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Review

On the theory of mental representation block. a novel perspective on learning and behavior

Pages 41-50 | Received 02 Feb 2021, Accepted 01 Mar 2021, Published online: 12 Mar 2021

References

  • Ploog BO, Conditioning C, Encyclopedia of Human Behavior (Second Edition),Elsevier Inc., 2012: pp. 484–491. doi:https://doi.org/10.1016/B978-0-12-375000-6.00090-2.
  • Lachman SJ. Learning is a process: toward an improved definition of learning. J Psychol. 1997;131(5):477–480.
  • Rouleau N, Karbowski LM, Persinger MA. Experimental Evidence of Classical Conditioning and Microscopic Engrams in an Electroconductive Material. PLoS One. 2016;11(10):e0165269.
  • Staddon JER, Cerutti DT. Operant Conditioning. Annu Rev Psychol. 2003;54(1):115–144.
  • Badyal D, Singh T. Learning theories: the basics to learn in medical education. Int J App Basic Med Res. 2017;7(5):1.
  • Torre DM, Daley BJ, Sebastian JL, et al. Overview of Current Learning Theories for Medical Educators. Am J Med. 2006;119(10):903–907.
  • Crossley MJ, Ashby FG, Maddox WT. Erasing the engram: the unlearning of procedural skills. J Exp Psychol. 2013;142(3):710–741.
  • Alberini CM, Ledoux JE. Memory reconsolidation. Curr Biol. 2013;23(17):R746–R750.
  • Alberini CM. The Role of Reconsolidation and the Dynamic Process of Long-Term Memory Formation and Storage. Front Behav Neurosci. 2011;5:12.
  • McKenzie S, Eichenbaum H. Consolidation and Reconsolidation: two Lives of Memories? Neuron. 2011;71(2):224–233.
  • McGaugh JL. Memory - A century of consolidation. Science. 2000;287(5451):248–251.
  • Dudai Y. The Neurobiology of Consolidations, Or, How Stable is the Engram? Annu Rev Psychol. 2004;55(1):51–86.
  • Tyng CM, Amin HU, Saad MNM, et al. The influences of emotion on learning and memory. Front Psychol. 2017;8. DOI:https://doi.org/10.3389/fpsyg.2017.01454..
  • McGaugh JL. Consolidating Memories. Annu Rev Psychol. 2015;66(1):1–24.
  • Nader K, Schafe GE, Le Doux JE. Fear memories require protein synthesis in the amygdala for reconsolidation after retrieval. Nature. 2000;406(6797):722–726.
  • Inda MC, Muravieva EV, Alberini CM. Memory retrieval and the passage of time: from reconsolidation and strengthening to extinction. J Neurosci. 2011;31:1635–1643
  • Alberini CM. Mechanisms of memory stabilization: are consolidation and reconsolidation similar or distinct processes? Trends Neurosci. 2005;28(1):51–56.
  • Milekic MH, Alberini CM. Temporally graded requirement for protein synthesis following memory reactivation. Neuron. 2002;36(3):521–525.
  • Eisenberg M, Dudai Y. Reconsolidation of fresh, remote, and extinguished fear memory in medaka: old fears don’t die. Eur J Neurosci. 2004;20(12):3397–3403.
  • Suzuki A, Josselyn SA, Frankland PW, et al. Memory reconsolidation and extinction have distinct temporal and biochemical signatures. J Neurosci. 2004;24(20):4787–4795.
  • Boccia MM. Post-retrieval effects of icv infusions of hemicholinium in mice are dependent on the age of the original memory. Learn Memory. 2006;13(3):376–381.
  • Robinson MJF, Franklin KBJ. Reconsolidation of a morphine place preference: impact of the strength and age of memory on disruption by propranolol and midazolam. Behav Brain Res. 2010;213(2):201–207.
  • Lattal KM, Lattal KA. Facets of Pavlovian and operant extinction. Behav Processes. 2012;90(1):1–8.
