Abstract

It is known that patients with severe motor and intellectual disabilities (SMID) showed sudden unexplained death (SUD), in which autopsy failed to identify causes of death. Although the involvement of brainstem dysfunction is speculated, the detailed neuropathological analysis still remains to be performed. In order to clarify pathogenesis, we investigated the brainstem functions in autopsy cases of SMID showing SUD. We immunohistochemically examined expressions of tyrosine hydroxylase, tryptophan hydroxylase, substance P, methionine-enkephalin, and c-fos in the serial sections of the midbrain, pons, and medulla oblongata in eight SUD cases and seven controls, having neither unexplained death nor pathological changes in the brain. Expressions of tyrosine hydroxylase and tryptophan hydroxylase were reduced in two of eight cases, and those of substance P and/or methionine-enkephalin were augmented in the pons and medulla oblongata in seven of eight cases, including the aforementioned two cases, when compared with those in controls. The hypoglossal nucleus and/or the dorsal vagal nucleus demonstrated increased neuronal immunoreactivity for c-fos in seven of eight cases, although there was no neuronal loss or gliosis in both the nuclei. Controls rarely showed immunoreactivity for c-fos in the medulla oblongata. These data suggest the possible involvement of brainstem dysfunction in SUD in patients with SMID, and consecutive neurophysiological evaluation of brainstem functions, such as all-night polysomnography and blink reflex, may be useful for the prevention of SUD, because some parameters in the neurophysiological examination are known to be related to the brainstem catecholamine neurons and the spinal tract nucleus of trigeminal nerve.

Highlights

  • Severe motor and intellectual disabilities (SMID) describe a heterogeneous group of disorders with severe physical disabilities and profound mental retardation [1, 2]

  • Dysfunction is speculated in sudden infant death syndrome (SIDS) [7,8,9], and disturbances of brainstem catecholamine neurons were involved in sudden death in developmental brain disorders, such as SIDS and Fukuyama-type congenital muscular dystrophy (FCMD) [10, 11]

  • We performed the comprehensive immunohistochemistry on the brainstem lesions in autopsy cases, in order to clarify the pathogenesis of sudden unexplained death (SUD) in patients with SMID, and discussed the possibility of monitoring SUD using neurophysiological examination

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Summary

INTRODUCTION

Severe motor and intellectual disabilities (SMID) describe a heterogeneous group of disorders with severe physical disabilities and profound mental retardation [1, 2]. For immunohistochemical staining of the brainstem, sections with thickness of 5 μm were serially cut in the upper and lower parts of the midbrain, and the upper, middle, and lower parts of the pons, and medulla oblongata They were deparaffinized, quenched with 1% hydrogen peroxide, and treated after microwave antigen retrieval with the following antibodies: mouse monoclonal antibodies to glial fibrillary acidic protein (GFAP, Dako, Glostrup, Denmark), tyrosine hydroxylase (Affinity Bioreagents, Inc., Golden, CO, USA), and tryptophan hydroxylase (Oncogen Research Product, Cambridge, MA, USA), in addition to rabbit polyclonal antibodies to substance P (Zymed Laboratories, Foster City, CA, USA), methionineenkephalin (Chemikon International, Inc., Temecula, CA, USA), and c-fos (Santa Cruz Biotechnology, CA, USA) at the following concentrations: 1:50 (GFAP, substance P), 1:100 (tryptophan hydroxylase), 1:400 (tyrosine hydroxylase), 1:1000 (methionineenkephalin, c-fos).

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