Department of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland 21205.
Department of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland 21205
J Neurosci. 2023 Mar 29;43(13):2326-2337. doi: 10.1523/JNEUROSCI.1831-22.2023. Epub 2023 Feb 17.
To maintain stable posture of the head and body during our everyday activities, the brain integrates information across multiple sensory systems. Here, we examined how the primate vestibular system, independently and in combination with visual sensory input, contributes to the sensorimotor control of head posture across the range of dynamic motion experienced during daily life. We recorded activity of single motor units in the splenius capitis and sternocleidomastoid muscles in rhesus monkeys during yaw rotations spanning the physiological range of self-motion (up to 20 Hz) in darkness. Splenius capitis motor unit responses continued to increase with frequency up to 16 Hz in normal animals, and were strikingly absent following bilateral peripheral vestibular loss. To determine whether visual information modulated these vestibular-driven neck muscle responses, we experimentally controlled the correspondence between visual and vestibular cues of self-motion. Surprisingly, visual information did not influence motor unit responses in normal animals, nor did it substitute for absent vestibular feedback following bilateral peripheral vestibular loss. A comparison of muscle activity evoked by broadband versus sinusoidal head motion further revealed that low-frequency responses were attenuated when low- and high-frequency self-motion were experienced concurrently. Finally, we found that vestibular-evoked responses were enhanced by increased autonomic arousal, quantified via pupil size. Together, our findings directly establish the vestibular system's contribution to the sensorimotor control of head posture across the dynamic motion range experienced during everyday activities, as well as how vestibular, visual, and autonomic inputs are integrated for postural control. Our sensory systems enable us to maintain control of our posture and balance as we move through the world. Notably, the vestibular system senses motion of the head and sends motor commands, via vestibulospinal pathways, to axial and limb muscles to stabilize posture. By recording the activity of single motor units, here we show, for the first time, that the vestibular system contributes to the sensorimotor control of head posture across the dynamic motion range experienced during everyday activities. Our results further establish how vestibular, autonomic, and visual inputs are integrated for postural control. This information is essential for understanding both the mechanisms underlying the control of posture and balance, and the impact of the loss of sensory function.
为了在日常活动中保持头部和身体的稳定姿势,大脑整合了来自多个感觉系统的信息。在这里,我们研究了灵长类动物前庭系统如何独立地以及与视觉感觉输入相结合,有助于控制头部姿势在日常生活中经历的各种动态运动范围内的运动感觉。我们在黑暗中记录了猕猴斜方肌和胸锁乳突肌的单个运动单位的活动,这些运动单位的活动跨越了自主运动的生理范围(高达 20 Hz)进行了侧摆旋转。在正常动物中,斜方肌运动单位的反应在 16 Hz 之前会继续随频率增加,而在双侧外周前庭丧失后则明显消失。为了确定视觉信息是否调节了这些前庭驱动的颈部肌肉反应,我们实验性地控制了自我运动的视觉和前庭线索的对应关系。令人惊讶的是,在正常动物中,视觉信息并没有影响运动单位的反应,也没有在双侧外周前庭丧失后替代缺失的前庭反馈。进一步比较宽带和正弦头部运动引起的肌肉活动表明,当同时经历低频和高频自运动时,低频反应会减弱。最后,我们发现前庭诱发的反应会随着自主警觉性的增加而增强,通过瞳孔大小来量化。总的来说,我们的研究结果直接确立了前庭系统在控制日常活动中经历的动态运动范围内的头部姿势的感觉运动中的贡献,以及前庭、视觉和自主输入如何整合进行姿势控制。我们的感觉系统使我们能够在移动时保持对姿势和平衡的控制。值得注意的是,前庭系统感知头部的运动,并通过前庭脊髓途径发送运动指令,以稳定姿势轴向和肢体肌肉。通过记录单个运动单位的活动,我们首次表明,前庭系统有助于在日常活动中经历的动态运动范围内控制头部姿势的感觉运动。我们的研究结果进一步确立了前庭、自主和视觉输入如何整合进行姿势控制。这些信息对于理解姿势和平衡控制的机制以及感觉功能丧失的影响至关重要。