Brenner Michael J, Moradzadeh Arash, Myckatyn Terence M, Tung Thomas H H, Mendez Allen B, Hunter Daniel A, Mackinnon Susan E
Department of Otolaryngology-Head & Neck Surgery, Washington University School of Medicine, Saint Louis, MO, USA.
Microsurgery. 2008;28(4):265-72. doi: 10.1002/micr.20483.
Small animal models are indispensable for research on nerve injury and reconstruction, but their superlative regenerative potential may confound experimental interpretation. This study investigated time-dependent neuroregenerative phenomena in rodents. Forty-six Lewis rats were randomized to three nerve allograft groups treated with 2 mg/(kg day) tacrolimus; 5 mg/(kg day) Cyclosporine A; or placebo injection. Nerves were subjected to histomorphometric and walking track analysis at serial time points. Tacrolimus increased fiber density, percent neural tissue, and nerve fiber count and accelerated functional recovery at 40 days, but these differences were undetectable by 70 days. Serial walking track analysis showed a similar pattern of recovery. A "blow-through" effect is observed in rodents whereby an advancing nerve front overcomes an experimental defect given sufficient time, rendering experimental groups indistinguishable at late time points. Selection of validated time points and corroboration in higher animal models are essential prerequisites for the clinical application of basic research on nerve regeneration.
小动物模型对于神经损伤与重建的研究不可或缺,但它们超强的再生潜能可能会混淆实验结果的解读。本研究调查了啮齿动物中随时间变化的神经再生现象。46只Lewis大鼠被随机分为三组,分别接受2毫克/(千克·天)他克莫司、5毫克/(千克·天)环孢素A或安慰剂注射的神经同种异体移植治疗。在连续的时间点对神经进行组织形态计量学和行走轨迹分析。他克莫司在40天时增加了纤维密度、神经组织百分比和神经纤维数量,并加速了功能恢复,但在70天时这些差异无法检测到。连续行走轨迹分析显示出类似的恢复模式。在啮齿动物中观察到一种“穿透”效应,即如果给予足够的时间,前进的神经前沿会克服实验缺陷,导致实验组在后期时间点无法区分。选择经过验证的时间点并在高等动物模型中进行验证,是神经再生基础研究临床应用的基本前提。