Isolation of the antidiarrhoeal tiliroside and its derivative from Waltheria indica leaf extract

B. Ayinde, J. Owolabi, I. Uti, P. C. Ogbeta, M. Choudhary
{"title":"Isolation of the antidiarrhoeal tiliroside and its derivative from Waltheria indica leaf extract","authors":"B. Ayinde, J. Owolabi, I. Uti, P. C. Ogbeta, M. Choudhary","doi":"10.4314/njnpm.v25i1.10","DOIUrl":null,"url":null,"abstract":"The antidiarrhoeal effect of Waltheria indica methanol extract and fractions have been reported earlier but, the present work examined the intestinal relaxant effects of two flavonoid-phenyl propanoids isolated from the methanol extract. The active aqueous fraction was subjected to vacuum liquid chromatography using dichloromethane with increasing concentration of ethyl acetate, and that of methanol and water successively. The ten (10) fractions obtained were combined to give seven (7). The fraction 2 (C, D) was subjected to preparative thin layer chromatography on silica gel GF254 (10-40μm) using CHCl3-CH3OH (8:2) to obtain compound coded F2. Fraction 4 (F) was subjected to column chromatography using silica gel (60-120μm mesh) and eluted with  dichloromethane with increasing concentrations of methanol. Fractions 9-28 were combined and subjected to column  chromatography using chloroform with increasing concentration of methanol. The fractions 1-16 of these were purified on Sephadex LH-20 to obtain compound BAA. The identities of the two compounds were established using spectroscopic methods. The  antidiarrheal effect of compound F2 was evaluated on mice using charcoal transit (100,200, 400mg/kg), castor oil (40, 60 mg/kg)  while the two compounds were examined for their inhibitory effects on Ach-induced ileum contraction. The effects of the  compounds were compared with loperamide (3mg/kg) and atropine (80μg). Compounds F2 and BAA were identified as tiliroside and 3’’’, 5’’’-dimethoxy tiliroside respectively. Tiliroside inhibited the charcoal transition in the animals in a dose dependent pattern with 400mg/ mL eliciting 63.41% inhibition compared to 59.23% produced by loperamide. The compound also elicited significantly (P<0.05) prolonged onset of stooling and reduced the number and weight of stools produced lower than the control. The two  compounds drastically inhibited the Ach-induced contractions of the ileum. The compound, tiliroside at 10mg, completely abolished  the contraction by Ach unlike 3’’’, 5’’’-dimethoxy tiliroside which reduced the contraction to 1.92% at 20mg. The identified compounds seem to be responsible for the ethnomedicinal use of the plant in treating diarrhea.","PeriodicalId":19356,"journal":{"name":"Nigerian Journal of Natural Products and Medicine","volume":"50 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nigerian Journal of Natural Products and Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4314/njnpm.v25i1.10","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The antidiarrhoeal effect of Waltheria indica methanol extract and fractions have been reported earlier but, the present work examined the intestinal relaxant effects of two flavonoid-phenyl propanoids isolated from the methanol extract. The active aqueous fraction was subjected to vacuum liquid chromatography using dichloromethane with increasing concentration of ethyl acetate, and that of methanol and water successively. The ten (10) fractions obtained were combined to give seven (7). The fraction 2 (C, D) was subjected to preparative thin layer chromatography on silica gel GF254 (10-40μm) using CHCl3-CH3OH (8:2) to obtain compound coded F2. Fraction 4 (F) was subjected to column chromatography using silica gel (60-120μm mesh) and eluted with  dichloromethane with increasing concentrations of methanol. Fractions 9-28 were combined and subjected to column  chromatography using chloroform with increasing concentration of methanol. The fractions 1-16 of these were purified on Sephadex LH-20 to obtain compound BAA. The identities of the two compounds were established using spectroscopic methods. The  antidiarrheal effect of compound F2 was evaluated on mice using charcoal transit (100,200, 400mg/kg), castor oil (40, 60 mg/kg)  while the two compounds were examined for their inhibitory effects on Ach-induced ileum contraction. The effects of the  compounds were compared with loperamide (3mg/kg) and atropine (80μg). Compounds F2 and BAA were identified as tiliroside and 3’’’, 5’’’-dimethoxy tiliroside respectively. Tiliroside inhibited the charcoal transition in the animals in a dose dependent pattern with 400mg/ mL eliciting 63.41% inhibition compared to 59.23% produced by loperamide. The compound also elicited significantly (P<0.05) prolonged onset of stooling and reduced the number and weight of stools produced lower than the control. The two  compounds drastically inhibited the Ach-induced contractions of the ileum. The compound, tiliroside at 10mg, completely abolished  the contraction by Ach unlike 3’’’, 5’’’-dimethoxy tiliroside which reduced the contraction to 1.92% at 20mg. The identified compounds seem to be responsible for the ethnomedicinal use of the plant in treating diarrhea.
獐牙菜叶提取物中抗腹泻药tiliroside及其衍生物的分离
早前已经报道了印度白刺草甲醇提取物和馏分的抗腹泻作用,但本研究检查了从甲醇提取物中分离的两种类黄酮-苯丙素的肠道松弛作用。活性水馏分采用二氯甲烷真空液相色谱法,依次增加乙酸乙酯、甲醇和水的浓度。将得到的十(10)个馏分合并得到七(7)个。馏分2 (C, D)在硅胶GF254 (10-40μm)上用CHCl3-CH3OH(8:2)制备薄层色谱,得到编码为F2的化合物。馏分4 (F)采用硅胶(60-120μm目)柱层析,并用二氯甲烷随着甲醇浓度的增加洗脱。馏分9-28混合,用氯仿增加甲醇浓度进行柱层析。在Sephadex LH-20上纯化得到化合物BAA。用光谱方法确定了这两个化合物的性质。采用木炭转运(100、200、400mg/kg)、蓖麻油转运(40、60 mg/kg)对小鼠进行化合物F2的止泻作用,并观察两种化合物对疼痛诱导的回肠收缩的抑制作用。并与洛哌丁胺(3mg/kg)、阿托品(80μg)的作用进行比较。化合物F2和BAA分别鉴定为铁力苷和3′,5′-二甲氧基铁力苷。tilroside对动物体内炭转化的抑制呈剂量依赖性,400mg/ mL的抑制率为63.41%,而loperamide的抑制率为59.23%。与对照组相比,该化合物显著延长了排便时间(P<0.05),减少了排便数量和重量。这两种化合物能显著抑制疼痛引起的回肠收缩。该化合物,在10mg时,完全消除了乙酰胆碱对乙酰胆碱的收缩作用,而3 ' ',5 ' ' -二甲氧基铁力苷在20mg时将收缩率降低到1.92%。鉴定的化合物似乎是负责的民族医学使用的植物在治疗腹泻。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信