Suppr超能文献

从甘松中提取的倍半萜类化合物马兜铃烯-1(10)-烯-9-醇经吸入给药,通过γ-氨基丁酸能系统产生镇静作用。

Inhalation administration of the sesquiterpenoid aristolen-1(10)-en-9-ol from Nardostachys chinensis has a sedative effect via the GABAergic system.

作者信息

Takemoto Hiroaki, Ito Michiho, Asada Yoshihisa, Kobayashi Yoshinori

机构信息

School of Pharmacy, Kitasato University, Tokyo, Japan.

Graduate School of Pharmaceutical Sciences, Kyoto University, Kyoto, Japan.

出版信息

Planta Med. 2015 Mar;81(5):343-7. doi: 10.1055/s-0035-1545725. Epub 2015 Mar 23.

Abstract

Spikenard, the dried roots of Nardostachys chinensis, contains sesquiterpenoids and is widely used as an herbal tranquilizer. We previously demonstrated that spikenard vapor showed a sedative effect when administered by inhalation, and we identified hydrocarbon sesquiterpenoids as active components. Here we investigated the other components that contribute to the effects of spikenard. Six oxygenated sesquiterpenoids, including aristolane- and guaiane-types, were isolated from an acetone extract of spikenard. We evaluated the sedative activities of these oxygenated compounds using an inhalation administration method in a caffeine-treated excitatory mouse model. We identified aristolen-1(10)-en-9-ol and patchouli alcohol as highly effective sedative components. These compounds inhibited locomotion in mice by approximately 60% at a dose of 300 µg/cage. In addition, aristolen-1(10)-en-9-ol prolonged pentobarbital-induced sleep to the same extent as 1 mg/kg diazepam. This effect completely disappeared with the administration of the GABAA-benzodiazepine receptor antagonist flumazenil (3 mg/kg), suggesting that the sedative effect of aristolen-1(10)-en-9-ol is expressed via the GABAergic system. Furthermore, differently from diazepam, inhalation of aristolen-1(10)-en-9-ol for 1 h did not affect the motor coordination in the rota-rod test. In the present study, we identified active components and provided evidence supporting the traditional sedative use of spikenard. Our research suggests that aristolen-1(10)-en-9-ol may be an effective aromatherapy, providing mild sedation.

摘要

甘松,即甘松(Nardostachys chinensis)的干燥根,含有倍半萜类化合物,被广泛用作草药镇静剂。我们之前证明,甘松挥发物通过吸入给药时具有镇静作用,并且我们确定烃类倍半萜为活性成分。在此,我们研究了其他对甘松药效有贡献的成分。从甘松的丙酮提取物中分离出六种含氧倍半萜,包括马兜铃烷型和愈创木烷型。我们在咖啡因处理的兴奋性小鼠模型中使用吸入给药方法评估了这些含氧化合物的镇静活性。我们确定马兜铃-1(10)-烯-9-醇和广藿香醇为高效镇静成分。这些化合物在剂量为300μg/笼时可使小鼠运动减少约60%。此外,马兜铃-1(10)-烯-9-醇可使戊巴比妥诱导的睡眠时间延长至与1mg/kg地西泮相同的程度。给予GABAA-苯二氮䓬受体拮抗剂氟马西尼(3mg/kg)后,这种作用完全消失,表明马兜铃-1(10)-烯-9-醇的镇静作用是通过GABA能系统发挥的。此外,与地西泮不同,吸入马兜铃-1(10)-烯-9-醇1小时对转棒试验中的运动协调性没有影响。在本研究中,我们确定了活性成分,并为甘松传统的镇静用途提供了证据支持。我们的研究表明,马兜铃-1(10)-烯-9-醇可能是一种有效的芳香疗法,可提供轻度镇静作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验