Prenatal removal of frontal association cortex in the fetal rhesus monkey: Anatomical and functional consequences in postnatal life

Anatomical and behavioral consequences were examined following bilateral or unilateral resections of the presumptive dorsolateral prefrontal cortex in 4 rhesus monkey fetuses at E102 (102nd embryonic day), E104, E106 and E119, with subsequent replacement in utero and delivery at later stages of development. Unoperated monkeys of appropriate pre- and postnatal ages served as controls for certain features of morphogenesis and tectogenesis. Monkeys given comparable unilateral or bilateral lesions at selected postnatal ages were used as controls for the behavioral effects of prenatal resection as well as for neuropathological examination. The behavioral evaluation provided evidence for extraordinary preservation of function after frontal cortical resection in the prenatal period. During the entire course of its postnatal development, a monkey that sustained bilateral resection as a fetus at E106 performed surprisingly well and clearly with the competence of unoperated monkeys of identical or older ages on tasks selective for dorsolateral prefrontal cortical function; it did not exhibit deficits characteristic of animals that have comparable or even smaller resections as juveniles or adults. Following either unilateral or bilateral resection prior to E106, ectopic sulci and gyri appeared in intact regions of the frontal lobe of each hemisphere, as well as in locations at a considerable distance from the lesions, such as the temporal and occipital lobes. The cytoarchitectonic characteristics of the cortex in these anomalous gyri were typical of adjacent cortex in the regions in which they appeared. Examination of the parvocellular subdivision of the mediodorsal thalamic nucleus yielded the novel finding that this principal source of essential projections to the dorsolateral prefrontal cortex contained a virtually normal number of neurons in postnatal monkeys, following unilateral or bilateral lesions performed at or before E106, and exhibited only a partial loss of neurons after surgery at E119. The same cells regularly degenerate following comparable resections in the postnatal period. The survival of these neurons in prenatally operated monkeys is unprecedented, and can be explained by several hypotheses, including the possibility that their axons become rerouted to their structures in the absence of their normal targets. The present results thus demonstrate that ablation of a circumscript area of the frontal cortex in a non-human primate a full two months before birth may leave the functions later to be subserved by that area unaffected. Such early surgical intervention results in significant alteration in the gross morphological characteristics of the cortex, and apparently induces a functionally compensatory reorganization of thalamocortical connections. Similar principles may account for sparing of function following early damage to the human brain.

[1]  W. Nauta,et al.  Columnar distribution of cortico-cortical fibers in the frontal association, limbic, and motor cortex of the developing rhesus monkey , 1977, Brain Research.

[2]  M. Dennis,et al.  Selective impairments of visuo-spatial abilities in infantile hemiplegics after right cerebral hemidecortication. , 1974, Neuropsychologia.

[3]  P. S. Goldman,et al.  Postnatal maturation of subcortical projections from the prefrontal cortex in the rhesus monkey , 1976, The Journal of comparative neurology.

[4]  H. E. Rosvold,et al.  Analysis of the delayed-alternation deficit produced by dorsolateral prefrontal lesions in the rhesus monkey. , 1971, Journal of comparative and physiological psychology.

[5]  B. J. Winer Statistical Principles in Experimental Design , 1992 .

[6]  P. Rakić,et al.  Timing of major ontogenetic events in the visual cortex of the rhesus monkey. , 1975, UCLA forum in medical sciences.

[7]  Giorgio M. Innocenti,et al.  Exuberant projection into the corpus callosum from the visual cortex of newborn cats , 1977, Neuroscience Letters.

[8]  P. Rakic Prenatal genesis of connections subserving ocular dominance in the rhesus monkey , 1976, Nature.

[9]  W. Kahle Zur ontogenetischen Entwicklung der Brodmannschen Rindenfelder , 1966 .

[10]  Doreen Berman,et al.  Auditory thresholds in monkeys asphyxiated at birth. , 1971, Experimental neurology.

[11]  M. Kennard Age and other factors in motor recovery from precentral lesions in monkeys. , 1936 .

