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口服可卡因自我给药:运动活性与药代动力学的关系。

Oral cocaine self-administration: relation of locomotor activity to pharmacokinetics.

作者信息

Lau C E, Falk J L, King G R

机构信息

Department of Psychology, Rutgers University, New Brunswick, NJ 08903.

出版信息

Pharmacol Biochem Behav. 1992 Sep;43(1):45-51. doi: 10.1016/0091-3057(92)90637-u.

Abstract

Rats were exposed to daily schedule-induced polydipsia sessions in which solutions of cocaine HCl were available. Both cocaine solution concentration (0.08-0.32 mg/ml) and session duration (0.25-3 h) were varied to determine their effects on locomotor activity rate. Additional animals were used to determine the effect of session length on serum cocaine and metabolite levels when drinking 0.32 mg/ml cocaine solution. Changes in locomotor activity rate were related to serum cocaine concentration by a linear concentration-effect model. By estimation from the linear model, the serum cocaine concentration threshold for increasing locomotor activity was about 0.01 microgram/ml. Under these schedule-induction conditions, there was no evidence for the development of acute tolerance to the locomotor-stimulating activity of cocaine.

摘要

将大鼠暴露于每日定时诱导的多饮实验中,实验期间可获得盐酸可卡因溶液。改变可卡因溶液浓度(0.08 - 0.32毫克/毫升)和实验持续时间(0.25 - 3小时),以确定它们对运动活动率的影响。使用额外的动物来确定当饮用0.32毫克/毫升可卡因溶液时,实验时长对血清可卡因和代谢物水平的影响。运动活动率的变化通过线性浓度-效应模型与血清可卡因浓度相关。根据线性模型估计,增加运动活动的血清可卡因浓度阈值约为0.01微克/毫升。在这些定时诱导条件下,没有证据表明对可卡因的运动刺激活性产生急性耐受性。

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