Factors influencing frontal cortex development and recovery from early frontal injury

References

• Uylings H, Groenewegen H, Kolb B. Does the rat have a prefrontal cortex?. Behavioural Brain Research 2003; 146: 3–17
   PubMed Web of Science ®Google Scholar
• Kolb B, Stewart J. Sex-related differences in dendritic branching of cells in the prefrontal cortex of rats. Journal of Neuroendocrinology 1991; 3: 95–99
   PubMed Web of Science ®Google Scholar
• Robinson TE, Kolb B. Structural plasticity associated with drugs of abuse. Neuropharmacology 2004; 47(Suppl 1)33–46
   PubMed Web of Science ®Google Scholar
• Brown RW, Kolb B. Nicotine sensitization increases dendritic length and spine density in the nucleus accumbens and cingulate cortex. Brain Research 2001; 899: 94–100
   PubMed Web of Science ®Google Scholar
• Gonzalez CLR, Gharbawie OA, Kolb B. Chronic low-dose administration of nicotine facilitates recovery and synaptic change after focal ischemia in rats. Neuropharmacology 2006; 50: 777–787
   PubMed Web of Science ®Google Scholar
• Jacobs B, Schall M, Scheibel AB. A quantitative dendritic analysis of Wernicke's area in humans: II. Gender, hemispheric, and environmental factors. Journal of Comparative Neurology 1993; 327: 97–111
   PubMed Web of Science ®Google Scholar
• Greenough WT, Chang FF. Plasticity of synapse structure and pattern in the cerebral cortex. Cerebral cortex, A Peters, EG Jones. Plenum Press, New York 1989; 7: 391–440
   Google Scholar
• Siervaag AM, Greenough WT. A multivariate statistical summary of synaptic plasticity meaures in rats exposed to complex, social, and individual environments. Brain Research 1988; 441: 386–392
   PubMed Web of Science ®Google Scholar
• Kolb B, Gibb R, Gorny G. Experience-dependent changes in dendritic arbor and spine density in neocortex vary with age and sex. Neurobiology of Learning and Memory 2003; 79: 1–10
   PubMed Web of Science ®Google Scholar
• Comeau WL, Kolb B. Early methylphendiate exposure inhibits experience-induced plasticity of complex housing in rats, Manuscript in submission
   Google Scholar
• Comeau WL, McDonald R, Kolb B. Learning-induced alterations in prefrontal cortical circuitry. 2009, Manuscript in submission
   Google Scholar
• Bell H, Pellis S, Kolb B. Number of social partners and juvenile peer play experience affect brain development in orbital and medial prefrontal cortices in rats. 2009, Manuscript in submission
   Google Scholar
• Kolb B, Gibb R. Tactile stimulation after posterior parietal cortical injury in infant rats stimulates functional recovery and altered cortical morphology. 2009, Manuscript in submission
   Google Scholar
• Gibb R, Kolb B. Tactile-stimulation that facilitates functional recovery after perinatal cortical injury is mediated by FGF-2. 2009, Manuscript in submission
   Google Scholar
• Liston C, Miller MM, Goldwater DS, Radley JJ, Rocher AB, Hof PR, Morrison JH, McEwen BS. Stress-induced alterations in prefrontal cortical dendritic morphology predict selective impairments in perceptual attentional set-shifting. Journal of Neuroscience 2006; 26: 7870–7874
   PubMed Web of Science ®Google Scholar
• Halliwell C, Tees RC, Kolb B. Neonatal dietary choline supplementation facilitates functional recovery and morphological change after neonatal frontal or parietal lesions in rats. 2009, Manuscript in submission
   Google Scholar
• Diaz Heijtz R, Kolb B, Forssberg H. Can a therapeutic dose of amphetamine during pre-adolescence modify the pattern of synaptic organization in the brain?. European Journal of Neuroscience 2003; 18: 3394–3399
   PubMed Web of Science ®Google Scholar
• Comeau WL, Diaz Heijtz R, Butt A, Hess S, Kolb B. Enduring effects of early methylphenidate use in rats: Anatomical correlates of modified behavior, Manuscript in submission
   Google Scholar
• Kolb B, Gorny G, Li Y, Samaha AN, Robinson TE. Amphetamine or cocaine limits the ability of later experience to promote structural plasticity in the neocortex and nucleus accumbens. Proceedings of the National Academy of Sciences (USA) 2003; 100: 10523–10528
