• 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

肺纤维化治疗用肺部康复混合物的药效动力学和药代动力学评估。

Pharmacodynamic and pharmacokinetic assessment of pulmonary rehabilitation mixture for the treatment of pulmonary fibrosis.

机构信息

School of Pharmaceutical Sciences, Binzhou Medical University, Yantai, PR China.

出版信息

Sci Rep. 2017 Jun 14;7(1):3458. doi: 10.1038/s41598-017-02774-1.

DOI:10.1038/s41598-017-02774-1
PMID:28615638
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5471221/
Abstract

Pulmonary rehabilitation mixture (PRM), a Chinese herbal medicine formula, has been used to treat pulmonary fibrosis for decades. In this study, we systematically evaluated the pharmacodynamic and pharmacokinetic performance of PRM. The pharmacodynamic results showed that PRM could improve the condition of CoCl-stimulated human type II alveolar epithelial cells, human pulmonary microvascular endothelial cells, human lung fibroblasts and pulmonary fibrosis rats induced by bleomycin, PRM treatment reduced the expression of platelet-derived growth factor, fibroblast growth factor, toll-like receptor 4, high-mobility group box protein 1 and hypoxia-inducible factor 1α. In the pharmacokinetic study, an accurate and sensitive ultra-high performance liquid chromatography tandem mass spectrometry method was developed and validated for the simultaneous determination of calycosin, calycosin-7-O-glucoside, formononetin, ononin and mangiferin of PRM in the rat plasma for the first time. The method was then successfully applied to the comparative pharmacokinetic study of PRM in normal and pulmonary fibrosis rats. The five constituents could be absorbed in the blood after the oral administration of PRM and exhibited different pharmacokinetic behaviors in normal and pulmonary fibrosis rats. In summary, PRM exhibited a satisfactory pharmacodynamic and pharmacokinetic performance, which highlights PRM as a potential multi-target oral drug for the treatment of pulmonary fibrosis.

摘要

肺康复合剂(PRM)是一种中药方剂,已用于治疗肺纤维化数十年。在这项研究中,我们系统地评估了 PRM 的药效学和药代动力学性能。药效学结果表明,PRM 可改善 CoCl 刺激的人 II 型肺泡上皮细胞、人肺微血管内皮细胞、人肺成纤维细胞和博莱霉素诱导的肺纤维化大鼠的状况,PRM 治疗可降低血小板衍生生长因子、成纤维细胞生长因子、Toll 样受体 4、高迁移率族蛋白 1 和缺氧诱导因子 1α 的表达。在药代动力学研究中,首次建立并验证了一种用于同时测定大鼠血浆中 PRM 中的毛蕊异黄酮、毛蕊异黄酮-7-O-葡萄糖苷、芒柄花素、大豆苷元和芒果苷的准确灵敏的超高效液相色谱-串联质谱法。该方法随后成功应用于 PRM 在正常和肺纤维化大鼠中的比较药代动力学研究。口服 PRM 后,这五种成分可以被血液吸收,并在正常和肺纤维化大鼠中表现出不同的药代动力学行为。总之,PRM 表现出令人满意的药效学和药代动力学性能,这突出了 PRM 作为一种潜在的多靶点口服药物,可用于治疗肺纤维化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5abc/5471221/2ad898d6a587/41598_2017_2774_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5abc/5471221/50246f547368/41598_2017_2774_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5abc/5471221/2d358519f441/41598_2017_2774_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5abc/5471221/e38c38ebe6c3/41598_2017_2774_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5abc/5471221/0a0150b6cc7b/41598_2017_2774_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5abc/5471221/7e0c2f2a968d/41598_2017_2774_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5abc/5471221/f35c9377f839/41598_2017_2774_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5abc/5471221/7b7d929cde3f/41598_2017_2774_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5abc/5471221/2ad898d6a587/41598_2017_2774_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5abc/5471221/50246f547368/41598_2017_2774_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5abc/5471221/2d358519f441/41598_2017_2774_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5abc/5471221/e38c38ebe6c3/41598_2017_2774_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5abc/5471221/0a0150b6cc7b/41598_2017_2774_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5abc/5471221/7e0c2f2a968d/41598_2017_2774_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5abc/5471221/f35c9377f839/41598_2017_2774_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5abc/5471221/7b7d929cde3f/41598_2017_2774_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5abc/5471221/2ad898d6a587/41598_2017_2774_Fig8_HTML.jpg

