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Journal articles on the topic 'Postnatal neurogenesis'

Author: Grafiati

Published: 4 June 2021

Last updated: 11 March 2023

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1

Walton, R. M. "Postnatal Neurogenesis." Veterinary Pathology 49, no. 1 (2011): 155–65. http://dx.doi.org/10.1177/0300985811414035.

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Bond, Allison M., Daniel A. Berg, Stephanie Lee, et al. "Differential Timing and Coordination of Neurogenesis and Astrogenesis in Developing Mouse Hippocampal Subregions." Brain Sciences 10, no. 12 (2020): 909. http://dx.doi.org/10.3390/brainsci10120909.

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Neocortical development has been extensively studied and therefore is the basis of our understanding of mammalian brain development. One fundamental principle of neocortical development is that neurogenesis and gliogenesis are temporally segregated processes. However, it is unclear how neurogenesis and gliogenesis are coordinated in non-neocortical regions of the cerebral cortex, such as the hippocampus, also known as the archicortex. Here, we show that the timing of neurogenesis and astrogenesis in the Cornu Ammonis (CA) 1 and CA3 regions of mouse hippocampus mirrors that of the neocortex; ne

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3

Swayne, Leigh Anne, and Leigh Wicki-Stordeur. "Ion channels in postnatal neurogenesis." Channels 6, no. 2 (2012): 69–74. http://dx.doi.org/10.4161/chan.19721.

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4

Bartkowska, Katarzyna, Beata Tepper, Krzysztof Turlejski, and Ruzanna Djavadian. "Postnatal and Adult Neurogenesis in Mammals, Including Marsupials." Cells 11, no. 17 (2022): 2735. http://dx.doi.org/10.3390/cells11172735.

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In mammals, neurogenesis occurs during both embryonic and postnatal development. In eutherians, most brain structures develop embryonically; conversely, in marsupials, a number of brain structures develop after birth. The exception is the generation of granule cells in the dentate gyrus, olfactory bulb, and cerebellum of eutherian species. The formation of these structures starts during embryogenesis and continues postnatally. In both eutherians and marsupials, neurogenesis continues in the subventricular zone of the lateral ventricle (SVZ) and the dentate gyrus of the hippocampal formation th

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5

Mustafin, Rustam N., and Elza K. Khusnutdinova. "Postnatal neurogenesis in the human brain." Morphology 159, no. 2 (2022): 37–46. http://dx.doi.org/10.17816/1026-3543-2021-159-2-37-46.

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Recently, a lot of data has been gathered which demonstrates neurogenesis in the brain of adult humans. In genetics, findings have been obtained that not only prove, but also elucidate the molecular mechanisms of neurogenesis. In some publications, however, morphology disputes neuronal renewal in adulthood. Therefore, this review presents the modern achievements of epigenetics, morphology, and physiology, which confirm and characterize postnatal neurogenesis in detail. We suggest that the introduction of molecular genetic technologies into morphological studies will be the starting point for t

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6

Asrican, Brent, Patricia Paez-Gonzalez, Joshua Erb, and Chay T. Kuo. "Cholinergic circuit control of postnatal neurogenesis." Neurogenesis 3, no. 1 (2016): e1127310. http://dx.doi.org/10.1080/23262133.2015.1127310.

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7

Seress, László. "Postnatal neurogenesis in the rat hypothalamus." Developmental Brain Research 22, no. 1 (1985): 156–60. http://dx.doi.org/10.1016/0165-3806(85)90080-x.

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8

Vaz, Andreia, Inês Ribeiro, and Luísa Pinto. "Frontiers in Neurogenesis." Cells 11, no. 22 (2022): 3567. http://dx.doi.org/10.3390/cells11223567.

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One of the most intriguing dogmas in neurosciences—the empirical lack of brain neuronal regeneration in adulthood onwards to late life—began to be debunked initially by research groups focused on understanding postnatal (early days/weeks of murine and guinea pigs) neurodevelopmental and neuroplastic events [...]

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9

Semenov, Mikhail. "Proliferative Capacity of Adult Mouse Brain." International Journal of Molecular Sciences 22, no. 7 (2021): 3449. http://dx.doi.org/10.3390/ijms22073449.