  • Quirk GJ, Paré D, Richardson R, et al. Erasing fear memories with extinction training, in: journal of Neuroscience. Soc Neurosci. 2010;pp. 14993–14997. https://doi.org/10.1523/JNEUROSCI.4268-10.2010.
  • McClelland JL, McNaughton BL, O’Reilly RC. Why there are complementary learning systems in the hippocampus and neocortex: insights from the successes and failures of connectionist models of learning and memory.. Psychol Rev. 1995;102(3):419–457.
  • Squire LR, Alvarez P. Retrograde amnesia and memory consolidation: a neurobiological perspective. Curr Opin Neurobiol. 1995;5(2):169–177.
  • Liu Y, Lin W, Liu C, et al. Memory consolidation reconfigures neural pathways involved in the suppression of emotional memories. Nat Commun. 2016;7(1):1–12.
  • Bayley PJ, Hopkins RO, Squire LR. The fate of old memories after medial temporal lobe damage. J Neurosci. 2006;26(51):13311–13317.
  • Tobore TO. On Energy Efficiency and the Brain’s Resistance to Change: the Neurological Evolution of Dogmatism and Close-Mindedness. Psychol Rep. 2019;122(6):2406–2416.
  • Alberini CM. The role of protein synthesis during the labile phases of memory: revisiting the skepticism. Neurobiol Learn Mem. 2008;89(3):234–246.
  • Scharf MT, Woo NH, Matthew Lattal K, et al. Protein synthesis is required for the enhancement of long-term potentiation and long-term memory by spaced training. J Neurophysiol. 2002;87(6):2770–2777.
  • Jarome TJ, Helmstetter FJ. Protein degradation and protein synthesis in long-term memory formation. Front Mol Neurosci. 2014;7:61.
  • Peng J-Y, Li B-M. Protein synthesis is essential not only for consolidation but also for maintenance and post-retrieval reconsolidation of acrobatic motor skill in rats. Molecular Brain. 2009;2(1):12.
  • Lindqvist LM, Tandoc K, Topisirovic I, et al. Cross-talk between protein synthesis, energy metabolism and autophagy in cancer. Curr Opin Genet Dev. 2018;48:104–111.
  • Karbowski J. Metabolic constraints on synaptic learning and memory. J Neurophysiol. 2019;122(4):1473–1490.
  • Okano H, Hirano T, Balaban E, Learning and memory. The Proceedings of the National Academy of Sciences (PNAS), the official journal of the National Academy of Sciences (NAS). 2000;97:12403–12404. https://www.pnas.org/content/97/23/12403
  • Stuchlik A. Dynamic learning and memory, synaptic plasticity and neurogenesis: an update. Front Behav Neurosci. 2014;8:106.
  • Harris JJ, Jolivet R, Attwell D. Synaptic Energy Use and Supply. Neuron. 2012;75(5):762–777.
  • Herculano-Houzel S, Perc M. Scaling of Brain Metabolism with a Fixed Energy Budget per Neuron: implications for Neuronal Activity, Plasticity and Evolution. PLoS ONE. 2011;6(3):e17514.
  • Boshes B, Moody RR, Kupersmith MJ, et al. The role of monoamines in learning and memory consolidation.. Int J Neurol. 1975;10(1–4):172–177.
  • Jacome LF, Gautreaux C, Inagaki T, et al. Estradiol and ERβ agonists enhance recognition memory, and DPN, an ERβ agonist, alters brain monoamines. Neurobiol Learn Mem. 2010;94(4):488–498.
  • Inagaki T, Gautreaux C, Luine V. Acute estrogen treatment facilitates recognition memory consolidation and alters monoamine levels in memory-related brain areas. Horm Behav. 2010;58(3):415–426.
  • Makkar SR, Zhang SQ, Cranney J. Behavioral and neural analysis of GABA in the acquisition, consolidation, reconsolidation, and extinction of fear memory. Neuropsychopharmacology. 2010;35:1625–1652.