相似文献

1
Pharmacodynamic and pharmacokinetic assessment of pulmonary rehabilitation mixture for the treatment of pulmonary fibrosis.肺纤维化治疗用肺部康复混合物的药效动力学和药代动力学评估。
Sci Rep. 2017 Jun 14;7(1):3458. doi: 10.1038/s41598-017-02774-1.
2
Protective roles of pulmonary rehabilitation mixture in experimental pulmonary fibrosis in vitro and in vivo.肺康复合剂在实验性肺纤维化体内外的保护作用
Braz J Med Biol Res. 2015 Jun;48(6):545-52. doi: 10.1590/1414-431X20144301. Epub 2015 May 8.
3
Simultaneous determination of calycosin-7-O-β-D-glucoside, ononin, calycosin, formononetin, astragaloside IV, and astragaloside II in rat plasma after oral administration of Radix Astragali extraction for their pharmacokinetic studies by ultra-pressure liquid chromatography with tandem mass spectrometry.采用超高效液相色谱-串联质谱法同时测定大鼠口服黄芪提取物后血浆中毛蕊异黄酮葡萄糖苷、芒柄花苷、毛蕊异黄酮、芒柄花素、黄芪甲苷和黄芪乙苷,用于其药代动力学研究。
Cell Biochem Biophys. 2014 Sep;70(1):677-86. doi: 10.1007/s12013-014-9972-x.
4
Tissue distribution of six major bio-active components after oral administration of Zhenqi Fuzheng capsules to rats using ultra-pressure liquid chromatography-tandem mass spectrometry.采用超高效液相色谱-串联质谱法研究贞芪扶正胶囊灌胃大鼠后六种主要生物活性成分的组织分布。
J Chromatogr B Analyt Technol Biomed Life Sci. 2015 Apr 1;986-987:44-53. doi: 10.1016/j.jchromb.2015.01.033. Epub 2015 Feb 9.
5
Determination of paeoniflorin, calycosin-7-O-β-D-glucoside, ononin, calycosin and formononetin in rat plasma after oral administration of Buyang Huanwu decoction for their pharmacokinetic study by liquid chromatography-mass spectrometry.采用液相色谱-质谱联用技术测定大鼠口服补阳还五汤后血浆中芍药苷、毛蕊异黄酮-7-O-β-D-葡萄糖苷、芒柄花苷、毛蕊异黄酮和刺芒柄花素,以进行其药代动力学研究。
Biomed Chromatogr. 2011 Apr;25(4):450-7. doi: 10.1002/bmc.1466. Epub 2010 Aug 23.
6
Simultaneous determination of calycosin-7-O-β-d-glucoside, calycosin, formononetin, astragaloside IV and schisandrin in rat plasma by LC-MS/MS: application to a pharmacokinetic study after oral administration of Shenqi Wuwei chewable tablets.采用液相色谱-串联质谱法同时测定大鼠血浆中毛蕊异黄酮葡萄糖苷、毛蕊异黄酮、芒柄花素、黄芪甲苷和五味子醇甲:应用于参芪五味咀嚼片口服给药后的药代动力学研究
Biomed Chromatogr. 2014 Aug;28(8):1118-25. doi: 10.1002/bmc.3128. Epub 2014 Mar 21.
7
Study of pharmacokinetic profiles and characteristics of active components and their metabolites in rat plasma following oral administration of the water extract of Astragali radix using UPLC-MS/MS.采用超高效液相色谱-串联质谱法研究黄芪水提取物口服给药后大鼠血浆中活性成分及其代谢产物的药代动力学特征和特性。
J Ethnopharmacol. 2015 Jul 1;169:183-94. doi: 10.1016/j.jep.2015.04.019. Epub 2015 Apr 23.
8
The pharmacokinetic screening of multiple components of the Nao Mai Tong formula in rat plasma by liquid chromatography tandem mass spectrometry combined with pattern recognition method and its application to comparative pharmacokinetics.采用液相色谱串联质谱联用技术结合模式识别方法对脑脉通方多成分进行大鼠血浆药代动力学筛选及其在比较药代动力学中的应用
J Pharm Biomed Anal. 2016 Nov 30;131:345-354. doi: 10.1016/j.jpba.2016.09.011. Epub 2016 Sep 9.
9
Simultaneous Determination of Multiple Components in Guanjiekang in Rat Plasma via the UPLC-MS/MS Method and Its Application in Pharmacokinetic Study.采用 UPLC-MS/MS 法同时测定大鼠血浆中的冠心康中多种成分及其药代动力学研究。
Molecules. 2016 Dec 16;21(12):1732. doi: 10.3390/molecules21121732.
10
Pharmacokinetic comparison of seven major bio-active components in normal and blood deficiency rats after oral administration of Danggui Buxue decoction by UPLC-TQ/MS.采用超高效液相色谱-串联四极杆质谱法(UPLC-TQ/MS)对正常大鼠和血虚大鼠口服当归补血汤后七种主要生物活性成分的药代动力学比较
J Ethnopharmacol. 2014 Apr 11;153(1):169-77. doi: 10.1016/j.jep.2014.02.004. Epub 2014 Feb 26.

