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Hypothesis on Remote Memory Forming from Heterosynaptic LTD-Mediated Neuronal Degeneration

DOI: 10.4236/oalib.1105442, PP. 1-6

Subject Areas: Developmental Biology, Linguistics, Neuroscience, Cell Biology

Keywords: Remote Memory, Homosynaptic LTP, Heterosynaptic LTD, Neuronal Degeneration

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Abstract

In this article, it is hypothesized a new mechanism for the formation of stable remote memory in brain comprising the important memory acquired during childhood and the common words in language. It has been demonstrated that the memory forms concurrently at both homosynaptic long term potentiation (LTP) and heterosynaptic long term depression (LTD). It is pointed out that the repeated LTD may result in neuronal degeneration as evidenced at molecular and cellular level, becoming long lasting throughout the lifespan. Besides, it is further supported by the consequent storage of remote memory directly on the information pathway, as evidenced by the degenerative ocular dominance plasticity and the storage of common words/grammar within the linguistic areas of brain. Accordingly, it is herein completed the hypothesis on the formation of remote memory from the heterosynaptic LTD-mediated neuronal degeneration in brain so long as the homosynaptic pathway does not degenerate from such causes as aging and so on, while supplementing a new form of neuronal plasticity for memory in addition to the contemporary LTP and LTD.

Cite this paper

Cai, Z. (2019). Hypothesis on Remote Memory Forming from Heterosynaptic LTD-Mediated Neuronal Degeneration. Open Access Library Journal, 6, e5442. doi: http://dx.doi.org/10.4236/oalib.1105442.

