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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Restricted neural plasticity in vestibulospinal pathways after unilateral labyrinthectomy as the origin for scoliotic deformations
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Restricted neural plasticity in vestibulospinal pathways after unilateral labyrinthectomy as the origin for scoliotic deformations

机译:在单侧迷宫切除术后,在门外障碍后的神经可塑性作为脊柱菌变形的起源

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摘要

Adolescent idiopathic scoliosis in humans is often associated with vestibulomotor deficits. Compatible with a vestibular origin, scoliotic deformations were provoked in adult Xenopus frogs by unilateral labyrinthectomy (UL) at larval stages. The aquatic ecophysiology and absence of body-weight-supporting limb proprioceptive signals in amphibian tadpoles as a potential sensory substitute after UL might be the cause for a persistent asymmetric descending vestibulospinal activity. Therefore, peripheral vestibular lesions in larval Xenopus were used to reveal the morphophysiological alterations at the cellular and network levels. As a result, spinal motor nerves that were modulated by the previously intact side before UL remained permanently silent during natural vestibular stimulation after the lesion. In addition, retrograde tracing of descending pathways revealed a loss of vestibular neurons on the ipsilesional side with crossed vestibulospinal projections. This loss facilitated a general mass imbalance in descending premotor activity and a permanent asymmetric motor drive to the axial musculature. Therefore, we propose that the persistent asymmetric contraction of trunk muscles exerts a constant, uncompensated differential mechanical pull on bilateral skeletal elements that enforces a distortion of the soft cartilaginous skeletal elements and bone shapes. This ultimately provokes severe scoliotic deformations during ontogenetic development similar to the human syndrome.
机译:人类的青少年特发性脊柱侧凸常与前院运动缺陷有关。与前庭血管结合术中的牙龈血液切除术(UL)在幼儿阶段刺激了脊髓灰质炎。水生生物学与体重支持的肢体蝌蚪中的肢体类血管活性信号作为UL后的潜在感官替代物,可能是持续不对称下降前列腺活性的原因。因此,幼虫外围口腔病变用于揭示细胞和网络水平的语气生理改变。结果,在UL之前先前完整的侧面调节的脊柱电机神经在病变后的天然前庭刺激期间保持永久性沉默。此外,降途途径的逆行追踪揭示了在Ipsilessional侧的前庭神经元的丧失,具有交叉的前颈孔突起。这种损失促进了在下降前运动活性和永久的不对称电动机驱动器中的一般质量不平衡,以及轴向肌肉组织。因此,我们提出躯干肌肉的持续不对称收缩施加恒定的未致密的差分机械拉力,双侧骨骼元素施加柔软的软骨骨骼元素和骨形状的变形。这最终在血细胞生殖发育期间引起严重的微杆菌变形,类似于人类综合征。

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    Centre d'Etude de la SensoriMotricité Centre National de la Recherche Scientifique Unité Mixte de;

    Centre d'Etude de la SensoriMotricité Centre National de la Recherche Scientifique Unité Mixte de;

    Centre d'Etude de la SensoriMotricité Centre National de la Recherche Scientifique Unité Mixte de;

    Department Biology II Ludwig-Maximilians-University Munich 82152 Planegg Germany;

    Centre d'Etude de la SensoriMotricité Centre National de la Recherche Scientifique Unité Mixte de;

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  • 正文语种 eng
  • 中图分类 人体生理学;
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