Hara Hideaki, Ise Yasuaki, Morimoto Nobutaka, Shimazawa Masamitsu, Ichihashi Koji, Ohyama Masayoshi, Iinuma Munekazu
Department of Biofunctional Evaluation, Molecular Pharmacology, Gifu Pharmaceutical University, Japan.
Biosci Biotechnol Biochem. 2008 Feb;72(2):335-45. doi: 10.1271/bbb.70361. Epub 2008 Feb 7.
We investigated the laxative activity of an extract of agarwood leaves from Aquilaria sinensis. The laxative activity was measured in mice by counting the stool frequency and stool weight, and the drugs were orally administered. An acetone extract of agarwood leaves and senna (a representative laxative drug) both increased the stool frequency and weight, but a methanol extract did not. The laxative effect of the acetone extract was milder than that of the anthraquinoid laxative, senna, and the former did not induce diarrhea as a severe side effect. We identified the main constituent contributing to the laxative effect of the acetone extract as genkwanin 5-O-beta-primeveroside (compound 4). Compound 4 strengthened the spontaneous motility and induced contraction in the ileum. This ileal contraction induced by compound 4 was inhibited by atropine, but not by azasetron, suggesting that the effect of compound 4 was mediated by acetylcholine receptors, and not by serotonin. The laxative mechanism for compound 4 may in part involve stimulation of intestinal motility via acetylcholine receptors.
我们研究了白木香叶提取物的通便活性。通过计算小鼠的粪便频率和粪便重量来测定通便活性,药物通过口服给药。沉香叶的丙酮提取物和番泻叶(一种典型的泻药)均增加了粪便频率和重量,但甲醇提取物则没有。丙酮提取物的通便作用比蒽醌类泻药番泻叶更为温和,且前者不会引起严重的腹泻副作用。我们确定丙酮提取物通便作用的主要成分是芫花素5-O-β-樱草糖苷(化合物4)。化合物4增强了自发运动并诱导回肠收缩。化合物4诱导的这种回肠收缩被阿托品抑制,但不被阿扎司琼抑制,这表明化合物4的作用是由乙酰胆碱受体介导的,而不是由5-羟色胺介导的。化合物4的通便机制可能部分涉及通过乙酰胆碱受体刺激肠道运动。