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Autoradiographic and histological evidence of postnatal hippocampal neurogenesis in rats
Abstract
In the autoradiograms of young rats injected with thymidine‐H 3 many of the granule cells of the dentate gyrus were found labeled. The number of labeled cells declined rapidly with increased age at the time of injection. Histological studies showed the presence in young rats of a large germinal matrix of mitotic cells in the ependymal and subependymal layers of the third and lateral ventricles. The areal extent and cell population of this germinal pool declined rapidly from birth on, with a transient rise with a peak at about 15 days. During this latter period the number of “undifferentiated” cells near the granular layer of the dentate gyrus showed a rapid rise with a subsequent decline. The decline in the number of “undifferentiated” cells was accompanied by a rise in the number of differentiated granule cells. Cell counts in homologous parts of the dentate gyrus indicated a six‐fold increase in the number of differentiated granule cells from birth to three months. We postulated that undifferentiated cells migrate postnatally from the forebrain ventricles to the hippocampus where they become differentiated. The possible functional significance of delayed hippocampal neurogenesis is discussed with reference to our finding of incorporation of testosterone‐H 3 by cells of the hippocampus, implicating that they may function as receptors of gonadal hormones.
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“The dentate gyrus of the hippocampus is the brain region where the most active neurogenesis has been documented to take place23–25.”
From Therapeutically viable generation of neurons with antisense oligonucleotide suppression of PTB (2021) · cites this paper as [23]
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“since adult neurogenesis within the DG is well-established in rodents (Altman & Das 1965).”
From Perineuronal net deglycosylation associates with tauopathy‐induced gliosis and neurodegeneration (2024) · cites this paper as Altman & Das 1965
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Metadata
- Authors
- Altman, J., & Das, G. D.
- Affiliations
- Massachusetts Institute of Technology (US)
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1965-06
- Volume
- 124
- Issue
- 3
- Pages
- 319-335
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W1980499453
- Cited by
- 3,592
- References
- 18
- Citations by year
- 2026: 55 · 2025: 79 · 2024: 66 · 2023: 92 · 2022: 112 · 2021: 131 · 2020: 130 · 2019: 136 · 2018: 116 · 2017: 128 · 2016: 132 · 2015: 143 · 2014: 142 · 2013: 145 · 2012: 160
- FWCI
- 6.21
- 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 › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- dentate gyrus granule cells, germinal matrix, ependymal layer, undifferentiated cells, cell migration, rat brain development
- MeSH terms
- Animals, Animals, Newborn, Autoradiography, Cell Differentiation, Hippocampus, Testosterone, Thymidine, Tritium, Rats, In Vitro Techniques
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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