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We studied cell proliferation in the postnatal mouse brain between the ages of 2 and 30 months and identified four compartments with different densities of proliferating cells. The first identified compartment corresponds to the postnatal pallial neurogenic (PPN) zone in the telencephalon; the second to the subpallial postnatal neurogenic (SPPN) zone in the telencephalon; the third to the white matter bundles in the telencephalon; and the fourth to all brain parts outside of the other three compartments. We estimated that about 3.4 million new cells, including 0.8 million in the subgranular zo

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Morgun, A. V., E. D. Osipova, E. B. Boytsova та ін. "Astroglia-mediated regulation of cell development in the model of neurogenic niche in vitro treated with Aβ1-42". Biomeditsinskaya Khimiya 65, № 5 (2019): 366–73. http://dx.doi.org/10.18097/pbmc20196505366.

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Neurogenesis is a complex process which governs embryonic brain development and is importants for brain plasticity throughout the whole life. Postnatal neurogenesis occurs in neurogenic niches that regulate the processes of proliferation and differentiation of stem and progenitor cells under the action of stimuli that trigger the mechanisms of neuroplasticity. Cells of glial and endothelial origin are the key regulators of neurogenesis. It is known that physiological neurogeneses is crucial for memory formation, whereas reparative neurogenesis provides partial repair of altered brain structure

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11

González-Martínez, Jorge A., William E. Bingaman, Steven A. Toms, and Imad M. Najm. "Neurogenesis in the postnatal human epileptic brain." Journal of Neurosurgery 107, no. 3 (2007): 628–35. http://dx.doi.org/10.3171/jns-07/09/0628.

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Object The normal adult human telencephalon does not reveal evidence of spontaneous neuronal migration and differentiation despite the robust germinal capacity of the subventricular zone (SVZ) astrocyte ribbon that contains neural stem cells. This might be because it is averse to accepting new neurons into an established neuronal network, probably representing an evolutionary acquisition to prevent the formation of anomalous neuronal circuits. Some forms of epilepsy, such as malformations of cortical development, are thought to be due to abnormal corticogenesis during the embryonic and early p

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12

Goranova, Vanya. "Application of BrdU in studying postnatal neurogenesis." Scripta Scientifica Medica 45, no. 1 (2013): 24. http://dx.doi.org/10.14748/ssm.v45i1.333.

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13

Papile, L. A. "Sedative and Anticonvulsant Drugs Suppress Postnatal Neurogenesis." Yearbook of Neonatal and Perinatal Medicine 2009 (January 2009): 114–15. http://dx.doi.org/10.1016/s8756-5005(09)79008-0.

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14

Andreotti, Julia P., Pedro H. D. M. Prazeres, Luiz A. V. Magno, Marco A. Romano‐Silva, Akiva Mintz, and Alexander Birbrair. "Neurogenesis in the postnatal cerebellum after injury." International Journal of Developmental Neuroscience 67, no. 1 (2018): 33–36. http://dx.doi.org/10.1016/j.ijdevneu.2018.03.002.

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15

Namaka, Michael P., Mike Sawchuk, Stephen C. MacDonald, Larry M. Jordan, and Shawn Hochman. "Neurogenesis in Postnatal Mouse Dorsal Root Ganglia." Experimental Neurology 172, no. 1 (2001): 60–69. http://dx.doi.org/10.1006/exnr.2001.7761.

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16

Stefovska, Vanya G., Ortrud Uckermann, Miroslaw Czuczwar, et al. "Sedative and anticonvulsant drugs suppress postnatal neurogenesis." Annals of Neurology 64, no. 4 (2008): 434–45. http://dx.doi.org/10.1002/ana.21463.

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17

Elliott, Terry. "D'Arcy Wentworth Thompson, interindividual variation, and postnatal neuronal growth." Behavioral and Brain Sciences 24, no. 2 (2001): 284. http://dx.doi.org/10.1017/s0140525x01283952.