   PubMed Web of Science ®Google Scholar
• Frost DO, Cerceo S, Carroll C, Kolb B. Early exposure to haloperidol or olanzapine induces long-term alterations of dendritic form. 2009, Synapse in press
   Google Scholar
• Kolb B, Gibb R, Pearce S, Tanguay R. Prenatal exposure to prescription medication alters recovery following early brain injury in rats. Society for Neuroscience Abstracts 2008; 34: 349.5
   Google Scholar
• Goldstein JM, Seidman LJ, Horton NJ, Makris N, Kennedy DN, Caviness VS, Jr, Faraone SV, Tsuang MT. Normal sexual dimorphism of the adult human brain assessed by in vivo magnetic resonance imaging. Cerebral Cortex 2001; 11: 490–499
   PubMed Web of Science ®Google Scholar
• Goldman PS. An alternative to development plasticity: Heterology of CNS structures in infants and adults. Plasticity and Recovery of Function in the Central Nervous System, DG Stein, JJ Rosen, N Butters. Academic Press, New York, NYUSA 1974; 14974
   Google Scholar
• Schneider GD. Is it really better to have your brain lesion early? A revision of the ‘Kennard principle’. Neuropsychologia 1979; 17: 557–583
   PubMed Web of Science ®Google Scholar
• Goldman PS, Galkin TW. Prenatal removal of frontal association cortex in the fetal rhesus monkey: Anatomical and functional consequences in postnatal life. Brain Research 1978; 152: 451–485
   PubMed Web of Science ®Google Scholar
• Kolb B. Recovery from early cortical damage in rats. I. Differential behavioral and anatomical effects of frontal lesions at different ages of neural maturation. Behavioural Brain Research 1987; 25: 205–220
   PubMed Web of Science ®Google Scholar
• Kolb B, Petrie B, Cioe J. Recovery from early cortical damage in rats. VII. Comparison of the behavioural and anatomical effects of medial prefrontal lesions at different ages of neural maturation. Behavioural Brain Research 1996; 79: 1–13
   PubMed Web of Science ®Google Scholar
• Schmanke TD, Villablanca JR. A critical maturational period of reduced brain vulnerability to injury. A study of cerebral glucose metabolism in cats. Developmental Brain Research 2001; 26: 127–141
   Google Scholar
• Villablanca JR, Hovda DA, Jackson GF, Infante C. Neurological and behavioral effects of a unilateral frontal cortical lesion in fetal kittens: II. Visual system tests, and proposing a ‘critical period’ for lesion effects. Behavioural Brain Research 1993; 57: 79–92
   PubMed Web of Science ®Google Scholar
• Kolb B. Brain plasticity and behavior. Erlbaum, Mahwah, NJ 1995
   Google Scholar
• Anderson V, Spencer-Smith M, Leventer R, Coleman L, Anderson P, Williams J, Greeham M, Jacobs R. Childhood brain insult: can age at insult help us predict outcome?. Brain 2009; 132: 45–56
   PubMed Web of Science ®Google Scholar
• Kolb B, Whishaw IQ. Neonatal frontal lesions in the rat: Sparing of learned but not species-typical behavior in the presence of reduced brain weight and cortical thickness. Journal of Comparative and Physiological Psychology 1981; 95: 863–879
   PubMed Web of Science ®Google Scholar
• Kolb B, Gibb R, van der Kooy D. Neonatal frontal cortical lesions in rats alter cortical structure and connectivity. Brain Research 1994; 645: 85–97
   PubMed Web of Science ®Google Scholar
• Kolb B, Gibb R, van der Kooy D. Neonatal frontal cortical lesions in rats alter cortical structure and connectivity. Brain Research 1994; 645: 85–97
   PubMed Web of Science ®Google Scholar
• Kolb B, Cioe J, Whishaw IQ. Is there an optimal age for recovery from unilateral motor cortex lesions? Behavioural and anatomical sequelae of unilateral motor cortex lesions in rats on postnatal days 1, 10, and in adulthood. Restorative Neurology and Neuroscience 2000; 17: 61–70
   Web of Science ®Google Scholar
• Sherren N, Akins L, Kolb B. Functional outcome and anatomical correlates of focal unilateral medial frontal cortex lesions at different developmental ages in neonatal rats. Society for Neuroscience Abstracts 2005; 31: 835.11
   Google Scholar
• Frost DO, Boire D, Gingras G, Ptito M. Surgically created neural pathways mediate visual pattern discrimination. Proceedings of the National Academy of Sciences (USA) 2000; 97: 11068–11073
