一种有意识Göttingen微型猪的微创连续脑脊液取样模型

A. Bergadano, E. M. Amen, B. Jacobsen, S. Belli, Anthony Vandjour, Christelle Rapp, C. Senn
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引用次数: 5

摘要

脑脊液(CSF)中的药物浓度通常被用作其在中枢神经系统中可用性的替代测量,动物研究中的CSF穿透性用于评估早期临床前药物开发中的中枢神经系统药物递送。在临床前研究中,迷你猪是狗和非人灵长类动物作为非啮齿动物的有效替代品,但该物种具有解剖学上的特殊性,使得CSF的系列收集在技术上具有挑战性。在临床前研究中,建立了一种通过蛛网膜下腔导管在有意识的小型猪体内进行微创连续脑脊液采集模型,以评估药物在中枢神经系统中的纵向药代动力学。不久,麻醉后的迷你猪用Tuohy针穿刺进入蛛网膜下腔;当脑脊液流过针头时,将导管推进,然后穿隧固定在背部。在清醒的动物中进行皮下给药肽A的PK,并在长达48小时的时间内取样脑脊液。与血浆动力学数据相比,Pept的消除期有明显差异。A来自脑脊液,在脑脊液中的平均终末半衰期明显更长。通过减少中枢神经系统药代动力学分析所需的动物数量,提高模型的有效性,避免因麻醉、血液污染和个体间变异性造成的偏差,可以解决3r问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A minimally-invasive serial cerebrospinal fluid sampling model in conscious Göttingen minipigs
Drug concentrations in cerebrospinal fluid (CSF) are typically used as a as a surrogate measure of their availability in the CNS, and CSF penetration in animal studies are used for assessment of CNS drug delivery in early preclinical drug development. The minipig is a valid alternative to dogs and non-human primates as non-rodent species in preclinical research, but this species presents anatomical peculiarities that make the serial collection of CSF technically challenging. A minimally-invasive serial cerebrospinal fluid collection model via catheterization of the subarachnoid space in conscious minipigs was developed allowing assessment of longitudinal drug pharmacokinetics in the central nervous system in preclinical research. Shortly, the subarachnoid space was accessed in the anesthetized minipig by puncture with a Tuohy needle; when CSF was flowing through the needle a catheter was advanced and thereafter tunneled and fixed on the back. The PK of peptide A administered subcutaneously was performed and CSF could be sampled in the conscious animals for up to 48 h. When compared to the plasma kinetic data, there was a clear difference in the elimination phase of Pept. A from CSF, with an apparent longer average terminal half-life in CSF. The 3Rs are addressed by reducing the number of animals needed for a pharmacokinetic profile in central nervous system and by improving the validity of the model avoiding biases due to anesthesia, blood contamination, and inter-individual variability.
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