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It is suggested that a connection between neurogenesis and brain part size is unsurprising. It is argued that neurogenesis cannot, however, be the only factor contributing to brain size. Highly individual post-natal experience radically shapes individual brains, leading to dramatic increases in brain size. The role of comparatively coarse statistical techniques in addressing these subtle biological issues is questioned.

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Hovorka, Michelle, David Ewing, and David S. Middlemas. "Chronic SSRI Treatment, but Not Norepinephrine Reuptake Inhibitor Treatment, Increases Neurogenesis in Juvenile Rats." International Journal of Molecular Sciences 23, no. 13 (2022): 6919. http://dx.doi.org/10.3390/ijms23136919.

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There has been growing recognition that major depressive disorder is a serious medical disorder that also affects children. This has been accompanied by an increased use of antidepressant drugs in adolescents; however, not all classes of antidepressants are effective in children and adolescents. There is an increasing need to understand the differences in antidepressant action in different developmental stages. There are some data indicating that the behavioral effect of chronic antidepressant treatment in adult rodents is dependent on hippocampal neurogenesis; however, it is not known which c

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19

LaDage, Lara D. "Broadening the functional and evolutionary understanding of postnatal neurogenesis using reptilian models." Journal of Experimental Biology 223, no. 15 (2020): jeb210542. http://dx.doi.org/10.1242/jeb.210542.

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ABSTRACTThe production of new neurons in the brains of adult animals was first identified by Altman and Das in 1965, but it was not until the late 20th century when methods for visualizing new neuron production improved that there was a dramatic increase in research on neurogenesis in the adult brain. We now know that adult neurogenesis is a ubiquitous process that occurs across a wide range of taxonomic groups. This process has largely been studied in mammals; however, there are notable differences between mammals and other taxonomic groups in how, why and where new neuron production occurs.

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Lievajová, Kamila, Marcela Martončíková, Juraj Blaško, Judita Orendáčová, Viera Almašiová, and Enikő Račeková. "Early stress affects neurogenesis in the rat rostral migratory stream." Open Life Sciences 5, no. 6 (2010): 757–64. http://dx.doi.org/10.2478/s11535-010-0062-9.

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AbstractStressful experience during the early postnatal period may influence processes associated with neurogenesis (i.e. proliferation, cell death, appearance of astrocytes or cell differentiation) in the neonatal rat rostral migratory stream (RMS). To induce stress, pups were subjected to maternal deprivation daily for three hours, starting from the first postnatal day till the seventh postnatal day. Immunohistochemical methods were used to visualize proliferating cells and astrocytes; dying cells and nitrergic cells were visualized using histochemical staining. Quantitative analysis showed

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21

Isaev, Nickolay K., Elena V. Stelmashook, and Elisaveta E. Genrikhs. "Neurogenesis and brain aging." Reviews in the Neurosciences 30, no. 6 (2019): 573–80. http://dx.doi.org/10.1515/revneuro-2018-0084.

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AbstractHuman aging affects the entire organism, but aging of the brain must undoubtedly be different from that of all other organs, as neurons are highly differentiated postmitotic cells, for the majority of which the lifespan in the postnatal period is equal to the lifespan of the entire organism. In this work, we examine the distinctive features of brain aging and neurogenesis during normal aging, pathological aging (Alzheimer’s disease), and accelerated aging (Hutchinson-Gilford progeria syndrome and Werner syndrome).

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22

Akter, Mariyam, Naoko Kaneko, Vicente Herranz-Pérez, et al. "Dynamic Changes in the Neurogenic Potential in the Ventricular–Subventricular Zone of Common Marmoset during Postnatal Brain Development." Cerebral Cortex 30, no. 7 (2020): 4092–109. http://dx.doi.org/10.1093/cercor/bhaa031.

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Abstract Even after birth, neuronal production continues in the ventricular–subventricular zone (V–SVZ) and hippocampus in many mammals. The immature new neurons (“neuroblasts”) migrate and then mature at their final destination. In humans, neuroblast production and migration toward the neocortex and the olfactory bulb (OB) occur actively only for a few months after birth and then sharply decline with age. However, the precise spatiotemporal profiles and fates of postnatally born neurons remain unclear due to methodological limitations. We previously found that common marmosets, small nonhuman

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23

Bonfanti, Luca. "The (Real) Neurogenic/Gliogenic Potential of the Postnatal and Adult Brain Parenchyma." ISRN Neuroscience 2013 (February 6, 2013): 1–14. http://dx.doi.org/10.1155/2013/354136.

