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首页> 外文期刊>Japanese Journal of Pharmacology >ANALGESIC POTENCIES OF NON-NARCOTIC, NARCOTIC AND ANESTHETIC DRUGS AS DETERMINED BY THE BRADYKININ-INDUCED BITING-LIKE RESPONSES IN RATS
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ANALGESIC POTENCIES OF NON-NARCOTIC, NARCOTIC AND ANESTHETIC DRUGS AS DETERMINED BY THE BRADYKININ-INDUCED BITING-LIKE RESPONSES IN RATS

机译:缓激肽诱导的类似行为的反应确定非麻醉性,麻醉性和麻醉性药物的止痛潜力

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摘要

References(13) Cited-By(4) Aversive (nociceptive) biting-like responses induced by micro-application of bradykinin solution onto rat tooth pulp were dose-dependently suppressed by nonnarcotic drugs such as baclofen and lidocaine as well as carbamazepine and phenytoin, which are employed for clinical treatment of trigeminal neuralgia. The potency order of these drugs on a molar basis is baclofen (4.20)carbamazepine (1.00)lidocaine (0.94)phenytoin (0.19). Such responses were also inhibited by morphine, pentazocine and cyclazocine (potency ratio of the three general analgesics, 1.00:0.46:8.11 ), indomethacin (a non-narcotic and anti-inflammatory analgesic) and α-chloralose (an anesthetic). The latter drug produced an analgesic effect at doses much lower than those used for anesthesia. These findings suggest that our method is feasible for evaluating the activities of general and particular analgesic drugs in the trigeminal regions.
机译:参考文献(13)被引用的By(4)由缓激肽溶液微滴于大鼠牙髓引起的厌恶(伤害性)咬合反应被巴氯芬和利多卡因等非麻醉药以及卡马西平和苯妥英钠剂量依赖性地抑制,用于临床治疗三叉神经痛。这些药物的摩尔效价比为巴氯芬(4.20)>卡马西平(1.00)>利多卡因(0.94)>苯妥英钠(0.19)。此类反应也被吗啡,喷他佐辛和环唑嗪(三种普通镇痛药的药效比为1.00:0.46:8.11),消炎痛(一种非麻醉和消炎镇痛药)和α-氯草胺(麻醉药)抑制。后一种药物产生的镇痛作用远低于麻醉所用的剂量。这些发现表明我们的方法对于评估三叉神经区域的一般和特定止痛药的活性是可行的。

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