引用本文的文献

1
Mechanism of Lung Fibrosis Caused by Rare Earth Samarium Oxide Through Hippo Signaling Pathway and the Intervention of GBE.稀土氧化钐通过Hippo信号通路致肺纤维化的机制及银杏叶提取物的干预作用
Biol Trace Elem Res. 2025 Mar 18. doi: 10.1007/s12011-025-04571-8.
2
Perspective for Studying the Relationship of miRNAs with Transposable Elements.研究微小RNA与转座元件关系的视角
Curr Issues Mol Biol. 2023 Apr 5;45(4):3122-3145. doi: 10.3390/cimb45040204.
3
Anti- Activity of Ononin and Other Secondary Metabolites from MART.来自MART的芒柄花苷及其他次生代谢产物的抗活性

本文引用的文献

1
The potential role of mangiferin in cancer treatment through its immunomodulatory, anti-angiogenic, apoptopic, and gene regulatory effects.芒果苷通过其免疫调节、抗血管生成、凋亡诱导和基因调控作用在癌症治疗中的潜在作用。
Biofactors. 2016 Sep 10;42(5):475-491. doi: 10.1002/biof.1299. Epub 2016 May 24.
2
Gastroesophageal Reflux in Idiopathic Pulmonary Fibrosis: More than a Gut Feeling?特发性肺纤维化中的胃食管反流:不止是一种直觉?
Respiration. 2016;91(1):1-2. doi: 10.1159/000443183. Epub 2016 Jan 5.
3
Formononetin promotes angiogenesis through the estrogen receptor alpha-enhanced ROCK pathway.
Metabolites. 2022 Oct 24;12(11):1014. doi: 10.3390/metabo12111014.
4
Calycosin Ameliorates Bleomycin-Induced Pulmonary Fibrosis via Suppressing Oxidative Stress, Apoptosis, and Enhancing Autophagy.毛蕊异黄酮通过抑制氧化应激、细胞凋亡及增强自噬改善博来霉素诱导的肺纤维化。
Evid Based Complement Alternat Med. 2022 Oct 11;2022:9969729. doi: 10.1155/2022/9969729. eCollection 2022.
5
The SIRT1-HMGB1 axis: Therapeutic potential to ameliorate inflammatory responses and tumor occurrence.SIRT1-HMGB1轴:改善炎症反应和肿瘤发生的治疗潜力。
Front Cell Dev Biol. 2022 Aug 19;10:986511. doi: 10.3389/fcell.2022.986511. eCollection 2022.
6
Ginkgo biloba Extract EGb761 Attenuates Bleomycin-Induced Experimental Pulmonary Fibrosis in Mice by Regulating the Balance of M1/M2 Macrophages and Nuclear Factor Kappa B (NF-κB)-Mediated Cellular Apoptosis.银杏叶提取物 EGb761 通过调节 M1/M2 巨噬细胞平衡和核因子-κB(NF-κB)介导的细胞凋亡减轻博来霉素诱导的小鼠实验性肺纤维化。
Med Sci Monit. 2020 Aug 16;26:e922634. doi: 10.12659/MSM.922634.
7
Chinese Herbal Formula, Huayu Tongbi Fang, Attenuates Inflammatory Proliferation of Rat Synoviocytes Induced by IL-1 by Regulating Proliferation and Differentiation of T Lymphocytes.中药复方化瘀通痹方通过调节T淋巴细胞增殖分化减轻白细胞介素-1诱导的大鼠滑膜细胞炎性增殖