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During the last two decades basic research in neuroscience has remarkably expanded due to the discovery of neural stem cells (NSCs) and adult neurogenesis in the mammalian central nervous system (CNS). The existence of such unexpected plasticity triggered hopes for alternative approaches to brain repair, yet deeper investigation showed that constitutive mammalian neurogenesis is restricted to two small “neurogenic sites” hosting NSCs as remnants of embryonic germinal layers and subserving homeostatic roles in specific neural systems. The fact that in other classes of vertebrates adult neurogen

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24

Millichap, J. Gordon. "Anticonvulsant Suppression of Postnatal Neurogenesis in Laboratory Animals." Pediatric Neurology Briefs 22, no. 12 (2008): 92. http://dx.doi.org/10.15844/pedneurbriefs-22-12-4.

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25

Lozano-Ureña, Anna, Raquel Montalbán-Loro, Anne C. Ferguson-Smith, and Sacri R. Ferrón. "Genomic Imprinting and the Regulation of Postnatal Neurogenesis." Brain Plasticity 3, no. 1 (2017): 89–98. http://dx.doi.org/10.3233/bpl-160041.

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26

Inta, Dragos, Juan M. Lima-Ojeda, Peter Gass, and Paolo Fusar-Poli. "Postnatal Neurogenesis and Dopamine Alterations in Early Psychosis." Recent Patents on CNS Drug Discovery 7, no. 3 (2012): 236–42. http://dx.doi.org/10.2174/157488912803251998.

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27

Angelova, Alexandra, Marie-Catherine Tiveron, Harold Cremer, and Christophe Beclin. "Neuronal Subtype Generation During Postnatal Olfactory Bulb Neurogenesis." Journal of Experimental Neuroscience 12 (January 2018): 117906951875567. http://dx.doi.org/10.1177/1179069518755670.

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28

Chen, Yanan, and Bor Luen Tang. "The amyloid precursor protein and postnatal neurogenesis/neuroregeneration." Biochemical and Biophysical Research Communications 341, no. 1 (2006): 1–5. http://dx.doi.org/10.1016/j.bbrc.2005.12.150.

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29

Platel, Jean-Claude, Séverine Stamboulian, Ivy Nguyen, and Angélique Bordey. "Neurotransmitter signaling in postnatal neurogenesis: The first leg." Brain Research Reviews 63, no. 1-2 (2010): 60–71. http://dx.doi.org/10.1016/j.brainresrev.2010.02.004.

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30

Kowalchuk, Angelica M., Kate A. Maurer, Farnaz Shoja-Taheri, and Nadean L. Brown. "Requirements for Neurogenin2 during mouse postnatal retinal neurogenesis." Developmental Biology 442, no. 2 (2018): 220–35. http://dx.doi.org/10.1016/j.ydbio.2018.07.020.

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31

Khodak, T. V., V. O. Tykholaz, and V. M. Shevchenko. "Postnatal neurogenesis in the neuroproliferative areas of the brain." Reports of Vinnytsia National Medical University 26, no. 4 (2022): 676–80. http://dx.doi.org/10.31393/reports-vnmedical-2022-26(4)-27.

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Annotation. The purpose of the work is to systematize and analyze existing problematic aspects in the study of postnatal neurogenesis in neuroproliferative areas of the brain. The relevance of this problem is due to the growing share of neurodegenerative diseases and the search for the possibility of their treatment. From the databases PubMed, ScienceDirect, UpToDate, Web of science, Scopus, 28 sources on this problem were selected for consideration, regardless of age, with a predominance of publications from the last 10 years. The state of research related to the study of postnatal neurogenes

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32

Káradóttir, Ragnhildur T., and Chay T. Kuo. "Neuronal Activity-Dependent Control of Postnatal Neurogenesis and Gliogenesis." Annual Review of Neuroscience 41, no. 1 (2018): 139–61. http://dx.doi.org/10.1146/annurev-neuro-072116-031054.

