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来自婆罗洲的药用植物多杜蓬朴(Fagraea racemosa)的药理活性成分。

Pharmacologically active components of Todopon Puok (Fagraea racemosa), a medicinal plant from Borneo.

作者信息

Okuyama E, Suzumura K, Yamazaki M

机构信息

Faculty of Pharmaceutical Sciences, Chiba University, Japan.

出版信息

Chem Pharm Bull (Tokyo). 1995 Dec;43(12):2200-4. doi: 10.1248/cpb.43.2200.

Abstract

The lignans of (+)-pinoresinol, (+)-epipinoresinol, (+)-lariciresinol and (+)-isolariciresinol together with phenols such as syringaldehyde and 7,8-dihydro-7-oxy-coniferyl alcohol were isolated from Todopon Puok (Fagraea racemosa Jack ex Wall), a medicinal plant from Borneo, using a bioassay of the relaxation effect on norepinephrine (NE)-induced contraction in rat aortic strips. The plant extract also exhibited analgesic properties in the acetic acid-induced writhing and tail pressure tests in mice, with the activity being concentrated in the lignan fraction. (+)-Pinoresinol showed analgesic effect on writhing symptoms in mice which were dose-dependent, and produced local anesthesia in guinea pigs.

摘要

从婆罗洲的药用植物托多蓬普奥克(Fagraea racemosa Jack ex Wall)中分离出了(+)-松脂醇、(+)-表松脂醇、(+)-落叶松脂醇和(+)-异落叶松脂醇的木脂素,以及诸如丁香醛和7,8-二氢-7-氧代松柏醇等酚类物质,采用对大鼠主动脉条中去甲肾上腺素(NE)诱导的收缩的松弛作用生物测定法。该植物提取物在小鼠的醋酸诱导扭体和尾压试验中也表现出镇痛特性,活性集中在木脂素部分。(+)-松脂醇对小鼠的扭体症状显示出镇痛作用,且呈剂量依赖性,并在豚鼠中产生局部麻醉作用。

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