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Muscarinic receptor activation facilitates the induction of long-term potentiation (LTP) in the rat dentate gyrus

Burgard, Edward C., Sarvey, John M.·1990·Neuroscience Letters

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Abstract

Bath application of two different concentrations of muscarine produced two different effects on evoked responses in the dentate gyrus of rat hippocampal slices. A concentration of 1 microM muscarine did not affect the evoked population spike or excitatory postsynaptic potential (EPSP), but facilitated the induction of LTP. In contrast, a concentration of 10 microM muscarine depressed both the population spike and EPSP, but had no effect on LTP induction. The M1 muscarinic receptor antagonist pirenzepine (1 microM) blocked the muscarine-induced facilitation of LTP, but had no effect on the depression of evoked responses. These data suggest that activation of M1 receptors can facilitate the induction of LTP.

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Long‐lasting potentiation of synaptic transmission in the dentate area of the unanaesthetized rabbit following stimulation of the perforant path
Bliss, T. V. P., & Gardner-Medwin, A. R. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010274 · Cited by 7,424
Pirenzepine distinguishes between different subclasses of muscarinic receptors
Hammer, R., Berrie, C. P., Birdsall, N. J. M., Burgen, A. S. V., & Hulme, E. C. (1980) · Nature · doi:10.1038/283090a0 · Cited by 1,273
Differential regulation of PI hydrolysis and adenylyl cyclase by muscarinic receptor subtypes
Peralta, E. G., Ashkenazi, A., Winslow, J. W., Ramachandran, J., & Capon, D. J. (1988) · Nature · doi:10.1038/334434a0 · Cited by 658
Cholinergic innervation of the rat hippocampus as revealed by choline acetyltransferase immunocytochemistry: A combined light and electron microscopic study
Frotscher, M., & Léránth, C. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902390210 · Cited by 600
Localization of a family of muscarinic receptor mRNAs in rat brain
Buckley, N. J., Bonner, T. I., & Brann, M. R. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-12-04646.1988 · Cited by 478
Selectivity of muscarinic antagonists in radioligand and in vivo experiments for the putative M1, M2 and M3 receptors.
Doods, H. N., Mathy, M. J., Davidesko, D., van Charldorp, K. J., Jonge, A. D., & van Zwieten, P. A. (1987) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)39062-2 · Cited by 440
Acetylcholine Mediates a Slow Synaptic Potential in Hippocampal Pyramidal Cells
Cole, A. E., & Nicoll, R. A. (1983) · Science · doi:10.1126/science.6612345 · Cited by 374
Autoradiographic localization of M1 and M2 muscarine receptors in the rat brain
Mash, D. C., & Potter, L. T. (1986) · Neuroscience · doi:10.1016/0306-4522(86)90280-0 · Cited by 316
The role of protein kinase C in long-term potentiation: a testable model
Linden, D. J., & Routtenberg, A. (1989) · Brain Research Reviews · doi:10.1016/0165-0173(89)90004-0 · Cited by 291
Muscarinic cholinergic receptor subtypes in the human brain. II. Quantitative autoradiographic studies
Cortés, R., Probst, A., Tobler, H.-J., & Palacios, J. M. (1986) · Brain Research · doi:10.1016/0006-8993(86)90449-x · Cited by 286

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Burgard, 1989, Muscarinic receptor activation modulates long-term potentiation (LTP) and isoproterenol-induced long-lasting potentiation (ILLP) in rat dentate gyrus, Pharmacologist, 31, 135

