To deliberate, remember; to anticipate, forget: Cognitive deliberation profiles underpinning active forgetting-dependent everyday-like memory performance in young and aged mice

Recalling a specific past episode that will enable us to decide which action is suited to a given present situation is a core element of everyday life. A wealth of research has demonstrated that such selective remembering is dependent upon a capacity to inhibit or provisionally ‘forget’ related yet inappropriate memory episodes which could orient behavior in unwilled directions. Everyday-like memory (EdM) refers to this type of common organizational mnemonic capacity, known to deteriorate significantly with age, putatively as a result of decline in the cognitive capacity for selective inhibition or ‘active forgetting’. Moreover, this memory retrieval-concomitant active forgetting comes at the cost of genuine amnesic weakening of the inhibited episodes, a phenomenon referred to as retrieval-induced forgetting (RIF). In the present study, we introduce a novel characterization of our previously validated mouse model of EdM in terms of the existing active forgetting and RIF literature. We also introduce novel behavioral analyses of the deliberation processes elicited by EdM challenge and use detailed multi-factorial explorations to reveal how these processes are impacted by age, temporal retention demand, difficulty of EdM challenge, and anticipation of trial outcome. Our observations indicate that deliberation requires remembering while accurate anticipation—in which a critical age-related deficit is also observed—requires active forgetting. Our results represent a significant advance towards unifying our understanding of the neurocognitive processes underpinning everyday-like memory, RIF, mnemonic deliberation, anticipatory function, and how they all are impacted by the physiological ageing process. In parallel, we present preliminary results using a transgenic mouse model which point to a fundamental role for the endocannabinoid system (eCS) in active forgetting and EdM, thereby demonstrating that deeper investigation of previously characterized age-related decline of the eCS should be a pre-clinical priority with a view to developing treatments for age-related decline of EdM function.

[1]  P. Dux,et al.  Knowledge generalization and the costs of multitasking , 2022, Nature Reviews Neuroscience.

[2]  Bárður H Joensen,et al.  Targeted memory reactivation during sleep can induce forgetting of overlapping memories , 2022, Learning & memory.

[3]  K. Wassum Amygdala-cortical collaboration in reward learning and decision making , 2022, eLife.

[4]  David P. Tomàs,et al.  Noise correlations in neural ensemble activity limit the accuracy of hippocampal spatial representations , 2022, Nature Communications.

[5]  V. Lagani,et al.  Age-related changes in medial septal cholinergic and GABAergic projection neurons and hippocampal neurotransmitter receptors: relationship with memory impairment , 2022, Experimental Brain Research.

[6]  V. Sohal,et al.  Top-down control of hippocampal signal-to-noise by prefrontal long-range inhibition , 2021, Cell.

[7]  R. Faull,et al.  The effect of age and sex on the expression of GABA signaling components in the human hippocampus and entorhinal cortex , 2021, Scientific Reports.

[8]  L. Medina,et al.  Refocusing neuroscience: moving away from mental categories and towards complex behaviours , 2021, Philosophical Transactions of the Royal Society B.

[9]  N. Schmitzer-Torbert,et al.  Vicarious Trial-and-Error Is Enhanced During Deliberation in Human Virtual Navigation in a Translational Foraging Task , 2021, Frontiers in Behavioral Neuroscience.

[10]  M. Costanzi,et al.  Forgetting Unwanted Memories: Active Forgetting and Implications for the Development of Psychological Disorders , 2021, Journal of personalized medicine.

[11]  T. Hnasko,et al.  Mechanism for differential recruitment of orbitostriatal transmission during actions and outcomes following chronic alcohol exposure , 2021, eLife.

[12]  M. Walton,et al.  Complementary task representations in hippocampus and prefrontal cortex for generalizing the structure of problems , 2021, bioRxiv.

[13]  Michael C. Anderson,et al.  Active Forgetting: Adaptation of Memory by Prefrontal Control. , 2020, Annual review of psychology.

[14]  Jaime Fern'andez del R'io,et al.  Array programming with NumPy , 2020, Nature.

[15]  J. Changeux,et al.  Conscious Processing and the Global Neuronal Workspace Hypothesis , 2020, Neuron.

[16]  T. Shackelford,et al.  Encyclopedia of Animal Cognition and Behavior , 2020 .

