Jae-Hwan Choi, Eun Hye Oh, Hyun Sung Kim, Ji-Yun Park, Suk-Min Lee, Seo Young Choi, Hyo Jung Kim, Jeong-Yoon Choi, Ji-Soo Kim, Jorge Otero-Millan, Kwang-Dong Choi
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When Alexander's law is violated, the time constant (Tc) was larger than that in the controls (median [interquartile range, IQR]: 14.4s [6.4-38.9] vs 9.0s [IQR 5.5-12.6], p = 0.036) while the Tc did not differ between the groups when Alexander' law is obeyed (9.6s [3.6-16.1] vs 9.0s [5.5-12.6], p = 0.924). To test the study hypothesis that an unstable neural integrator may generate nystagmus violating Alexander's law, we utilized the gaze-holding neural integrator model incorporating brainstem leaky neural integrator and negative velocity feedback loop via the cerebellum. The lesion-induced changes included false rotational cue, primarily attributed to central vestibular imbalance, and unstable neural integrator, examined in two ways: hyperexcitable brainstem neural integrator and paradoxical excitatory effect of Purkinje cells. With normal integrator function, the false rotational cue generated nystagmus consistent with Alexander's law. 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引用次数: 0
摘要
亚历山大定律指出,注视快相方向时自发性眼球震颤增加,注视慢相方向时自发性眼球震颤减少。在中枢性眼球震颤中偶尔观察到对亚历山大定律的不服从,但潜在的神经回路机制尚不清楚。在对2652例后循环卒中患者的回顾性分析中,我们发现17例单侧外侧髓质病变影响前庭核的患者在一个或两个方向侧视违反亚历山大定律。前庭神经炎患者作为对照。违反亚历山大定律时,时间常数(Tc)大于对照组(中位数[四分位数间距,IQR]: 14.4s [6.4-38.9] vs . 9.0s [IQR 5.5-12.6], p = 0.036),而遵守亚历山大定律时,各组Tc无差异(9.6s [3.6-16.1] vs . 9.0s [5.5-12.6], p = 0.924)。为了验证不稳定的神经积分器可能导致违反亚历山大定律的眼球震颤的研究假设,我们采用了包含脑干漏性神经积分器和小脑负速度反馈回路的注视神经积分器模型。病变引起的改变包括假旋转提示,主要归因于前庭中枢失衡,以及不稳定的神经整合器,通过两种方式检查:过度兴奋的脑干神经整合器和浦肯野细胞的矛盾兴奋效应。在正常积分器功能下,假旋转提示产生的眼球震颤符合亚历山大定律。然而,两种类型的不稳定的神经整合测试都会产生眼球震颤,这违反了亚历山大定律。我们认为,当神经积分器不稳定,脑干神经积分器本身或浦肯野细胞与脑干前庭核之间的神经突触受损时,眼球震颤违反亚历山大定律。违反亚历山大定律的自发性眼球震颤可能是鉴别中枢性前庭综合征的有用线索。
Spontaneous Nystagmus Violating the Alexander's Law: Neural Substrates and Mechanisms.
Alexander's law states that spontaneous nystagmus increases when looking in the direction of fast-phase and decreases during gaze in slow-phase direction. Disobedience to Alexander's law is occasionally observed in central nystagmus, but the underlying neural circuit mechanisms are poorly understood. In a retrospective analysis of 2,652 patients with posterior circulations stroke, we found a violation of Alexander's law in one or both directions of lateral gaze in 17 patients with lesions of unilateral lateral medulla affecting the vestibular nucleus. Patients with vestibular neuritis served as a control. When Alexander's law is violated, the time constant (Tc) was larger than that in the controls (median [interquartile range, IQR]: 14.4s [6.4-38.9] vs 9.0s [IQR 5.5-12.6], p = 0.036) while the Tc did not differ between the groups when Alexander' law is obeyed (9.6s [3.6-16.1] vs 9.0s [5.5-12.6], p = 0.924). To test the study hypothesis that an unstable neural integrator may generate nystagmus violating Alexander's law, we utilized the gaze-holding neural integrator model incorporating brainstem leaky neural integrator and negative velocity feedback loop via the cerebellum. The lesion-induced changes included false rotational cue, primarily attributed to central vestibular imbalance, and unstable neural integrator, examined in two ways: hyperexcitable brainstem neural integrator and paradoxical excitatory effect of Purkinje cells. With normal integrator function, the false rotational cue generated nystagmus consistent with Alexander's law. However, both types of unstable neural integrators tested produced nystagmus that violated Alexander's law. We propose that when the neural integrator is unstable with lesions in the brainstem neural integrator itself or the neural synapse between Purkinje cells and the brainstem vestibular nucleus, nystagmus violates Alexander's law. The spontaneous nystagmus violating Alexander's law may be the useful clue for identifying central vestibular syndrome.
期刊介绍:
Official publication of the Society for Research on the Cerebellum devoted to genetics of cerebellar ataxias, role of cerebellum in motor control and cognitive function, and amid an ageing population, diseases associated with cerebellar dysfunction.
The Cerebellum is a central source for the latest developments in fundamental neurosciences including molecular and cellular biology; behavioural neurosciences and neurochemistry; genetics; fundamental and clinical neurophysiology; neurology and neuropathology; cognition and neuroimaging.
The Cerebellum benefits neuroscientists in molecular and cellular biology; neurophysiologists; researchers in neurotransmission; neurologists; radiologists; paediatricians; neuropsychologists; students of neurology and psychiatry and others.