[12]  G. Schneider,et al.  Mechanisms of functional recovery following lesions of visual cortex or superior colliculus in neonate and adult hamsters. , 1970, Brain, behavior and evolution.

[13]  H. E. Rosvold,et al.  The effects of selective caudate lesions in infant and juvenile Rhesus monkeys. , 1972, Brain research.

[14]  H. Harlow,et al.  Analysis of frontal and posterior association syndromes in brain-damaged monkeys. , 1952, Journal of comparative and physiological psychology.

[15]  V. Caviness,et al.  Mechanical model of brain convolutional development. , 1975, Science.

[16]  P. Rakić Prenatal development of the visual system in rhesus monkey. , 1977, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[17]  P. S. Goldman Functional development of the prefrontal cortex in early life and the problem of neuronal plasticity. , 1971, Experimental neurology.

[18]  A. Brodal,et al.  MODIFICATION OF GUDDEN METHOD FOR STUDY OF CEREBRAL LOCALIZATION , 1940 .

[19]  O. Marburg,et al.  PORENCEPHALY: II. STUDIES IN PHLEBOTHROMBOSIS AND PHLEBOSTASIS , 1945 .

[20]  R. Bleier Retrograde transsynaptic cellular degeneration in mammillary and ventral tegmental nuclei following limbic decortication in rabbits of various ages. , 1969, Brain research.

[21]  P. Rakić,et al.  Genesis of the dorsal lateral geniculate nucleus in the rhesus monkey: Site and time of origin, kinetics of proliferation, routes of migration and pattern of distribution of neurons , 1977, The Journal of comparative neurology.

[22]  D. Pandya,et al.  A search for the spatial engram within the frontal lobes of monkeys. , 1972, Acta neurobiologiae experimentalis.

[23]  V. Hamburger Cell death in the development of the lateral motor column of the chick embryo , 1975, The Journal of comparative neurology.

[24]  P. S. Goldman Maturation of the Mammalian Nervous System and the Ontogeny of Behavior1 , 1976 .

[25]  C. J. Connolly,et al.  External morphology of the primate brain , 1950 .

[26]  F. Gilles,et al.  Gyral development of the human brain , 1977, Transactions of the American Neurological Association.

[27]  Egdahl Rh,et al.  The performance of complex fetal operations in utero without amniotic fluid loss or other disturbances of fetal-maternal relationships. , 1960 .

[28]  P. Yakovlev,et al.  Schizencephalies; a study of the congenital clefts in the cerebral mantle; clefts with fused lips. , 1946, Journal of neuropathology and experimental neurology.

[29]  S. Wise,et al.  Prenatal development of sensorimotor cortical projections in cats , 1977, Brain Research.

[30]  H. Teuber,et al.  Behaviour after Cerebral Lesions in Children and Adults , 1962, Developmental medicine and child neurology.

[31]  A. J. Blomquist,et al.  Learning in rhesus monkeys after varying amounts of prefrontal lobe destruction during infancy and adolescence. , 1970, Brain research.

[32]  M. Dennis,et al.  Comprehension of syntax in infantile hemiplegics after cerebral hemidecortication: Left-hemisphere superiority , 1975, Brain and Language.

[33]  G. Bonin,et al.  The neocortex of Macaca mulatta , 1947 .

[34]  H. E. Rosvold,et al.  Delayed Recovery of Function follwing Orbital Prefrontal Lesions in Infant Monkeys , 1973, Science.

[35]  A. Berman,et al.  Delayed response deficits in neonatally asphyxiated rhesus monkeys. , 1970, Experimental neurology.

[36]  W. Nauta,et al.  An intricately patterned prefronto‐caudate projection in the rhesus monkey , 1977, The Journal of comparative neurology.

[37]  W. Cowan,et al.  The development of the isthmo‐optic tract in the chick, with special reference to the occurrence and correction of developmental errors in the location and connections of isthmo‐optic neurons , 1976, The Journal of comparative neurology.

[38]  G Raisman,et al.  Neuronal plasticity in the septal nuclei of the adult rat. , 1969, Brain research.

