丙泊西泮对不同炎症模型的抗炎作用

N. Golovenko, T. A. Kabanova, S. Andronati, O. I. Halimova, V. Larionov, A. Reder
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引用次数: 7

摘要

背景丙氧西泮,7-溴-5-(2-氯苯基)-3-丙氧基-1H-苯并[e][1,4]二氮杂-2(3H)-酮,是一种很有前途的镇痛和抗惊厥剂,目前正在进行临床前试验。客观的本研究旨在研究丙泊酚的抗炎镇痛作用。方法。通过卡拉胶诱导的大鼠足水肿、甲醛诱导的小鼠舔爪反应和缓激肽诱导的大白鼠疼痛反应来评价其抗炎作用。后果首次确定,当在不同的体内化学诱导炎症实验模型中进行测试时,即卡拉胶、缓激肽和福尔马林诱导的炎症测试中,给予丙氧西泮会产生显著的抗炎活性。结论。丙泊酚显著减轻急性和亚急性炎症,并证明其疗效和类似的抗炎作用。
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ANTI-INFLAMMATORY EFFECTS OF PROPOXAZEPAM ON DIFFERENT MODELS OF INFLAMMATION
Background. Propoxazepam, 7-bromo-5-(2-chlorophenyl)-3-propoxy-1H-benzo[e][1,4]diazepin-2(3H)-one, is a promising analgesic and anticonvulsant and is on preclinical trial. Objective. The aim of the research was to study the anti-inflammatory and analgesic action of Propoxazepam. Methods. The anti-inflammatory action was evaluated by carrageenan induced rat paw edema, formalininduced paw licking response in mice and bradykinin-induced pain response in rat models. Results. It was established for the first time that the administration of Propoxazepam caused a significant anti-inflammatory activity when tested in different in vivo chemical experimental models of induced inflammation, i.e. carrageenan-, bradykininand formalin-induced inflammation tests. Conclusions. Propoxazepam significantly reduced acute and sub-acute inflammation and proved its efficacy and similar to anti-inflammatory action.
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发文量
14
审稿时长
36 weeks
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