{"id":201764,"date":"2024-12-17T01:15:35","date_gmt":"2024-12-17T07:15:35","guid":{"rendered":"https:\/\/lifeboat.com\/blog\/2024\/12\/membrane-potential-states-gate-synaptic-consolidation-in-human-neocortical-tissue"},"modified":"2024-12-17T01:15:35","modified_gmt":"2024-12-17T07:15:35","slug":"membrane-potential-states-gate-synaptic-consolidation-in-human-neocortical-tissue","status":"publish","type":"post","link":"https:\/\/lifeboat.com\/blog\/2024\/12\/membrane-potential-states-gate-synaptic-consolidation-in-human-neocortical-tissue","title":{"rendered":"Membrane potential states gate synaptic consolidation in human neocortical tissue"},"content":{"rendered":"<p><a class=\"aligncenter blog-photo\" href=\"https:\/\/lifeboat.com\/blog.images\/membrane-potential-states-gate-synaptic-consolidation-in-human-neocortical-tissue.jpg\"><\/a><\/p>\n<p>As humans, we have the ability to recall detailed information, even from years in the past, indicating a powerful memory system. Newly encoded explicit memories initially depend on the hippocampus<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Kitamura, T. et al. Engrams and circuits crucial for systems consolidation of a memory. Science 356, 73&ndash;78 (2017).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR1\" id=\"ref-link-section-d71592232e683\">1<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Klinzing, J. G., Niethard, N. & Born, J. Mechanisms of systems memory consolidation during sleep. Nat. Neurosci. 22, 1598&ndash;1610 (2019).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR2\" id=\"ref-link-section-d71592232e683_1\">2<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Corkin, S. What\u2019s new with the amnesic patient H.M.? Nat. Rev. Neurosci. 3153&ndash;160 (2002).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR3\" id=\"ref-link-section-d71592232e683_2\">3<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 4\" title=\"Frankland, P. W. & Bontempi, B. The organization of recent and remote memories. Nat. Rev. Neurosci. 6119&ndash;130 (2005).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#ref-CR4\" id=\"ref-link-section-d71592232e686\">4<\/a><\/sup>. Memory reactivation, mediated by a hippocampo-cortical dialog, leads to a gradual maturation of neocortical engrams over time<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Buzsaki, G. The hippocampo-neocortical dialogue. Cereb. Cortex 6, 81&ndash;92 (1996).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR5\" id=\"ref-link-section-d71592232e690\">5<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Siapas, A. G. & Wilson, M. A. Coordinated interactions between hippocampal ripples and cortical spindles during slow-wave sleep. Neuron 21, 1123&ndash;1128 (1998).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR6\" id=\"ref-link-section-d71592232e690_1\">6<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Buzsaki, G. Hippocampal sharp wave-ripple: a cognitive biomarker for episodic memory and planning. Hippocampus 25, 1073&ndash;1188 (2015).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR7\" id=\"ref-link-section-d71592232e690_2\">7<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Ji, D. & Wilson, M. A. Coordinated memory replay in the visual cortex and hippocampus during sleep. Nat. Neurosci. 10100&ndash;107 (2007).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR8\" id=\"ref-link-section-d71592232e690_3\">8<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 9\" title=\"Logothetis, N. K. et al. Hippocampal-cortical interaction during periods of subcortical silence. Nature 491547&ndash;553 (2012).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#ref-CR9\" id=\"ref-link-section-d71592232e693\">9<\/a><\/sup>. After this systems consolidation process, the neocortex can store information for decades.<\/p>\n<p>It is well established that consolidation relies on non-rapid eye movement (NREM) sleep<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Diekelmann, S. & Born, J. The memory function of sleep. Nat. Rev. Neurosci. 11114&ndash;126 (2010).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR10\" id=\"ref-link-section-d71592232e700\">10<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Huber, R., Ghilardi, M. F., Massimini, M. & Tononi, G. Local sleep and learning. Nature 430, 78&ndash;81 (2004).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR11\" id=\"ref-link-section-d71592232e700_1\">11<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Girardeau, G. & Lopes-Dos-Santos, V. Brain neural patterns and the memory function of sleep. Science 374560&ndash;564 (2021).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR12\" id=\"ref-link-section-d71592232e700_2\">12<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Krause, A. J. et al. The sleep-deprived human brain. Nat. Rev. Neurosci. 