• 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

克罗恩病与 CYP3A4 和 P-糖蛋白蛋白表达降低有关。

Crohn's Disease Is Associated with Decreased CYP3A4 and P-Glycoprotein Protein Expression.

出版信息

Mol Pharm. 2019 Sep 3;16(9):4059-4064. doi: 10.1021/acs.molpharmaceut.9b00459. Epub 2019 Aug 19.

DOI:10.1021/acs.molpharmaceut.9b00459
PMID:31393129
Abstract

Cytochrome P450 (CYP) 3A4 and P-glycoprotein (P-gp) have broad substrate overlap and are involved in the metabolism and transport of nearly 50% of currently prescribed medications. In the intestine, CYP3A4 and P-gp are coexpressed in the enterocytes at the intestinal villous tip and act in a coordinated manner to limit drug and xenobiotic oral bioavailability prior to further metabolism and disposition in the liver. Crohn's disease (CD), a form of inflammatory bowel disease, introduces a transmural intestinal insult that disrupts the intestinal barrier function; it therefore has the potential to affect intestinal drug metabolism and transport. We hypothesized that individuals with CD have reduced intestinal expression of CYP3A4 and P-gp. We obtained intestinal biopsy samples from individuals with and without CD and quantified the expression of CYP3A4 and P-gp. When we carried out Western analysis for protein expression, we observed a significant reduction in ileal (45% decrease) and colonic (78% decrease) CYP3A4 protein expression in subjects with CD compared with those without. Similarly, an 85% reduction in colonic P-gp protein expression was seen in the CD patients. Our data highlight important and novel findings pertaining to CD-associated changes to the intestinal expression of CYP3A4 and P-gp that are of relevance to better predict substrate drug dosing for patients with CD.

摘要

细胞色素 P450(CYP)3A4 和 P-糖蛋白(P-gp)具有广泛的底物重叠,参与近 50%的当前处方药物的代谢和转运。在肠道中,CYP3A4 和 P-gp 在肠绒毛尖端的肠上皮细胞中共同表达,并以协调的方式作用,以限制药物和外源性物质在肝脏进一步代谢和处置之前的口服生物利用度。克罗恩病(CD)是一种炎症性肠病,会造成肠壁损伤,破坏肠道屏障功能;因此,它有可能影响肠道药物代谢和转运。我们假设 CD 患者的肠道 CYP3A4 和 P-gp 表达减少。我们从 CD 患者和无 CD 患者中获取肠道活检样本,并定量检测 CYP3A4 和 P-gp 的表达。当我们进行蛋白质表达的 Western 分析时,与无 CD 患者相比,CD 患者的回肠(减少 45%)和结肠(减少 78%)CYP3A4 蛋白表达显著降低。同样,在 CD 患者中也观察到结肠 P-gp 蛋白表达降低 85%。我们的数据突出了与 CD 相关的、对 CYP3A4 和 P-gp 肠道表达的重要和新颖的发现,这与更好地预测 CD 患者的底物药物剂量有关。

相似文献

1
Crohn's Disease Is Associated with Decreased CYP3A4 and P-Glycoprotein Protein Expression.克罗恩病与 CYP3A4 和 P-糖蛋白蛋白表达降低有关。
Mol Pharm. 2019 Sep 3;16(9):4059-4064. doi: 10.1021/acs.molpharmaceut.9b00459. Epub 2019 Aug 19.
2
CYP3A4 Activity is Markedly Lower in Patients with Crohn's Disease.克罗恩病患者的CYP3A4活性显著降低。
Inflamm Bowel Dis. 2017 May;23(5):804-813. doi: 10.1097/MIB.0000000000001062.
3
Impact of inflammation on the duodenal mRNA expression of CYP3A and P-glycoprotein in children with Crohn's disease.炎症对克罗恩病患儿十二指肠中CYP3A和P-糖蛋白mRNA表达的影响。
Inflamm Bowel Dis. 2006 Aug;12(8):745-9. doi: 10.1097/00054725-200608000-00011.
4
Effect of Crohn's Disease on Villous Length and CYP3A4 Expression in the Pediatric Small Intestine.克罗恩病对儿科小肠绒毛长度和 CYP3A4 表达的影响。
Clin Transl Sci. 2021 Mar;14(2):729-736. doi: 10.1111/cts.12938. Epub 2020 Dec 16.
5
Cytochrome P450 3A4 and P-glycoprotein expression in human small intestinal enterocytes and hepatocytes: a comparative analysis in paired tissue specimens.细胞色素P450 3A4和P-糖蛋白在人小肠肠上皮细胞和肝细胞中的表达:配对组织标本的比较分析
Clin Pharmacol Ther. 2004 Mar;75(3):172-83. doi: 10.1016/j.clpt.2003.10.008.
6
Variation in oral clearance of saquinavir is predicted by CYP3A5*1 genotype but not by enterocyte content of cytochrome P450 3A5.沙奎那韦口服清除率的差异由CYP3A5*1基因型预测,而非细胞色素P450 3A5的肠细胞含量预测。
Clin Pharmacol Ther. 2005 Dec;78(6):605-18. doi: 10.1016/j.clpt.2005.08.014.
7
The consequence of regional gradients of P-gp and CYP3A4 for drug-drug interactions by P-gp inhibitors and the P-gp/CYP3A4 interplay in the human intestine ex vivo.P-糖蛋白(P-gp)和细胞色素P450 3A4(CYP3A4)的区域梯度对P-gp抑制剂引起的药物相互作用以及人离体肠道中P-gp/CYP3A4相互作用的影响。
Toxicol In Vitro. 2017 Apr;40:26-33. doi: 10.1016/j.tiv.2016.12.002. Epub 2016 Dec 7.
8
Unmasking the dynamic interplay between intestinal P-glycoprotein and CYP3A4.揭示肠道P-糖蛋白与细胞色素P450 3A4之间的动态相互作用。
J Pharmacol Exp Ther. 2002 Mar;300(3):1036-45. doi: 10.1124/jpet.300.3.1036.
9
Effect of variations in the amounts of P-glycoprotein (ABCB1), BCRP (ABCG2) and CYP3A4 along the human small intestine on PBPK models for predicting intestinal first pass.沿人体小肠的 P-糖蛋白(ABCB1)、BCRP(ABCG2)和 CYP3A4 量的变化对预测肠道首过的 PBPK 模型的影响。
Mol Pharm. 2010 Oct 4;7(5):1596-607. doi: 10.1021/mp100015x. Epub 2010 Aug 4.
10
P-glycoprotein and cytochrome P450 3A act together in restricting the oral bioavailability of paclitaxel.P-糖蛋白和细胞色素 P450 3A 共同作用限制紫杉醇的口服生物利用度。
Int J Cancer. 2013 May 15;132(10):2439-47. doi: 10.1002/ijc.27912. Epub 2012 Nov 14.