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The addition of new neurons and oligodendroglia in the postnatal and adult mammalian brain presents distinct forms of gray and white matter plasticity. Substantial effort has been devoted to understanding the cellular and molecular mechanisms controlling postnatal neurogenesis and gliogenesis, revealing important parallels to principles governing the embryonic stages. While during central nervous system development, scripted temporal and spatial patterns of neural and glial progenitor proliferation and differentiation are necessary to create the nervous system architecture, it remains unclear

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Ares, S., J. Quero, and G. Morreale de Escobar. "Thyroid Hormones and the Psychomotor Development of the Newborn." European Psychiatry 24, S1 (2009): 1. http://dx.doi.org/10.1016/s0924-9338(09)70390-6.

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Iodine is a trace element which is essential for the synthesis of thyroid hormones. If maternal iodine deficiency in pregnancy is severe, fetal brain damage will occur. This damage is irreversible after birth. Mild/moderate iodine deficiency during pregnancy and early postnatal life is associated with neuro/psycho-intellectual deficits in infants and children. The severity is not only related to the degree of iodine deficiency, but also to the developmental phase during which it is suffered, the most severe being the consequence of iodine deficiency during the first two trimesters of pregnancy

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34

Belachew, Shibeshih, Ramesh Chittajallu, Adan A. Aguirre, et al. "Postnatal NG2 proteoglycan–expressing progenitor cells are intrinsically multipotent and generate functional neurons." Journal of Cell Biology 161, no. 1 (2003): 169–86. http://dx.doi.org/10.1083/jcb.200210110.

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Neurogenesis is known to persist in the adult mammalian central nervous system (CNS). The identity of the cells that generate new neurons in the postnatal CNS has become a crucial but elusive issue. Using a transgenic mouse, we show that NG2 proteoglycan–positive progenitor cells that express the 2′,3′-cyclic nucleotide 3′-phosphodiesterase gene display a multipotent phenotype in vitro and generate electrically excitable neurons, as well as astrocytes and oligodendrocytes. The fast kinetics and the high rate of multipotent fate of these NG2+ progenitors in vitro reflect an intrinsic property,

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35

Tsupykov, O. "Neural stem cell niches in the adult mammalian brain." Cell and Organ Transplantology 3, no. 2 (2015): 190–94. http://dx.doi.org/10.22494/cot.v3i2.13.

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Stem cells of the central nervous system have received a great deal of attention in neurobiology in the last decade. It has been shown that neurogenesis occurs in the postnatal period in specialized niches of the adult mammalian brain. The niche is a key regulator of stem cell behavior. Recent data underscore the complexity and heterogeneity of the different components of the niche, and the presence of local signaling microdomain. The review is devoted to recent views on the structural organization of neurogenic niches and regulatory factors involved at different stages of neurogenesis in the

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36

Li, Jingzheng, Yafang Shang, Lin Wang, et al. "Genome integrity and neurogenesis of postnatal hippocampal neural stem/progenitor cells require a unique regulator Filia." Science Advances 6, no. 44 (2020): eaba0682. http://dx.doi.org/10.1126/sciadv.aba0682.

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Endogenous DNA double-strand breaks (DSBs) formation and repair in neural stem/progenitor cells (NSPCs) play fundamental roles in neurogenesis and neurodevelopmental disorders. NSPCs exhibit heterogeneity in terms of lineage fates and neurogenesis activity. Whether NSPCs also have heterogeneous regulations on DSB formation and repair to accommodate region-specific neurogenesis has not been explored. Here, we identified a regional regulator Filia, which is predominantly expressed in mouse hippocampal NSPCs after birth and regulates DNA DSB formation and repair. On one hand, Filia protects stall

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37

Bordey, Angélique. "The Postnatal Subventricular Zone: A Source of New Cells in This Old Brain." Nepal Journal of Neuroscience 2, no. 1 (2005): 12–23. http://dx.doi.org/10.3126/njn.v2i1.19977.