18404&ndash;418 (2017).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR13\" id=\"ref-link-section-d71592232e700_3\">13<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Rasch, B., Buchel, C., Gais, S. & Born, J. Odor cues during slow-wave sleep prompt declarative memory consolidation. Science 315, 1426&ndash;1429 (2007).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR14\" id=\"ref-link-section-d71592232e700_4\">14<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 15\" title=\"Staresina, B. P. Coupled sleep rhythms for memory consolidation. Trends Cogn. Sci. 28339&ndash;351 (2024).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#ref-CR15\" id=\"ref-link-section-d71592232e703\">15<\/a><\/sup>. This brain state gives rise to characteristic patterns in the electroencephalogram, including slow waves (\u223c 0.5\u20134 Hz), sleep spindles (\u223c 10\u201316 Hz) and hippocampal ripple oscillations (\u223c 80\u2013120 Hz in humans)<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Buzsaki, G., Horvath, Z., Urioste, R., Hetke, J. & Wise, K. High-frequency network oscillation in the hippocampus. Science 256, 1025&ndash;1027 (1992).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR16\" id=\"ref-link-section-d71592232e707\">16<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Dickey, C. W. et al. Cortical ripples during NREM sleep and waking in humans. J. Neurosci. 42, 7931&ndash;7946 (2022).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR17\" id=\"ref-link-section-d71592232e707_1\">17<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 18\" title=\"Staresina, B. P., Niediek, J., Borger, V., Surges, R. & Mormann, F. How coupled slow oscillations, spindles and ripples coordinate neuronal processing and communication during human sleep. Nat. Neurosci. 26, 1429&ndash;1437 (2023).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#ref-CR18\" id=\"ref-link-section-d71592232e710\">18<\/a><\/sup>. During slow wave activity (SWA), neocortical neurons exhibit synchronous membrane potential changes, referred to as UP and DOWN states<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Steriade, M., Timofeev, I. & Grenier, F. Natural waking and sleep states: a view from inside neocortical neurons. J. Neurophysiol. 85, 1969&ndash;1985 (2001).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR19\" id=\"ref-link-section-d71592232e714\">19<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Nir, Y. et al. Regional slow waves and spindles in human sleep. Neuron 70153&ndash;169 (2011).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR20\" id=\"ref-link-section-d71592232e714_1\">20<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Csercsa, R. et al. Laminar analysis of slow wave activity in humans. Brain 133, 2814&ndash;2829 (2010).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR21\" id=\"ref-link-section-d71592232e714_2\">21<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 22\" title=\"Adamantidis, A. R., Gutierrez Herrera, C. & Gent, T. C. Oscillating circuitries in the sleeping brain. Nat. Rev. Neurosci. 20746&ndash;762 (2019).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#ref-CR22\" id=\"ref-link-section-d71592232e717\">22<\/a><\/sup>. UP states are periods of increased neural activity, giving rise to depolarization of neurons<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 23\" title=\"Timofeev, I., Grenier, F., Bazhenov, M., Sejnowski, T. J. & Steriade, M. Origin of slow cortical oscillations in deafferented cortical slabs. Cereb. Cortex 10, 1185&ndash;1199 (2000).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#ref-CR23\" id=\"ref-link-section-d71592232e721\">23<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 24\" title=\"Shu, Y., Hasenstaub, A. & McCormick, D. A. Turning on and off recurrent balanced cortical activity. Nature 423288&ndash;293 (2003).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#ref-CR24\" id=\"ref-link-section-d71592232e724\">24<\/a><\/sup>. Conversely, DOWN states are silent periods, associated with hyperpolarization<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 25\" title=\"Timofeev, I., Grenier, F. & Steriade, M. Disfacilitation and active inhibition in the neocortex during the natural sleep-wake cycle: an intracellular study. Proc. Natl. Acad. Sci. USA 98, 1924&ndash;1929 (2001).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#ref-CR25\" id=\"ref-link-section-d71592232e728\">25<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 26\" title=\"Cash, S. S. et al. The human K-complex represents an isolated cortical down-state. Science 324, 1084&ndash;1087 (2009).