Brains from 32 neonatal autopsies from the Seychelles were examined hi
stologically and analyzed for mercury levels. Six brain regions were s
ampled: frontal and occipital cortex, temporal cortex with hippocampus
, basal ganglia with thalamus, cerebellum, and pens with medulla. Tiss
ue blocks for histology and mercury analysis were taken from opposing
faces to provide for correlation of findings. Similar studies were per
formed on 12 reference neonatal brains from Rochester, New York. No cl
ear-cut developmental abnormality was found, but some brains exhibited
low-grade, non-specific destructive changes. Total mercury levels, mo
st of it in the organic form, were elevated in many of the Seychelles
specimens. No correlation was demonstrated between mercury levels and
degree or type of histologic change. There was considerable variabilit
y in total mercury for each anatomic region among the 32 Seychelles ca
ses, as well as from one region to another in individual brains. All v
alues of total mercury were under 300 ppb. Statistical analysis of mea
n mercury levels for each region demonstrated higher values in deep su
bcortical nuclei, brain stem, and cerebellum, phylogenetically older p
arts of the brain. When total mercury concentration of each region was
paired with all other areas in the same brain and the paired values p
lotted for the entire group of brains, high correlations were obtained
for all brain pairs, suggesting a strong concentration-dependent rela
tionship between mercury intake and brain content Analysis of mercury
levels in separately dissected blocks of grey and white matter from 12
specimens revealed no significant differences between grey and white.
In comparison with other human developmental studies and with experim
ental developmental studies in animals, where toxicity has been demons
trated with total mercury brain levels above 1,000 ppb, this study fou
nd no evidence of toxicity within a range of mercury levels below 300
ppb. Submicroscopic changes, subcellular alterations, subtle disturban
ces in the unfolding of brain architectonics - none of these are exclu
ded with methods used in this report Further studies of threshold effe
cts of MeHg on fetal brain are essential. That approximately half of t
he mercury resides in glial elements in white matter reinforces the ne
ed to focus attention upon glia as well as neurons during development.
(C) 1995 Inter Press, Inc.