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先天性功能性肌梭缺失的运动感觉控制。

Sensorimotor control in the congenital absence of functional muscle spindles.

机构信息

Department of Neuroscience, Monash University, Melbourne, Victoria, Australia.

School of Medicine, Western Sydney University, Sydney, New South Wales, Australia.

出版信息

Exp Physiol. 2024 Jan;109(1):27-34. doi: 10.1113/EP090768. Epub 2023 Apr 8.

DOI:10.1113/EP090768
PMID:37029664
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10988665/
Abstract

Hereditary sensory and autonomic neuropathy type III (HSAN III), also known as familial dysautonomia or Riley-Day syndrome, results from an autosomal recessive genetic mutation that causes a selective loss of specific sensory neurones, leading to greatly elevated pain and temperature thresholds, poor proprioception, marked ataxia and disturbances in blood pressure control. Stretch reflexes are absent throughout the body, which can be explained by the absence of functional muscle spindle afferents - assessed by intraneural microelectrodes inserted into peripheral nerves in the upper and lower limbs. This also explains the greatly compromised proprioception at the knee joint, as assessed by passive joint-angle matching. Moreover, there is a tight correlation between loss of proprioceptive acuity at the knee and the severity of gait impairment. Surprisingly, proprioception is normal at the elbow, suggesting that participants are relying more on sensory cues from the overlying skin; microelectrode recordings have shown that myelinated tactile afferents in the upper and lower limbs appear to be normal. Nevertheless, the lack of muscle spindles does affect sensorimotor control in the upper limb: in addition to poor performance in the finger-to-nose test, manual performance in the Purdue pegboard task is much worse than in age-matched healthy controls. Unlike those rare individuals with large-fibre sensory neuropathy, in which both muscle spindle and cutaneous afferents are absent, those with HSAN III present as a means of assessing sensorimotor control following the selective loss of muscle spindle afferents.

摘要

遗传性感觉运动神经病 III 型(HSAN III),也称为家族性自主神经异常或赖利-戴综合征,是由常染色体隐性遗传突变引起的,导致特定感觉神经元选择性丧失,从而导致痛觉和温度阈值显著升高、本体感觉差、明显的共济失调和血压控制障碍。全身的牵张反射消失,可以通过插入上肢和下肢周围神经的神经内微电极评估功能肌梭传入纤维缺失来解释。这也解释了膝关节本体感觉严重受损,通过被动关节角度匹配进行评估。此外,膝关节本体感觉锐度丧失与步态障碍的严重程度之间存在紧密的相关性。令人惊讶的是,肘部的本体感觉正常,这表明参与者更多地依赖于来自覆盖皮肤的感觉提示;微电极记录显示,上肢和下肢的有髓触觉传入似乎正常。然而,肌梭的缺失确实会影响上肢的运动感觉控制:除了手指到鼻子测试表现不佳外,在普渡钉板任务中的手动操作明显比年龄匹配的健康对照组差。与那些罕见的大纤维感觉神经病患者不同,后者的肌梭和皮肤传入纤维均缺失,而那些患有 HSAN III 的患者则是评估选择性肌梭传入纤维丧失后运动感觉控制的一种手段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32e3/10988665/1509eb41acf5/EPH-109-27-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32e3/10988665/056ecfc40cd8/EPH-109-27-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32e3/10988665/643b61e46c02/EPH-109-27-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32e3/10988665/a78afc54475a/EPH-109-27-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32e3/10988665/1509eb41acf5/EPH-109-27-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32e3/10988665/056ecfc40cd8/EPH-109-27-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32e3/10988665/643b61e46c02/EPH-109-27-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32e3/10988665/a78afc54475a/EPH-109-27-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32e3/10988665/1509eb41acf5/EPH-109-27-g002.jpg

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