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大鼠对麻醉药品慢性恒定剂量治疗的运动反应。

Motility response of rats to chronic constant-dose treatment with narcotics.

作者信息

Davis W M, Hemnani K L, Pace H B

出版信息

Pharmacol Biochem Behav. 1982 Sep;17(3):489-94. doi: 10.1016/0091-3057(82)90309-4.

Abstract

The changes in effects on motor activity of rats upon repeated (48 day) dosing with four narcotic analgesics were determined. The following were administered IP once daily in a.m.: morphine sulfate (MOR), 20 mg/kg: dl-methadone HCl (MET), 5 mg/kg: meperidine HCl (MEP), 10 mg/kg; and pentazocine lactate (PEN), 20 mg/kg. Motility was measured in photocell actometers every 4 days for 6 hr after dosing. Activity was elevated after the initial dose as follows: for MOR at hours 3-5, for MET at hours 2-5, for MEP and PEN at hours 2-3. Time of peak response showed no systematic change over days. For all 4 drugs there occurred, upon repeated dosing, a considerable increase in motility over the initial acute response. For MOR the greatest increment occurred between days 12 and 16, but regression analysis showed a strong linear trend of increasing activity from day 1 through day 48. For MET and MEP, activity rose considerably between days 4 and 12 to a maximum, after which the activity trended downward for MET, but showed no continuing fall or climb for MEP. For PEN the greatest increases were from days 4 to 8 and 44 to 48, with an intervening period of relative stability. These results seem to be more readily explainable in terms of increasing sensitivity to the motor excitatory actions of these agents than merely by a development of tolerance to motor-inhibitory actions.

摘要

测定了四种麻醉性镇痛药重复给药(48天)对大鼠运动活性的影响变化。以下药物于上午每天一次腹腔注射给药:硫酸吗啡(MOR),20毫克/千克;盐酸消旋美沙酮(MET),5毫克/千克;盐酸哌替啶(MEP),10毫克/千克;乳酸喷他佐辛(PEN),20毫克/千克。给药后每4天在光电活动计中测量6小时的运动能力。初始给药后活性升高情况如下:MOR在给药后3 - 5小时,MET在给药后2 - 5小时,MEP和PEN在给药后2 - 3小时。峰值反应时间在数天内未显示出系统性变化。对于所有4种药物,重复给药后,运动能力较初始急性反应有相当大的增加。对于MOR,最大增幅出现在第12天至第16天之间,但回归分析显示从第1天到第48天活性有强烈的线性增加趋势。对于MET和MEP,活性在第4天至第12天之间大幅上升至最大值,此后MET的活性呈下降趋势,但MEP的活性未持续下降或上升。对于PEN,最大增幅出现在第4天至第8天和第44天至第48天之间,中间有一段相对稳定期。这些结果用对这些药物运动兴奋作用的敏感性增加来解释似乎比仅仅用对运动抑制作用的耐受性发展来解释更容易。

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