Azari Michael F, Lopes Elizabeth C, Stubna Chantelle, Turner Bradley J, Zang Dawei, Nicola Nicos A, Kurek John B, Cheema Surindar S
Department of Anatomy and Cell Biology, Faculty of Medicine, P.O. Box 13C, Monash University, 3800 Victoria, Australia.
Brain Res. 2003 Aug 22;982(1):92-7. doi: 10.1016/s0006-8993(03)02989-5.
We investigated the anatomical and behavioural effects of daily intraperitoneal injection of 25 microg/kg of LIF in the SOD1(G93A G1H) mouse model of familial ALS. We found some subtle beneficial behavioural changes in LIF treated mice. These included later onset of clinical disease in females as determined by clinical scoring; better grip strength in males; and delayed development of motor impairment in males as determined by the rotarod test. However, we found no significant rescue of motoneurons or prolongation of survival as a result of this systemic dose of LIF in these mice.
我们在家族性肌萎缩侧索硬化症(ALS)的SOD1(G93A G1H)小鼠模型中,研究了每日腹腔注射25微克/千克白血病抑制因子(LIF)的解剖学和行为学效应。我们发现接受LIF治疗的小鼠有一些细微的有益行为变化。这些变化包括:通过临床评分确定,雌性小鼠临床疾病发病较晚;雄性小鼠握力更强;通过转棒试验确定,雄性小鼠运动功能障碍的发展延迟。然而,我们发现,在这些小鼠中,这种全身剂量的LIF并未显著挽救运动神经元或延长生存期。