Evid Based Complement Alternat Med. 2020 May 19;2020:1706837. doi: 10.1155/2020/1706837. eCollection 2020.
8
Total extract of Xin Jia Xuan Bai Cheng Qi decoction inhibits pulmonary fibrosis via the TGF-β/Smad signaling pathways in vivo and in vitro.新加宣白承气汤总提取物通过TGF-β/Smad信号通路在体内外抑制肺纤维化。
Drug Des Devel Ther. 2019 Aug 19;13:2873-2886. doi: 10.2147/DDDT.S185418. eCollection 2019.
9
Feifukang ameliorates pulmonary fibrosis by inhibiting JAK-STAT signaling pathway.肺复康通过抑制 JAK-STAT 信号通路改善肺纤维化。
BMC Complement Altern Med. 2018 Aug 9;18(1):234. doi: 10.1186/s12906-018-2297-3.
大豆苷元通过雌激素受体α增强的ROCK途径促进血管生成。
Sci Rep. 2015 Nov 16;5:16815. doi: 10.1038/srep16815.
4
Suppression of A549 cell proliferation and metastasis by calycosin via inhibition of the PKC‑α/ERK1/2 pathway: An in vitro investigation.毛蕊异黄酮通过抑制PKC-α/ERK1/2信号通路抑制A549细胞增殖和转移的体外研究
Mol Med Rep. 2015 Dec;12(6):7992-8002. doi: 10.3892/mmr.2015.4449. Epub 2015 Oct 15.
5
Protective effect of calycosin-7-O-β-D-glucopyranoside against oxidative stress of BRL-3A cells induced by thioacetamide.毛蕊异黄酮葡萄糖苷对硫代乙酰胺诱导的BRL-3A细胞氧化应激的保护作用
Pharmacogn Mag. 2015 Jul-Sep;11(43):524-32. doi: 10.4103/0973-1296.160461.
6
Effects of Traditional Chinese Medicine Huangqi Injection (Radix astragali) on Random Skin Flap Survival in Rats.中药黄芪注射液对大鼠随意皮瓣存活的影响。
J Reconstr Microsurg. 2015 Oct;31(8):565-70. doi: 10.1055/s-0035-1555142. Epub 2015 Jun 30.
7
Protective roles of pulmonary rehabilitation mixture in experimental pulmonary fibrosis in vitro and in vivo.肺康复合剂在实验性肺纤维化体内外的保护作用
Braz J Med Biol Res. 2015 Jun;48(6):545-52. doi: 10.1590/1414-431X20144301. Epub 2015 May 8.
8
Study of pharmacokinetic profiles and characteristics of active components and their metabolites in rat plasma following oral administration of the water extract of Astragali radix using UPLC-MS/MS.采用超高效液相色谱-串联质谱法研究黄芪水提取物口服给药后大鼠血浆中活性成分及其代谢产物的药代动力学特征和特性。
J Ethnopharmacol. 2015 Jul 1;169:183-94. doi: 10.1016/j.jep.2015.04.019. Epub 2015 Apr 23.
9
Pharmacologic therapies for idiopathic pulmonary fibrosis, past and future.特发性肺纤维化的药物治疗:过去与未来
Ann Med. 2015 Mar;47(2):100-5. doi: 10.3109/07853890.2014.991751. Epub 2015 Jan 22.
10
The diagnosis and treatment of idiopathic pulmonary fibrosis.特发性肺纤维化的诊断与治疗
Dtsch Arztebl Int. 2013 Dec 23;110(51-52):875-81. doi: 10.3238/arztebl.2013.0875.