No abstract

No abstract

No abstract

The relationship between the neurotoxicity caused by excess amounts of synthetic amino acid preparations and serum levels of a certain amino acid was examined using suckling mice and kittens. Three preparations, two of which contained aspartic acid and glutamic acid, were injected intraperitoneally into neonatal mice. Almost all the animals which were treated with the preparations containing aspartic acid and glutamic acid at a dosage of more than 40 μl/g body weight (b.w.) showed hypothalamic lesions. The severity of these increased according to each dose increment. On the other hand, none of the animals treated with the preparation containing neither aspartic acid nor glutamic acid sustained hypothalamic lesions. All kittens injected intravenously with the preparation containing aspartic acid and glutamic acid at dosages of more than 20 μl/g b.w. also showed hypothalamic lesions, but none of the kittens treated with dosages of less than 10 μl/g b.w. did. Serum levels of each amino acid reached their highest values as early as 5 min after injection and then returned abruptly to the control value within 3 h.

This study was undertaken to elucidate morphological changes in the synaptic area of the Purkinje cell dendritic spines when granule cells were decreased in number. The mice were injected s.c. with 30 mg/kg b.w. of cytosine arabinoside on days 2, 3, and 4, and on days 7, 8 and 9, and were designated as group I and group II, respectively. The mice injected with saline on days 2, 3, and 4 served as control. The cerebella of the mice in each group were examined by electron microscopy on days 30, 60, and 90. Using photographs thus obtained, the synaptic length and area of Purkinje cell dendritic spines which participated in synapses with axons of granule cells were measured by computer. In the controls, these spines did not increase significantly either in synaptic length or in spine area in the duration from 30 to 90 days after birth. In the 90-day-old mice belonging to group I and group II, however, they increased by about 20% in the synaptic length and by about 35% in the spine area as compared to those in age-matched control. The elongation and enlargement show that the synaptic surface on the spine spreads to compensate for synapses lost by reduction in number of granule cells in experimental groups.