Gonzalez Deniselle Maria Claudia, Garay Laura, Gonzalez Susana, Guennoun Rachida, Schumacher Michael, De Nicola Alejandro F
Laboratory of Neuroendocrine Biochemistry, Instituto de Biología y Medicina Experimental, and Department of Biochemistry, Faculty of Medicine, University of Buenos, Obligado 2490, 1428 Buenos Aires, Argentina.
Exp Neurol. 2005 Oct;195(2):518-23. doi: 10.1016/j.expneurol.2005.06.015.
The Wobbler mouse, a mutant characterized by motoneuron degeneration in the cervical spinal cord, has been used to test the efficacy of novel treatments for human motoneuron diseases (HMD). Previous reports have shown that slow axonal transport is impaired in Wobblers and other models of HMD. Since progesterone (PROG) corrects some morphological, molecular, and functional abnormalities of Wobbler mice, we studied if steroid exposure for 8 weeks restored retrograde axonal transport by measuring motoneuron labeling after injection of fluorogold into the limb muscles. The dye was injected into forelimb biceps bracchii and flexor or into the rearlimb gastrocnemius muscles; 6 days later, the number of fluorescent motoneurons and the total number of cresyl violet stained motoneurons were counted in the cervical (C5-T1) or lumbar (L3-L5) spinal cord regions. A pronounced reduction (- 42.2%) of the percent of fluorescent motoneurons in Wobbler mice cervical cord was noted, which was significantly corrected after PROG treatment. In contrast, labeling of lumbar motoneurons was not reduced in Wobbler mice and was not affected by PROG treatment. In no case PROG showed an effect in control mice. Concomitantly, PROG slightly but significantly increased biceps weight of Wobbler mice. Behaviorally, PROG-treated Wobblers performed better on a motor test (hanging time from a horizontal rope) compared to untreated counterparts. We postulate a dual role for PROG in the Wobbler mouse, in part by prevention of motoneuron degeneration and also by enhancement of axonal transport. The latter mechanism could improve the traffic of neurotrophic factors from the forelimb muscles into the ailing motoneurons, improving neuromuscular function in this murine model of HMD.
摆动小鼠是一种以颈脊髓运动神经元变性为特征的突变体,已被用于测试新型人类运动神经元疾病(HMD)治疗方法的疗效。先前的报告表明,摆动小鼠和其他HMD模型中轴突慢运输受损。由于孕酮(PROG)可纠正摆动小鼠的一些形态、分子和功能异常,我们通过测量向肢体肌肉注射荧光金后运动神经元的标记情况,研究了8周的类固醇暴露是否能恢复逆行轴突运输。将染料注射到前肢肱二头肌和屈肌或后肢腓肠肌中;6天后,在颈(C5-T1)或腰(L3-L5)脊髓区域计数荧光运动神经元的数量和甲酚紫染色运动神经元的总数。注意到摆动小鼠颈髓中荧光运动神经元百分比显著降低(-42.2%),PROG治疗后得到显著纠正。相比之下,摆动小鼠腰运动神经元的标记未减少,且不受PROG治疗影响。在任何情况下,PROG对对照小鼠均无作用。同时,PROG使摆动小鼠的肱二头肌重量略有但显著增加。在行为上,与未治疗的摆动小鼠相比,经PROG治疗的摆动小鼠在运动测试(从水平绳索悬挂的时间)中表现更好。我们推测PROG在摆动小鼠中具有双重作用,部分是通过预防运动神经元变性,也通过增强轴突运输。后一种机制可以改善神经营养因子从前肢肌肉向患病运动神经元的运输,改善这种HMD小鼠模型中的神经肌肉功能。