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#ref-CR26\" id=\"ref-link-section-d71592232e731\">26<\/a><\/sup>. In the human neocortex, prominent SWA occurs in supragranular layers 2 &amp; 3<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 21\" title=\"Csercsa, R. et al. Laminar analysis of slow wave activity in humans. Brain 133, 2814&ndash;2829 (2010).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#ref-CR21\" id=\"ref-link-section-d71592232e736\">21<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 27\" title=\"Dickey, C. W. et al. Travelling spindles create necessary conditions for spike-timing-dependent plasticity in humans. Nat. Commun. 12, 1027 (2021).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#ref-CR27\" id=\"ref-link-section-d71592232e739\">27<\/a><\/sup>. Several studies have demonstrated that precise temporal coupling of spindles and ripples to SWA promotes engram reactivation<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Diba, K. & Buzsaki, G. Forward and reverse hippocampal place-cell sequences during ripples. Nat. Neurosci. 10, 1241&ndash;1242 (2007).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR28\" id=\"ref-link-section-d71592232e743\">28<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Peigneux, P. et al. Are spatial memories strengthened in the human hippocampus during slow wave sleep? Neuron 44535&ndash;545 (2004).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR29\" id=\"ref-link-section-d71592232e743_1\">29<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Wilson, M. A. & McNaughton, B. L. Reactivation of hippocampal ensemble memories during sleep. Science 265676&ndash;679 (1994).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR30\" id=\"ref-link-section-d71592232e743_2\">30<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Schreiner, T., Petzka, M., Staudigl, T. & Staresina, B. P. Endogenous memory reactivation during sleep in humans is clocked by slow oscillation-spindle complexes. Nat. Commun. 12, 3112 (2021).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR31\" id=\"ref-link-section-d71592232e743_3\">31<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Jiang, X. et al. Replay of large-scale spatio-temporal patterns from waking during subsequent NREM sleep in human cortex. Sci. Rep. 7, 17380 (2017).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR32\" id=\"ref-link-section-d71592232e743_4\">32<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Peyrache, A., Khamassi, M., Benchenane, K., Wiener, S. I. & Battaglia, F. P. Replay of rule-learning related neural patterns in the prefrontal cortex during sleep. Nat. Neurosci. 12919&ndash;926 (2009).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR33\" id=\"ref-link-section-d71592232e743_5\">33<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 34\" title=\"Skelin, I. et al. Coupling between slow waves and sharp-wave ripples engages distributed neural activity during sleep in humans. Proc. Natl. Acad. Sci. USA 118, e2012075118 (2021).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#ref-CR34\" id=\"ref-link-section-d71592232e746\">34<\/a><\/sup> and determines success of memory consolidation<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 18\" title=\"Staresina, B. P., Niediek, J., Borger, V., Surges, R. & Mormann, F. How coupled slow oscillations, spindles and ripples coordinate neuronal processing and communication during human sleep. Nat. Neurosci. 26, 1429&ndash;1437 (2023).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#ref-CR18\" id=\"ref-link-section-d71592232e750\">18<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Bergmann, T. O. & Born, J. Phase-amplitude coupling: a general mechanism for memory processing and synaptic plasticity? Neuron 97, 10&ndash;13 (2018).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR35\" id=\"ref-link-section-d71592232e753\">35<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Helfrich, R. F., Mander, B. A., Jagust, W. J., Knight, R. T. & Walker, M. P. Old brains come uncoupled in sleep: slow wave-spindle synchrony, brain atrophy, and forgetting. Neuron 97221&ndash;230 e224 (2018).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR36\" id=\"ref-link-section-d71592232e753_1\">36<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Hahn, M. A., Heib, D., Schabus, M., Hoedlmoser, K. & Helfrich, R. F. Slow oscillation-spindle coupling predicts enhanced memory formation from childhood to adolescence. Elife 9, e53730 (2020).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR37\" id=\"ref-link-section-d71592232e753_2\">37<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 38\" title=\"Muehlroth, B. E. et al. Precise slow oscillation-spindle coupling promotes memory consolidation in younger and older adults. Sci. Rep. 9, 1940 (2019).