Isoliquiritigenin, a Flavonoid from Licorice, plays a Dual Role in regulating Gastrointestinal Motility in vitro and in vivo

被引:58
作者
Chen, Gang [1 ]
Zhu, Lingxin [1 ]
Liu, Yang [1 ]
Zhou, Qian [1 ]
Chen, Hao [1 ]
Yang, Jing [1 ]
机构
[1] Wuhan Univ, Dept Pharmacol, Sch Med, Wuhan 430071, Peoples R China
关键词
Glycyrrhiza glabra; isoliquiritigenin; spasmogenic; muscarinic receptors; spasmolytic; calcium antagonist; ANTAGONIST CONSTITUENTS; CALCIUM-CHANNEL; SMOOTH-MUSCLE; RATS; PRINCIPLES; INTESTINE; DIARRHEA; RELEASE; ROOTS; COLON;
D O I
10.1002/ptr.2660
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Licorice root has been used for years to regulate gastrointestinal function in traditional Chinese medicine. This study reveals the gastrointestinal effects of isoliquiritigenin, a flavonoid isolated from the roots of Glycyrrhiza glabra (a kind of Licorice). In vivo, isoliquiritigenin produced a dual dose-related effect on the charcoal meal travel, inhibitory at the low doses, while prokinetic at the high doses. In vitro, isoliquiritigenin showed an atropine-sensitive concentration-dependent spasmogenic effect in isolated rat stomach fundus. However, a spasmolytic effect was observed in isolated rabbit jejunums, guinea pig ileums and atropinized rat stomach fundus, either as noncompetitive inhibition of agonist concentration-response curves, inhibition of high K+ (80 mM)-induced contractions, or displacement of Ca2+ concentration-response curves to the right, indicating a calcium antagonist effect. Pretreatment with N-omega-nitro-L-arginine methyl ester (L-NAME; 30 mu M), indomethacin (10 mu M), methylene blue (10 mu M), tetraethylammonium chloride (0.5 mM), glibenclamide (1 mu M), 4-aminopyridine (0.1 mM), or clotrimazole (1 mu M) did not inhibit the spasmolytic effect. These results indicate that isoliquiritigenin plays a dual role in regulating gastrointestinal motility, both spasmogenic and spasmolytic. The spasmogenic effect may involve the activating of muscarinic receptors, while the spasmolytic effect is predominantly due to blockade of the calcium channels. Copyright (C) 2008 John Wiley & Sons, Ltd.
引用
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页码:498 / 506
页数:9
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