Abstract

ABSTRACTPostmortem investigation of methamphetamine (MA) abuse is an important task in forensic pathology. The present study investigated morphological changes in the astrocytes in the parietal cerebral cortex of MA abusers. Glial fibrillary acidic protein immunoreactivity in the cerebral cortex was examined in forensic autopsy cases for MA-detected group and control group. Clasmatodendrotic astrocytes (including those with swollen cell bodies and disintegrating distal processes) were frequently observed in the cerebral cortex of MA abusers. Quantitative analysis using a colour image processor showed a concomitant increase in the astrocyte area and astrocyte-to-vessel area ratio (size and number of astrocytes) in the grey matter in acute MA fatality and other MA-involved cases, although the astrocyte area (size) was also increased in cases of asphyxiation. The total astrocyte area (size) in the white matter was significantly higher in MA fatalities and asphyxia than in the other groups involving MA abusers. Those indices were independent of blood MA level, age, sex, survival or postmortem time. These observations suggest the increasing number and hypertrophic changes of astrocytes in the grey matter in MA abusers can be the outcome of long-term abuse, while disintegrating distal processes may exist only in acute fatal MA intoxication.

Highlights

  • Drug abuse is a worldwide social problem related to crime, traffic and non-traffic accidents and physical and psychological hazards

  • glial fibrillary acidic protein (GFAP) immunohistochemistry demonstrated that hypertrophic astrocytes could be seen in layers IV, V, and VI in the parietal cerebral cortex of MA abusers (Figure 1), and this result could not be clearly obtained by HE

  • The present study suggests that an increase in the number and hypertrophic changes of astrocytes in the grey matter in MA abusers can be the outcome of long-term abuse, while disintegrating distal processes may exist only in acute fatal MA intoxication

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Summary

Introduction

Drug abuse is a worldwide social problem related to crime, traffic and non-traffic accidents and physical and psychological hazards. Acute MA dosing causes a variety of physical and mental disorders including restlessness, confusion, anxiety, hallucinations, cardiac arrhythmias, hypertensive crises, hyperthermia, metabolic acidosis, circulatory collapse, convulsions and coma. Both short-term and long-term serial and parallel toxic processes may cause neuronal metabolic deterioration involving an increase in oxidative stress, which can be enhanced by hyperthermia, and result in apoptosis and neuronal necrosis [10,11,12,13,14,15]. Astrocytic morphological changes in the cerebral cortex of MA abusers were quantitatively analysed to investigate the neuropathological effects of MA abuse in humans

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