4.3 Article

The Mesencephalic Periaqueductal Gray, a Further Structure Involved in Breathing Failure Underlying Sudden Infant Death Syndrome

Journal

ASN NEURO
Volume 13, Issue -, Pages -

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/17590914211048260

Keywords

neuropathology; periaqueductal gray; brainstem; sudden infant death syndrome; tyrosine hydroxylase; dopamine

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This study focused on investigating the involvement of the periaqueductal gray (PAG) in Sudden Infant Death Syndrome (SIDS), revealing hypoplasia of the PAG subnucleus medialis in 65% of SIDS cases but not in controls, and significantly higher expression of tyrosine hydroxylase in controls than in SIDS. The findings also showed a significant correlation between PAG and substantia nigra abnormalities, suggesting a common involvement in the sleep-arousal phase failure leading to SIDS.
The aim of this study was to investigate the involvement of the periaqueductal gray (PAG), an area of gray matter surrounding the cerebral aqueduct of Sylvius, in the pathogenetic mechanism of SIDS, a syndrome frequently ascribed to arousal failure from sleep. We reconsidered the same samples of brainstem, more precisely midbrain specimens, taken from a large series of sudden infant deaths, namely 46 cases aged from 1 to about 7 months, among which 26 SIDS and 20 controls, in which we already highlighted significant developmental alterations of the substantia nigra, another mesencephalic structure with a critical role in breath and awakening regulation. Specific histological and immunohistochemical methods were applied to examine the PAG cytoarchitecture and the expression of the tyrosine hydroxylase, a marker of catecholaminergic neurons. Hypoplasia of the PAG subnucleus medialis was observed in 65% of SIDS but never in controls; tyrosine hydroxylase expression was significantly higher in controls than in SIDS. A significant correlation was found between these findings and those related to the substantia nigra, demonstrating a link between these neuronal centers and the brainstem respiratory network and a common involvement in the sleep-arousal phase failure leading to SIDS.

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