首页> 外文期刊>Clinical and experimental pharmacology & physiology >Pharmacokinetics and pharmacodynamics of indomethacin: effects on cerebral blood flow in anaesthetized sheep.
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Pharmacokinetics and pharmacodynamics of indomethacin: effects on cerebral blood flow in anaesthetized sheep.

机译:消炎痛的药代动力学和药效学:对麻醉羊脑血流的影响。

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1. Indomethacin has been used to manage raised intracranial pressure (ICP) in humans during neuroanaesthesia and neurosurgery. Indomethacin causes cerebral vasoconstriction and reduces cerebral blood flow (CBF) and, therefore, ICP. 2. The systemic kinetics, cerebral kinetics and cerebral dynamics of indomethacin (0.2 mg/kg) were measured and modelled using a population approach. Data were collected using an instrumented sheep preparation with raised ICP and under either isoflurane or propofol anaesthesia to parallel the clinical use of indomethacin in neurosurgery. 3. The systemic kinetics of indomethacin could be described by a two-compartment model, with small distribution volumes and a clearance of 0.68 L/min. The cerebral kinetics of indomethacin could be described using a model with a cerebral distribution volume between 5 and 8 mL and a loss term of 3.3 mL/min, the latter probably representing slow diffusion across the blood-brain barrier. 4. The changes in CBF lagged behind the blood concentrations of indomethacin. Indirect response models with turnover times of 1.70-4.08 min were generally better able to describe the effect of indomethacin on CBF than effect compartment models. 5. There was a non-linear concentration-effect relationship, with the maximum possible reduction in CBF being to 73-74% of baseline. 6. The data and model support the concept of indomethacin having limited uptake into the brain, with its effect on CBF being the result of its action on the endothelium, where it indirectly modifies the turnover of a compound regulating vascular tone.
机译:1.吲哚美辛已被用于在神经麻醉和神经外科手术中控制人颅内压升高(ICP)。消炎痛可引起脑血管收缩并减少脑血流量(CBF),因此引起ICP。 2.使用人口方法对吲哚美辛(0.2 mg / kg)的全身动力学,脑动力学和脑动力学进行了测量和建模。使用仪器仪表的绵羊制备物,其ICP升高,并在异氟烷或异丙酚麻醉下收集数据,以与吲哚美辛在神经外科中的临床应用相平行。 3.吲哚美辛的全身动力学可以用两室模型描述,其分布体积小,清除率为0.68 L / min。吲哚美辛的脑动力学可以用大脑分布体积在5到8 mL之间且损失项为3.3 mL / min的模型来描述,后者可能代表了跨血脑屏障的缓慢扩散。 4. CBF的变化落后于消炎痛的血药浓度。与效应区室模型相比,周转时间为1.70-4.08分钟的间接响应模型更能描述吲哚美辛对CBF的作用。 5.存在非线性浓度-效应关系,脑血流量的最大可能降低为基线的73-74%。 6.数据和模型支持吲哚美辛对大脑的吸收有限的概念,其对CBF的影响是其对内皮的作用的结果,在内皮中它间接改变了调节血管紧张度的化合物的更新。

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