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Age- and sex-related oculomotor manifestation of dopamine deficiency in Segawa disease.
Terao, Yasuo; Fukuda, Hideki; Hikosaka, Okihide; Yugeta, Akihiro; Matsuda, Shun-Ichi; Fisicaro, Francesco; Ugawa, Yoshikazu; Hoshino, Kyoko; Nomura, Yoshiko.
Afiliação
  • Terao Y; Department of Neurology, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan; Department of Medical Physiology, Kyorin University, 6-20-2 Shinkawa, Mitaka, Tokyo 181-8611, Japan. Electronic address: yterao@ks.kyorin-u.ac.jp.
  • Fukuda H; Segawa Memorial Neurological Clinic for Children, 2-8 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-0062, Japan.
  • Hikosaka O; Section of Neuronal Networks, Laboratory of Sensorimotor Research, National Eye Institute, 49 Convent Drive, Bethesda 20892-4435, MD, USA.
  • Yugeta A; Department of Neurology, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.
  • Matsuda SI; Department of Neurology, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan.
  • Fisicaro F; Department of Biomedical and Biotechnological Sciences, University of Catania, Catania, Piazza Università, 2, 95131 Catalina, Italy.
  • Ugawa Y; Department of Human Neurophysiology, School of Medicine, Fukushima Medical University, 1 Hikarigaoka, Fukushima 960-1295, Japan.
  • Hoshino K; Segawa Memorial Neurological Clinic for Children, 2-8 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-0062, Japan.
  • Nomura Y; Yoshiko Nomura Neurological Clinic for Children, Tokyo 113-0034, Japan.
Clin Neurophysiol ; 157: 73-87, 2024 01.
Article em En | MEDLINE | ID: mdl-38064930
ABSTRACT

OBJECTIVE:

To investigate the oculomotor manifestations of Segawa disease (SD), considered to represent mild dopamine deficiency and discuss their pathophysiological basis.

METHODS:

We recorded visually- (VGS) and memory-guided saccade (MGS) tasks in 31 SD patients and 153 age-matched control subjects to study how basal ganglia (BG) dysfunction in SD evolves with age for male and female subjects.

RESULTS:

SD patients were impaired in initiating MGS, showing longer latencies with occasional failure. Patients showed impaired ability to suppress reflexive saccades; saccades to cues presented in MGS were more frequent and showed a shorter latency than in control subjects. These findings were more prominent in male patients, particularly between 13 and 25 years. Additionally, male patients showed larger delay in MGS latency in trials preceded by saccades to cue than those unpreceded.

CONCLUSIONS:

The findings can be explained by a dysfunction of the BG-direct pathway impinging on superior colliculus (SC) due to dopamine deficiency. The disturbed inhibitory control of saccades may be explained by increased SC responsivity to visual stimuli.

SIGNIFICANCE:

Oculomotor abnormalities in SD can be explained by dysfunction of the BG inhibitory pathways reaching SC, with a delayed maturation in male SD patients, consistent with previous pathological/physiological studies.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dopamina / Sinais (Psicologia) Limite: Female / Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dopamina / Sinais (Psicologia) Limite: Female / Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article