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阿魏洛芬的解热和局麻作用 被引量:4

ANTIPYRETIC AND ANESTHETIC ACTIVITY OF FERULOFEN
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摘要 肌注阿魏洛芬45mg和200mg/kg对伤寒、副伤寒三联菌苗和酵母粉悬液引起家兔和大鼠的发热反应具有明显的解热作用,其强度分别与肌注阿斯匹林35mg和100mg/kg基本相当。1%阿魏洛芬局部用药除对家兔角膜反射无影响外,在蟾蜍离体坐骨神经动作电位和豚鼠皮内丘疹痛觉反应中其阻滞强度明显弱于同浓度普鲁卡因和利多卡因,但均显示有一定的可逆性局麻效应。上述作用与前文结果进一步说明阿魏洛芬可能成为抗炎解热镇痛新药。 Ferulof en ( FL, 45mg and 200mg/kg im ) showed marked antipyretic effect on rabbit fever induced by typho-paratyhoid vaccine and on rat fever induced by yeast powder suspension respectively. Their potency and action phase were similar to those of aspirin ( 35mg and 100mg/kg) . Furthermore, it blocked the action potential of sciatic nerve in toad to some extent and had a certain local anesthetic effect on guinea pigs in intradermic wheal test, but much weaker than procaine and lidocaine at the same concentration. It had no obvious influence on corneal reflex in rabbits. It can be concluded from these findings that together with the results of previous paper the findings of this paper further indicated FL may be proved to be a new antiinflammatory, antipyretic and analgesic drug.
出处 《中国药理学通报》 CAS CSCD 北大核心 1990年第6期367-370,共4页 Chinese Pharmacological Bulletin
关键词 阿魏洛芬 解热 局麻 拾炎药 Ferulofen Non-steroidal antiinflammatory drug Antipyretic effect Local anesthetic activity
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同被引文献24

  • 1於传斌,吴华璞,葛敏,余晨光,赵明敏,陶明飞,隋治华,周淑兰,张琳萍,计志忠.阿魏洛芬的抗炎镇痛抗肿瘤作用[J].中国药理学通报,1989,5(5). 被引量:8
  • 2黄英,曾经泽.反相高效液相层析法测定人血浆中阿魏酸哌嗪含量[J].药物分析杂志,1989,9(4):194-196. 被引量:2
  • 3王秋娟,李运曼,李璐,燕金沛.风湿康Ⅰ号的镇痛和部分抗炎作用研究[J].中国药科大学学报,1996,27(2):111-114. 被引量:1
  • 4董怡.非甾体抗炎药的新进展[J].辽宁医学杂志,1997,11(1):16-17. 被引量:4
  • 5於传斌,中国药理学通报,1989年,5卷,5期,303页
  • 6郭玉麟,华西药学杂志,1987年,2卷,1期,54页
  • 7许景峰,药学通报,1987年,22卷,10期,618页
  • 8HAMBURGER M,HOSTETTMANN K.Glycosidic constituents of some European polygala species[J].J Nat Prod,1986,49(3):557.
  • 9KATSUMI I,KONDO H,YAMASHITA K,et al.Studies on styrene derivatives.I.Synthesis and antiinflammatory activities of α-benzylidene-γ-butyrolactone derivatives[J].Chem Pharm Bull,1986,34(1):121.
  • 10HIDAKA T,HOSOE K,ARIKI Y,et al.Pharmacological properties of a new anti-inflammatory compound,α-(3,5-di-tert-butyl-4-hydroxy-benzylidene)-γ-butyrolactone(KME-4),and its inhibitory effects on prostaglandin synthetase and 5-lipoxygenase[J].Jpn J Pharmacol,1984,36(1):77.

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