Brain development, experience, and behavior

Pediatric Blood and Cancer

Volumn 61, Issue 10, 2014, Pages 1720-1723

  Kolb, Bryan ^a   Mychasiuk, Richelle ^a   Gibb, Robbin ^a  

^a UNIVERSITY OF LETHBRIDGE   (Canada)

Author keywords

Brain development; Cerebral plasticity; Environmental stimulation; Epigenetics

Indexed keywords

PRESCRIPTION DRUG; PSYCHOTROPIC AGENT;

BEHAVIOR; BRAIN DEVELOPMENT; CHILD PARENT RELATION; DRUG ABUSE; EXPERIENCE; HUMAN; LOW CALORY DIET; NONHUMAN; PEER GROUP; PRENATAL DRUG EXPOSURE; PRIORITY JOURNAL; PROTEIN DIET; REVIEW; STRESS; VITAMIN SUPPLEMENTATION;

BRAIN DEVELOPMENT; CEREBRAL PLASTICITY; ENVIRONMENTAL STIMULATION; EPIGENETICS;

BRAIN; CHILD; CHILD BEHAVIOR; ENVIRONMENT; HUMANS; NEUROGENESIS; NEURONAL PLASTICITY;

EID: 84908506680     PISSN: 15455009     EISSN: 15455017     Source Type: Journal    
DOI: 10.1002/pbc.24908     Document Type: Review

References (52)

