Meyding-Lamadé U, Ehrhart K, de Ruiz H L, Kehm R, Lamadé W
Department of Neurology, University of Heidelberg, Germany.
J Exp Anim Sci. 1996;38(2):77-81.
This report describes a new technique for obtaining cerebrospinal fluid from the living mouse (SJL/NBom) in a model of herpes simplex virus encephalitis which is also applicable to other mouse models. The puncture technique was performed in living animals which had been infected with Herpes Simplex Virus Type I strain F in the living animal. The cisterna magna was micro-surgically prepared: The neck muscles were dissected microscopically down to the dura which subsequently was punctured by a glass micropipette. This newly developed minimally invasive technique was performed in a group of living animals (n = 20) and results compared with those of a second group of perfusion fixed animals (n = 20). For the first time, repeated cerebrospinal fluid punctures of individual, living animals are possible. This is of great value for the assessment of new therapeutic and diagnostic strategies in experimental research using mouse models. In addition, this refined methodology significantly reduces the number of experimental animals.
本报告描述了一种在单纯疱疹病毒性脑炎模型中从活体小鼠(SJL/NBom)获取脑脊液的新技术,该技术也适用于其他小鼠模型。穿刺技术在活体动物身上进行,这些动物在活体状态下感染了I型单纯疱疹病毒F株。对枕大池进行显微手术处理:在显微镜下解剖颈部肌肉直至硬脑膜,随后用玻璃微量移液器穿刺硬脑膜。这种新开发的微创技术在一组活体动物(n = 20)中进行,并将结果与第二组灌注固定动物(n = 20)的结果进行比较。首次实现了对个体活体动物进行重复脑脊液穿刺。这对于评估使用小鼠模型的实验研究中的新治疗和诊断策略具有重要价值。此外,这种改进的方法显著减少了实验动物的数量。