References

[1]  Cai, Z.-J. (1990) The Neural Mechanism of Declarative Memory Consolidation and Retrieval: A Hypothesis. Neuroscience & Bi-obehavioral Reviews, 14, 295-304.
https://doi.org/10.1016/S0149-7634(05)80039-9
[2]  Cai, Z.-J. (2018) The Limbic-Reticular Coupling Theory of Memory Processing in the Brain and Its Greater Compatibility Over Other Theories. Dementia & Neuropsychologia, 12, 105-113. https://doi.org/10.1590/1980-57642018dn12-020002
[3]  Moscovitch, M., Rosenbaum, R.S., Gil-boa, A., Addis, D.R., Westmacott, R., Grady, C., McAndrews, M.P., Levine, B., Black, S., Winocur, G. and Nadel, L. (2005) Func-tional Neuroanatomy of Remote Episodic, Semantic and Spatial Memory: A Unified Account Based on Multiple Trace Theory. Journal of Anatomy, 207, 35-66.
https://doi.org/10.1111/j.1469-7580.2005.00421.x
[4]  Squire, L.R. (1987) Memory and Brain. Oxford University Press, Oxford.
[5]  Cai, Z.-J. (2015) Semantic Memory Association, Procedural Grammar Syntax and Episodic Modality Coordination as Three Interactive Neural Processes Organizing Language: A Model. Open Access Library Journal, 2, e1718.
https://doi.org/10.4236/oalib.1101718
[6]  Cai, Z.-J. (2017) The Neurobiological Models of Language: An Updated Review. Psychology & Neuroscience, 10, 297-306. https://doi.org/10.1037/pne0000101
[7]  Moser, M.B. (2014) Nobel Lecture: Grid Cells, Place Cells and Memory. Nobelprize.org, Nobel Media AB.
[8]  Muller, D., Hefft, S. and Figurov, A. (1995) Heterosynaptic Interactions between LTP and LTD in CA1 Hippocampal Slices. Neuron, 14, 599-605.
https://doi.org/10.1016/0896-6273(95)90316-X
[9]  Abraham, W.C., Mason-Parker, S.E., Irvine, G.I., Logan, B. and Gill, A.I. (2006) Induction and Activity-Dependent Reversal of Persistent LTP and LTD in Lateral Perforant Path Synapses in Vivo. Neu-robiology of Learning and Memory, 86, 82-90.
https://doi.org/10.1016/j.nlm.2005.12.007
[10]  Abraham, W.C. and Goddard, G.V. (1983) Asymmetric Relationships between Homosynaptic Long-Term Potentiation and Heterosynaptic Long-Term Depression. Nature, 305, 717-719. https://doi.org/10.1038/305717a0
[11]  Jedlicka, P., Benuskova, L. and Abraham, W.C. (2015) A Volt-age-Based STDP Rule Combined with Fast BCM-Like Metaplasticity Accounts for LTP and Concurrent “Heterosynaptic” LTD in the Dentate Gyrus in Vivo. PLOS Computational Biology, 11, e1004588. https://doi.org/10.1371/journal.pcbi.1004588
[12]  Kosub, K.A., Do, V.H. and Derrick, B.E. (2005) NMDA Receptor Antagonists Block Heterosynaptic Long-Term Depression (LTD) But Not Long-Term Potentiation (LTP) in the CA3 Region Following Lateral Perforant Path Stimulation. Neuroscience Letters, 374, 29-34. https://doi.org/10.1016/j.neulet.2004.10.028
[13]  Abraham, W.C., Logan, B., Wolff, A. and Benuskova, L. (2007) “Heterosynaptic” LTD in the Dentate Gyrus of Anesthetized Rat Requires Homosynaptic Activity. Journal of Neurophysiology, 98, 1048-1051. https://doi.org/10.1152/jn.00250.2007
[14]  Chen, J., Tan, Z., Zeng, L., Zhang, X., He, Y., Gao, W., Wu, X., Li, Y., Bu, B., Wang, W. and Duan, S. (2013) Heterosynaptic Long-Term Depression Mediated by ATP Released from Astrocytes. Glia, 61, 178-191. https://doi.org/10.1002/glia.22425
[15]  Arami, M.K., Sohya, K., Sarihi, A., Jiang, B., Yanagawa, Y. and Tsumoto, T. (2013) Recip-rocal Homosynaptic and Heterosynaptic Long-Term Plasticity of Corticogeniculate Projection Neurons in Layer VI of the Mouse Visual Cortex. The Journal of Neuroscience, 33, 7787-7798. https://doi.org/10.1523/JNEUROSCI.5350-12.2013
[16]  Chiu, C.Q., Puente, N., Grandes, P. and Castillo, P.E. (2010) Dopaminergic Modulation of Endocannabinoid-Mediated Plasticity at GABAergic Synapses in the Prefrontal Cortex. The Journal of Neuroscience, 30, 7236-7248.
https://doi.org/10.1523/JNEUROSCI.0736-10.2010
[17]  Hansen, N. and Manahan-Vaughan, D. (2015) Locus Coeruleus Stimulation Facilitates Long-Term Depression in the Dentate Gyrusthat Requires Activation of β-Adrenergic Receptors. Cerebral Cortex, 25, 1889-1896.
https://doi.org/10.1093/cercor/bht429
[18]  Toyoda, H. (2018) Nicotine Facilitates Synaptic Depression in Layer V Pyramidal Neurons of the Mouse Insular Cortex. Neuroscience Letters, 672, 78-83.
https://doi.org/10.1016/j.neulet.2018.02.046
[19]  Sidorov, M.S., Kaplan, E.S., Osterweil, E.K., Lindemann, L. and Bear, M.F. (2015) Metabotropic Glutamate Receptor Signaling Is Required for NMDA Receptor-Dependent Ocular Dominance Plasticity and LTD in Visual Cortex. Proceedings of the National Academy of Sciences of the United States of America, 112, 12852-12857. https://doi.org/10.1073/pnas.1512878112
[20]  Jenks, K.R., Kim, T., Pastuzyn, E.D., Okuno, H., Taibi, A.V., Bito, H., Bear, M.F. and Shepherd, J.D. (2017) Arc Restores Juvenile Plasticity in Adult Mouse Visual Cortex. Proceedings of the National Academy of Sciences of the United States of America, 114, 9182-9187. https://doi.org/10.1073/pnas.1700866114
[21]  Czarnecki, A., Birtoli, B. and Ulrich, D. (2007) Cellular Mechanisms of Burst Firing-Mediated Long-Term Depression in Rat Neocortical Pyramidal Cells. The Journal of Physiology, 578, 471-479. https://doi.org/10.1113/jphysiol.2006.123588
[22]  González-Rueda, A., Pedrosa, V., Feord, R.C., Clopath, C. and Paulsen, O. (2018) Activity-Dependent Downscaling of Subthreshold Synaptic Inputs during Slow-Wave- Sleep-Like Activity in Vivo. Neuron, 97, 1244-1252.e5.
https://doi.org/10.1016/j.neuron.2018.01.047
[23]  Rasch, B. and Born, J. (2013) About Sleep’s Role in Memory. Physiological Reviews, 93, 681-766. https://doi.org/10.1152/physrev.00032.2012
[24]  Inostroza, M. and Born, J. (2013) Sleep for Preserving and Transforming Episodic Memory. Annual Review of Neuroscience, 36, 79-102.
https://doi.org/10.1146/annurev-neuro-062012-170429
[25]  Hunt, D.L., Linaro, D., Si, B., Romani, S. and Spruston, N. (2018) A Novel Pyramidal Cell Type Promotes Sharp-Wave Synchronization in the Hippocampus. Nature Neuroscience, 21, 985-995. https://doi.org/10.1038/s41593-018-0172-7

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