1. Blumberg MS, Freeman JH, Robinson SR. A new frontier for developmental behavioral neuroscience. In: Blumberg MS, Freeman JH, Robinson SR, editors. Oxford handbook of developmental behavioral neuroscience. New York: Oxford University Press; 2010. pp 1-6.
2. Petanjek Z, Judas M, Simic G, et al. Kostovic I extraordinary neoteny of synaptic spines in the human prefrontal cortex. Proc Natl Acad Sci USA 2011; 108:13281-13286.
3. Paus T, Keshavan M, Giedd JN. Why do many psychiatric disorders emerge during adolescence? Nat Rev Neurosci 2008; 9:947-957.
4. Sirevaag AM, Greenough WT. A multivariate statistical summary of synaptic plasticity measures in rats exposed to complex, social and individual environments. Brain Res 1987; 441:386-392.
5. Kolb B, Whishaw IQ. Brain plasticity and behavior. Ann Rev Psychol 1998; 49:43-64.
6. Mychasiuk R, Zahir S, Schmold N, et al. Parental enrichment and offspring development: Modifications to brain, behavior and the epigenome. Behav Brain Res 2012; 228:294-298.
7. Kolb B, Gibb R. Tactile stimulation facilitates functional recovery and dendritic change after neonatal medial frontal or posterior parietal lesions in rats. Behav Brain Res 2010; 214:115-120.
8. Richards S, Mychasiuk R, Kolb B, et al. Tactile stimulation during development alters behavior and neuronanatomical organization in normal rats. Behav Brain Res 2012; 231:86-91.
9. Anda RF, Felitti VJ, Bremner JD, et al. The enduring effects of abuse and related adverse experiences in childhood. A convergence of evidence from neurobiology and epidemiology. Eur Arch Psychiat Clin Neurosc 2006; 256:174-186.
10. Van den Bergh BR, Marcoen A. High antenatal maternal anxiety is related to ADHD symptoms, externalizing problems, and anxiety in 8- and 9-year-olds. Child Dev 2004; 75:1085-1097.
11. Weinstock M. The long-term behavioural consequences of prenatal stress. Neurosc Biobehav Rev 2008; 32:1073-1086.
12. Muhammad A, Kolb B. Mild prenatal stress modulates behaviour and neuronal spine density without affecting amphetamine sensitization. Dev Neurosci 2011; 33:85-98.
13. Murmu M, Salomon S, Biala Y, et al. Changes in spine density and dendritic complexity in the prefrontal cortex in offspring of mothers exposed to stress during pregnancy. Eur J Neurosc 2006; 24:1477-1487.
14. Bock J, Gruss M, Becker S, et al. Experience-indcued changes of dendritic spine densities in the prefronal and sensory cortex: Correlation with developmental time windows. Cereb Cortex 2005; 15:802-808.
15. Martinez-Tellez RI, Hernandez-Torres E, Gamboa C, et al. Prenatal stress alters sppine density and dendrtiic length of nucleus accumbens and hippocampus neurons in rat offspring. Synapse 2009; 63:794-804.
16. Mychasiuk R, Ilnytskyy S, Kovalchuk O, et al. Intensity matters: Brain, behaviour and the epigenome of prenatally stressed rats. Neurosci 2011; 180:105-110.
17. Robinson TE, Kolb B. Structural plasticity associated with drugs of abuse. Neuropharm 2004; 47:33-46.
18. Frost DO, Cerceo S, Carroll C, et al. Early exposure to haloperidol or olanzapine induces long-term alterations of dendritic form. Synapse 2009; 64:191-199.
19. Muhammad A, Mychasiuk R, Nakahashi A, et al. Prenatal nicotine alters neuroanatomical organization of the developing brain. Synapse 2012; 66:950-954.
20. Lawrence RC, Otero NKH, Kelly SJ. 2011; Selective effects of perinatal ethanol exposure in medial prefrontal cortex and nucleus accumbens. Neurotoxicol Teratol 34:128-135.
21. Hofer MA, Sullivan RM. Toward a neurobiology of attachment. In: Nelson CA, Luciana M, editors. Handbook of developmental cognitive neuroscience. Cambridge, MA: MIT Press; 2008. pp 787-806.
22. Myers MM, Brunelli SA, Squire JM, et al. Maternal behavior of SHR rats in its relationship to offspring blood pressure. Dev Psychobiol 1989; 22:29-53.
23. Weaver ICG, Cervoni N, Champagne FA, et al. Epigenetic programming by maternal behavior. Nat Neurosci 2004; 7:847-854.
24. Weaver ICG, Meaney M, Szyf M. Maternal care effects on the maternal transcriptome and anxiety-mediated behaviors in the offspring that are reversible in adulthood. Proc Natl Acad Sci USA 2006; 103:3480-3486.
25. Fenoglio KA, Brunson KL, Baram TZ. Hippocampal neuroplasticity induced by early-life stress: Functional and molecular aspects. Front Neuroendocrin 2006; 27:180-192.
26. Helmeke C, Seidel K, Poegfel G, et al. Paternal deprivation during infancy results in dendrite- and time-specific changes of dendritic development and spine formation in the orbitofrontal cortex of the biparental rodent Octodon degus. Neurosci 2009; 163:790-798.