  • Myhrer T. Neurotransmitter systems involved in learning and memory in the rat: a meta-analysis based on studies of four behavioral tasks. Brain Res Rev. 2003;41(2–3):268–287.
  • Seyedabadi M, Fakhfouri G, Ramezani V, et al. The role of serotonin in memory: interactions with neurotransmitters and downstream signaling. Exp Brain Res. 2014;232(3):723–738.
  • Pinto‐Duarte A, Roberts AJ, Ouyang K, et al., Impairments in remote memory caused by the lack of Type 2 IP 3 receptors. Glia. 2019;67:23679.
  • Gibbs ME, Hutchinson D, Hertz L. Astrocytic involvement in learning and memory consolidation. Neurosci Biobehav Rev. 2008;32(5):927–944.
  • Alberini CM, Cruz E, Descalzi G, et al. Astrocyte glycogen and lactate: new insights into learning and memory mechanisms. GLIA. 2018;66:1244–1262.
  • Fields RD, Araque A, Johansen-Berg H, et al. Glial biology in learning and cognition. The Neuroscientist. 2014;20(5):426–431.
  • Koeppen J, Nguyen AQ, Nikolakopoulou AM, et al. Functional consequences of synapse remodeling following astrocyte-specific regulation of ephrin-B1 in the adult hippocampus. The Journal of Neuroscience. 2018;38(25):5710–5726.
  • Weber B, Barros LF. The astrocyte: powerhouse and recycling center. Cold Spring Harb Perspect Biol. 2015;7. DOI:https://doi.org/10.1101/cshperspect.a020396..
  • Klinzing JG, Niethard N, Born J. Mechanisms of systems memory consolidation during sleep. Nat Neurosci. 2019;22:1598–1610. https://www.nature.com/articles/s41593-019-0467–3
  • Rasch B, Born J. About sleep’s role in memory. Physiol Rev. 2013;93:681–766.
  • Wei Y, Krishnan GP, Bazhenov M. Synaptic mechanisms of memory consolidation during sleep slow oscillations. The Journal of Neuroscience. 2016;36(15):4231–4247.
  • DiNuzzo M, Nedergaard M. Brain energetics during the sleep–wake cycle. Curr Opin Neurobiol. 2017;47:65–72.
  • Wehr TA. A brain-warming function for REM sleep. Neurosci Biobehav Rev. 1992;16(3):379–397.
  • Plaçais P-Y, De Tredern É, Scheunemann L, et al. Upregulated energy metabolism in the Drosophila mushroom body is the trigger for long-term memory. Nat Commun. 2017;8(1). DOI:https://doi.org/10.1038/ncomms15510.
  • Laughlin SB. Energy as a constraint on the coding and processing of sensory information. Curr Opin Neurobiol. 2001;11(4):475–480.
  • Hasenstaub A, Otte S, Callaway E, et al., Metabolic cost as a unifying principle governing neuronal biophysics. Proceedings of the National Academy of Sciences of the United States of America. 2010;107:12329–12334. https://www.pnas.org/content/early/2010/06/22/0914886107
  • Laughlin SB, Sejnowski TJ. Commun Neuronal Net Sci. 2003;301:1870–1874.
  • Niven JE, Laughlin SB. Energy limitation as a selective pressure on the evolution of sensory systems. J Exp Biol. 2008;211:1792–1804.
  • Levy WB, Baxter RA. Energy Efficient Neural Codes. Neural Comput. 1996;8(3):531–543.
  • Attwell D, Laughlin SB. An Energy Budget for Signaling in the Grey Matter of the Brain, Journal of Cerebral Blood Flow &. Metabolism. 2001;21:1133–1145.
  • Alle H, Roth A, Geiger JRP. Energy-efficient action potentials in hippocampal mossy fibers. Science. 2009;325(5946):1405–1408.
  • Mitchison G. Neuronal branching patterns and the economy of cortical wiring, Proceedings of the Royal Society of London. Series B: Biological Sciences. 1991;245:151–158.
