Teiger D G
J Pharmacol Exp Ther. 1976 May;197(2):311-6.
Ethylenediamine tetraacetic acid (EDTA) was used as a nociceptive stimulus intradermally in the guinea pig. The responses evoked by EDTA included vocalization, biting and scratching at the site of injection and escape behavior. Nociception by EDTA was shown to be the result of its cation chelating activity. The suppression of EDTA-induced responses proved to be a rapid and effective antinociceptive test. The narcotic analgesics morphine, codeine, meperidine and methadone and the narcotic antagonist analgesics cyclazocine, cyclorphan, nalorphine and pentazocine were active. The slopes of the dose-response curves of the narcotic antagonist analgesics were significantly shallower than those of the narcotic analgesics. The test was highly specific for these analgesics. Antipyretic analgesics and various nonanalgesic drugs were inactive.
在豚鼠身上,乙二胺四乙酸(EDTA)被用作皮内伤害性刺激物。EDTA引发的反应包括发声、在注射部位啃咬和抓挠以及逃避行为。已证明EDTA引起的伤害感受是其阳离子螯合活性的结果。对EDTA诱导反应的抑制被证明是一种快速有效的抗伤害感受测试。麻醉性镇痛药吗啡、可待因、哌替啶和美沙酮以及麻醉性拮抗镇痛药环唑辛、环芬太尼、烯丙吗啡和喷他佐辛都有活性。麻醉性拮抗镇痛药的剂量-反应曲线斜率明显比麻醉性镇痛药的斜率更平缓。该测试对这些镇痛药具有高度特异性。解热镇痛药和各种非镇痛药无活性。