首页> 外文期刊>Journal of Ethnopharmacology: An Interdisciplinary Journal Devoted to Bioscientific Research on Indigenous Drugs >Effects of an Atractylodes lancea rhizome extract and a volatile component β-eudesmol on gastrointestinal motility in mice
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Effects of an Atractylodes lancea rhizome extract and a volatile component β-eudesmol on gastrointestinal motility in mice

机译:白术根茎提取物和挥发性成分β-大麦醇对小鼠胃肠运动的影响

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Aim of the study: The rhizomes of Atractylodes lancea DC (Compositae) are used clinically to treat gastrointestinal symptoms, including functional dyspepsia and gastroparesis, in China and Japan, but their influence and mechanism on gastrointestinal motility are not yet proven in detail. Materials and methods: This study examined the effects of an Atractylodes lancea extract, and isolated β-eudesmol, on gastric emptying and small intestinal motility in atropine-, dopamine-, and 5-hydroxytryptamine (5-HT)-treated mice. Results and conclusions: The extract (500 or 1000 mg/kg) and β-eudesmol (50 or 100 mg/kg), as well as itopride hydrochloride (a dopamine D 2 receptor antagonist, 10 or 50 mg/kg), stimulated small intestinal motility in normal mice. They inhibited reductions in gastric emptying and gastrointestinal motility induced by dopamine (1 mg/kg, intraperitoneal injection, ip). The extract (1000 mg/kg) and β-eudesmol (100 mg/kg) inhibited the atropine-induced decrease in small intestinal motility, but not gastric emptying. Furthermore, the extract (500 or 1000 mg/kg) and β-eudesmol (25, 50, or 100 mg/kg) inhibited reductions in gastric emptying and small intestinal motility caused by 5-HT (4 mg/kg, ip) or the 5-HT 3 receptor agonist 1-(3-chlorophenyl) biguanide (0.5 mg/kg, ip), but not a 5-HT 2C receptor agonist. These findings suggest that the extract of Atractylodes lancea and β-eudesmol may stimulate gastric emptying or small intestinal motility by inhibiting the dopamine D 2 receptor and 5-HT 3 receptor.
机译:研究的目的:在中国和日本,白术的根茎在临床上用于治疗胃肠道症状,包括功能性消化不良和胃轻瘫,但它们对胃肠道蠕动的影响和机制尚未得到详细证实。材料和方法:这项研究检查了白术提取物和分离的β-大麦醇对阿托品,多巴胺和5-羟色胺(5-HT)处理的小鼠的胃排空和小肠蠕动的影响。结果与结论:提取物(500或1000 mg / kg)和β-乌地甜(50或100 mg / kg),以及盐酸伊托必利(10或50 mg / kg的多巴胺D 2受体拮抗剂)刺激小。正常小鼠的肠蠕动。它们抑制多巴胺(1 mg / kg,腹膜内注射,腹膜内注射)引起的胃排空和胃肠蠕动的减少。提取物(1000 mg / kg)和β-eudesmol(100 mg / kg)抑制了阿托品引起的小肠蠕动降低,但没有抑制胃排空。此外,提取物(500或1000 mg / kg)和β-eudesmol(25、50或100 mg / kg)抑制了由5-HT(4 mg / kg,腹腔注射)或HT引起的胃排空和小肠蠕动的减少。 5-HT 3受体激动剂1-(3-氯苯基)双胍(0.5 mg / kg,ip),但不是5-HT 2C受体激动剂。这些发现表明,白术和β-迷迭香提取物可能通过抑制多巴胺D 2受体和5-HT 3受体而刺激胃排空或小肠蠕动。

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