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Findings over the past decades demonstrating persistent neurogenesis in the adult brain have challenged the view of a fixed circuitry and raise hopes for self-renewal following brain injury. The subventricular zone (SVZ, also called subependymal layer, SEL) lining the lateral wall of the lateral ventricle is the largest germinal center where stem cells displaying astrocytic traits have been identified. These astrocyte-like cells ensheath neuroblasts, which migrate throughout the SVZ and along the rostral migratory stream to the olfactory bulb where they differentiate into interneurons. The cel

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Hara, Yoshinobu, Jonas Frisen, and Noriko Osumi. "The function of Ephrin-Eph signaling in postnatal neurogenesis." Neuroscience Research 58 (January 2007): S209. http://dx.doi.org/10.1016/j.neures.2007.06.957.

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Huang, Jing, Sheng Jing, Xi Chen, et al. "Propofol Administration During Early Postnatal Life Suppresses Hippocampal Neurogenesis." Molecular Neurobiology 53, no. 2 (2015): 1031–44. http://dx.doi.org/10.1007/s12035-014-9052-7.

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40

Mooney, Sandra M., and Michael W. Miller. "Prenatal exposure to ethanol affects postnatal neurogenesis in thalamus." Experimental Neurology 223, no. 2 (2010): 566–73. http://dx.doi.org/10.1016/j.expneurol.2010.02.003.

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41

Lopez-Garcia, C., A. Molowny, J. M. Garcia-Verdugo, and I. Ferrer. "Delayed postnatal neurogenesis in the cerebral cortex of lizards." Developmental Brain Research 43, no. 2 (1988): 167–74. http://dx.doi.org/10.1016/0165-3806(88)90096-x.

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42

Ban, Jelena, and Miranda Mladinic. "Spinal cord neural stem cells heterogeneity in postnatal development." STEMedicine 1, no. 1 (2020): e19. http://dx.doi.org/10.37175/stemedicine.v1i1.19.

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Neural stem cells are capable of generating new neurons during development as well as in the adulthood and represent one of the most promising tools to replace lost or damaged neurons after injury or neurodegenerative disease. Unlike the brain, neurogenesis in the adult spinal cord is poorly explored and the comprehensive characterization of the cells that constitute stem cell neurogenic niche is still missing. Moreover, the terminology used to specify developmental and/or anatomical CNS regions, where neurogenesis in the spinal cord occurs, is not consensual and the analogy with the brain is

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Komada, Munekazu, Tetsuji Nagao, and Nao Kagawa. "Prenatal and postnatal bisphenol A exposure inhibits postnatal neurogenesis in the hippocampal dentate gyrus." Journal of Toxicological Sciences 45, no. 10 (2020): 639–50. http://dx.doi.org/10.2131/jts.45.639.

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Niklison-Chirou, Maria Victoria, Massimiliano Agostini, Ivano Amelio, and Gerry Melino. "Regulation of Adult Neurogenesis in Mammalian Brain." International Journal of Molecular Sciences 21, no. 14 (2020): 4869. http://dx.doi.org/10.3390/ijms21144869.

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Adult neurogenesis is a multistage process by which neurons are generated and integrated into existing neuronal circuits. In the adult brain, neurogenesis is mainly localized in two specialized niches, the subgranular zone (SGZ) of the dentate gyrus and the subventricular zone (SVZ) adjacent to the lateral ventricles. Neurogenesis plays a fundamental role in postnatal brain, where it is required for neuronal plasticity. Moreover, perturbation of adult neurogenesis contributes to several human diseases, including cognitive impairment and neurodegenerative diseases. The interplay between extrins

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Wang, Ning, Yang Lu, Kui Wang, et al. "Simvastatin Attenuates Neurogenetic Damage and Improves Neurocongnitive Deficits Induced by Isoflurane in Neonatal Rats." Cellular Physiology and Biochemistry 46, no. 2 (2018): 618–32. http://dx.doi.org/10.1159/000488630.