[17]  T. Taniuchi,et al.  Directed forgetting in rats: Evidence for active memory control? , 2019, Learning & Behavior.

[18]  Karel Butz Rehearsal , 2019, Achieving Musical Success in the String Classroom.

[19]  Paul Cisek,et al.  The Urge to Decide and Act: Implications for Brain Function and Dysfunction , 2019, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.

[20]  M. Kliegel,et al.  Examining the role of rehearsal in old–old adults’ working memory , 2019, European journal of ageing.

[21]  Jozsef Csicsvari,et al.  Assembly Responses of Hippocampal CA1 Place Cells Predict Learned Behavior in Goal-Directed Spatial Tasks on the Radial Eight-Arm Maze , 2019, Neuron.

[22]  R. Faull,et al.  Sex- and age-related changes in GABA signaling components in the human cortex , 2019, Biology of Sex Differences.

[23]  Michael C. Anderson,et al.  A retrieval-specific mechanism of adaptive forgetting in the mammalian brain , 2018, Nature Communications.

[24]  G. Marsicano,et al.  Hippocampal CB1 Receptors Control Incidental Associations , 2018, Neuron.

[25]  Brian M. Sweis,et al.  Mice learn to avoid regret , 2018, PLoS biology.

[26]  H. Eichenbaum What Versus Where: Non-spatial Aspects of Memory Representation by the Hippocampus. , 2016, Current topics in behavioral neurosciences.

[27]  Michael C. Anderson,et al.  Hippocampal GABA enables inhibitory control over unwanted thoughts , 2017, Nature Communications.

[28]  Sara E. Morrison,et al.  Limbic-motor integration by neural excitations and inhibitions in the nucleus accumbens. , 2017, Journal of neurophysiology.

[29]  T. Ulas,et al.  A chronic low dose of Δ9-tetrahydrocannabinol (THC) restores cognitive function in old mice , 2017, Nature Medicine.

[30]  Alice Shaam Al Abed,et al.  Estradiol enhances retention but not organization of hippocampus-dependent memory in intact male mice , 2016, Psychoneuroendocrinology.

[31]  Karl J. Friston,et al.  Active Inference, epistemic value, and vicarious trial and error , 2016, Learning & memory.

[32]  K. Deisseroth,et al.  Endocannabinoid Modulation of Orbitostriatal Circuits Gates Habit Formation , 2016, Neuron.

[33]  Michael R. Dulas,et al.  Age-related changes in overcoming proactive interference in associative memory: The role of PFC-mediated executive control processes at retrieval , 2016, NeuroImage.

[34]  J. Krakauer,et al.  The basal ganglia: from motor commands to the control of vigor , 2016, Current Opinion in Neurobiology.

[35]  Michael C. Anderson,et al.  Inducing amnesia through systemic suppression , 2016, Nature Communications.

[36]  W. Schultz Dopamine reward prediction error coding , 2016, Dialogues in clinical neuroscience.

[37]  M. Mather The Affective Neuroscience of Aging. , 2016, Annual review of psychology.

[38]  Önder Albayram,et al.  Physiological impact of CB1 receptor expression by hippocampal GABAergic interneurons , 2016, Pflügers Archiv - European Journal of Physiology.

[39]  M. Yassa,et al.  Neurocognitive Aging and the Hippocampus across Species , 2015, Trends in Neurosciences.

[40]  C. Lustig,et al.  Questions of age differences in interference control: When and how, not if? , 2015, Brain Research.

[41]  Michael C. Anderson,et al.  Retrieval induces adaptive forgetting of competing memories via cortical pattern suppression , 2015, Nature Neuroscience.

[42]  Blake S. Porter,et al.  Hippocampal Representation of Related and Opposing Memories Develop within Distinct, Hierarchically Organized Neural Schemas , 2014, Neuron.

[43]  A. Redish,et al.  Behavioral and neurophysiological correlates of regret in rat decision-making on a neuroeconomic task , 2014, Nature Neuroscience.

[44]  Hervé Abdi,et al.  Memory Reactivation in Healthy Aging: Evidence of Stimulus-Specific Dedifferentiation , 2014, The Journal of Neuroscience.

[45]  Jennifer C. Weeks,et al.  The disruptive – and beneficial – effects of distraction on older adults’ cognitive performance , 2014, Front. Psychol..

