...
首页> 外文期刊>Japanese Journal of Pharmacology >ALGESIOGENIC AND ANALGESIC ACTIVITIES OF SYNTHETIC SUBSTANCE P
【24h】

ALGESIOGENIC AND ANALGESIC ACTIVITIES OF SYNTHETIC SUBSTANCE P

机译:合成物质P的代孕和止痛活性

获取原文
           

摘要

References(24) Cited-By(10) The objective of our study was to determine whether the pure synthetic substance P(SP) is algesiogenic or analgesic when administered centrally or peripherally. The relationships between SP-induced analgesia and the content of morphine-like factor (MLF) in the brain were also studied. Intracarotid arterial administration of SP (20-200 μg) produced no pseudoaffective responses to pain in six out of nine rats, but in the remaining three, there was an exhibition of these responses. Chlorpheniramine pretreatment antagonized these responses. On cantharidin blister base experiments in humans, SP (10-3 g/ml) produced slight pain and an itchy sensation. SP given intracerebroventricularly produced an analgesia in mice in a dose of 5 ng/mouse, as determined by the acetic acid-induced writhing and hot plate methods. These SP-induced analgesia were antagonized by naloxone pretreatment. SP did not alter the content of MLF in the mouse whole brain. However, SP5-11 not only produced an analgesia but also increased the content of MLF. These results suggest that SP has a slight algesiogenic activity which might be mediated by histamine and a slight analgesic activity which might be mediated by MLF.
机译:参考文献(24)被引依据(10)我们的研究目的是确定纯合成物质P(SP)在中央或周边给药时是否具有镇痛作用或止痛作用。还研究了SP诱导的镇痛作用与脑中吗啡样因子(MLF)含量之间的关系。颈动脉内注射SP(20-200μg)在9只大鼠中有6只对疼痛没有产生假情感反应,但在其余3只中,这些反应均表现出来。氯苯那敏预处理可拮抗这些反应。在人体中的斑din素水泡基础实验中,SP(10-3 g / ml)产生轻微的疼痛和发痒的感觉。通过乙酸诱发的扭体法和热板法测定,脑室内SP小鼠以5 ng /小鼠的剂量产生镇痛作用。纳洛酮预处理可拮抗这些SP诱导的镇痛作用。 SP不会改变小鼠全脑中MLF的含量。但是,SP5-11不仅产生镇痛作用,而且增加了MLF的含量。这些结果表明SP具有可能由组胺介导的轻微的镇痛活性和可能由MLF介导的轻微的镇痛活性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号