Response of the three main types of glial cells of cortex nad corpus callosum in rats handled during suckling or exposed to enriched, control and impoverished environments following weaning
Abstract
The cell populations of the occipital cortex were examined in young rats subjected to different sensory experiences. In one series recently weaned animals were reared in enriched, impoverished or control environments. The enriched environment was obtained by keeping the animals among “toys” and other rats; the impoverished environment, by rearing the animals one pr cage in a darkened, quiet room; and the control environment, by housing the animals three per cage under animal room conditions. Six recently weaned rats were kept ini each environment for 30 days and ten, for 80 days. In a second series suckling rats for 15 minutes per day during the first ten days after birth; twelve rats were studied, six handled and six unhandled controls. In the two series, the animals were sacrificed under anesthesia by perfusion with mixed aldehydes. Semithin epon sections of occipital cortex ere stained with toluidine blue; neurons and the three main types of glia were enumerated. In addition, the thickness of the cortex was measured and the glial cells of corpus callosum counted in the animals exposed to the three environments for 80 days. Under the influence of the enriched environment, the occipital cortex enlarged, the number of oligodendrocytes increased over the controls by 27‐33% in the 30‐ and 80‐day groups and the number of astrocytes, by 13% in the 80‐day grup. Within the cortex, only certain layers showed the increase in glial numbers. In the corpus callosum, however, the numbers of glial cells did not differ from those in controls. In the animals exposed to the impoverished environment, neither the size of the cortex nor the number of oligodendrocytes and astrocytes differed from controls. The animals subjected to handling also showed evidence of cortical enlargement, but the only significant change in glial cells was a 12% increase in astrocytes. It is concluded that handling and enrichment produce changes in anatomical indices of neural function including depth of cortex and numbers of glial cells. The glial response was specific to the type of manipulation since astrocytes were predominantly affected by handling and oligodendrocytes, by enrichment. The effect of handling on astrocytes may be attributed to the stimulation being applied at a time of astrocyte proliferation, whereas the effect of the enriched environment on oligodendrocytes occurred at a time of active production of these cells. The differences in cell numbers were explained by changes in the rate of cell population growth; since the impoverished did not differ from the control animals, the changes probably consisted of growth acceleration in the enriched animals rather than dimiution in the impoverished ones.
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The glia-neuron ratio increases with greater environmental enrichment and stimulation in rodents.
“Several experimental studies in rodents, furthermore, have demonstrated that the glia–neuron ratio increases with greater environmental enrichment and stimulation (15, 16).”
From Evolution of increased glia–neuron ratios in the human frontal cortex (2006) · cites this paper as [16]
Cites
The effects of an enriched environment on the histology of the rat cerebral cortex
Diamond, M. C., Krech, D., & Rosenzweig, M. R. (1964) · Journal of Comparative Neurology · doi:10.1002/cne.901230110 · Cited by 584 · see citing works
Pattern of dendritic branching in occipital cortex of rats reared in complex environments
Greenough, W. T., & Volkmar, F. R. (1973) · Experimental Neurology · doi:10.1016/0014-4886(73)90090-3 · Cited by 536 · see citing works
Mori, S., & Leblond, C. P. (1970) · The Journal of Comparative Neurology · doi:10.1002/cne.901390102 · Cited by 466 · see citing works
Self-citationIncreases in cortical depth and glia numbers in rats subjected to enriched environment
Diamond, M. C., Law, F., Rhodes, H., Lindner, B., Rosenzweig, M. R., Krech, D., & Bennett, E. L. (1966) · Journal of Comparative Neurology · doi:10.1002/cne.901280110 · Cited by 419 · see citing works
Ling, E., Paterson, J. A., Privat, A., Mori, S., & Leblond, C. P. (1973) · The Journal of Comparative Neurology · doi:10.1002/cne.901490104 · Cited by 402 · see citing works
Self-citationPostnatal development of the cerebral cortex in the rat.
