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应用脑内微透析技术研究药物在大鼠脑内的区域分布动力学。

Application of intracerebral microdialysis to study regional distribution kinetics of drugs in rat brain.

作者信息

de Lange E C, Bouw M R, Mandema J W, Danhof M, de Boer A G, Breimer D D

机构信息

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

出版信息

Br J Pharmacol. 1995 Nov;116(5):2538-44. doi: 10.1111/j.1476-5381.1995.tb15107.x.

Abstract
  1. The purpose of the present study was to determine whether intracerebral microdialysis can be used for the assessment of local differences in drug concentrations within the brain. 2. Two transversal microdialysis probes were implanted in parallel into the frontal cortex of male Wistar rats, and used as a local infusion and detection device respectively. Within one rat, three different concentrations of atenolol or acetaminophen were infused in randomized order. By means of the detection probe, concentration-time profiles of the drug in the brain were measured at interprobe distances between 1 and 2 mm. 3. Drug concentrations were found to be dependent on the drug as well as on the interprobe distance. It was found that the outflow concentration from the detection probe decreased with increasing lateral spacing between the probes and this decay was much steeper for acetaminophen than for atenolol. A model was developed which allows estimation of kbp/Deff (transfer coefficient from brain to blood/effective diffusion coefficient in brain extracellular fluid), which was considerably larger for the more lipohilic drug, acetaminophen. In addition, in vivo recovery values for both drugs were determined. 4. The results show that intracerebral microdialysis is able to detect local differences in drug concentrations following infusion into the brain. Furthermore, the potential use of intracerebral microdialysis to obtain pharmacokinetic parameters of drug distribution in brain by means of monitoring local concentrations of drugs in time is demonstrated.
摘要
  1. 本研究的目的是确定脑内微透析是否可用于评估脑内药物浓度的局部差异。2. 将两根横向微透析探针平行植入雄性Wistar大鼠的额叶皮质,分别用作局部输注和检测装置。在一只大鼠体内,以随机顺序输注三种不同浓度的阿替洛尔或对乙酰氨基酚。通过检测探针,在探针间距为1至2毫米的情况下测量脑内药物的浓度-时间曲线。3. 发现药物浓度既取决于药物,也取决于探针间距。发现检测探针的流出浓度随着探针之间横向间距的增加而降低,并且对乙酰氨基酚的这种衰减比对阿替洛尔陡峭得多。建立了一个模型,该模型可以估计kbp/Deff(从脑到血的转运系数/脑细胞外液中的有效扩散系数),对于亲脂性更强的药物对乙酰氨基酚,该值要大得多。此外,还测定了两种药物的体内回收率。4. 结果表明,脑内微透析能够检测到药物注入脑内后药物浓度的局部差异。此外,还证明了通过及时监测脑内局部药物浓度,脑内微透析在获取药物在脑内分布的药代动力学参数方面的潜在用途。

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