接筋藤醇提物初步安全性及镇痛抗炎实验研究
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云南省药物研究所/云南白药创新研发中心/云南省中药和民族药新药创制企业重点实验室,云南 昆明 650111

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R285.5

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* 基金项目: 云南省科技厅科技重大专项(2015Z703)
收稿日期: 2017 - 05- 05
作者简介: 张梦麒(1987-),男,云南个旧人,理学硕士,助理工程师,研究方向:天然药物药效学活性筛选。
△通信作者:苏梅,E-mail:smkms@126.com


Study on Acute Toxicity and Analgesic and Anti-inflammatory Effects of the Ethnol Extractionof Lepidogrammitis Drymoglossoides (Baker) Ching
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Yunnan Institute of Materia Medica/Yunnan Baiyao Group Innovation and R&D Center/Yunnan Province Company KeyLaboratory for TCM and Ethnic Drug of New Drug Creation, Kunming 650111, China

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    摘要:

    目的 研究接筋藤醇提物的小鼠灌胃给药急性毒性及镇痛抗炎作用,为接筋藤醇提物的临床安全及开发提供实验依据。方法 采用最大耐受量及最小致死量实验观察接筋藤醇提物的急性毒性,采用冰醋酸致小鼠扭体反应观察接筋藤醇提物的镇痛作用,用二甲苯致小鼠耳肿胀法研究其抗炎作用。结果 本实验所设计剂量范围及条件下,接筋藤醇提物24h内单次给药小鼠急性毒性实验的最小致死量为30.91g/kg·bw(相当于生药154.86 g/kg·bw);最大耐受量为24.73g/kg·bw(相当于生药123.90g/kg·bw)。接筋藤醇提物能抑制醋酸所致小鼠扭体性疼痛,并能抑制二甲苯所致小鼠耳廓肿胀。结论 本实验所设计剂量范围及条件下,接筋藤醇提物最小致死量为30.91g/kg·bw,最大耐受量为24.73g/kg·bw;接筋藤醇提物具有明显的镇痛抗炎作用。

    Abstract:

    Objective To study the acute toxicity and analgesic and anti-inflammatory effects of the ethnol extraction of Lepidogrammitis drymoglossoides(Baker) Ching in mice. Methods The acute toxicity was observed by maximum tolerance dose(MTD)experiment in mice, observed analgesic effect in mice by writhing reaction induced by glacial acetic acid, and to study the anti-inflammatory effect using the model of auricle edema in mice induced by xylene. Results The minimum lethal dose of the ethnol extraction of Lepidogrammitis drymoglossoides(Baker) Ching in mice is 30.91g/kg·bw, and the maximum tolerance dose of that is 24.73g/kg·bw. The ethnol extraction of Lepidogrammitis drymoglossoides(Baker) Ching could inhibit writhing pain induced by glacial acetic acid, and also could inhibit auricle edema induced by xylene in mice. Conclusion The minimum lethal dose of the ethnol extraction of Lepidogrammitis drymoglossoides(Baker) Ching in mice is 30.91g/kg·bw, and the maximum tolerance dose of that is 24.73g/kg·bw. The ethnol extraction of Lepidogrammitis drymoglossoides(Baker) Ching has significant analgesic anti-inflammatory effect.

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