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附子配伍甘草后对附子生物碱类成分大鼠在体肠吸收特性的影响
引用本文:李文,杨晓琴,章津铭,傅超美,游宇,林彦君,陈海红.附子配伍甘草后对附子生物碱类成分大鼠在体肠吸收特性的影响[J].中国实验方剂学杂志,2018,24(22):11-16.
作者姓名:李文  杨晓琴  章津铭  傅超美  游宇  林彦君  陈海红
作者单位:成都中医药大学药学院
基金项目:国家自然科学基金青年基金项目(81403123)
摘    要:目的:研究附子-甘草配伍前后附子中6种生物碱类成分的大鼠在体肠吸收特征。方法:采用大鼠在体肠灌注模型,以紫外分光光度法测定酚红质量浓度,利用LC-MS测定灌注液中乌头碱、次乌头碱、新乌头碱、苯甲酰乌头原碱、苯甲酰次乌头原碱、苯甲酰新乌头原碱的质量浓度,分别研究附子单煎液、附子-甘草合煎液、附子-甘草合并液3种配伍方式对上述6种生物碱类成分肠吸收的影响。结果:与附子单煎液相比,苯甲酰乌头原碱在附子-甘草合煎液、附子-甘草合并液中的吸收速率常数(Ka)和单位时间吸收率(A)呈下降趋势;苯甲酰新乌头原碱在附子-甘草合煎液、附子单煎液中的Ka和A相比附子-甘草合并液有所减少;附子-甘草合煎液中次乌头碱的Ka和A相比附子单煎液呈下降趋势,附子-甘草合并液中次乌头碱的Ka和A相比附子单煎液均呈升高趋势,附子-甘草合煎液中苯甲酰次乌头原碱、乌头碱和新乌头碱的吸收相比附子单煎液中均有所降低。结论:附子配伍甘草后6种乌头碱类成分在大鼠十二指肠中的吸收均有一定程度的降低,为阐释"附子得甘草而后缓"的配伍理论提供了实验依据。

关 键 词:附子  甘草  苯甲酰乌头原碱  乌头碱  次乌头碱  新乌头碱  在体肠吸收  原位肠灌注模型
收稿时间:2018/2/5 0:00:00

Effect of Aconiti Lateralis Radix Praepareta Combined with Glycyrrhizae Radix et Rhizoma on in situ Intestinal Absorption of Alkaloids in Aconiti Lateralis Radix Praepareta
LI Wen,YANG Xiao-qin,ZHANG Jin-ming,FU Chao-mei,YOU Yu,LIN Yan-jun and CHEN Hai-hong.Effect of Aconiti Lateralis Radix Praepareta Combined with Glycyrrhizae Radix et Rhizoma on in situ Intestinal Absorption of Alkaloids in Aconiti Lateralis Radix Praepareta[J].China Journal of Experimental Traditional Medical Formulae,2018,24(22):11-16.
Authors:LI Wen  YANG Xiao-qin  ZHANG Jin-ming  FU Chao-mei  YOU Yu  LIN Yan-jun and CHEN Hai-hong
Affiliation:College Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China,College Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China,College Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China,College Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China,College Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China,College Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China and College Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China
Abstract:Objective:To study on the intestinal absorption of six alkaloids in Aconiti Lateralis Radix Praepareta(ALRP)-Glycyrrhizae Radix et Rhizoma(GRR) before and after their compatibility by in situ perfusion method in rats. Method:A rat intestinal perfusion model was used,the mass concentration of phenol red was measured by ultraviolet spectrophotometry,and the contents of aconitine,hypaconitine,mesaconitine,benzoylaconine,benzoylhypaconine,benzoylmesaconine in the perfusate were measured by LC-MS.Effect of three modes of compatibility on intestinal absorption of six alkaloids in ALRP decoction,ALRP-GRR combined decoction and ALRP-GRR separated decoction were investigated. Result:Compared with ALRP decoction,absorption rate constant(Ka) and absorption rate per unit time(A) of benzoylaconine in ALRP-GRR combined decoction and ALRP-GRR separated decoction showed a downward trend.Compared with ALRP-GRR separated decoction,Ka and A of benzoylmesaconine in ALRP-GRR combined decoction and ALRP decoction was decreased.Compared with ALRP decoction,Ka and A of hypaconitine in ALRP-GRR combined decoction showed a decreasing trend,Ka and A of hypaconitine in ALRP-GRR separated decoction showed a increasing trend.Compared with ALRP decoction,absorption of benzoylhypacoitine,aconitine and mesaconitine in ALRP-GRR combined decoction was in decline. Conclusion:Absorption of six alkaloids from ALRP in duodenum of rats decreases to some extent after combined with GRR.This study provides an experimental basis for the interpretation of the compatibility theory of "ALRP used with GRR can be absorbed slowly".
Keywords:Aconiti Lateralis Radix Praepareta  Glycyrrhizae Radix et Rhizoma  benzoylaconine  aconitine  hypaconitine  mesaconitine  in situ intestinal absorption  in situ intestinal perfusion model
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