 10.1055/s-2007-967120. Epub 2007 Feb 22.
8
Fatty acid synthase inhibitory activity of dibenzocyclooctadiene lignans isolated from Schisandra chinensis.从五味子中分离得到的二苯并环辛二烯木脂素对脂肪酸合酶的抑制活性。
Phytother Res. 2010 Jun;24 Suppl 2:S225-8. doi: 10.1002/ptr.3149.
9
Molecular mechanism of apoptosis induced by schizandrae-derived lignans in human leukemia HL-60 cells.五味子木脂素诱导人白血病HL-60细胞凋亡的分子机制
Food Chem Toxicol. 2008 Feb;46(2):590-7. doi: 10.1016/j.fct.2007.08.048. Epub 2007 Sep 14.
10
Growth inhibition and cell cycle arrest in the G0/G1 by schizandrin, a dibenzocyclooctadiene lignan isolated from Schisandra chinensis, on T47D human breast cancer cells.五味子丙素,从五味子属植物中分离得到的二苯并环辛烯木脂素,对 T47D 人乳腺癌细胞在 G0/G1 期的生长抑制和细胞周期阻滞。
Phytother Res. 2010 Feb;24(2):193-7. doi: 10.1002/ptr.2907.

引用本文的文献

1
A comprehensive review of Schisandra chinensis lignans: pharmacokinetics, pharmacological mechanisms, and future prospects in disease prevention and treatment.五味子木脂素的综合综述:药代动力学、药理机制及疾病防治的未来前景
Chin Med. 2025 Apr 9;20(1):47. doi: 10.1186/s13020-025-01096-z.
2
A Comprehensive Review of the Main Lignan Components of Schisandra chinensis (North Wu Wei Zi) and Schisandra sphenanthera (South Wu Wei Zi) and the Lignan-Induced Drug-Drug Interactions Based on the Inhibition of Cytochrome P450 and P-Glycoprotein Activities.基于细胞色素P450和P-糖蛋白活性抑制作用的五味子(北五味子)和华中五味子(南五味子)主要木脂素成分及木脂素诱导的药物相互作用的综合综述
Front Pharmacol. 2022 Mar 11;13:816036. doi: 10.3389/fphar.2022.816036. eCollection 2022.
3
Plant Adaptogens-History and Future Perspectives.植物适应原——历史与未来展望。
Nutrients. 2021 Aug 20;13(8):2861. doi: 10.3390/nu13082861.
4
Wuzhi capsule increased systemic exposure to methotrexate by inhibiting the expression of OAT1/3 and P-gp.乌脂胶囊通过抑制OAT1/3和P-糖蛋白的表达增加了甲氨蝶呤的全身暴露量。
Ann Transl Med. 2021 May;9(10):845. doi: 10.21037/atm-21-1303.
5
Phytochemicals: Potential Lead Molecules for MDR Reversal.植物化学物质:多药耐药逆转的潜在先导分子
Front Pharmacol. 2020 Jun 19;11:832. doi: 10.3389/fphar.2020.00832. eCollection 2020.
6
Potential for pharmacokinetic interactions between Schisandra sphenanthera and bosutinib, but not imatinib: in vitro metabolism study combined with a physiologically-based pharmacokinetic modelling approach.五味子与博舒替尼之间存在药代动力学相互作用的可能性,但与伊马替尼不存在:体外代谢研究结合基于生理学的药代动力学建模方法。
Br J Clin Pharmacol. 2020 Oct;86(10):2080-2094. doi: 10.1111/bcp.14303. Epub 2020 May 13.
7
Pharmacokinetic Comparison of 20(R)- and 20(S)-Ginsenoside Rh1 and 20(R)- and 20(S)-Ginsenoside Rg3 in Rat Plasma following Oral Administration of Radix Ginseng Rubra and Sheng-Mai-San Extracts.口服红参和生脉散提取物后大鼠血浆中20(R)-和20(S)-人参皂苷Rh1以及20(R)-和20(S)-人参皂苷Rg3的药代动力学比较
Evid Based Complement Alternat Med. 2017;2017:6451963. doi: 10.1155/2017/6451963. Epub 2017 May 23.
8
Extraction and Separation of Active Ingredients in Schisandra chinensis (Turcz.) Baill and the Study of their Antifungal Effects.五味子有效成分的提取分离及其抗真菌作用研究
PLoS One. 2016 May 6;11(5):e0154731. doi: 10.1371/journal.pone.0154731. eCollection 2016.
9
Schisandra chinensis regulates drug metabolizing enzymes and drug transporters via activation of Nrf2-mediated signaling pathway.五味子通过激活Nrf2介导的信号通路来调节药物代谢酶和药物转运体。
Drug Des Devel Ther. 2014 Dec 17;9:127-46. doi: 10.2147/DDDT.S68501. eCollection 2015.
10
Pharmacokinetic compatibility of ginsenosides and Schisandra Lignans in Shengmai-san: from the perspective of p-glycoprotein.生脉散中人参皂苷与五味子木脂素的药代动力学相容性:从P-糖蛋白角度探讨
PLoS One. 2014 Jun 12;9(6):e98717. doi: 10.1371/journal.pone.0098717. eCollection 2014.