Alterations in Brainstem and Cortical Organization of Rats Sustaining Prenatal Vibrissa Follicle Lesions

References

• Bates C., Killackey H. P. The organization of the neonatal rat's connections in the parietal cortex of the rat. J. Comp. Neurol. 1985; 181: 513–538
   Google Scholar
• Belford G. R., Killackey H. P. The sensitive period in the development of the trigeminal system of the neonatal rats. J. Comp. Neurol. 1980; 193: 335–350
   PubMed Web of Science ®Google Scholar
• Bennett-Clarke C. A., Chiaia N. L., Crissman R. S., Rhoades R. W. The source of the transient serotoninergic input to the developing visual and somatosensory cortices in rat. Neuroscience 1991; 43: 163–183
   Google Scholar
• Blakemore C., Van Sluyters R. C. Reversal of the physiological effects of monocular deprivation in kittens: Further evidence for a sensitive period. J. Physiol. (Lond.) 1974; 237: 195–216
   Google Scholar
• Blue M. E., Erzurumlu R. S., Jhaveri S. A comparison of pattern formation by thalamocortical and serotonergic afferents in the rat barrel field cortex. Cerebral Cortex 1991; 1: 380–389
   Google Scholar
• Bronchti G., Schönenberger N., Welker E., Van der Loos H. Barrelfield expansion after neonatal eye removal in mice. Neuro I. Rep. 1992; 3: 489–492
   PubMedGoogle Scholar
• Chiaia N. L., Bennett-Clarke C. A., Eck M., White F. A., Crissman R. S., Rhoades R. W. Evidence for prenatal competition among the central arbors of trigeminal primary afferent neurons. J. Neurosci. 1992; 12: 62–76
   PubMed Web of Science ®Google Scholar
• Chiaia N. L., Bennett-Clarke C. A., Rhoades R. W. Effects of cortical and thalamic lesions upon primary afferent terminations, distributions of projection neurons, and the cytochrome oxidase pattern in the trigeminal brainstem complex. J. Comp. Neurol. 1991; 303: 600–616
   PubMedGoogle Scholar
• Cynader M., Timney B. N., Mitchell D. E. Period of susceptibility of kitten visual cortex to the effects of monocular deprivation extends beyond six months of age. Brain Res. 1980; 191: 545–550
   Google Scholar
• D'Amato R. J., Blue M. E., Largent B. L., Lynch D. R., Ledbetter D. J., Molliver M. E., Snyder S. H. Ontogeny of the serotonergic projection to rat neocortex: Transient expression of a dense innervation to primary sensory areas. Proc. Natl. Acad. Sci. USA 1987; 84: 4322–4326
   PubMed Web of Science ®Google Scholar
• Dehay C., Horsburgh G., Berland M., Killackey H., Kennedy H. The effects of bilateral enucleation in the primate fetus on the parcellation of visual cortex. Dev. Brain Res. 1991; 62: 137–141
   Google Scholar
• Durham D., Woolsey T. A. Effects of neonatal whisker lesions on mouse central trigeminal pathways. J. Comp. Neurol. 1984; 223: 424–447
   PubMedGoogle Scholar
• Erzurumlu R. S., Jhaveri S. Thalamic axons confer a blueprint of the sensory periphery onto the developing rat somatosensory cortex. Dev. Brain Res. 1990; 56: 229–234
   PubMedGoogle Scholar
• Erzurumlu R., Killackey H. P. Development of order in the rat trigeminal system. J. Comp. Neurol. 1983; 213: 365–380
   PubMed Web of Science ®Google Scholar
• Gyllensten L., Malmfors T., Norlin M. L. Effects of visual deprivation on the optic centers of growing and adult mice. J. Comp. Neurol. 1966; 126: 463–470
   PubMed Web of Science ®Google Scholar
• Hubel D. H., Wiesel T. N. The period of susceptibility to the physiological effects of unilateral eye closure in kittens. J. Physiol. (Lond.) 1970; 206: 419–436
   Google Scholar
• Jeanmonod D., Rice F. L., Van der Loos H. Mouse somatosensory cortex: Alterations in the barrelfield following receptor injury at different early postnatal ages. Neuroscience 1981; 66: 1503–1535
   Google Scholar
• Jensen K. F., Killackey H. P. Terminal arbors of axons projecting to the somatosensory cortex of the adult rat: I. The normal morphology of specific thalamocortical afferents. J. Neurosci. 1987; 7: 3529–3543
   Google Scholar
• Killackey H. P. Anatomical evidence for cortical subdivisions based on vertically discrete thalamic projections from the ventral posterior nucleus to cortical barrels in the rat. Brain Res. 1973; 51: 326–331
   PubMed Web of Science ®Google Scholar
• Killackey H. P., Belford G., Ryugo R., Ryugo D. K. Anomalous organization of thalamocortical projections consequent to vibrissae removal in the newborn rat and mouse. Brain Res. 1976; 104: 309–315
   PubMed Web of Science ®Google Scholar
• Killackey H. P., Dawson D. R. Expansion of the central hindpaw representation following fetal forelimb removal in the rat. Eur. J. Neurosci. 1989; 1: 210–221
   PubMed Web of Science ®Google Scholar
• Killackey H. P., Jacquin M. F., Rhoades R. W. Development of somatosensory system structures. Development of Sensory Systems in Mammals, J. R. Coleman. Wiley, New York 1990; 403–429
   Google Scholar
• Killackey H. P., Shinder A. Central correlates of peripheral pattern alterations in the trigeminal system of the rat: II. The effect of nerve section. Dev. Brain Res. 1981; 1: 121–126
   Google Scholar