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Goldstein, L. B. (2006) · NeuroRx · doi:10.1016/j.nurx.2006.07.010 · Cited by 41
Strategies That Support Declining Cholinergic Neurotransmission in Alzheimer’s Disease Patients
Sirviö, J. (1999) · Gerontology · doi:10.1159/000052759 · Cited by 40
Alteration of Neurotrophins in the Hippocampus and Cerebral Cortex of Young Rats Exposed to Chlorpyrifos and Methyl Parathion
Betancourt, A. M., Filipov, N. M., & Carr, R. L. (2007) · Toxicological Sciences · doi:10.1093/toxsci/kfm248 · Cited by 39
Biochemical Correlates of Long-Term Potentiation in Hippocampal Synapses
Otani, S., & Ben‐Ari, Y. (1993) · International review of neurobiology · doi:10.1016/s0074-7742(08)60567-x · Cited by 40
SDZ ENS 163, a selective muscarinic M1 receptor agonist, facilitates the induction of long-term potentiation in rat hippocampal slices
Boddeke, E., Enz, A., & Shapiro, G. (1992) · European Journal of Pharmacology · doi:10.1016/0014-2999(92)90457-f · Cited by 38
θ-activity-dependent and -independent muscarinic facilitation of long-term potentiation in guinea pig hippocampal slices.
Natsume, K., & Kometani, K. (1997) · Neuroscience Research · doi:10.1016/s0168-0102(97)01167-x · Cited by 34
Cellular Mechanisms Of Long-Term Potentiation: Late Maintenance
Frey, U. (1997) · Advances in psychology · doi:10.1016/s0166-4115(97)80092-1 · Cited by 33
Cholinergic responses of morphologically and electrophysiologically characterized neurons of the basolateral complex in rat amygdala slices
Yajeya, J., Juan, A. D. L. F., Merchán, M. Á., Riolobos, A. S., Heredia, M., & Criado, J. M. (1997) · Neuroscience · doi:10.1016/s0306-4522(96)00614-8 · Cited by 33
NMDA receptor activation enhances the release of a cholinergic differentiation peptide (HCNP) from hippocampal neurons in vitro
Ojika, K., Tsugu, Y., Mitake, S., Otsuka, Y., & Katada, E. (1998) · Developmental Brain Research · doi:10.1016/s0165-3806(98)00014-5 · Cited by 32
Selective cholinergic immunolesioning affects synaptic plasticity in developing visual cortex
Kuczewski, N., Aztiria, E., Leanza, G., & Domenici, L. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04014.x · Cited by 32
Activation of the medial septal area attenuates LTP of the lateral perforant path and enhances heterosynaptic LTD of the medial perforant path in aged rats
Pang, K. C. H., Williams, M. J., & Olton, D. S. (1993) · Brain Research · doi:10.1016/0006-8993(93)91150-q · Cited by 30
Muscarinic potentiation of IK in hippocampal neurons: electrophysiological characterization of the signal transduction pathway
Zhang, L., Weiner, J. L., & Carlen, P. L. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-11-04510.1992 · Cited by 31
Muscarinic acetylcholine receptor-dependent induction of persistent synaptic enhancement in rat hippocampus in vivo
Li, S., Cullen, W. K., Anwyl, R., & Rowan, M. J. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.10.001 · Cited by 30

Authors: Burgard, E. C., & Sarvey, J. M.
Affiliations: Uniformed Services University of the Health Sciences (US)
Corresponding author: Sarvey, John M.
Venue: Neuroscience Letters
Publisher: Elsevier BV
Published: 1990-08
Volume: 116
Issue: 1-2
Pages: 34-39
ISSN: 0304-3940 (ISSN-L)
DOI: 10.1016/0304-3940(90)90382-j
OpenAlex: W2072926455
Cited by: 188
References: 24
Citations by year: 2026: 2 · 2023: 1 · 2022: 1 · 2021: 1 · 2020: 3 · 2019: 4 · 2018: 3 · 2017: 2 · 2016: 1 · 2015: 1 · 2014: 5 · 2013: 1 · 2012: 10
FWCI: 2.97
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Neuroscience Letters (publishedVersion)
PubMed (publishedVersion)
Funders: National Institutes of Health (5r01ns023865-07)
National Institute of Neurological Disorders and Stroke (NS-23865)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
Keywords: muscarinic receptors, M1 muscarinic receptor, long-term potentiation, LTP induction, dentate gyrus, hippocampus, muscarine, pirenzepine, excitatory postsynaptic potentials, synaptic plasticity
MeSH terms: Animals, Electric Stimulation, Evoked Potentials, Hippocampus, Kinetics, Muscarine, Pirenzepine, Receptors, Muscarinic, Rats, In Vitro Techniques

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Muscarinic receptor activation facilitates the induction of long-term potentiation (LTP) in the rat dentate gyrus

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