Tang F, Cheung A, Vacca-Galloway L L
Department of Physiology, Faculty of Medicine, University of Hong Kong.
Brain Res. 1990 Jun 4;518(1-2):329-33. doi: 10.1016/0006-8993(90)90992-k.
The Wobbler mouse (wr) exhibits the loss of motoneurons especially in the cervical spinal cord, and thus has been studied as a model for human motoneuron diseases. Wobbler mice selected at various ages and stages during the disease process show increased levels of thyrotropin releasing hormone and substance P in spinal cord and brainstem (medulla). Enkephalins (methionine and leucine) also increase in the spinal cord and brainstem. Somatostatin increases in hypothalamus, perhaps accounting partly for the small size of this mutant mouse via its effect on growth hormone.
摇摆小鼠(wr)表现出运动神经元丧失,尤其是在颈脊髓,因此已被作为人类运动神经元疾病的模型进行研究。在疾病过程中的不同年龄和阶段选择的摇摆小鼠显示,脊髓和脑干(延髓)中促甲状腺激素释放激素和P物质的水平升高。脑啡肽(甲硫氨酸和亮氨酸)在脊髓和脑干中也增加。生长抑素在下丘脑中增加,这可能部分解释了这种突变小鼠体型小的原因,因为它对生长激素有影响。