   PubMed Web of Science ®Google Scholar
• Payne BR, Lomber S. Reconstructing functional systems afer lesions of the cerebral cortex. Nature Reviews, Neuroscience 2001; 2: 911–919
   PubMed Web of Science ®Google Scholar
• Castro A. Plasticity in the motor system. Cerebral cortex of the rat, B Kolb, R Tees. MIT Press, Cambridge, MA 1990; 563–588
   Google Scholar
• Whishaw IQ, Kolb B. Sparing of skilled forelimb reaching and corticospinal projections after neonatal motor cortex removal or hemidecortication in the rat: Support for the Kennard Doctrine. Brain Research 1988; 451: 97–114
   PubMed Web of Science ®Google Scholar
• Villablanca JR, Gomez-Pinilla F. Novel crossed corticothalamic projections after neonatal cerebral hemispherectomy. A quantitative autoradiography study in cats. Brain Research 1987; 410: 219–231
   PubMed Web of Science ®Google Scholar
• Comeau W, Hastings E, Kolb B. Differential effect of pre and postnatal FGF-2 following medial prefrontal cortical injury. Behavioural Brain Research 2007; 180: 18–27
   PubMed Web of Science ®Google Scholar
• Monfils M-H, Driscoll I, Kamitakahara H, Wilson B, Flynn C, Teskey GC, Kleim JA, Kolb B. FGF-2-induced cell proliferation stimulates anatomical, neurophysiological, and functional recovery from neonatal motor cortex injury. European Journal of Neuroscience 2006; 24: 739–749
   PubMed Web of Science ®Google Scholar
• Monfils M-H, Kolb B, Faoud K. FGF-2 promotes restoration of functional corticospinal neurons after neonatal motor cortex injury. Experimental Brain Research 2008; 185: 453–460
   PubMed Web of Science ®Google Scholar
• Meck WH, Williams CL. Metabolic imprinting of choline by its availability during gestation: Implications for memory and attentional processing across the lifespan. Neuroscience and Biobehavioral Reviews 2003; 27: 385–399
   PubMed Web of Science ®Google Scholar
• Meck WH, Smith RA, Williams CL. Organizational changes in cholinergic activity and enhanced visuospatial memory as a function of choline administered prenatally or postnatally or both. Behavioral Neuroscience 1988; 103: 1234–1241
   Web of Science ®Google Scholar
• Tees RC, Mohammadi E. The effects of neonatal choline dietary supplementation on adult spatial and configural memory in rats. Developmental Psychobiology 1999; 35: 226–240
   PubMed Web of Science ®Google Scholar
• Sandstrom MJ, Loy R, Williams CL. Prentaal choline supplementation increases NGF levels in hippocampus and frontal cortex of young and adult rats. Brain Research 2002; 947: 9–16
   PubMed Web of Science ®Google Scholar
• Thomas JD, Biane JS, O'Bryan KA, O'Neill TM, Dominguez HD. Choline supplementation following third-trimester-equivalent alcohol exposure attenuates behavioral alterations in rats. Behavioral Neuroscience 2007; 121: 120–130
   PubMed Web of Science ®Google Scholar
• Kolb B, Gorny G, Cote S, Ribeiro-da-Silva A, Cuello AC. Nerve growth factor stimulates growth of cortical pyramidal neurons in young adult rats. Brain Research 1997; 751: 289–294
   PubMed Web of Science ®Google Scholar
• Halliwell C, Kolb B. Vitamin and mineral supplementation facilitates functional recovery and morphological change after neonatal medial frontal lesions in rats. 2009, Manuscript in submission
   Google Scholar
• Diaz Heijtz R, Kolb B, Forssberg H. Can a therapeutic dose of amphetamine during pre-adolescence modify the pattern of synaptic organization in the brain?. European Journal of Neuroscience 2003; 18: 3394–3399
   PubMed Web of Science ®Google Scholar
• Kolb B, Elliott W. Recovery from early cortical damage in rats. II. Effects of experience on anatomy and behavior following frontal lesions at 1 or 5 days of age. Behavioural Brain Research 1987; 26: 47–56
   PubMed Web of Science ®Google Scholar
• Halliwell CI, Checknita D, Kolb B, Gibb R. The effects of vitamin and mineral supplementation on recovery from early cortical injury at postnatal day 10 in prenatally stressed rats. Society for Neuroscience Abstracts 2008; 34: 349.1
   Google Scholar