Loss of glutamate immunoreactivity from mouse first somatosensory (SI) cortex following neonatal vibrissal lesion.

Whisker follicles were surgically ablated (lesioned) on two entire rows (B and C) of the left snout of two groups of Swiss mice, in the first 2 days after birth (neonatally lesioned) with the animals being allowed to survive for 4 weeks. In the second group at 8 weeks of age (adults), the whisker follicles of rows B and C were similarly lesioned and a survival period of 3 days allowed. Glutamate-immunoreactivity (Glu-IR) was examined in tangential sections of the first somatosensory (SI) 'barrel' cortex of these two groups (at which time it was also confirmed that the follicles had not regrown). In the neonatally lesioned mice, barrel rows B and C were more poorly defined in the right (experimental) hemisphere sections and a semi-quantitative study showed that there was a decrease in Glu-IR cell number (up to 41%) in rows B and C of the right hemisphere compared to the spared barrel rows (A and D). The loss appears to occur over almost the entire area of each deprived barrel rather than being confined to the sides or hollows. In contrast to neonatally lesioned animals, the barrels of the adult-lesioned mice appeared intact and visually similar in both the experimental (right) and control hemispheres (left). The only notable change in Glu-IR observed in the adult-lesioned animals was a decrease of 38% in the number of Glu-IR cells in the sides between the two deafferented rows of barrels (B and C), compared to the cell number between the unaffected barrels (D and E), a change also seen in the neonatally lesioned mice.(ABSTRACT TRUNCATED AT 250 WORDS)