Muramatsu Ken, Niimi Naoko, Ikutomo Masako, Shimo Satoshi, Tamaki Toru, Niwa Masatoshi, Sango Kazunori
Department of Physical Therapy, Kyorin University, Mitaka-City, Tokyo, Japan.
Diabetic Neuropathy Project, Department of Diseases and Infection, Tokyo Metropolitan Institute of Medical Science, Setagaya-Ku, Tokyo, Japan.
Exp Neurol. 2023 May;363:114357. doi: 10.1016/j.expneurol.2023.114357. Epub 2023 Feb 26.
Diabetes disrupts the corticospinal tract (CST) system components that control hindlimb and trunk movement, resulting in weakness of the lower extremities. However, there is no information about a method to improve these disorders. This study aimed to investigate the rehabilitative effects of 2 weeks of aerobic training (AT) and complex motor skills training (ST) on motor disorders in streptozotocin-induced type 1 diabetic rats. In this study, electrophysiological mapping of the motor cortex showed that the diabetes mellitus (DM)-ST group had a larger motor cortical area compared to the DM-AT group and sedentary diabetic animals. Moreover, hand grip strength and rotarod latency increased in the DM-ST group; however, these two parameters did not change in the DM-AT group, as well as in control and sedentary diabetic rats. Furthermore, in the DM-ST group, cortical stimulation-induced and motor-evoked potentials were preserved after the interception of the CST; however, this potential disappeared after additional lesions were made on lateral funiculus, suggesting that their function extends to activating motor descending pathways other than the CST locating lateral funiculus. According to immunohistochemical analysis, the larger fibers present on the dorsal part of the lateral funiculus, which corresponds to the rubrospinal tract of the DM-ST group, expressed the phosphorylated growth-associated protein, 43 kD, which is a specific marker of axons with plastic changes. Additionally, electrical stimulation of the red nucleus revealed expansion of the hindlimb-responsible area and increased motor-evoked potentials of the hindlimb in the DM-ST group, suggesting a strengthening of synaptic connections between the red nucleus and spinal interneurons driving motoneurons. These results reveal that ST induces plastic changes in the rubrospinal tract in a diabetic model, which can compensate for diabetes by disrupting the CST system components that control the hindlimb. This finding suggests that ST can be a novel rehabilitation strategy to improve motor dysfunctions in diabetic patients.
糖尿病会破坏控制后肢和躯干运动的皮质脊髓束(CST)系统组件,导致下肢无力。然而,目前尚无关于改善这些病症方法的相关信息。本研究旨在探讨为期2周的有氧训练(AT)和复杂运动技能训练(ST)对链脲佐菌素诱导的1型糖尿病大鼠运动障碍的康复效果。在本研究中,运动皮层的电生理图谱显示,与糖尿病-有氧训练组和久坐的糖尿病动物相比,糖尿病-复杂运动技能训练组具有更大的运动皮层面积。此外,糖尿病-复杂运动技能训练组的握力和转棒试验潜伏期增加;然而,这两个参数在糖尿病-有氧训练组以及对照和久坐的糖尿病大鼠中并未改变。此外,在糖尿病-复杂运动技能训练组中,切断CST后,皮层刺激诱发的运动诱发电位得以保留;然而,在外侧索进行额外损伤后,这种电位消失,这表明其功能延伸至激活除位于外侧索的CST之外的运动下行通路。根据免疫组织化学分析,外侧索背侧存在的较大纤维,对应于糖尿病-复杂运动技能训练组的红核脊髓束,表达了磷酸化的生长相关蛋白43 kD,这是具有可塑性变化的轴突的特异性标志物。此外,对红核的电刺激显示糖尿病-复杂运动技能训练组中后肢负责区域扩大且后肢运动诱发电位增加,这表明红核与驱动运动神经元的脊髓中间神经元之间的突触连接增强。这些结果表明,在糖尿病模型中,复杂运动技能训练可诱导红核脊髓束发生可塑性变化,通过破坏控制后肢的CST系统组件来补偿糖尿病。这一发现表明,复杂运动技能训练可能是改善糖尿病患者运动功能障碍的一种新的康复策略。