Tarczyluk-Wells Marta A, Salzlechner Christoph, Najafi Allison R, Lim Ming J, Smith David, Platt Frances M, Williams Brenda P, Cooper Jonathan D
Department of Basic and Clinical Neuroscience, King's College London, Institute of Psychiatry, Psychology and Neuroscience, Maurice Wohl Clinical Neuroscience Institute, London, United Kingdom.
Department of Pediatrics, David Geffen School of Medicine at UCLA, Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, CA, United States.
Front Neurol. 2019 Sep 11;10:963. doi: 10.3389/fneur.2019.00963. eCollection 2019.
Batten disease, or juvenile NCL, is a fatal neurodegenerative disorder that occurs due to mutations in the gene. Because the function of CLN3 remains unclear, experimental therapies for JNCL have largely concentrated upon the targeting of downstream pathomechanisms. Neuron loss is preceded by localized glial activation, and in this proof-of-concept study we have investigated whether targeting this innate immune response with ibuprofen in combination with the neuroprotective agent lamotrigine improves the previously documented beneficial effects of immunosuppressants alone. Drugs were administered daily to symptomatic mice over a 3 month period, starting at 6 months of age, and their impact was assessed using both behavioral and neuropathological outcome measures. During the treatment period, the combination of ibuprofen and lamotrigine significantly improved the performance of mice on the vertical pole test, slowing the disease-associated decline, but had less of an impact upon their rotarod performance. There were also moderate and regionally dependent effects upon astrocyte activation that were most pronounced for ibuprofen alone, but there was no overt effect upon microglial activation. Administering such treatments for longer periods will enable testing for any impact upon the neuron loss that occurs later in disease progression. Given the partial efficacy of these treatments, it will be important to test further drugs of this type in order to find more effective combinations.
巴滕病,即青少年型神经元蜡样脂褐质沉积症(juvenile NCL),是一种致命的神经退行性疾病,由该基因的突变引起。由于CLN3的功能仍不清楚,青少年型神经元蜡样脂褐质沉积症(JNCL)的实验性治疗主要集中在针对下游致病机制。神经元丧失之前会出现局部胶质细胞活化,在这项概念验证研究中,我们研究了用布洛芬联合神经保护剂拉莫三嗪靶向这种先天免疫反应是否能改善之前记录的单独使用免疫抑制剂的有益效果。从6个月大开始,对有症状的小鼠每天给药3个月,使用行为和神经病理学结果指标评估其影响。在治疗期间,布洛芬和拉莫三嗪的联合用药显著改善了小鼠在垂直杆试验中的表现,减缓了与疾病相关的衰退,但对其转棒试验表现的影响较小。对星形胶质细胞活化也有中度且区域依赖性的影响,单独使用布洛芬时最为明显,但对小胶质细胞活化没有明显影响。延长此类治疗的给药时间将能够测试其对疾病进展后期发生的神经元丧失的任何影响。鉴于这些治疗的部分疗效,进一步测试此类药物以找到更有效的组合将很重要。