  • Bélanger M, Allaman I, Magistretti PJ. Brain energy metabolism: focus on Astrocyte-neuron metabolic cooperation. Cell Metab. 2011;14(6):724–738.
  • Preston AR, Eichenbaum H. Interplay of hippocampus and prefrontal cortex in memory. Curr Biol. 2013;23(17):R764–R773.
  • Van Kesteren MTR, Ruiter DJ, Fernández G, et al. How schema and novelty augment memory formation. Trends Neurosci. 2012;35(4):211–219.
  • Tse D, Langston RF, Kakeyama M, et al. Schemas and memory consolidation. Science. 2007;316(5821):76–82.
  • Shing YL, Brod G. Effects of Prior Knowledge on Memory: implications for Education. Mind Brain Educ. 2016;10(3):153–161.
  • Van Prooijen J-W, Krouwel APM. Extreme Political Beliefs Predict Dogmatic Intolerance. Social Psychol Personality Sci. 2017;8(3):292–300.
  • Ottati V, Price ED, Wilson C, et al. When self-perceptions of expertise increase closed-minded cognition: the earned dogmatism effect. J Exp Social Psychol. 2015;61:131–138.
  • Taber CS, Lodge M. Motivated Skepticism in the Evaluation of Political Beliefs. Am J Political Sci. 2006;50(3):755–769.
  • Seshadri KG. The neuroendocrinology of love. Indian J Endocrinol Metab. 2016;20(4):558–563.
  • Tobore TO. Towards a Comprehensive Theory of Love: the Quadruple Theory. Front Psychol. 2020;11. DOI:https://doi.org/10.3389/fpsyg.2020.00862..
  • Sternberg RJ, Sternberg K. The nature of hate. Cambridge, UK: Cambridge University Press; 2008. DOI:https://doi.org/10.1017/CBO9780511818707.
  • Timmermann WK. The Relationship between Hate Propaganda and Incitement to Genocide: a New Trend in International Law Towards Criminalization of Hate Propaganda? Leiden J Int Law. 2005;18(2):257–282.
  • Green, LL. Gender Hate Propaganda and Sexual Violence in the Rwandan Genocide: an Argument for Intersectionality in International Law. Columbia Human Rights Law Review. 2001;3:3. https://heinonline.org/HOL/Page?handle=hein.journals/colhr33&id=745&div=&collection=
  • Aviezer N. Intelligent Design versus Evolution. Rambam Maimonides Med J. 2010;1(1):e0007.
  • Carreño JE, Hansen F, Irarrázabal M, et al. Some considerations about the theory of intelligent design. Biological Res. 2009;42(2):223–232.
  • Pennock RT. C REATIONISM AND I NTELLIGENT D ESIGN. Annu Rev Genomics Hum Genet. 2003;4(1):143–163.
  • Jost, JT. Resistance to Change: a Social Psychological Perspective. Social Research: an International Quarterly. 2015;82:607–636. https://muse.jhu.edu/article/603152
  • Thorndyke PW, Yekovich FR. A critique of schema-based theories of human story memory. Poetics. 1980;9(1–3):23–49.
  • Plant KL, Stanton NA. The explanatory power of Schema Theory: theoretical foundations and future applications in Ergonomics. Ergonomics. 2013;56(1):1–15.
  • Massaad CA, Klann E. Reactive oxygen species in the regulation of synaptic plasticity and memory. Antioxid Redox Signaling. 2011;14(10):2013–2054.
  • Madore KP, Addis DR, Schacter DL. Creativity and Memory. Psychol Sci. 2015;26(9):1461–1468.
  • Andreasen NC, O’Leary DS, Cizadlo T, et al. Remembering the past: two facets of episodic memory explored with positron emission tomography. Am J Psychiatry. 1995;152:1576–1585.
  • Griffin A. Adolescent Neurological Development and Implications for Health and Well-Being. Healthcare. 2017;5(4):62.