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#ref-CR38\" id=\"ref-link-section-d71592232e756\">38<\/a><\/sup>. Consequently, brain stimulation methods that boost SWA or enhance coupling have a positive effect on memory performance in rodents and humans<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Marshall, L., Helgadottir, H., Molle, M. & Born, J. Boosting slow oscillations during sleep potentiates memory. Nature 444610&ndash;613 (2006).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR39\" id=\"ref-link-section-d71592232e760\">39<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Massimini, M. et al. Triggering sleep slow waves by transcranial magnetic stimulation. Proc. Natl. Acad. Sci. USA 104, 8496&ndash;8501 (2007).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR40\" id=\"ref-link-section-d71592232e760_1\">40<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Latchoumane, C. V., Ngo, H. V., Born, J. & Shin, H. S. Thalamic spindles promote memory formation during sleep through triple phase-locking of cortical, thalamic, and hippocampal rhythms. Neuron 95424&ndash;435.e426 (2017).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR41\" id=\"ref-link-section-d71592232e760_2\">41<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Maingret, N., Girardeau, G., Todorova, R., Goutierre, M. & Zugaro, M. Hippocampo-cortical coupling mediates memory consolidation during sleep. Nat. Neurosci. 19959&ndash;964 (2016).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR42\" id=\"ref-link-section-d71592232e760_3\">42<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Geva-Sagiv, M. et al. Augmenting hippocampal-prefrontal neuronal synchrony during sleep enhances memory consolidation in humans. Nat. Neurosci. 26, 1100&ndash;1110 (2023).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#Sec6#ref-CR43\" id=\"ref-link-section-d71592232e760_4\">43<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 44\" title=\"Ngo, H. V., Martinetz, T., Born, J. & Molle, M. Auditory closed-loop stimulation of the sleep slow oscillation enhances memory. Neuron 78545&ndash;553 (2013).\" href=\"https:\/\/www.nature.com\/articles\/s41467-024-53901-2#ref-CR44\" id=\"ref-link-section-d71592232e763\">44<\/a><\/sup>. These observations suggest that SWA and the underlying membrane potential UP and DOWN states initiate mechanisms that augment memory functions. However, in the human brain such mechanisms remain elusive.<\/p>\n<p>One possibility is that UP and DOWN states modulate excitatory synapses in the neocortex to increase synaptic strength during SWA-coupled neural activity. While action potentials (AP) are necessary to initiate transmission in the mammalian neocortex, it has been demonstrated in laboratory animals that presynaptic signals below the AP-threshold (i.e., subthreshold signals) have a modulatory effect on synaptic strength<sup>45,46,47,48,49,50,51,52,53,54<\/sup>. For instance, at synapses between neocortical pyramidal neurons in ferrets<sup>46<\/sup> and rats<sup>47<\/sup> a 1-second-long subthreshold depolarization preceding an AP leads to an increase in synaptic amplitude. Through such mechanisms, UP and DOWN states could tune local synaptic networks to promote long-term synaptic plasticity, which is believed to be fundamental for memory consolidation<sup>2,55<\/sup>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>As humans, we have the ability to recall detailed information, even from years in the past, indicating a powerful memory system. Newly encoded explicit memories initially depend on the hippocampus1,2,3,4. Memory reactivation, mediated by a hippocampo-cortical dialog, leads to a gradual maturation of neocortical engrams over time5,6,7,8,9. After this systems consolidation process, the neocortex can [\u2026]<\/p>\n","protected":false},"author":427,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[47],"tags":[],"class_list":["post-201764","post","type-post","status-publish","format-standard","hentry","category-neuroscience"],"_links":{"self":[{"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/posts\/201764","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/users\/427"}],"replies":[{"embeddable":true,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/comments?post=201764"}],"version-history":[{"count":0,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/posts\/201764\/revisions"}],"wp:attachment":[{"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/media?parent=201764"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/categories?post=201764"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/tags?post=201764"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}