TRANSNEURONAL DEGENERATION OF THALAMIC NEURONS FOLLOWING DEAFFERENTATION - QUANTITATIVE STUDIES USING [H-3] THYMIDINE AUTORADIOGRAPHY

被引:10
作者
OH, LJ
KIM, G
YU, J
ROBERTSON, RT
机构
[1] UNIV CALIF IRVINE, COLL MED, DEPT ANAT & NEUROBIOL, IRVINE, CA 92717 USA
[2] UNIV CALIF IRVINE, COLL MED, DEPT PHYSIOL MED & REHABIL, IRVINE, CA 92717 USA
来源
DEVELOPMENTAL BRAIN RESEARCH | 1991年 / 63卷 / 1-2期
关键词
DEAFFERENTATION; DEVELOPMENT; ENUCLEATION; THALAMUS; THYMIDINE AUTORADIOGRAPHY; TRANSNEURONAL DEGENERATION;
D O I
10.1016/0165-3806(91)90078-W
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Transneuronal degeneration of thalamic neurons following partial deafferentation was studied using [H-3]thymidine autoradiography. Timedpregnant female Sprague-Dawley rats received systemic injections of [H-3]thymidine on embryonic day (E) 13, 14 and/or 15. On the day of birth, pups were anesthetized by hypothermia and subjected to unilateral enucleation, unilateral removal of the inferior colliculus or sham lesion. Animals were sacrificed on postnatal day 10 or 30 and the brains processed for autoradiography. Material from sham-lesioned animals demonstrates that neurons destined for the dorsal lateral geniculate nucleus (LGd) undergo final mitoses on E13, 14 and 15. Neurons in the ventral medial geniculate nucleus (MGv) undergo final mitoses on E13 and 14. Thirty days following neonatal unilateral eye removal, the contralateral LGd displays a loss of approximately 30-35% of [H-3]thymidine labeled neurons. Neonatal unilateral removal of the inferior colliculus results in a loss of approximately 30-40% of labeled neurons in MGv. For both LGd and MGv, shorter survival times reveal less severe cell loss. Late generated (E15) LGd neurons show less severe loss following enucleation than do earlier generated neurons. These results document the degree of cell loss in sensory thalamic nuclei following deafferentation and demonstrate that [H-3]thymidine autoradiography provides a useful quantitative method for assessing anterograde transneuronal cell los in targeted populations of neurons in the developing central nervous system.
引用
收藏
页码:191 / 200
页数:10
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