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作为一种测定大鼠脑内药物药代动力学的技术,脑微透析的关键因素。

Critical factors of intracerebral microdialysis as a technique to determine the pharmacokinetics of drugs in rat brain.

作者信息

de Lange E C, Danhof M, de Boer A G, Breimer D D

机构信息

Leiden/Amsterdam Center for Drug Research, Division of Pharmacology, Sylvius Laboratory, The Netherlands.

出版信息

Brain Res. 1994 Dec 12;666(1):1-8. doi: 10.1016/0006-8993(94)90276-3.

Abstract

The purpose of this investigation was to determine the effect of experimental conditions on the concentrations of atenolol and acetaminophen in brain microdialysate, and to investigate the feasibility of performing repeated experiments within individual rats. Following intravenous bolus administration, reproducible concentration-time profiles were obtained in plasma and in brain dialysate. Based on corrections for in vitro recoveries of the intracerebral probe, the estimated ratio of the AUC in brain extracellular fluid (AUCbrain ECF) over the AUC in plasma (AUCplasma) +/- S.E.M. was 3.8 +/- 0.6% (n = 6) for atenolol and 18 +/- 2% (n = 6) for acetaminophen. Upon intracerebroventricular administration, interanimal differences in kinetics of acetaminophen in brain dialysate were observed while the concentrations of atenolol were below the detection limit of the assay. The influence of the use of isotonic versus hypotonic perfusate solutions on AUCbrain ECF values after intravenous bolus administration of both drugs was determined. Repeated experiments with the isotonic perfusate (24, 48 and 78 h post-surgery) resulted in AUCbrain ECF values with the ratio of 100: 98: 76% for acetaminophen and 100: 103: 98% for atenolol. Using a hypotonic perfusion solution the ratio of AUCbrain ECF values was 100: 154: 114% for acetaminophen and 100: 378: 427% for atenolol. A clear effect of the temperature of the hypotonic perfusate (24 vs 38 degrees C) on acetaminophen AUCbrain ECF values was revealed. The ratio of AUCbrain ECF values obtained at 24: 38 degrees C was 192: 100%.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究的目的是确定实验条件对脑微透析液中阿替洛尔和对乙酰氨基酚浓度的影响,并研究在个体大鼠体内进行重复实验的可行性。静脉推注给药后,在血浆和脑透析液中获得了可重复的浓度-时间曲线。基于脑内探针体外回收率的校正,脑细胞外液中AUC(AUCbrain ECF)与血浆中AUC(AUCplasma)的估计比值±标准误,阿替洛尔为3.8±0.6%(n = 6),对乙酰氨基酚为18±2%(n = 6)。脑室内给药后,观察到脑透析液中对乙酰氨基酚动力学的动物间差异,而阿替洛尔的浓度低于检测限。确定了等渗与低渗灌注液对两种药物静脉推注给药后AUCbrain ECF值的影响。使用等渗灌注液进行重复实验(术后24、48和78小时),对乙酰氨基酚的AUCbrain ECF值比值为100:98:76%,阿替洛尔为100:103:98%。使用低渗灌注液时,对乙酰氨基酚的AUCbrain ECF值比值为100:154:114%,阿替洛尔为100:378:427%。揭示了低渗灌注液温度(24℃与38℃)对对乙酰氨基酚AUCbrain ECF值的明显影响。在24℃:38℃下获得的AUCbrain ECF值比值为192:100%。(摘要截断于250字)

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