R. Pamphlett et Fy. Png, SHRINKAGE OF MOTOR AXONS FOLLOWING SYSTEMIC EXPOSURE TO INORGANIC MERCURY, Journal of neuropathology and experimental neurology, 57(4), 1998, pp. 360-366
Systemically-administered inorganic mercury localizes to motor neurons
, but it is not known if mercury injures these neurons. We therefore l
ooked for signs of damage to the motor and sensory neurons of mice tha
t had been exposed to inorganic mercury. Young adult mice were injecte
d intraperitoneally with either 1 or 2 mu g/g of mercuric chloride and
perfused 1 or 30 weeks later. The cellular distribution of mercury in
the spinal cord was examined with silver nitrate autometallography. T
he numbers and sizes of myelinated axons in the L5 anterior and poster
ior roots were quantitated using an image analysis program. Mercury wa
s found throughout the cytoplasm of motor neuron cell bodies after 1 w
eek and in paranuclear aggregations after 30 weeks. Thirty weeks after
exposure to either 1 or 2 mu g/g of mercury, fewer large myelinated a
xons were seen in mercury-injected groups than in controls, though tot
al numbers of myelinated axons did not differ between groups. A slight
increase in numbers of small axons was seen in the posterior roots of
mice exposed to 1 mu g/g of mercury. In conclusion, inorganic mercury
remains within mouse neurons for prolonged periods and causes a reduc
tion in the size of myelinated axons in the anterior root and to a les
ser extent the posterior spinal root. Inorganic mercury within motor n
eurons therefore appears to behave as a slowly-acting neurotoxin that
shrinks motor axons.