• Lee K. J., Woolsey T. A. A proportional relationship between peripheral innervation density and cortical neuron number in the somatosensory system of the mouse. Brain Res. 1975; 99: 349–353
   PubMed Web of Science ®Google Scholar
• Lee P. H., Weaver W. R., Henderson T. A., Sonty R. V., Woolsey T. A., Jacquin M. F. Activity-dependent competitive interactions in the developing whisker-barrel neuraxis. Soc. Neurosci. Abstr. 1991; 17: 10
   Google Scholar
• McCasland J. S., Bernardo K. L., Probst K. L., Woolsey T. A. Cortical local circuit axons do not mature after early deafferentation. Proc. Natl. Acad. Sci. USA 1992; 89: 1832–1836
   PubMedGoogle Scholar
• Necker R., Rehkämper G., Nevo E. Electrophysiological mapping of body representation in the cortex of the blind mole rat. Neurol. Rep. 1992; 3: 505–508
   Google Scholar
• Olavarria J., Malach R., Van Sluyters R. C. Development of visual callosal connections in neonatally enucleated rats. J. Comp. Neurol. 1987; 260: 321–348
   PubMed Web of Science ®Google Scholar
• Olson C. R., Freeman R. D. Profile of the sensitive period for monocular deprivation in kittens. Exp. Brian Res. 1980; 39: 1721
   Google Scholar
• Rakic P. Specification of cerebral cortical areas. Science 1988; 241: 170–176
   PubMed Web of Science ®Google Scholar
• Rakic P., Suñer I., Williams R. W. A novel cytoarchitectonic area induced experimentally within the primate visual cortex. Proc. Natl. Acad. Sci. USA 1991; 88: 2083–2087
   Google Scholar
• Rauschecker J. P., Tian B., Korte M., Egert U. Crossmodal changes in the somatosensory vibrissa/barrel system of visually deprived animals. Proc Natl. Acad. Sci. USA 1992; 89: 5063–5067
   PubMed Web of Science ®Google Scholar
• Rhoades R. W., Bennett-Clarke C. A., Chiaia N. L., White F. A., MacDonald G. J., Haring J. H., Jacquin M. F. Development and lesion induced reorganization of the cortical representation of the rat's body surface as revealed by immunocytochemistry for serotonin. J. Comp. Neurol. 1990; 293: 190–207
   PubMed Web of Science ®Google Scholar
• Rice F. L., Van der Loos H. Development of the barrels and barrelfield in the somatic sensory cortex of the mouse. J. Comp. Neurol. 1977; 71: 545–560
   Google Scholar
• Riddle D., Richards A., Zsuppan F., Purves D. Growth of the rat somatic sensory cortex and its constituent parts during postnatal development. J. Neurosci. 1992; 12: 3509–3524
   Google Scholar
• Schlagger B. J., O'Leary D. D. M. An activity-dependent component of plasticity in the developing rat neocortex. Soc. Neurosci. Abstr. 1992; 18: 57
   Google Scholar
• Senft S. L., Woolsey T. A. Growth of thalamic afferents into mouse barrel cortex. Cerebral Cortex 1991; 1: 308–335
   PubMed Web of Science ®Google Scholar
• Ungewitter L. H. A urea silver nitrate method for nerve fibers and nerve endings. Stain Technol. 1951; 26: 73–76
   PubMed Web of Science ®Google Scholar
• Van der Loos H., Woolsey T. A. Somatosensory cortex: Structural alterations following early injury to sense organs. Science 1973; 179: 395–398
   PubMed Web of Science ®Google Scholar
• Waite P. M. E. Plasticity in cranial somatosensory pathways. Information Processing in Mammalian Auditory and Tactile Systems, M. Rowe, L. Aitkin. Alan R. Liss, New York 1990; 237–251
   Google Scholar
• Waite P. M. E., de Permentier P. The rat's postero-orbital sinus hair: I. Brainstem projections and the effect of infraorbital nerve section at different ages. J. Comp. Neurol. 1991; 312: 325–340
   Google Scholar
• Welker E., Van der Loos H. Quantitative correlation between barrel-field size and the sensory innervation of the whiskerpad: A comparative study in six strains of mice bred for different patterns of mystacial vibrissae. J. Neurosci. 1986; 6: 3355–3373
   PubMedGoogle Scholar
• Wong-Riley M. T. T. Changes in the visual system of monocularly sutured or enucleated cats demonstrable with cytochrome oxidase histochemistry. Brain Res. 1979; 160: 134–138
   PubMedGoogle Scholar
• Wong-Riley M. T. T., Welt C. Histochemical changes in cytochrome oxidase of cortical barrels after vibrissal removal in neonatal and adult mice. Proc. Natl. Acad. Sci. USA 1980; 77: 2333–2337
   PubMed Web of Science ®Google Scholar
• Woolsey T. A. Peripheral alteration and somatosensory development. Development of Sensory Systems in Mammals, J. R. Coleman. Wiley, New York 1990; 461–516
   Google Scholar
• Woolsey T. A., Anderson J. R., Wann J. R., Stanfield B. B. Effects of early vibrissae damage on neurons in the ventrobasal (VB) thalamus of the mouse. J. Comp. Neurol. 1979; 184: 363–380
   PubMed Web of Science ®Google Scholar
• Woolsey T. A., Vander Loos H. The structural organization of layer IV in the somatosensory region (SI) of the mouse cerebral cortex. Brain Res. 1970; 17: 205–242
   PubMed Web of Science ®Google Scholar
• Woolsey T. A., Wann J. R. Areal changes in mouse cortical barrels following vibrissal damage at different postnatal ages. J. Comp. Neurol. 1976; 170: 53–66
   PubMedGoogle Scholar