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Antidiarrheal mechanism of Carpolobia lutea leaf fractions in rats

机译:黄果叶部分的止泻机制

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Context: Carpolobia lutea G. Don (Polygalaceae) leaf is reputable as an antidiarrheal agent among the Efik and Ibibio tribe of Akwa Ibom State, Nigeria. The crude extract is reported to show antidiarrheal and antiulcer effects in rodents. Objective: The isolation and characterization of drug molecules from the leaf fraction with antidiarrheal bioactivity and determination of mechanism of action are reported. Material and methods: Gradient extraction by maceration yielding n-hexane, chloroform, ethyl acetate, and ethanol fractions (770?mg/kg) were used to establish the fractions suitable for drug discovery. The antidiarrheal effect of the leaf fractions of Carpolobia lutea was evaluated using castor oil–induced diarrhea, castor oil–induced intestinal transit, and enteropooling. Results: Results indicate that all fractions produced a significant (p??0.01–0.001) decrease in castor oil–induced diarrhea in rats. This effect was not antagonized by isosorbide dinitrate (150?mg/kg, p.o), diphenoxylate (5?×?10?3 mg/kg p.o) and yohimbine (1?mg/kg, s.c.) except for the chloroform fraction. The ethyl acetate fraction produced 100% inhibition of intestinal transit, an effect greater than pure drug. Phytochemical analysis of the ethyl acetate fraction yielded polyphenolic compounds. Conclusion: The leaf fractions contain two types of antidiarrheal agents, one mediating its effect through α1-presynaptic adrenoceptor while the other does not. Polyphenols isolated may in part lend credence for observed antidiarrheal activity.
机译:背景:在尼日利亚阿克瓦伊博姆州的Efik和Ibibio部落中,黄花茄叶(Polygalaceae)被认为是止泻药。据报道,粗提物在啮齿动物中显示出止泻和抗溃疡作用。目的:报道了具有抗腹泻生物活性的叶级分中的药物分子的分离,表征以及作用机理的确定。材料和方法:通过浸提法进行梯度萃取,得到正己烷,氯仿,乙酸乙酯和乙醇馏分(770?mg / kg),用于建立适合药物发现的馏分。使用蓖麻油引起的腹泻,蓖麻油引起的肠运输和肠蓄积来评估黄果叶的叶级分的止泻作用。结果:结果表明,所有成分均导致蓖麻油诱发的大鼠腹泻明显减少(p <0.01〜0.001)。硝酸异山梨酯(150?mg / kg,口服),苯乙氧基化物(5?×?10 ?3 mg / kg口服)和育亨宾(1?mg / kg,sc)不能拮抗这一作用。除了氯仿馏分。乙酸乙酯级分产生100%的肠道运输抑制作用,其作用比纯药物大。乙酸乙酯馏分的植物化学分析产生多酚化合物。结论:叶级分含有两种类型的止泻药,一种通过α 1 -突触前肾上腺素受体介导其作用,而另一种则没有。分离出的多酚可部分证明其所观察到的止泻活性。

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