Summary
After permanent ligation of the middle cerebral artery the motor function of rats housed in an enriched environment, i.e. cages with opportunities for various activities but not forcing the rats to do any particular task, is significantly better than in rats housed in individual cages. Rats kept in an enriched environment before and after MCA ligation improved sooner and slightly more than those placed in the enriched environment after ischemia but with no lasting significant difference except for climbing. Preliminary studies suggest that social stimulation is more important than physical activity. Rats with fetal neocortical grafts implanted into the infarct cavity performed better if exposed to enriched environment than grafted control rats housed in standard laboratory cages with 5 rats in each cage. However, they did not perform better than non-grafted rats housed in the same enriched environment. The infarct size did not differ between rats housed in an enriched environment and control rats. There was no correlation between infarct size and performance in rats exposed to an enriched environment. The improved motor function suggests that a rich environment may stimulate mechanisms that enhance brain plasticity.
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References
Bachy-Rita P (1990) Receptor plasticity and volume transmission in the brain: emerging concepts with reference to neurological rehabilitation. J Neuro Rehab 4: 121–128
Brailowsky S, Knight RT, Blood K, Scabini D (1986) Yaminobutyric acid-induced potentiation of cortical hemiplegia. Brain Res 362: 322–330
Calford MB, Tweedale R (1990) Interhemispheric transfer of plasticity in the cerebral cortex. Science 249: 805–807
Chino YM, Kaas JH, Smith III EL, Langston AL, Cheng H (1992) Rapid reorganization of cortical maps in adult cats following restricted deafferentation in retina. Vision Res 32: 789–796
Chollet F, DiPiero V, Wise RJS, Brook DJ, Dolan RJ, Frackowiak RSJ (1991) The functional anatomy of motor recovery after stroke in humans: a study with positron emission tomography. Ann Neurol 29: 63–71
Cohen LG, Brasil-Neto JP, Pascual-Leone A, Hallett M (1993) Plasticity of cortical motor output organization following deafferentation, cerebral lesions, and skill acquisition. Adv Neurol 63: 187–200
Cornell-Bell AH, Finkbeiner SM, Cooper MS, Smith SJ (1990) Glutamate induces calcium waves in cultured astrocytes: long-range glial signaling. Science 247: 470–473
Coyle P (1982) Middle cerebral artery occlusion in the young rat. Stroke 13: 855–859
De Ryck M, Van Reempts J, Borgers M, Wauquier A, Janssen AJ (1989) Photochemical stroke model: flunarizine prevents sensorimotor deficits after neocortical infarcts in rats. Stroke 20: 1383–1389
Ernst E (1990) A review of stroke rehabilitation and physiotherapy. Stroke 21: 1081–1085
Feeney DM, Gonzalez A, Law WA (1982) Amphetamine, haloperidole and experience interact to affect the rate of recovery after motor cortex injuries. Science 217: 855–857
Feeney DM (1991) Pharmacologic modulation of recovery after brain injury: a reconsideration of diaschisis. J Neurol Rehab 5: 113–128
Fries W, Danek A, Scheidtmann K, Hamburger C (1993) Motor recovery following capsular stroke. Brain 116: 369–382
Gage FH, Olejniczak P, Armstrong DM (1988) Astrocytes are important for sprouting in the septohippocampal circuit. Exp Neurol 102: 2–13
Goldstein LB (1991) Pharmacologic modulation of recovery after stroke: clinical data. J Neurol Rehab 5: 129–140
Goldstein LB, Davis JN (1990) Post-lesion practice and amphetamine-facilitated recovery of beam-walking in the rat. Restor Neurol Neurosci 1: 311–314
Grabowski M, Brundin P, Johansson BB (1993) Paw-reaching, sensorimotor, and rotational behavior after brain infarction in rats. Stroke 24: 889–895
Grabowski M, Brundin P, Johansson BB (1993) Functional integration of cortical grafts placed in brain infarcts of rats. Ann Neurol 34: 362–368
Grabowski M, Sorensen J C, Mattson B, Zimmer J, Johansson BB (1995) Influence of an enriched environment and cortical grafting on functional outcome in brain infarcts of adult rats. Exp Neurol 133: 1–7
Jenkins WM, Merzenich MM (1987) Reorganization of neocortical representations after brain injury: a neurophysiological model of the bases of recovery from stroke. Prog Brain Res 71: 249–266
Jenkins WM, Merzenich MM, Ochs MT, Allard T, GuÃc-Robles E (1990) Functional reorganization of primary somatosensory cortex in adult owl monkeys after behaviorally controlled tactile stimulation. J Neurophysiol 63: 82–104
Jenkins WM, Merzenich MM, Recanzone G (1990) Neocortical representational dynamics in adult primates: implications for neuropsychology. Neuropsychologia 28: 573–584
Johansson BB (1993) Has sensory stimulation a role in stroke rehabilitation ? Scand J Rehab Med 29: 87–96
Johansson BB, Grabowski M (1994) Functional recovery after brain infarction: Plasticity and neural transplantation. Brain Pathol 4: 85–95
Johansson BB (1995) Functional recovery after brain infarction. A review of animal data. Cerebrovasc Dis 5: 278–281
