The nucleus raphe interpositus in spinocerebellar ataxia type 3 (Machado-Joseph disease)

被引:31
|
作者
Rüb, U
Brunt, ER
Gierga, K
Schultz, C
Paulson, H
de Vos, RAI
Braak, H
机构
[1] Univ Frankfurt, Dept Clin Neuroanat, D-60590 Frankfurt, Germany
[2] Lab Pathol Oost Nederaland, NL-7512 AD Enschede, Netherlands
[3] Univ Iowa, Coll Med, Dept Neurol, Iowa City, IA 52242 USA
[4] Univ Groningen Hosp, Dept Neurol, NL-5970 RB Groningen, Netherlands
关键词
brain stem; oculomotor system; omnipause neurons; saccades; SCA3;
D O I
10.1016/S0891-0618(02)00099-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The nucleus raphe interpositus (RIP) plays an important role in the premotor network for saccades. Its omnipause neurons gate the activity of the burst neurons for vertical saccades lying within the rostral interstitial nucleus of the medial longitudinal fascicle and that for horizontal saccades residing in the caudal subnucleus of the pontine reticular formation. In the present study we investigated the RIP in five patients with clinically diagnosed and genetically confirmed spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease. Polyethylene glycol-embedded 100 mum serial sections stained for lipofuscin pigment and Nissl material as well as paraffin-embedded Nissl stained thin sections revealed the hitherto overlooked involvement of this pontine nucleus in the degenerative process underlying SCA3, whereby in four of our SCA3 patients the RIP underwent a conspicuous loss of presumed omnipause neurons. As observed in other affected brain structures, the RIP of all our SCA3 patients displayed reactive astrocytes and activated microglial cells, while some of the few of its surviving neurons harbored an ataxin-3-immunopositive intranuclear inclusion body. The findings of the present pathoanatomical study suggest that (1) neurodegeneration in the brain stem of terminal SCA3 patients is more widespread than previously thought and is not confined to cranial nerve nuclei involved in the generation of saccades but likewise involves the premotor network for saccades and (2) damage to the RIP may contribute to slowing of horizontal saccades in SCA3 patients but is not associated with saccadic oscillations as occasionally speculated. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:115 / 127
页数:13
相关论文
共 50 条
  • [1] Spinocerebellar ataxia type 3 (Machado-Joseph disease)
    Dulski, Jaroslaw
    Al-Shaikh, Rana Hanna
    Sulek, Anna
    Kasprzak, Jakub
    Slawek, Jaroslaw
    Wszolek, Zbigniew K.
    POLISH ARCHIVES OF INTERNAL MEDICINE-POLSKIE ARCHIWUM MEDYCYNY WEWNETRZNEJ, 2022, 132 (10):
  • [2] The Neuropathology of Spinocerebellar Ataxia Type 3/Machado-Joseph Disease
    Koeppen, Arnulf H.
    POLYGLUTAMINE DISORDERS, 2018, 1049 : 233 - 241
  • [3] Spinocerebellar ataxia type 3 (Machado-Joseph disease) and varenicline
    Young, Pablo
    Finn, Barbara C.
    Giuliani, Franco
    Reisin, Ricardo
    REVISTA MEDICA DE CHILE, 2015, 143 (09) : 1221 - 1222
  • [4] Degeneration of the external cuneate nucleus in spinocerebellar ataxia type 3 (Machado-Joseph disease)
    Rüb, U
    de Vos, RAI
    Brunt, ER
    Schultz, C
    Paulson, H
    Del Tredici, K
    Braak, H
    BRAIN RESEARCH, 2002, 953 (1-2) : 126 - 134
  • [5] Spinocerebellar ataxia type 3 (Machado-Joseph disease):: severe destruction of the lateral reticular nucleus
    Rüb, U
    de Vos, RAI
    Schultz, C
    Brunt, ER
    Paulson, H
    Braak, H
    BRAIN, 2002, 125 : 2115 - 2124
  • [6] Mouse Models of Spinocerebellar Ataxia Type 3 (Machado-Joseph Disease)
    Colomer Gould, Veronica F.
    NEUROTHERAPEUTICS, 2012, 9 (02) : 285 - 296
  • [7] A new classification of spinocerebellar ataxia type 3 (Machado-Joseph disease)
    Teive, HA
    Arruda, WO
    Werneck, LC
    MOVEMENT DISORDERS, 2004, 19 : S25 - S25
  • [8] Diagnosis of Spinocerebellar Ataxia type 3 (Machado-Joseph disease) in Chile
    Miranda C, Marcelo
    REVISTA MEDICA DE CHILE, 2015, 143 (01) : 126 - 127
  • [9] Mouse Models of Spinocerebellar Ataxia Type 3 (Machado-Joseph Disease)
    Veronica F. Colomer Gould
    Neurotherapeutics, 2012, 9 : 285 - 296
  • [10] Spinocerebellar ataxia type 3/Machado-Joseph disease starting before adolescence
    Donis, Karina Carvalho
    Morales Saute, Jonas Alex
    Krum-Santos, Ana Carolina
    Furtado, Gabriel Vasata
    Mattos, Eduardo Preusser
    Saraiva-Pereira, Maria Luiza
    Torman, Vanessa Leotti
    Jardim, Laura Bannach
    NEUROGENETICS, 2016, 17 (02) : 107 - 113