  • Kuzawa CW, Chugani HT, Grossman LI, et al., Metabolic costs and evolutionary implications of human brain development. The Proceedings of the National Academy of Sciences (PNAS), the official journal of the National Academy of Sciences (NAS). 2014;111:13010–13015.
  • Kuzawa CW, Blair C, A hypothesis linking the energy demand of the brain to obesity risk. The Proceedings of the National Academy of Sciences (PNAS), the official journal of the National Academy of Sciences (NAS). 2019;116:13266–13275.
  • Gino F, Wiltermuth SS. Evil Genius? How Dishonesty Can Lead to Greater Creativity. Psychol Sci. 2014;25(4):973–981.
  • Gino F, Ariely D. The dark side of creativity: original thinkers can be more dishonest. J Pers Soc Psychol. 2012;102(3):445–459.
  • Ludwig AM, Mental illness and creative activity in female writers. Am J Psychiatry. 1994;151:1650–1656. https://pubmed.ncbi.nlm.nih.gov/7943456/
  • Andreasen NC. Creativity and mental illness: prevalence rates in writers and their first-degree relatives. Am J Psychiatry. 1987;144:1288–1292.
  • Paus T, Keshavan M, Giedd JN. Why do many psychiatric disorders emerge during adolescence? Nat Rev Neurosci. 2008;9(12):947–957.
  • Meyer HC, Lee FS. Translating Developmental Neuroscience to Understand Risk for Psychiatric Disorders. Am J Psychiatry. 2019;176(3):179–185.
  • Žliobaitė I. AI minds need to think about energy constraints. Nat Mach Intell. 2019;1(8):335.
  • Strubell E, Ganesh A, McCallum A, Energy and Policy Considerations for Deep Learning in NLP, ACL 2019-57th Annual Meeting of the Association for Computational Linguistics, Proceedings of the Conference.  Florence, Italy. 2019; 3645–3650. http://arxiv.org/abs/1906.02243 ( accessed 2021 Feb 28).
  • Watson D. The Rhetoric and Reality of Anthropomorphism in Artificial Intelligence. Minds Mach. 2019;29(3):417–440.
  • Cao J, Galinsky AD, Maddux WW. Does Travel Broaden the Mind? Breadth of Foreign Experiences Increases Generalized Trust. Social Psychol Personality Sci. 2014;5(5):517–525.
  • Campos JJ, Anderson DI, Barbu-Roth MA, et al. Travel Broadens the Mind. Infancy. 2000;1(2):149–219.
  • Yee Leung AK, Maddux WW, Galinsky AD, et al. Multicultural Experience Enhances Creativity: the When and How. Am Psychologist. 2008;63(3):169–181.
  • Maddux WW, Galinsky AD. Cultural borders and mental barriers: the relationship between living abroad and creativity. J Pers Soc Psychol. 2009;96(5):1047–1061.
  • Elsey JWB, Kindt M. Breaking boundaries: optimizing reconsolidation-based interventions for strong and old memories. Learn Memory. 2017;24(9):472–479.
  • Hernandez PJ, Abel T. The role of protein synthesis in memory consolidation: progress amid decades of debate. Neurobiol Learn Mem. 2008;89:293–311.
  • Frimer JA, Skitka LJ, Motyl M. Liberals and conservatives are similarly motivated to avoid exposure to one another’s opinions. J Exp Social Psychol. 2017;72:1–12.
  • Ditto PH, Lopez DF. Motivated Skepticism: use of Differential Decision Criteria for Preferred and Nonpreferred Conclusions. J Pers Soc Psychol. 1992;63(4):568–584.
  • Waddell C. Creativity and mental illness: is there a link? Can J Psychiatry. 1998;43(2):166–172.
  • Nader K, Einarsson EÖ. Memory reconsolidation: an update. Ann N Y Acad Sci. 2010;1191(1):27–41.
  • Debiec J, LeDoux JE, Nader K. Cellular and systems reconsolidation in the hippocampus. Neuron. 2002;36(3):527–538.