Role of the cholinergic system in regulating survival of newborn neurons in the adult mouse dentate gyrus and olfactory bulb
Abstract
Neurogenesis in the subgranular zone of the hippocampal dentate gyrus and olfactory bulbs continues into adulthood and has been implicated in the cognitive function of the adult brain. The basal forebrain cholinergic system has been suggested to play a role in regulating neurogenesis as well as learning and memory in these regions. Herein, we report that highly polysialylated neural cell adhesion molecule (PSA‐NCAM)‐positive immature cells as well as neuronal nuclei (NeuN)‐positive mature neurons in the dentate gyrus and olfactory bulb express multiple acetylcholine receptor subunits and make contact with cholinergic fibers. To examine the function of acetylcholine in neurogenesis, we used donepezil (Aricept), a potent and selective acetylcholinesterase inhibitor that improves cognitive impairment in Alzheimer's disease. Intraperitoneal administrations of donepezil significantly enhanced the survival of newborn neurons, but not proliferation of neural progenitor cells in the subgranular zone or the subventricular zone of normal mice. Moreover, donepezil treatment reversed the chronic stress‐induced decrease in neurogenesis. Taken together, these results suggest that activation of the cholinergic system promotes survival of newborn neurons in the adult dentate gyrus and olfactory bulb under both normal and stressed conditions.
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If newborn neurons do not receive sufficient stimulation, they become much less likely to survive to maturity.
“If these newborn neurons do not receive sufficient stimulation, they become much less likely to survive to maturity [17].”
From MiR-338-3p regulates neuronal maturation and suppresses glioblastoma proliferation. (2017) · cites this paper as [17]
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- Calza, L., Giuliani, A., Fernandez, M., Pirondi, S., D'Intino, G., Aloe, L. & Giardino, L. (2003) Neural stem cells and cholin- ergic neurons: regulation by immunolesion and treatment with mitogens, retinoic acid, and nerve growth factor. Proc. Natl. Acad. Sci. USA 100, 7325-7330.
- Doetsch, F. & Alvarez-Buylla, A. (1996) Network of tangential pathways for neuronal migration in adult mammalian brain. Proc. Natl. Acad. Sci. USA 93, 14895-14900.
- Fibiger, H.C. (1991) Cholinergic mechanisms in learning, memory and dementia: a review of recent evidence. Trends Neurosci. 14, 220-223.
- Gheusi, G., Cremer, H., McLean, H., Chazal, G., Vincent, J.D. & Lledo, P.M. (2000) Importance of newly generated neurons in the adult olfactory bulb for odor discrimination. Proc. Natl. Acad. Sci. USA 97, 1823 -1828.
- Leanza, G., Nilsson, O.G., Wiley, R.G. & Bjorklund, A. (1995) Selective lesioning of the basal forebrain cholinergic system by intraventricular 192 IgG-saporin: behavioural, biochemical and stereological studies in the rat. Eur. J. Neurosci. 7, 329 -343.
- Levey, A.I., Edmunds, S.M., Koliatsos, V., Wiley, R.G. & Heilman, C.J. (1995) Expression of m1-m4 muscarinic acetyl- choline receptor proteins in rat hippocampus and regulation by cholinergic innervation. J. Neurosci. 15, 4077-4092.
- van Praag, H., Christie, B.R., Sejnowski, T.J. & Gage, F.H. (1999) Running enhances neurogenesis, learning, and long-term poten- tiation in mice. Proc. Natl. Acad. Sci. USA 96, 13427-13431.
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- Authors
- Kaneko, N., Okano, H., & Sawamoto, K.
- Venue
- Genes to Cells
- Publisher
- Wiley
- Published
- 2006-08-25
- Volume
- 11
- Issue
- 10
- Pages
- 1145-1159
- ISSN
- 1356-9597
- 1365-2443
- Cited by
- 162
- References
- 0
- Language
- en
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