Chen Gang, Zhu Lingxin, Liu Yang, Zhou Qian, Chen Hao, Yang Jing
Department of Pharmacology, School of Medicine, Wuhan University, Donghu Road, Wuhan 430071, China.
Phytother Res. 2009 Apr;23(4):498-506. doi: 10.1002/ptr.2660.
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 Ca(2+) concentration-response curves to the right, indicating a calcium antagonist effect. Pretreatment with N(omega)-nitro-L-arginine methyl ester (L-NAME; 30 microM), indomethacin (10 microM), methylene blue (10 microM), tetraethylammonium chloride (0.5 mM), glibenclamide (1 microM), 4-aminopyridine (0.1 mM), or clotrimazole (1 microM) 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.
多年来,甘草根已被用于调节中医中的胃肠功能。本研究揭示了异甘草素的胃肠效应,异甘草素是从光果甘草(一种甘草)根中分离出的一种黄酮类化合物。在体内,异甘草素对炭末推进产生双相剂量相关效应,低剂量时具有抑制作用,而高剂量时具有促动力作用。在体外,异甘草素在离体大鼠胃底显示出对阿托品敏感的浓度依赖性致痉作用。然而,在离体兔空肠、豚鼠回肠和阿托品化的大鼠胃底观察到解痉作用,表现为对激动剂浓度-反应曲线的非竞争性抑制、对高钾(80 mM)诱导的收缩的抑制,或使钙浓度-反应曲线右移,表明具有钙拮抗剂作用。用N(ω)-硝基-L-精氨酸甲酯(L-NAME;30 μM)、吲哚美辛(10 μM)、亚甲蓝(10 μM)、四乙铵氯化物(0.5 mM)、格列本脲(1 μM)、4-氨基吡啶(0.1 mM)或克霉唑(1 μM)预处理均未抑制解痉作用。这些结果表明,异甘草素在调节胃肠动力方面发挥双重作用,既有致痉作用又有解痉作用。致痉作用可能涉及毒蕈碱受体的激活,而解痉作用主要是由于钙通道的阻断。