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丙泊酚和乙醇对小鼠产生相加的催眠和麻醉作用。

Propofol and ethanol produce additive hypnotic and anesthetic effects in the mouse.

作者信息

Garfield J M, Bukusoglu C

机构信息

Anesthesia Research Laboratories, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.

出版信息

Anesth Analg. 1996 Jul;83(1):156-61. doi: 10.1097/00000539-199607000-00027.

Abstract

The sedative and anesthetic effects of ethanol and propofol when these drugs are coadministered are not known. Accordingly, we investigated the nature of the pharmacological interaction between ethanol and propofol during hypnosis and anesthesia in the mouse. Propofol, ethanol, and mixtures of the two were administered through the tail vein in male CD-1 mice (n = 162). The loss of righting response occurring 10 s after injection and persisting at least 10 s thereafter was defined as hypnosis, and lack of a motor response to tail clamping 60 s after injection was defined as anesthesia. The 50% effective dose (ED50) values for the hypnotic and anesthetic actions of the drugs were determined with quantal dose-response curves, using probit analysis. The pharmacological interactions were identified by the locations of ED50 values on their corresponding hypnosis and anesthesia isoboles. For each drug alone, the hypnotic and anesthetic ED50 values with 0.95 confidence intervals were 16.70 (11.98, 23.20) mg/kg and 25.02 (20.27, 31.29) mg/kg for propofol and 0.88 (0.81, 0.95) g/kg and 1.80 (1.45, 2.23) g/kg for ethanol, respectively. For the drugs in combination, the ED50 values for hypnosis with 0.95 confidence intervals were 6.98 (6.50, 7.49) mg/kg propofol with 0.61 (0.57, 0.66) g/kg ethanol, and for anesthesia were 10.55 (9.76, 11.42) mg/kg propofol with 0.93 (0.86, 1.05) g/kg ethanol, respectively. When plotted isobolographically, we found these combinations to be behaviorally additive both for hypnosis and anesthesia. Although a finding of synergism would have excluded the possibility of an identical mechanism of action for the drugs, elucidation of the molecular basis of the additivity must await further studies.

摘要

乙醇和丙泊酚联合使用时的镇静和麻醉效果尚不清楚。因此,我们研究了小鼠催眠和麻醉期间乙醇与丙泊酚之间药理相互作用的性质。将丙泊酚、乙醇以及二者的混合物通过尾静脉注射给雄性CD-1小鼠(n = 162)。注射后10秒出现的翻正反射消失并持续至少10秒被定义为催眠,注射后60秒对夹尾无运动反应被定义为麻醉。使用概率分析,通过剂量反应曲线确定药物催眠和麻醉作用的50%有效剂量(ED50)值。通过ED50值在相应的催眠和麻醉等效线图上的位置来确定药理相互作用。对于每种单独的药物,丙泊酚催眠和麻醉的ED50值及0.95置信区间分别为16.70(11.98,23.20)mg/kg和25.02(20.27,31.29)mg/kg,乙醇分别为0.88(0.81,0.95)g/kg和1.80(1.45,2.23)g/kg。对于联合用药,催眠的ED50值及0.95置信区间为丙泊酚6.98(6.50,7.49)mg/kg与乙醇0.61(0.57,0.66)g/kg,麻醉的为丙泊酚10.55(9.76,11.42)mg/kg与乙醇0.93(0.86,1.05)g/kg。当以等效线图绘制时,我们发现这些组合在催眠和麻醉方面在行为上都是相加的。尽管协同作用的发现会排除药物作用机制相同的可能性,但相加性分子基础的阐明仍需进一步研究。

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