贵州医科大学学报2024,Vol.49Issue(7) :966-974.DOI:10.19367/j.cnki.2096-8388.2024.07.004

心肌缺血再灌注损伤大鼠体内荭草花活性成分的PK-PD研究

Study on PK-PD of active components of Polygonum orientale L.flower in rats with myocardial ischemia-reperfusion injury

杨青波 杨兴美 向文英 郑林 黄勇 迟明艳 蒲健
贵州医科大学学报2024,Vol.49Issue(7) :966-974.DOI:10.19367/j.cnki.2096-8388.2024.07.004

心肌缺血再灌注损伤大鼠体内荭草花活性成分的PK-PD研究

Study on PK-PD of active components of Polygonum orientale L.flower in rats with myocardial ischemia-reperfusion injury

杨青波 1杨兴美 2向文英 2郑林 3黄勇 3迟明艳 2蒲健2
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作者信息

  • 1. 贵州益佰制药股份有限公司 国家苗药工程技术研究中心,贵州 贵阳 550008
  • 2. 贵州医科大学 药学院,贵州 贵阳 550004;贵州医科大学 省部共建药用植物功效与利用国家重点实验室& 贵州省药物制剂重点实验室,贵州 贵阳 550004
  • 3. 贵州医科大学 省部共建药用植物功效与利用国家重点实验室& 贵州省药物制剂重点实验室,贵州 贵阳 550004;贵州医科大学 民族药与中药开发应用教育部工程研究中心,贵州 贵阳 550004
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摘要

目的 建立药代动力学-药效动力学(PK-PD)结合模型,探讨荭草花提取物在心肌缺血再灌注损伤(MIRI)模型大鼠体内活性成分的动态变化与其药效消长之间的关系.方法 荭草花药材经水煮醇沉、正丁醇萃取得荭草花提取物;取SD大鼠6只,采用冠脉结扎法制备MIRI模型,术前大鼠灌胃荭草花提取物86 g/kg,3次/d、连续5 d,于末次给药后5 min、10 min、15 min、30 min、1.0 h、1.5 h、2.0 h、4.0 h、6.0 h、8.0 h、10.0 h、12.0 h、24.0 h、36.0 h及48.0 h经尾静脉取血,采用高效液相色谱-串联质谱(HPLC-MS/MS)检测血浆样本中6种活性成分(原儿茶酸、槲皮苷、花旗松素、N-p香豆酰酪胺、山奈素-3-O-β-D-葡萄糖苷及山奈素-3-O-α-L-鼠李糖苷)的质量浓度,获取各成分血药浓度-时间曲线;采用试剂盒测定血浆样本中超氧化物歧化酶(SOD)、乳酸脱氢酶(LDH)、肌酸激酶同工酶(CK-MB)及心肌钙蛋白I(cTn-I)的浓度,获取效应-时间曲线;通过Winnonlin 6.4软件分别对药物浓度-时间与效应-时间进行拟合,建立PK-PD模型.结果 荭草花提取物中各有效成分均能够较好地与各药效指标拟合,以SOD为药效指标时,各成分的PK-PD模型以Sigmoid Emax拟合较优;以LDH、CK-MB及cTn-I为药效指标时,各成分的PK-PD模型以Inhibitory Effect拟合较优.结论 荭草花提取物中的原儿茶酸、槲皮苷、山奈素-3-O-β-D-葡萄糖苷及山奈素-3-O-α-L-鼠李糖苷、花旗松素、N-p香豆酰酪胺具有心肌缺血保护作用,其浓度与药效指标SOD、LDH、CK-MB及cTn-I的水平有相关性.

Abstract

Objective To establish a pharmacokinetic-pharmacodynamic (PK-PD) combined model and explore the correlation between dynamic changes of the active components of Polygonum orientale L.flower extract in rats with myocardial ischemia-reperfusion injury ( MIRI) model and the decline of its efficacy. Methods Polygonum orientale L. Flower extract was extracted by n-butanol after water extracting and alcohol precipitation. Six SD rats were used to establish MIRI model by coronary artery ligation. Before operation,the rats were given Polygonum orientale flower extract (86 g/kg),3 times a day for continuous5 days. Blood samples were collected from tail vein at 5 min,10 min,15 min,30 min,1.0h,1.5h,2.0h,4.0h,6.0h,8.0h,10.0h,12.0h,24.0h,36.0h,48. 0h after the last administration. High performance liquid chromatography-tandem mass spectrometry ( HPLC-MS/MS) was used to measure the mass concentrations of 6 active components ( protocatechuate,quercitrin,taxifolin,paprazine,kaempferol-3-O-β-D-glucopyranoside and kaempferol 3-O-α-L-rhamnoside) in plasma samples. The blood drug concentration-time curves of each component were obtained. Kits were used to measure the concentrations of superoxide dismutase ( SOD ),lactate dehydrogenase ( LDH),creatine kinase isoenzyme ( CK-MB ),and cardiac troponin I ( cTn-I ) in plasma samples to plot the effect-time curves. The drug concentration-time and effect-time were fitted by Winnonlin 6.4 software to establish PK-PD model. Results The active components in the Polygonum orientale L. Flower were well-fitted with each pharmacodynamic index. When SOD was used as a pharmacodynamic index,PK-PD binding model was well-fitted with Sigmoid Emax. When the pharmacodynamic indexes were LDH,CK-MB,and cTn-I,PK-PD binding model was well-fitted by inhibitory effect. Conclusion Protocatechuate,quercitrin,taxifolin,paprazine,kaempferol-3-O-β-D-glucopyranoside,and kaempferol 3-O-α-L-rhamnoside in Polygonum orientale L. Flower extract exert protective effects on MIRI. The concentrations of 6 active components are correlated with the levels of SOD,LDH,CK-MB,and cTn-I.

关键词

心肌缺血/再灌注损伤/药代动力学/荭草花提取物/高效液相色谱-串联质谱/药效动力学/PK-PD模型/活性成分/药效指标

Key words

myocardial ischemia/reperfusion injury/pharmacokinetics/Polygonum orientale L. flower extract/high performance liquid chromatography-tandem mass spectrometry/pharmacodynamics/PK-PD model/active component/pharmacodynamic index

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基金项目

国家自然科学基金(81360664)

贵州省科技计划项目(黔科合中引地[2023]006)

贵州省科技计划项目(黔科合平台人才-GCC[2022]031-1)

贵州省科技计划项目(黔科合平台人才-GXTD[2023]019)

出版年

2024
贵州医科大学学报
贵阳医学院

贵州医科大学学报

CSTPCD
影响因子:0.827
ISSN:2096-8388
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