留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码

苦地丁中紫堇灵和乙酰紫堇灵在急性肺损伤大鼠体内的药代动力学研究

陈燕 穆雪梅 蔡慧敏 邵华 郑啸

陈燕, 穆雪梅, 蔡慧敏, 邵华, 郑啸. 苦地丁中紫堇灵和乙酰紫堇灵在急性肺损伤大鼠体内的药代动力学研究[J]. 南京中医药大学学报, 2020, 36(6): 863-868.
引用本文: 陈燕, 穆雪梅, 蔡慧敏, 邵华, 郑啸. 苦地丁中紫堇灵和乙酰紫堇灵在急性肺损伤大鼠体内的药代动力学研究[J]. 南京中医药大学学报, 2020, 36(6): 863-868.
CHENYan, MUXue-mei, CAIHui-min, SHAOHua, ZHENGXiao. Pharmacokinetic Study of Corynoline and Acetylcorynoline in LPS-Induced Acute Lung Injury Rats After Oral Administration ofCorydalis Bungeana Turcz Extract[J]. Journal of Nanjing University of traditional Chinese Medicine, 2020, 36(6): 863-868.
Citation: CHENYan, MUXue-mei, CAIHui-min, SHAOHua, ZHENGXiao. Pharmacokinetic Study of Corynoline and Acetylcorynoline in LPS-Induced Acute Lung Injury Rats After Oral Administration ofCorydalis Bungeana Turcz Extract[J]. Journal of Nanjing University of traditional Chinese Medicine, 2020, 36(6): 863-868.

苦地丁中紫堇灵和乙酰紫堇灵在急性肺损伤大鼠体内的药代动力学研究

Pharmacokinetic Study of Corynoline and Acetylcorynoline in LPS-Induced Acute Lung Injury Rats After Oral Administration ofCorydalis Bungeana Turcz Extract

  • 摘要: 目的 研究苦地丁中主要活性成分紫堇灵和乙酰紫堇灵在急性肺损伤大鼠体内的药代动力学研究。方法 建立同时测定大鼠血浆中紫堇灵和乙酰紫堇灵的LC-MS/MS分析方法,血浆样品采用乙腈沉淀蛋白,在C18色谱柱下进行梯度洗脱。离子源为电喷雾离子源,采用多反应离子检测。同时对其专属性、线性及范围、准确度、精密度、稳定性、基质效应进行考察。采用滴鼻LPS诱导急性肺损伤大鼠模型,灌胃428 mg/kg苦地丁提取物后,测定大鼠血浆中紫堇灵和乙酰紫堇灵的血药浓度,采用DAS3.0计算其药代动力参数。结果 紫堇灵和乙酰紫堇灵在0.25~100.0 ng/mL和0.40~160.0 ng/mL之间有较好的线性(R2>0.995);同时批间及批内精密度和准确度、基质效应、回收率以及不同条件下的稳定性均符合要求。与正常组相比,急性肺损伤大鼠体内的紫堇灵暴露水平显著增加(AUC,P<0.01),而乙酰紫堇灵的暴露水平未见明显变化。结论 该方法具有快速、灵敏、准确的特点,可用于苦地丁提取物中紫堇灵和乙酰紫堇灵体内药代动力学研究,同时紫堇灵在急性肺损伤大鼠体内暴露水平显著增加,清除显著减弱。

     

  • [1] 李木子, 张浩, 朱粉霞. 苦地丁的化学成分研究[J]. 华西药学杂志, 2019, 34(3): 120-126.
    [2] 张浩, 李木子, 翟晓婷, 等. 紫堇灵的分离制备及抗炎活性[J]. 中国药科大学学报, 2017, 48(6): 715-720.
    [3] LIU Y, SONG M, ZHU G, et al. Corynoline attenuates LPS-induced acute lung injury in mice by activating Nrf2[J]. Int Immunopharmacol, 2017, 48: 96-101.
    [4] ZHAI XT, CHEN JQ, JIANG CH, et al.Corydalis bungeana Turcz. attenuates LPS-induced inflammatory responses via the suppression of NF-κB signaling pathwayin vitro andin vivo[J]. J Ethnopharmacol, 2016, 194: 153-161.
    [5] MAO X, PENG Y, ZHENG J.In vitro andin vivo characterization of reactive intermediates of corynoline[J]. Drug Metab Dispos, 2015, 43(10): 1491-1498.
    [6] LIU RJ, ZHENG L, CHENG ML, et al. Simultaneous determination of corynoline and acetylcorynoline in human urine by LC-MS/MS and its application to a urinary excretion study[J]. J Chromatogr B, 2016, 1014: 83-89.
    [7] YANG CJ, XIAO Y, WANG ZB, et al. UHPLC-ESI-MS/MS determination and pharmacokinetic study of two alkaloid components in rat plasma after oral administration of the extract ofCorydalis bungeana Turcz[J]. J Chromatogr B, 2014, 960: 59-66.
    [8] MAO X, ZHAO HM, WANG Q, et al. Metabolism-based herb-drug interaction ofCorydalis Bungeanae Herba with berberinein vitro andin vivo in rats[J]. Biomed Chromatogr, 2019, 33(7): e4514.
    [9] LIU RJ, ZHOU F, HE H, et al. Metabolism and bioactivation of corynoline with characterization of the glutathione/cysteine conjugate and evaluation of its hepatotoxicity in mice[J]. Front Pharmacol, 2018, 9: 1264.
    [10] ANWAR-MOHAMED A, ZORDOKY BNM, ABOUTABL ME, et al. Alteration of cardiac cytochrome P450-mediated arachidonic acid metabolism in response to lipopolysaccharide-induced acute systemic inflammation[J]. Pharmacol Res, 2010, 61(5): 410-418.
    [11] CHEN LW, LU Y, ZHAO LJ, et al. Curcumin attenuatesSepsis-induced acute organ dysfunction by preventing inflammation and enhancing the suppressive function of Tregs[J]. Int Immunopharmacol, 2018, 61: 1-7.
  • 加载中
计量
  • 文章访问数:  396
  • HTML全文浏览量:  17
  • PDF下载量:  289
  • 被引次数: 0
出版历程
  • 刊出日期:  2020-11-10

目录

    /

    返回文章
    返回