School of Medicine, University of Western Sydney, Locked Bag 1797, Penrith South DC, NSW 1797, Australia.
Exp Brain Res. 2010 Apr;202(2):291-8. doi: 10.1007/s00221-009-2131-8. Epub 2009 Dec 30.
We have previously shown that sinusoidal galvanic vestibular stimulation (sGVS), a means of a selectively modulating vestibular afferent input without affecting other inputs, can cause partial entrainment of muscle sympathetic nerve activity (MSNA). Given that motion sickness causes sweating and pallor, we tested the hypothesis that sGVS also entrains skin sympathetic nerve activity (SSNA), but that the optimal frequencies are closer to those associated with slow postural changes (0.2 Hz). SSNA was recorded via tungsten microelectrodes inserted into the common peroneal nerve in 11 awake-seated subjects. Bipolar binaural sinusoidal GVS (+/-2 mA, 200 cycles) was applied to the mastoid processes at frequencies of 0.2, 0.5, 0.8, 1.1, 1.4, 1.7 and 2.0 Hz. All subjects reported strong postural illusions of 'rocking in a boat' or 'swaying in a hammock'. Sinusoidal GVS caused a marked entrainment of SSNA at all frequencies. Measured as the modulation index, vestibular modulation ranged from 81.5 +/- 4.0% at 0.2 Hz to 76.6 +/- 3.6% at 1.7 Hz; it was significantly weaker at 2.0 Hz (63.2 +/- 5.4%). Interestingly, pulse-related modulation of SSNA, which is normally weak, increased significantly during sGVS but was stronger at 0.8 Hz (86.2 +/- 2.0%) than at 0.2 Hz (69.3 +/- 8.3%), the opposite of the pattern seen with vestibular modulation of MSNA. We conclude that vestibular inputs can entrain the firing of cutaneous sympathetic neurones and increase their normally weak pulse-related rhythmicity.
我们之前已经证明,正弦电流前庭刺激(sGVS)是一种选择性调节前庭传入输入而不影响其他输入的方法,可以引起肌肉交感神经活动(MSNA)的部分同步。由于运动病会导致出汗和苍白,我们假设 sGVS 也会同步皮肤交感神经活动(SSNA),但最佳频率更接近与缓慢姿势变化相关的频率(0.2 Hz)。通过将钨微电极插入腓总神经,在 11 名清醒坐姿的受试者中记录 SSNA。在频率为 0.2、0.5、0.8、1.1、1.4、1.7 和 2.0 Hz 时,将双极双耳正弦 GVS(+/-2 mA,200 个周期)施加到乳突上。所有受试者均报告出现强烈的姿势错觉,如“在船上摇晃”或“在吊床上摇摆”。正弦 GVS 导致 SSNA 在所有频率下均明显同步。以调制指数衡量,前庭调制范围从 0.2 Hz 时的 81.5 +/- 4.0%到 1.7 Hz 时的 76.6 +/- 3.6%;在 2.0 Hz 时明显较弱(63.2 +/- 5.4%)。有趣的是,在 sGVS 期间,通常较弱的 SSNA 脉冲相关调制显著增加,但在 0.8 Hz 时更强(86.2 +/- 2.0%),而不是在 0.2 Hz 时更强(69.3 +/- 8.3%),这与 MSNA 的前庭调制模式相反。我们得出结论,前庭输入可以同步皮肤交感神经元的放电并增加其通常较弱的脉冲相关节律性。