[39]  G. E. Alexander,et al.  Maturation of prefrontal cortex in the monkey revealed by local reversible cryogenic depression , 1977, Nature.

[40]  C. Courville Birth and brain damage : an investigation into the problems of antenatal and paranatal anoxia and allied disorders and their relation to the many lesion-complexes residual thereto , 1971 .

[41]  D. G. Lawrence,et al.  The development of motor control in the rhesus monkey: evidence concerning the role of corticomotoneuronal connections. , 1976, Brain : a journal of neurology.

[42]  H. Harlow,et al.  Learned Behavior of Rhesus Monkeys following Neonatal Bilateral Prefrontal Lobotomy , 1960, Science.

[43]  J. Sechzer Memory deficit in monkeys brain damaged by asphyxia neonatorum. , 1969, Experimental neurology.

[44]  A. Walker,et al.  A cytoarchitectural study of the prefrontal area of the macaque monkey , 1940 .

[45]  G. E. Alexander,et al.  Functional development of the dorsolateral prefrontal cortex: An analysis utilizing reversible cryogenic depression , 1978, Brain Research.

[46]  K. Nelson,et al.  Perinatal brain damage: porencephaly in a cynomolgous monkey. , 1973, Biology of the neonate.

[47]  L. Basser Hemiplegia of early onset and the faculty of speech with special reference to the effects of hemispherectomy. , 1962, Brain : a journal of neurology.

[48]  P. Rodier,et al.  The influence of a prenatal trauma on formation of Purkinje cells. , 1973, The American journal of anatomy.

[49]  R. Lund,et al.  Development of the geniculocortical pathway in rat , 1977, The Journal of comparative neurology.

[50]  K. Pribram,et al.  Analysis of the effects of frontal lesions in monkey. I. Variations of delayed alternation. , 1955, Journal of comparative and physiological psychology.

[51]  Aaron Smith,et al.  Development of above normal language and intelligence 21 years after left hemispherectomy , 1975, Neurology.

[52]  J. Walton Birth and Brain Damage , 1972 .

[53]  Walle J. H. Nauta,et al.  Autoradiographic demonstration of a projection from prefrontal association cortex to the superior colliculus in the rhesus monkey , 1976, Brain Research.

[54]  H. E. Rosvold,et al.  Localization of function within the dorsolateral prefrontal cortex of the rhesus monkey. , 1970, Experimental neurology.

[55]  Richard Passingham,et al.  Delayed matching after selective prefrontal lesions in monkeys (Macaca mulatta) , 1975, Brain Research.

[56]  L. T. Robertson,et al.  Effect of prosencephalectomy on the connections of the inferior olivary nucleus in fetal rhesus monkeys , 1976, Experimental Neurology.

[57]  G. Lynch,et al.  Developmental differences in post-lesion axonal growth in the hippocampus. , 1973, Brain research.

[58]  R. Thompson,et al.  Differential effects of cortical lesions in infant and adult cats on roughness discrimination. , 1959, Experimental neurology.

[59]  A. Kling,et al.  Differential effects of early and late lesions of frontal granular cortex in the monkey , 1967 .

[60]  K H PRIBRAM,et al.  A behavioral analysis of the organization of the parieto‐temporo‐preoccipital cortex , 1950, The Journal of comparative neurology.

[61]  Charles M. Butter,et al.  Perseveration in extinction and in discrimination reversal tasks following selective frontal ablations in Macaca mulatta , 1969 .

[62]  P. S. Goldman The role of experience in recovery of function following orbital prefrontal lesions in infant monkeys , 1976, Neuropsychologia.

[63]  W. Cowan,et al.  The time of origin and the pattern of survival of neurons in the isthmo‐optic nucleus of the chick , 1976, The Journal of comparative neurology.

[64]  I. Kostović,et al.  The development of synapses in cerebral cortex of the human fetus. , 1973, Brain research.

[65]  J. Mcfie THE EFFECTS OF HEMISPHERECTOMY ON INTELLECTUAL FUNCTIONING IN CASES OF INFANTILE HEMIPLEGIA , 1961, Journal of neurology, neurosurgery, and psychiatry.