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复方威茯急性毒性实验及抗炎镇痛作用观察

Study on Acute Toxicity,Anti-inflammatory and Analgesic Effects of Fufang Weifu
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摘要 研究复方威茯的急性毒性作用,并观察其抗炎镇痛作用。以最大给药量方法进行急性毒性实验,观察小鼠一般情况等,14 d后处死解剖,观察小鼠主要脏器组织病变情况。以二甲苯致小鼠耳廓肿胀、醋酸致小鼠腹腔毛细血管通透性增加,实验观察复方威茯抗炎作用。以冰醋酸致小鼠扭体、热板致小鼠疼痛探讨复方威茯镇痛作用。结果在急性毒性实验中,未见小鼠有中毒症状或死亡,外观表现未见异常,解剖后未见脏器异常;复方威茯可明显抑制二甲苯所致小鼠耳廓肿胀度和醋酸致腹腔毛细血管通透性的增高(P<0.05或P<0.01),可明显减少醋酸致小鼠扭体反应次数(P<0.01),可提高热板致小鼠疼痛的痛阈值(P<0.05或P<0.01)。说明复方威茯无明显的急性毒性作用,有明显的抗炎镇痛作用。 To study the acute toxicity, anti-inflammatory and analgesic effects of Fufang Weifu, the acute toxicity experiment of Fufang Weifu was done through maximum dose of stomach perfusion in mice to observe their general state,etc. 14d later, mice was dissected to observe the lesions of major organs and tissues, ter dissected, heart, liver and other major organs and tissues lesions. Models of acute inflammatory reactions edema caused by xylene in mouse ear and acetic acid-induced abdominal capillary permeability increases to observe anti-inflammatory of compound Weifu. Methods of acetic acid-induced writhing and hot-plate test in mice to observe analgesic of compound Weifu. In the acute toxicological test, no clinical signs or death were found in mice, the general conditions,major organs and tissues of mice were not abnormal. Fufang Weifu can significantly counteracted xylene-induced mouse ear edema and acetic acid-induced elevation of abdominal capillary permeability(P 〈 0. 05 or P 〈 0. 01 ). It could relieve the pain caused by acetic acid(P 〈0. 01) and hot-plate(P 〈0.05 or P 〈0. 01 ). It is conclused that Fufang Weifu showed no significant acute toxicity, but markedly anti-inflammatory and analgesic effects in the study .
出处 《科学技术与工程》 北大核心 2015年第16期141-143,148,共4页 Science Technology and Engineering
基金 广西中医药管理局中医药科技专项课题(GXYZ1136) 广西科技基础条件平台建设项目(13-051-06) 广西中药药效研究重点实验室开放课题(13-051-06-K2)资助
关键词 复方威茯 急性毒性 抗炎 镇痛 Fufang Weifu acute toxicity anti-inflammatory analgesic
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  • 1陈益华,张华杰,南发俊.Caspases抑制剂的研究进展[J].生命科学,2006,18(3):247-254. 被引量:13
  • 2朱深银,周远大,杜冠华.防治痛风药物的研究进展[J].医药导报,2006,25(8):803-806. 被引量:31
  • 3苑辉卿,薛克亮,任红玉.土茯苓的研究概况[J].中国中药杂志,1997,22(5):315-317. 被引量:15
  • 4余存.青霉素治疗痛风30例临床分析.综合临床医学,1996,12(2):108-108.
  • 5鲁子平.治疗痛风药物的临床应用研究[J].中国药房,2007,18(29):2313-2314. 被引量:5
  • 6ANZAI N, ENOMOTO A, ENDOU H. Renal urate handling clinical relevance of recent advances [ J ]. Curr Rheumatol Rep,2005,7 (3) 1227 - 234.
  • 7HEDIGER M A, JOHNSON R J, MIYAZAKI H, et al. Molecular physiology of urate transport [ J ]. Phy- siology (Bethesda) ;2005,20 (2) : 125 - 133.
  • 8HYON K C,DAVID B M,ANTHONY M R. Patho- genesis of gout[ J]. Ann Intern Meal,2005,143 ( 7 ) : 499 -516.
  • 9SATO Y, ARAI N, NEGISHI A. Expression of cy- clooxygenase genes and involvement of endogenous prostaglandin during osteogenesis in the rat tibial bone marrow cavity [ J ]. J Med Dent Sci, 1997,44 (4) :81 -92.
  • 10MORRIS I, VARUGHESE G, MATI'INGLY P. Col- chicine in acute gout [ J ]. Br Med J, 2003, 327 (7426): 1275 - 1276.

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