Loux J J, Smith S, Salem H
Arzneimittelforschung. 1978;28(9):1644-7.
Anti-writhing assays to detect analgesia or specific activity against selected agonists were performed on albino mice. Acetylcholine Cl, bradykinin triacetate, phenylquinone, and serotonin creatinine sulfate were used as agonists. 10 compounds, including 5 standard analgetics, were tested against each agonist. Attempts to study histamine phosphate as an agonist were not successful. Results of these investigations showed satisfactory analgetic acitivity for codeine phosphate and acteyl salicylic acid (ASA) in all assays. weaker analgetics displayed varying degrees of activity depending on the agonist tested. Acute oral toxicities were determined for the 10 test compounds and the analgetic ED50 vs the LD50 of each compound was compared. The data confirmed the nonspecificity for writhing assays as well as a variability in activity of the test compounds against the various agonist.
在白化小鼠身上进行了抗扭体试验,以检测镇痛效果或针对选定激动剂的特定活性。乙酰胆碱氯、缓激肽三乙酸盐、苯醌和血清素硫酸肌酐用作激动剂。针对每种激动剂测试了10种化合物,包括5种标准镇痛药。将磷酸组胺用作激动剂的研究未获成功。这些研究结果表明,在所有试验中,磷酸可待因和乙酰水杨酸(ASA)具有令人满意的镇痛活性。较弱的镇痛药根据所测试的激动剂显示出不同程度的活性。测定了10种受试化合物的急性口服毒性,并比较了每种化合物的镇痛半数有效量(ED50)与半数致死量(LD50)。数据证实了扭体试验的非特异性以及受试化合物针对各种激动剂的活性变异性。