引用本文的文献

1
Network pharmacology analysis of Lanatoside C: molecular targets and mechanisms in the treatment of ulcerative colitis.毛花苷C的网络药理学分析:治疗溃疡性结肠炎的分子靶点及机制
Front Mol Biosci. 2025 Mar 21;12:1552360. doi: 10.3389/fmolb.2025.1552360. eCollection 2025.
2
Variability in intestinal drug metabolizing enzymes and transporters in Crohn's disease and potential impact on oral drug absorption.克罗恩病中肠道药物代谢酶和转运体的变异性及其对口服药物吸收的潜在影响。
Br J Clin Pharmacol. 2025 Jul;91(7):2028-2044. doi: 10.1002/bcp.70019. Epub 2025 Mar 4.
3
Human Organ Chips Reveal New Inflammatory Bowel Disease Drivers.
人体器官芯片揭示炎症性肠病新驱动因素
Res Sq. 2025 Jan 29:rs.3.rs-5627712. doi: 10.21203/rs.3.rs-5627712/v1.
4
Gut microbiota trigger host liver immune responses that affect drug-metabolising enzymes.肠道微生物群引发影响药物代谢酶的宿主肝脏免疫反应。
Front Immunol. 2024 Dec 11;15:1511229. doi: 10.3389/fimmu.2024.1511229. eCollection 2024.
5
Inflammatory Bowel Disease Drivers Revealed in Human Organ Chips.人体器官芯片揭示炎症性肠病的驱动因素
medRxiv. 2024 Dec 8:2024.12.05.24318563. doi: 10.1101/2024.12.05.24318563.
6
Drug-disease interaction: Clinical consequences of inflammation on drugs action and disposition.药物-疾病相互作用:炎症对药物作用和处置的临床影响。
J Pharm Pharm Sci. 2023 Feb 6;26:11137. doi: 10.3389/jpps.2023.11137. eCollection 2023.
7
Assessment of potential drug-drug interactions among outpatients in a tertiary care hospital: focusing on the role of P-glycoprotein and CYP3A4 (retrospective observational study).三级护理医院门诊患者潜在药物相互作用的评估:聚焦于P-糖蛋白和CYP3A4的作用(回顾性观察研究)
Heliyon. 2022 Oct 28;8(11):e11278. doi: 10.1016/j.heliyon.2022.e11278. eCollection 2022 Nov.
8
The Role of CYP3A in Health and Disease.细胞色素P450 3A在健康与疾病中的作用
Biomedicines. 2022 Oct 24;10(11):2686. doi: 10.3390/biomedicines10112686.
9
Altered Bioavailability and Pharmacokinetics in Crohn's Disease: Capturing Systems Parameters for PBPK to Assist with Predicting the Fate of Orally Administered Drugs.克罗恩病的生物利用度和药代动力学改变:捕获 PBPK 系统参数以帮助预测口服药物的命运。
Clin Pharmacokinet. 2022 Oct;61(10):1365-1392. doi: 10.1007/s40262-022-01169-4. Epub 2022 Sep 3.
10
Prognostic value of using glucosylceramide synthase and cytochrome P450 family 1 subfamily A1 expression levels for patients with triple-negative breast cancer following neoadjuvant chemotherapy.新辅助化疗后,葡萄糖神经酰胺合酶和细胞色素P450家族1亚家族A1表达水平对三阴性乳腺癌患者的预后价值。
Exp Ther Med. 2021 Mar;21(3):247. doi: 10.3892/etm.2021.9678. Epub 2021 Jan 22.