Eayrs, J. T., & Goodhead, B. (1959) · Europe PMC (PubMed Central) · Cited by 375 · see citing works
Identification of microglia in light and electron microscopy
Mori, S., & Leblond, C. P. (1969) · Journal of Comparative Neurology · doi:10.1002/cne.901350104 · Cited by 330 · see citing works
Self-citationAn electron microscopic analysis of gliogenesis in rat optic nerves
Vaughn, J. E. (1969) · Cell and Tissue Research · doi:10.1007/bf00319179 · Cited by 321 · see citing works
Hormonal Influences on Brain Organization in Infant Rats
Levine, S., & Mullins, R. F. (1966) · Science · doi:10.1126/science.152.3729.1585 · Cited by 279 · see citing works
Paterson, J. A., Privat, A., Ling, E., & Leblond, C. P. (1973) · The Journal of Comparative Neurology · doi:10.1002/cne.901490106 · Cited by 276 · see citing works
Self-citationDiamond, M. C., Lindner, B., & Raymond, A. (1967) · Journal of Comparative Neurology · doi:10.1002/cne.901310305 · Cited by 260 · see citing works
Ling, E., & Leblond, C. P. (1973) · The Journal of Comparative Neurology · doi:10.1002/cne.901490105 · Cited by 223 · see citing works
Self-citationAltman, J., & Das, G. D. (1964) · Nature · doi:10.1038/2041161a0 · Cited by 223 · see citing works
Effects of environmental enrichment and impoverishment on rat cerebral cortex
Diamond, M. C., Rosenzweig, M. R., Bennett, E. L., Lindner, B., & Lyon, L. (1972) · Journal of Neurobiology · doi:10.1002/neu.480030105 · Cited by 211 · see citing works
Electron microscopic features and proliferation of astrocytes in the corpus callosum of the rat
Mori, S., & Leblond, C. P. (1969) · The Journal of Comparative Neurology · doi:10.1002/cne.901370206 · Cited by 206 · see citing works
Self-citationQuantitative Synaptic Changes With Differential Experience In Rat Brain
Møllgaard, K., Diamond, M. C., Bennett, E. L., Rosenzweig, M. R., & Lindner, B. (1971) · International Journal of Neuroscience · doi:10.3109/00207457109148764 · Cited by 192 · see citing works
Early Experience Effects upon Cortical Dendrites: A Proposed Model for Development
Schapiro, S., & Vukovich, K. R. (1970) · Science · doi:10.1126/science.167.3916.292 · Cited by 180 · see citing works
Molecular Approaches to Learning and Memory
Deutsch, J. A., & Byrne, W. L. (1971) · The American Journal of Psychology · doi:10.2307/1421369 · Cited by 134 · see citing works
The fine structure of pulse labeled (3H‐thymidine cells) in degenerating rat optic nerve
Skoff, R. P. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901610408 · Cited by 129 · see citing works
Chemical and Anatomical Plasticity of Brain: Replications and Extensions, 1970
Rosenzweig, M. R., Bennett, E. L., & Diamond, M. C. (1972) · Springer eBooks · doi:10.1007/978-1-4684-6042-1_12 · Cited by 128 · see citing works
Effects of infantile handling on morphological development of the rat brain: An exploratory study
Altman, J., Das, G. D., & Anderson, W. J. (1968) · Developmental Psychobiology · doi:10.1002/dev.420010104 · Cited by 113 · see citing works
Increased Adrenocortical Activity in the Neonatal Rat Following Handling
Denenberg, V. H., Brumaghim, J. T., Haltmeyer, G. C., & ZARROW, M. X. (1967) · Endocrinology · doi:10.1210/endo-81-5-1047 · Cited by 112 · see citing works
Contribution to steady potential shifts of slow depolarization in cells presumed to be glia
Castellucci, V. F., & Goldring, S. (1970) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(70)90178-1 · Cited by 101 · see citing works
"Infantile stimulation" in rodents: A consideration of possible mechanisms.
Russell, P. A. (1971) · Psychological Bulletin · doi:10.1037/h0030426 · Cited by 97 · see citing works
Glial metabolism: alteration by potassium levels comparable to those during neural activity
Orkand, P. M., Bracho, H., & Orkand, R. K. (1973) · Brain Research · doi:10.1016/0006-8993(73)90315-6 · Cited by 73 · see citing works
Watson, W. E. (1974) · Physiological Reviews · doi:10.1152/physrev.1974.54.2.245 · Cited by 70 · see citing works
Rr, S. (1974) · PubMed · Cited by 67 · see citing works
Slow hyperpolarization in cells presumed to be glia in cerebral cortex of cat.
Ransom, B. R., & Goldring, S. (1973) · Journal of Neurophysiology · doi:10.1152/jn.1973.36.5.879 · Cited by 67 · see citing works
Interactive Effects of Age and Duration of Infantile Experience on Adult Learning
Denenberg, V. H., & Karas, G. G. (1960) · Psychological Reports · doi:10.2466/pr0.1960.7.2.313 · Cited by 61 · see citing works
The effects of differential infantile stimulation of emotionality at weaning.