[46]  F. Pulvermüller How neurons make meaning: brain mechanisms for embodied and abstract-symbolic semantics , 2013, Trends in Cognitive Sciences.

[47]  R. Costa,et al.  Orbitofrontal and striatal circuits dynamically encode the shift between goal-directed and habitual actions , 2013, Nature Communications.

[48]  Lynn Hasher,et al.  Interference from previous distraction disrupts older adults' memory. , 2013, The journals of gerontology. Series B, Psychological sciences and social sciences.

[49]  L. Nadel,et al.  Decay happens: the role of active forgetting in memory , 2013, Trends in Cognitive Sciences.

[50]  Bérengère Staub,et al.  Sustained attention in the elderly: What do we know and what does it tell us about cognitive aging? , 2013, Ageing Research Reviews.

[51]  C. Lustig,et al.  Everyday memory errors in older adults , 2013, Neuropsychology, development, and cognition. Section B, Aging, neuropsychology and cognition.

[52]  A. Bilkei-Gorzo,et al.  The endocannabinoid system in normal and pathological brain ageing , 2012, Philosophical Transactions of the Royal Society B: Biological Sciences.

[53]  P. Dudchenko,et al.  The neural substrates of deliberative decision making: contrasting effects of hippocampus lesions on performance and vicarious trial-and-error behavior in a spatial memory task and a visual discrimination task , 2012, Front. Behav. Neurosci..

[54]  Wei Wang,et al.  Acute Cannabinoids Impair Working Memory through Astroglial CB1 Receptor Modulation of Hippocampal LTD , 2012, Cell.

[55]  Aline Marighetto,et al.  Studying the impact of aging on memory systems: contribution of two behavioral models in the mouse. , 2012, Current topics in behavioral neurosciences.

[56]  Beat Lutz,et al.  Role of CB1 cannabinoid receptors on GABAergic neurons in brain aging , 2011, Proceedings of the National Academy of Sciences.

[57]  Kenneth R. Light,et al.  Longitudinal attentional engagement rescues mice from age-related cognitive declines and cognitive inflexibility. , 2011, Learning & memory.

[58]  J. Changeux,et al.  Experimental and Theoretical Approaches to Conscious Processing , 2011, Neuron.

[59]  L. Panlilio,et al.  Automatic recording of mediating behavior in delayed matching- and nonmatching-to-position procedures in rats , 2011, Psychopharmacology.

[60]  Amanda M. Kutz,et al.  Increased memory load-related frontal activation after estradiol treatment in postmenopausal women , 2010, Hormones and Behavior.

[61]  Shauna M. Stark,et al.  Individual differences in spatial pattern separation performance associated with healthy aging in humans. , 2010, Learning & memory.

[62]  M. Gallagher,et al.  Bridging neurocognitive aging and disease modification: targeting functional mechanisms of memory impairment. , 2010, Current Alzheimer research.

[63]  A. Damasio Self comes to mind : constructing the conscious brain , 2010 .

[64]  N. Cohen,et al.  Relational Memory and the Hippocampus: Representations and Methods , 2009, Front. Neurosci..

[65]  Adam Johnson,et al.  Looking for cognition in the structure within the noise , 2009, Trends in Cognitive Sciences.

[66]  David G. Amaral,et al.  Neuroanatomy of the primate amygdala. , 2009 .

[67]  Eric A. Zilli,et al.  Modeling the role of working memory and episodic memory in behavioral tasks , 2008, Hippocampus.

[68]  N. Mons,et al.  Retinoid Hyposignaling Contributes to Aging-Related Decline in Hippocampal Function in Short-Term/Working Memory Organization and Long-Term Declarative Memory Encoding in Mice , 2008, The Journal of Neuroscience.

[69]  A. Marighetto,et al.  Comparative effects of the α7 nicotinic partial agonist, S 24795, and the cholinesterase inhibitor, donepezil, against aging-related deficits in declarative and working memory in mice , 2008, Psychopharmacology.

[70]  Adam Johnson,et al.  Neural Ensembles in CA3 Transiently Encode Paths Forward of the Animal at a Decision Point , 2007, The Journal of Neuroscience.

