Gastroprotective activity of the chloroform extract of the roots from Arctium lappa L.

被引:30
|
作者
dos Santos, Ana C. [2 ]
Baggio, Cristiane H. [2 ]
Freitas, Cristina S. [2 ]
Lepieszynski, Juliana [2 ]
Mayer, Barbara [2 ]
Twardowschy, Andre [2 ]
Missau, Fabiana C. [3 ]
dos Santos, Elide P. [4 ]
Pizzolatti, Moacir G. [3 ]
Marques, Maria C. A. [1 ,2 ]
机构
[1] Univ Fed Parana, Ctr Politecn Jardim Amer, Dept Pharmacol, BR-81531990 Curitiba, PR, Brazil
[2] Univ Fed Parana, Sect Biol Sci, Dept Pharmacol, BR-80060000 Curitiba, PR, Brazil
[3] Univ Fed Santa Catarina, Dept Chem, Florianopolis, SC, Brazil
[4] Univ Fed Parana, Sect Biol Sci, Dept Bot, BR-80060000 Curitiba, PR, Brazil
关键词
D O I
10.1211/jpp.60.6.0016
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Arctium lappa L. is used in folk medicine as a diuretic, depurative and digestive stimulant and in dermatological conditions. The objective of this study was to evaluate the effect and the possible mechanisms involved in the gastroprotective effects of a chloroform extract (CE) of the roots from A. lappa and its fractions. Oral pretreatment with CE (10, 30 and 100 mg kg(-1)) significantly reduced gastric lesions induced by ethanol by 61%, 70% and 76%, respectively. Oral administration of CE (100 mg kg(-1) per day for 7 days) reduced the chronic gastric ulceration induced by acetic acid by 52%. Intraduodenal CE (100, 300 and 600 mg kg(-1)) reduced the total acidity of gastric secretion by 22%, 22% and 33%, respectively, while i.p. administration (10, 30 and 100 mg kg(-1)) inhibited total acidity by 50%, 60% and 67%, respectively. In-vitro, CE inhibited H+, K+-ATPase activity with an EC50 of 53 mu g mL(-1) and fraction A (30 and 100 mu g mL(-1)) reduced this by 48% and 89%, respectively. CE had no effect on gastrointestinal motility. CE (250 mu g mL(-1)) and fraction B (100 and 250 mu g mL(-1)) had free-radical scavenging ability, inhibiting 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical activity by 50%, 20% and 55%, respectively. Collectively, the results show that the CE protects animals from gastric lesions by reducing gastric acid secretion via inhibition of gastric H+, K+-ATPase.
引用
收藏
页码:795 / 801
页数:7
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