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菊苣种子中的倍半萜糖苷——菊苣苷的抗肝毒性活性

Anti-hepatotoxic activity of cichotyboside, a sesquiterpene glycoside from the seeds of Cichorium intybus.

作者信息

Ahmed Bahar, Khan Shamshir, Masood Mubashir H, Siddique Anwarul H

机构信息

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Hamdard University, New Delhi, India.

出版信息

J Asian Nat Prod Res. 2008 Mar-Apr;10(3-4):223-31. doi: 10.1080/10286020701590764.

Abstract

The seeds of Cichorium intybus L. (Asteraceae) afforded a new guaianolide sesquiterpene glycoside, cichotyboside, which was characterized as 2alpha, 6beta, 7beta, 15-tetrahydroxy-1 (10), 4 (5)-diene-guaian-9alpha, 12-olide-7-O-beta-caffoyl-15-O-beta-D-glucoside (1) by means of spectral methods. Cichotyboside (1) exhibited a significant anti-hepatotoxic activity against CCl4 induced toxicity in Wistar rats, wherein it reduced the elevated levels of liver enzymes such as serum glutamate oxaloacetate transaminase (SGOT) by 52 units/ml; SGPT 38 units/ml; ALKP 24.97 units/ml and 7.54 g/dl, 5.48 g/dl increase in total protein and albumin, respectively. It was observed that cichotyboside (1) decreased the level of ALKP comparable with that of standard drug silymarin, exhibiting an 88% decrease in comparison to silymarin (92%) and increased the level of total albumin 85% in comparison to silymarin (89%) against intoxicated control. Whereas, the levels of SGOT and SGPT were also decreased considerably in comparison to standard and intoxicated control.

摘要

菊苣(菊科)种子中含有一种新的愈创木烷型倍半萜糖苷——菊苣苷,通过光谱方法将其确定为2α, 6β, 7β, 15 - 四羟基 - 1(10), 4(5) - 二烯 - 愈创木 - 9α, 12 - 内酯 - 7 - O - β - 咖啡酰 - 15 - O - β - D - 葡萄糖苷(1)。菊苣苷(1)对Wistar大鼠四氯化碳诱导的毒性表现出显著的抗肝毒性活性,其中它使血清谷氨酸草酰乙酸转氨酶(SGOT)等肝酶升高水平降低了52单位/毫升;SGPT降低了38单位/毫升;碱性磷酸酶(ALKP)降低了24.97单位/毫升,总蛋白增加了7.54克/分升,白蛋白增加了5.48克/分升。观察到菊苣苷(1)降低ALKP的水平与标准药物水飞蓟宾相当,与水飞蓟宾(92%)相比降低了88%,与中毒对照组相比,总白蛋白水平增加了85%(水飞蓟宾为89%)。而与标准药物组和中毒对照组相比SGOT和SGPT的水平也显著降低。

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