Jones TA, Schallert T (1992) Overgrowth and pruning of dendrites in adult rats recovering from neocortical damage. Brain Res 581: 156–160
Jones TA, Schauert T (1994) Use-dependent growth of pyramidal neurons after neocortical damage. J Neurosci 14: 2140–2152
Kelche C, Dalrymple-Alford JC, Will B (1988) Housing conditions modulate the effects of intracerebral grafts in rats with brain lesions. Behav Brain Res 28: 287–295
Kolb B (1992) Mechanisms underlying recovery from cortical injury: reflections on progress and directions for the future. In: Rose FD, Johnson DA (eds) Recovery from brain damage. Plenum, New York, pp 169–186
Kolb B, Gibb R (1991) Environmental enrichment and cortical injury: behavioral and anatomical consequences of frontal cortex lesions. Cereb Cortex 1: 189–198
Kotila M, Waltimo O, Niemi M-J, Laaksonen R, Lempinen M (1984) The profile of recovery from stroke and factors influencing outcome. Stroke 15: 1039–1044
Marrero H, Astion ML, Coles JA, Orkand RK (1989) Facilitation of voltage-gated ion channels in frog neuroglia by nerve impulses. Nature 339: 378–380
Merzenich MM, Recanzone G, Jenkins WM, Allard TT, Nudo RJ (1988) Cortical representational plasticity. In: Rakic P, Singer W (eds) Neurobiology of neocortex. Wiley, Berlin, pp 42–67
Mohammed AK, Winblad B, Ebendal T, Lärkfors L (1990) Environmental influence on behaviour and nerve growth factor in the brain. Brain Res 528: 62–72
Ohlsson A-L, Johansson BB (1995) The environment influences functional outcome of cerebral infarction in rats. Stroke 26: 644–649
Ottenbacher KJ, Jannell S (1993) The results of clinical trials in stroke rehabilitation research. Arch Neurol 50: 37–44
Pascual-Leone A, Grafman J, Hallett M (1994) Modulation of cortical motor output maps during development of implicit and explicit knowledge. Science 263: 1287–1289
Pascual-Leone A, Torres F (1993) Plasticity of the sensorimotor cortex representation of the readingfiger in Braille readers. Brain 116: 39–52
Pons TP, Garraghty PE, Mishkin M (1988) Lesion-induced plasticity in the second somatosensory cortex of adult macaques. Proc Natl Acad Sci USA 85: 5279–5281
Recanzone GH, Schreiner CE, Merzenich MM (1993) Plasticity in the frequency representation of primary auditory cortex following discrimination training in adult owl monkeys. J Neurosci 13: 87–103
Rose FD (1988) Environmental enrichment and recovery of function following brain damage in the rat. Med Sci Res 16: 257–263
Rose FD, Johnson DA (1992) Recovery from brain damage. Adv Exp Med Biol 325: 187–198
Rosenzweig MR (1984) Experience, memory, and the brain. Am Psychol 39: 365–376
Skilbeck CE, Wade DT, Langton Hewer R, Wood VA (1983) Recovery after stroke. J Neurol Neurosurg Psychiatry 14: 5–8
Schallert T, Hernandez TD, Barth TM (1986) Recovery of function after brain damage: severe and chronic disruption by diazepam. Brain Res 379: 104–111
Schallert T, Jones T, Weaver M, Shapior L, Crippens D, Fulton R (1992) Pharmacologic and anatomic considerations in recovery of function. In: Hanson S, Tucker DM (eds) Neuro-psychological assessment–physical medicine and rehabilitation: state of the art reviews 6: 375–393
Sanes JN, Wang J, Donoghue JP (1992) Immediate and delayed changes of rat motor cortical output representation with new forelimb configurations. Cereb Cortex 2: 141–152
Sirevaag AM, Greenough WT (1991) Plasticity of GFAP-immunoreactive astrocyte size and number in visual cortex of rats reared in complex environments. Brain Res 540: 273–278
Sutton RL, Feeney DM (1992) Noradrenergic agonists and antagonists affect recovery and maintenance of beam-walking ability after senorimotor cortex ablation in the rat. Rest Neurol Neurosci 4: 1–11
Usowicz MM, Gallo V, Cull-Candy SG (1989) Multiple conductance channels in type-2 cerebellar astrocytes activated by excitatory amino acids. Nature 339: 380–383
Wagennar RC, Meijer OG (1991) Effects of stroke rehabilitation (I). A critical review of the literature. J Rehab Sciences 4: 61–73
Walsh R (1981) Sensory environments, brain damage, and drugs: a review of interactions and mediating mechanisms. Int J Neurosci 14: 129–137
Weiller C, Chollet F, Friston KJ, Wise RJS, Frackowiak RSJ (1992) Functional reorganization of the brain in recovery from striatocapsular infarction in man. Ann Neurol 31: 463–472
Will B, Kelche C (1992) Environmental approaches to recovery of function from brain damage: a review of animal studies (1981–1991). Adv Exp Med Biol 325: 79–103
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Johansson, B. (1996). Environmental Influence on Outcome After Experimental Brain Infarction. In: Baethmann, A., Kempski, O.S., Plesnila, N., Staub, F. (eds) Mechanisms of Secondary Brain Damage in Cerebral Ischemia and Trauma. Acta Neurochirurgica, vol 66. Springer, Vienna. https://doi.org/10.1007/978-3-7091-9465-2_11
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DOI: https://doi.org/10.1007/978-3-7091-9465-2_11
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