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Do early lesions affect cell death in the central nervous system? A study on the effects of early cerebellar hemispherectomy in rats
Author(s) -
Gramsbergen A.,
IjkemaPaassen J.
Publication year - 1987
Publication title -
journal of comparative neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.855
H-Index - 209
eISSN - 1096-9861
pISSN - 0021-9967
DOI - 10.1002/cne.902550412
Subject(s) - nissl body , biology , hemispherectomy , cerebellum , nucleus , central nervous system , red nucleus , anatomy , neuroscience , epilepsy , staining , genetics
Cell death patterns in the lateral and interposed nuclei were compared in control rats and rats in whom a unilateral cerebellar hemispherectomy was performed at day 2 of life. Both groups were studied between days 2 and 20 of life. Pyknotic cells and live neuronal and glial cells were counted from Nissl stained sections. After correction of these values, pyknotic to live cell ratios were calculated. In the lateral nucleus of normal rats, around 14–28 pyknotic cells per 1,000 live cells occurred from day 2 to day 12. Thereafter this value decreased, and from day 16 less than 3 pyknotic/1,000 live cells were observed. In the interposed nuclei, 18–28 pyknotic cells/1,000 live cells occurred at day 2, and from this age onward values gradually decreased. At day 20 values ranged around 1.6/1,000. After unilateral cerebellar hemispherectomy, values in both nuclei began to decrease as early as from day 8. Results from the present study strongly suggest that these cells are prevented from dying because they find an aberrant synaptic target in the ipsilateral red nucleus. Our results demonstrate that early lesions interfere with the regulation of fundamental processes of neuro‐ontogeny.