Levine, S. (1959) · Canadian Journal of Psychology/Revue Canadienne de Psychologie · doi:10.1037/h0083784 · Cited by 43 · see citing works
Early experience and behavior : the psychobiology of development
Newton, G., & Levine, S. (1968) · C.C. Thomas eBooks · Cited by 42 · see citing works
Rr, S. (1975) · PubMed · Cited by 37 · see citing works
Infant Handling: Effects on Avoidance Learning, Brain Weight, and Cholinesterase Activity
Tapp, J. T., & Markowitz, H. (1963) · Science · doi:10.1126/science.140.3566.486 · Cited by 25 · see citing works
Paterson, J. A. (1977) · eScholarship@McGill (McGill) · doi:10.82308/1682 · Cited by 2 · see citing works
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Cited by
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Neural consequences of enviromental enrichment
van Praag, H., Kempermann, G., & Gage, F. H. (2000) · Nature Reviews Neuroscience · doi:10.1038/35044558 · Cited by 2,468 · see citing works
Glial reduction in the subgenual prefrontal cortex in mood disorders
Öngür, D., Drevets, W. C., & Price, J. L. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.22.13290 · Cited by 1,525 · see citing works
White matter in learning, cognition, and psychiatric disorders
Fields, R. D. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2008.04.001 · Cited by 1,337 · see citing works
Experience-driven brain plasticity: Beyond the synapse
MARKHAM, J. A., & GREENOUGH, W. T. (2004) · Neuron Glia Biology · doi:10.1017/s1740925x05000219 · Cited by 437 · see citing works
Evolution of increased glia–neuron ratios in the human frontal cortex
Sherwood, C. C., Stimpson, C. D., Raghanti, M. A., Wildman, D. E., Uddin, M., Grossman, L. I., Goodman, M., Redmond, J. C., Bonar, C. J., Erwin, J. M., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0605843103 · Cited by 342 · see citing works
Linking oligodendrocyte and myelin dysfunction to neurocircuitry abnormalities in schizophrenia
Takahashi, N., Sakurai, T., Davis, K. L., & Buxbaum, J. D. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2010.09.004 · Cited by 337 · see citing works
Quantitative Architecture Distinguishes Prefrontal Cortical Systems in the Rhesus Monkey
Dombrowski, S. M. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.10.975 · Cited by 240 · see citing works
Pham, T. M., Söderström, S., Winblad, B., & Mohammed, A. H. (1999) · Behavioural Brain Research · doi:10.1016/s0166-4328(99)00019-4 · Cited by 162 · see citing works
Glia:Neuron index: Review and hypothesis to account for different values in various mammals.
Reichenbach, A. (1989) · Glia · doi:10.1002/glia.440020202 · Cited by 97 · see citing works
Sciolino, N. R., Bortolato, M., Eisenstein, S. A., Fu, J., Oveisi, F., Hohmann, A. G., & Piomelli, D. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.04.007 · Cited by 89 · see citing works
Vibrissa-signaled eyeblink conditioning induces somatosensory cortical plasticity
Galvez, R., Weiss, C., Weible, A. P., & Disterhoft, J. F. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.5582-05.2006 · Cited by 66 · see citing works
Markham, J. A., Herting, M. M., Luszpak, A. E., Juraska, J. M., & Greenough, W. T. (2009) · Brain Research · doi:10.1016/j.brainres.2009.06.087 · Cited by 58 · see citing works
Major, D. E., Kesslak, J. P., Cotman, C. W., Finch, C. E., & Day, J. R. (1997) · Neurobiology of Aging · doi:10.1016/s0197-4580(97)00102-4 · Cited by 52 · see citing works
Enriched environment increases the myelinated nerve fibers of aged rat corpus callosum
Zhao, Y., Shi, X., Qiu, X., Lu, W., Yang, S., Li, C., Chen, L., Zhang, L., Cheng, G., & Tang, Y. (2012) · The Anatomical Record · doi:10.1002/ar.22446 · Cited by 41 · see citing works
- Authors
- Szeligo, F., & Leblond, C. P.
- Affiliations
- McGill University (CA)
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1977-03-15
- Volume
- 172
- Issue
- 2
- Pages
- 247-263
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2052460692
- Cited by
- 129
- References
- 35
- Citations by year
- 2024: 1 · 2023: 1 · 2022: 2 · 2020: 3 · 2019: 2 · 2018: 1 · 2017: 7 · 2016: 4 · 2015: 4 · 2014: 4 · 2013: 5 · 2012: 6
- FWCI
- 2.07
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Comparative Neurology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- glial cells, oligodendrocytes, astrocytes, corpus callosum, occipital cortex, environmental enrichment, impoverished environment, sensory deprivation, suckling rats, weaning, cortical thickness, glial cell proliferation, astrocyte proliferation, astrocyte differentiation, rat brain development
- MeSH terms
- Animals, Animals, Newborn, Cell Count, Cerebral Cortex, Corpus Callosum, Handling, Psychological, Neuroglia, Neurons, Occipital Lobe, Social Environment, Social Isolation, Sucking Behavior, Rats
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