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Background/Aims: Isoflurane inhibited neurogenesis and induced subsequent neurocognitive deficits in developing brain. Simvastatin exerts neuroprotection in a wide range of brain injury models. In the present study, we investigated whether simvastatin could attenuate neurogenetic inhibition and cognitive deficits induced by isoflurane exposure in neonatal rats. Methods: Sprague-Dawley rats at postnatal day (PND) 7 and neural stem cells (NSCs) were treated with either gas mixture, isoflurane, or simvastatin 60 min prior to isoflurane exposure, respectively. The rats were decapitated at PND 8 an

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Tran, Phu V., Stephanie J. B. Fretham, Jane Wobken, Bradley S. Miller, and Michael K. Georgieff. "Gestational-neonatal iron deficiency suppresses and iron treatment reactivates IGF signaling in developing rat hippocampus." American Journal of Physiology-Endocrinology and Metabolism 302, no. 3 (2012): E316—E324. http://dx.doi.org/10.1152/ajpendo.00369.2011.

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Gestational-neonatal iron deficiency, a common micronutrient deficiency affecting the offspring of more than 30% of pregnancies worldwide, leads to long-term cognitive and behavioral abnormalities. Preclinical models of gestational-neonatal iron deficiency result in reduced energy metabolism and expression of genes critical for neuronal plasticity and cognitive function, which are associated with a smaller hippocampal volume and abnormal neuronal dendrite growth. Because insulin-like growth factor (IGF) modulates early postnatal cellular growth, differentiation, and survival, we used a dietary

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Cuppini, Riccardo, Sandra Ciaroni, Tiziana Cecchini, et al. "Tocopherols Enhance Neurogenesis in Dentate Gyrus of Adult Rats." International Journal for Vitamin and Nutrition Research 72, no. 3 (2002): 170–76. http://dx.doi.org/10.1024/0300-9831.72.3.170.

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In the dentate gyrus of the mammalian hippocampus, neurogenesis carries on throughout postnatal life. The aim of this work was to identify an exogenous control factor of adult neurogenesis. Neurogenesis in the adult dentate gyrus was previously found to be enhanced in vitamin E-deficient rats. The effects of alpha- or beta-tocopherol supplementation on neurogenesis in the adult dentate gyrus were investigated by 5-bromo-2’-deoxyuridine labeling. Tocopherol was found to increase the survival of newborn cells and the total number of granule cells in the adult rat dentate gyrus. Newborn cells wer

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48

Abbott, Louise C., and Fikru Nigussie. "Mercury Toxicity and Neurogenesis in the Mammalian Brain." International Journal of Molecular Sciences 22, no. 14 (2021): 7520. http://dx.doi.org/10.3390/ijms22147520.

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The mammalian brain is formed from billions of cells that include a wide array of neuronal and glial subtypes. Neural progenitor cells give rise to the vast majority of these cells during embryonic, fetal, and early postnatal developmental periods. The process of embryonic neurogenesis includes proliferation, differentiation, migration, the programmed death of some newly formed cells, and the final integration of differentiated neurons into neural networks. Adult neurogenesis also occurs in the mammalian brain, but adult neurogenesis is beyond the scope of this review. Developing embryonic neu

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Gao, Hui, Xuejun Cheng, Junchen Chen, et al. "Fto-modulated lipid niche regulates adult neurogenesis through modulating adenosine metabolism." Human Molecular Genetics 29, no. 16 (2020): 2775–87. http://dx.doi.org/10.1093/hmg/ddaa171.

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Abstract Adult neurogenesis is regulated by diverse factors including the local environment, i.e. the neurogenic niche. However, whether the lipid in the brain regulates adult neurogenesis and related mechanisms remains largely unknown. In the present study, we found that lipid accumulates in the brain during postnatal neuronal development. Conditional knockout of Fto (cKO) in lipid not only reduced the level of lipid in the brain but also impaired the learning and memory of mice. In addition, Fto deficiency in lipid did not affect the proliferation of adult neural stem cells (aNSCs), but it d

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Lavenex, Pamela Banta, Pierre Lavenex, and Nicola S. Clayton. "Comparative studies of postnatal neurogenesis and learning: a critical review." Avian and Poultry Biology Reviews 12, no. 3 (2001): 103–25. http://dx.doi.org/10.3184/147020601783698495.

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