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Depletion of New Neurons by Image Guided Irradiation

Ionizing radiation continues to be a relevant tool in both imaging and the treatment of cancer. Experimental uses of focal irradiation have recently been expanded to studies of new neurons in the adult brain. Such studies have shown cognitive deficits following radiation treatment and raised caution...

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Autores principales: Tan, Y.-F., Rosenzweig, S., Jaffray, D., Wojtowicz, J. M.
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3083759/
https://www.ncbi.nlm.nih.gov/pubmed/21541259
http://dx.doi.org/10.3389/fnins.2011.00059
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author Tan, Y.-F.
Rosenzweig, S.
Jaffray, D.
Wojtowicz, J. M.
author_facet Tan, Y.-F.
Rosenzweig, S.
Jaffray, D.
Wojtowicz, J. M.
author_sort Tan, Y.-F.
collection PubMed
description Ionizing radiation continues to be a relevant tool in both imaging and the treatment of cancer. Experimental uses of focal irradiation have recently been expanded to studies of new neurons in the adult brain. Such studies have shown cognitive deficits following radiation treatment and raised caution as to possible unintentional effects that may occur in humans. Conflicting outcomes of the effects of irradiation on adult neurogenesis suggest that the effects are either transient or permanent. In this study, we used an irradiation apparatus employed in the treatment of human tumors to assess radiation effects on rat neurogenesis. For subjects we used adult male rats (Sprague-Dawley) under anesthesia. The irradiation beam was directed at the hippocampus, a center for learning and memory, and the site of neurogenic activity in adult brain. The irradiation was applied at a dose-rate 0.6 Gy/min for total single-fraction, doses ranging from 0.5 to 10.0 Gy. The animals were returned to home cages and recovered with no sign of any side effects. The neurogenesis was measured either 1 week or 6 weeks after the irradiation. At 1 week, the number of neuronal progenitors was reduced in a dose-dependent manner with the 50% reduction at 0.78 Gy. The dose–response curve was well fitted by a double exponential suggesting two processes. Examination of the tissue with quantitative immunohistochemistry revealed a dominant low-dose effect on neuronal progenitors resulting in 80% suppression of neurogenesis. This effect was partially reversible, possibly due to compensatory proliferation of the remaining precursors. At higher doses (>5 Gy) there was additional, nearly complete block of neurogenesis without compensatory proliferation. We conclude that notwithstanding the usefulness of irradiation for experimental purposes, the exposure of human subjects to doses often used in radiotherapy treatment could be damaging and cause cognitive impairments.
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spelling pubmed-30837592011-05-03 Depletion of New Neurons by Image Guided Irradiation Tan, Y.-F. Rosenzweig, S. Jaffray, D. Wojtowicz, J. M. Front Neurosci Neuroscience Ionizing radiation continues to be a relevant tool in both imaging and the treatment of cancer. Experimental uses of focal irradiation have recently been expanded to studies of new neurons in the adult brain. Such studies have shown cognitive deficits following radiation treatment and raised caution as to possible unintentional effects that may occur in humans. Conflicting outcomes of the effects of irradiation on adult neurogenesis suggest that the effects are either transient or permanent. In this study, we used an irradiation apparatus employed in the treatment of human tumors to assess radiation effects on rat neurogenesis. For subjects we used adult male rats (Sprague-Dawley) under anesthesia. The irradiation beam was directed at the hippocampus, a center for learning and memory, and the site of neurogenic activity in adult brain. The irradiation was applied at a dose-rate 0.6 Gy/min for total single-fraction, doses ranging from 0.5 to 10.0 Gy. The animals were returned to home cages and recovered with no sign of any side effects. The neurogenesis was measured either 1 week or 6 weeks after the irradiation. At 1 week, the number of neuronal progenitors was reduced in a dose-dependent manner with the 50% reduction at 0.78 Gy. The dose–response curve was well fitted by a double exponential suggesting two processes. Examination of the tissue with quantitative immunohistochemistry revealed a dominant low-dose effect on neuronal progenitors resulting in 80% suppression of neurogenesis. This effect was partially reversible, possibly due to compensatory proliferation of the remaining precursors. At higher doses (>5 Gy) there was additional, nearly complete block of neurogenesis without compensatory proliferation. We conclude that notwithstanding the usefulness of irradiation for experimental purposes, the exposure of human subjects to doses often used in radiotherapy treatment could be damaging and cause cognitive impairments. Frontiers Research Foundation 2011-04-21 /pmc/articles/PMC3083759/ /pubmed/21541259 http://dx.doi.org/10.3389/fnins.2011.00059 Text en Copyright © 2011 Tan, Rosenzweig, Jaffray and Wojtowicz. http://www.frontiersin.org/licenseagreement This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.
spellingShingle Neuroscience
Tan, Y.-F.
Rosenzweig, S.
Jaffray, D.
Wojtowicz, J. M.
Depletion of New Neurons by Image Guided Irradiation
title Depletion of New Neurons by Image Guided Irradiation
title_full Depletion of New Neurons by Image Guided Irradiation
title_fullStr Depletion of New Neurons by Image Guided Irradiation
title_full_unstemmed Depletion of New Neurons by Image Guided Irradiation
title_short Depletion of New Neurons by Image Guided Irradiation
title_sort depletion of new neurons by image guided irradiation
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3083759/
https://www.ncbi.nlm.nih.gov/pubmed/21541259
http://dx.doi.org/10.3389/fnins.2011.00059
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