27. Seidel K, Poeggel G, Holetschka R, et al. Paternal deprivation affects the development of corticotrophin-releasing factor-expressing neurons in prefrontal cortex, amygdala and hippocampus of the biparental Ocodon degus. J Neuroendocrinol 2011; 23:1166-1176.
28. Helmeke C, Otscharoff W, Poeggel G, et al. Juvenile emotional experience alters synaptic inputs on pyramidal neurons in the anterior cingulate cortex. Cereb Cortex 2001; 11:717-727.
29. Muhammad A, Kolb B. Maternal separation altered behavior and neuronal spine density without influencing amphetamine sensitization. Behav Brain Res 2011; 223:7-16.
30. Harlow HF, Harlow MK. The affectional systems. In: Schier A, Harlow HF, Stollnitz F, editors. Behaviour of nonhuman primates, Vol. 2. New York: Academic Press; 1965.
31. Pellis S, Pellis V. The playful brain. New York: Oneworld Publications; 2010. 542 p.
32. Pellis SM, Hastings E, Takeshi T, et al. The effects of orbital frontal cortex damage on the modulation of defensive responses by rats in playful and non-playful social contexts. Behav Neurosc 2006; 120:72-84.
33. Bell HC, Pellis SM, Kolb B. Juvenile peer play experience and the development of the orbitofrontal and medial prefrontal cortex. Behav Brain Res 2010; 207:7-13.
34. Björkholm B, Bok CM, Lundin A, et al. Intestinal microbiota regulate xenobiotic metabolism in the liver. PLoS ONE 2009; 4:e6958.
35. Finegold SM, Molitoris D, Song Y, et al. Gastrointestinal microflora studies in late-onset autism. Clin Infect Dis 2002; 35:S6-S16.
36. Mittal VA, Ellman LM, Cannon TD. Gene-environment interaction and covariation in schizophrenia: The role of obstetric complications. Schiz Bull 2008; 34:1083-1094.
37. Heijtz R, Wang S, Anuar F, et al. Normal gut microbiota modulates brain development and behavior. Proc Natl Acad Sc USA 2011; 108:3047-3052.
38. Christie LA, Acharya MM, Limoli CL. Quantifying cognitive decrements caused by cranial radiotherapy. J Vis Exp 2011; 56:3108.
39. Small BJ, Rawson KS, Walsh E, et al., Catechol-O-methyltransferase genotype modulates cancer treatment-related cognitive deficits in breast cancer survivors. Cancer 2011; 117:1369-1376.
40. Ilnytskyy Y, Koturbash I, Kovalchuk O. Radiation-induced bystander effects in vivo are epigenetically regulated in a tissue-specific manner. Environ Mol Mutagen 2009; 50:105-113.
41. Mancuso M, Pasquali E, Leonardi S, et al. Oncogenic bystander radiation effects in Patched heterozygous mouse cerebellum. Proc Natl Acad Sci USA 2008; 105:12445-12450.
42. Mancuso M, Pasquali E, Leonardi S, et al. Role of connexin43 and ATP in long-range bystander radiation damage and oncogenesis in vivo. Oncogene 2011; 30:4601-4608.
43. Parihar VK, Limoli CL. Cranial radiation compromises neuronal architecture in the hippocampus. Proc Natl Acad Sci USA 2013; 110:12822-12827.
44. Robinson KE, Kivesay KL, Campbell LK. Working memory in suvivors of childhood acute lymphocytic leukemia: Functional neuroimaging analyses. Pediatr Blood Cancer 2010; 54:585-590.
45. Campbell LK, Scaduto M, Van Slyke D. Executive function, coping and behavior of survivors of childhood acute lymphocytic leukemia. J Pediatr Psychol 2009; 34:317-327.
46. Lewis PD. Nutrition and anatomical development of the brain. In: van Gelder NM, Butterworth RF, Drujan BD, editors. (Mal)Nutrition and the infant brain. New York: Wiley-Liss; 1990. pp 89-109.
47. Meck WH, Williams CL. Metabolic imprinting of choline by its availability during gestation: Implications for memory and attentional processing across the lifespan. Neurosc Biobehav Rev 2003; 27:385-399.
48. Tees RC, Mohammadi E. The effects of neonatal choline dietary supplementation on adult spatial and configural learning and memory in rats. Dev Psychobiol 1999; 35:226-240.
49. Sandstrom NJ, Loy R, Williams CL. Prenatal choline supplementation increase NGF levels in the hippocampus and frontal cortex of young and adult rats. Brain Res 2002; 947:9-16.
50. Leung BM, Wiens KP, Kaplan BJ. Does prenatal micronutrient supplementation improve children's mental development? A systematic review. BCM Pregnancy Childbirth 2011; 11:1-12.
51. Mehl-Madrona L, Leung B, Kennedy C, et al. Micronutrients versus standard medication management in autism: A naturalistic case-control study. J Child Adolesc Psychopharm 2010; 20:95-103.
52. Kolb B, Mychasiuk R, Muhammad A, et al. 2012; Experience and the developing prefrontal cortex. Proc Nat Acad Sc USA 2012:17186-17193.