[71]  M. Tamosiunaite,et al.  Hippocampal CA1 Place Cells Encode Intended Destination on a Maze with Multiple Choice Points , 2007, The Journal of Neuroscience.

[72]  H. Eichenbaum,et al.  Neurocognitive aging: prior memories hinder new hippocampal encoding , 2006, Trends in Neurosciences.

[73]  Beat Lutz,et al.  The Endocannabinoid System Controls Key Epileptogenic Circuits in the Hippocampus , 2006, Neuron.

[74]  D. Tranel,et al.  Psychophysiological anticipation of positive outcomes promotes advantageous decision-making in normal older persons. , 2006, International journal of psychophysiology : official journal of the International Organization of Psychophysiology.

[75]  J. Rawlins,et al.  T-maze alternation in the rodent , 2006, Nature Protocols.

[76]  Antonio Damasio,et al.  The somatic marker hypothesis: A neural theory of economic decision , 2005, Games Econ. Behav..

[77]  Chris R Brewin,et al.  Working memory capacity and suppression of intrusive thoughts. , 2005, Journal of behavior therapy and experimental psychiatry.

[78]  H. Eichenbaum Hippocampus Cognitive Processes and Neural Representations that Underlie Declarative Memory , 2004, Neuron.

[79]  M. Shapiro,et al.  Prospective and Retrospective Memory Coding in the Hippocampus , 2003, Neuron.

[80]  J. Changeux,et al.  A neuronal network model linking subjective reports and objective physiological data during conscious perception , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[81]  K. Unsicker,et al.  Morphological alterations in the amygdala and hippocampus of mice during ageing , 2002, The European journal of neuroscience.

[82]  B. Baars The conscious access hypothesis: origins and recent evidence , 2002, Trends in Cognitive Sciences.

[83]  J. Gregory Trafton,et al.  Memory for goals: an activation-based model , 2002, Cogn. Sci..

[84]  A. Grace,et al.  Dopamine Attenuates Prefrontal Cortical Suppression of Sensory Inputs to the Basolateral Amygdala of Rats , 2001, The Journal of Neuroscience.

[85]  S A Deadwyler,et al.  Cannabinoids Reveal the Necessity of Hippocampal Neural Encoding for Short-Term Memory in Rats , 2000, The Journal of Neuroscience.

[86]  M. Ekker,et al.  A Highly Conserved Enhancer in the Dlx5/Dlx6Intergenic Region is the Site of Cross-Regulatory Interactions betweenDlx Genes in the Embryonic Forebrain , 2000, The Journal of Neuroscience.

[87]  C. Lebiere,et al.  The Atomic Components of Thought , 1998 .

[88]  J. Panksepp Affective Neuroscience: The Foundations of Human and Animal Emotions , 1998 .

[89]  B. Baars In the theater of consciousness : the workspace of the mind , 1997 .

[90]  D. Hu,et al.  A simple test of the vicarious trial-and-error hypothesis of hippocampal function. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[91]  Michael C. Anderson,et al.  Remembering can cause forgetting: retrieval dynamics in long-term memory. , 1994, Journal of experimental psychology. Learning, memory, and cognition.

[92]  Richard Reviewer-Granger Unified Theories of Cognition , 1991, Journal of Cognitive Neuroscience.

[93]  B. Baars A cognitive theory of consciousness , 1988 .

[94]  W. N. Dember,et al.  Spontaneous alternation behavior in animals: A review , 1986 .

[95]  J. Gibson The Ecological Approach to Visual Perception , 1979 .

[96]  B. Jaffe Cognitive Therapy and the Emotional Disorders , 1977 .

[97]  W. N. Dember,et al.  Spontaneous alternation behavior. , 1958, Psychological bulletin.

[98]  J. G. Taylor,et al.  Vicarious trial and error. , 1951, Psychological review.

[99]  E. Tolman Cognitive maps in rats and men. , 1948, Psychological review.

[100]  E. Tolman Prediction of vicarious trial and error by means of the schematic sowbug. , 1939 .

[101]  K. F. Muenzinger Vicarious Trial and Error at a Point of Choice: I. A General Survey of its Relation to Learning Efficiency , 1938 .

[102]  F. W. Irwin Purposive Behavior in Animals and Men , 1932, The Psychological Clinic.

[103]  William B. Borgers DEMOCRACY AND EDUCATION. , 1919 .