Modulation of memory storage
Abstract
For several decades, the concept of modulation of memory storage has significantly influenced research investigating neurobiological memory mechanisms. New evidence provides additional support for the view that stress hormones released during emotionally arousing situations modulate memory processes. Recent experiments have investigated the role of sympathetic adrenomedullary hormones in emotional memory in humans, as well as the role of adrenocortical hormones, primarily in animal studies. Further, it is becoming increasingly clear that the sympathetic adrenomedullary and the pituitary adrenocortical systems interact to modulate memory storage. Other new evidence emphasizes the role of peripheral influences to the brain on emotional memory, as well as the critical contribution of the amygdaloid complex in modulation of memory by emotional arousal.
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Acute mild stress exposure has no effect on or can actually improve memory consolidation functions of the hippocampus and amygdala.
“By contrast, acute mild stress exposure has no effect on or can actually improve the memory consolidation functions of the hippocampus and the amygdala35,36.”
From Stress signalling pathways that impair prefrontal cortex structure and function (2009) · cites this paper as [36]
Watching an upsetting video enhanced the memory consolidation of the emotionally charged events in the film.
“In contrast to the impairments in dlPFC working memory, an earlier study showed that watching an upsetting video enhanced the memory consolidation of the emotionally charged events in the film34.”
From Stress weakens prefrontal networks: molecular insults to higher cognition (2015) · cites this paper as [34]
This improvement in memory consolidation correlated with increased activity in the amygdala while the subject watched the video.
“This improvement in memory consolidation correlated with increased activity in the amygdala while the subject watched the video34.”
From Stress weakens prefrontal networks: molecular insults to higher cognition (2015) · cites this paper as [34]
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“Presumably, the stimulation of peripheral -adrenergic receptors during emotionally arousing events modulates the HR changes (Cahill and McGaugh, 1996).”
BackgroundCarvedilol affects the physiological and behavioral response to smoked cocaine in humans.
Sofuoglu, M., Brown, S., Babb, D. A., Pentel, P., & Hatsukami, D. K. (2000) · Drug and Alcohol Dependence · doi:10.1016/s0376-8716(00)80009-5 · Cited by 64 · see citing works
A Review of the Neural and Behavioral Consequences for Unitizing Emotional and Neutral Information
Murray, B. D., & Kensinger, E. A. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00042 · Cited by 61 · see citing works
“…role in the modulation of emotional memories – via its interaction with other MTL regions – has been well established (Gallagher and Chiba, 1996; Cahill and McGaugh, 1998; Kensinger and Schacter, 2006), and although its role has been investigated more thoroughly for memories that are…”
BackgroundOrr, S., Milad, M., Metzger, L., Lasko, N., Gilbertson, M., & Pitman, R. (2006) · Biological Psychology · doi:10.1016/j.biopsycho.2006.05.001 · Cited by 63 · see citing works
“Using an inhibitory avoidance procedure in animals, McGaugh and colleagues have shown that administration of propranolol, a b-adrenergic blocker, prior to, or immediately after, training inhibited the enhancement effects of norepinephrine on memory consolidation (Cahill and McGaugh, 1996; Miranda et al., 2003; Salinas…”
BackgroundMethodMottet, T., Parker‐Raley, J., Beebe, S. A., & Cunningham, C. B. (2007) · Communication Education · doi:10.1080/03634520601164259 · Cited by 62 · see citing works
“His conclusions are informed by Cahill and McGaugh (1998), who examined how arousal and stress impacted hormones and glucose levels, and ultimately learning.”
Background■ REVIEW : Stress and Sex Effects on Associative Learning: For Better or for Worse
Shors, T. (1998) · The Neuroscientist · doi:10.1177/107385849800400517 · Cited by 61 · see citing works
“They also experience neuron loss in the amygdala (6, 7), a brain structure involved in emotion and the modulation of memory by exposure to emotional events (8-10).”
BackgroundKindt, M., Van den Hout, M., & Buck, N. (2005) · Journal of Behavior Therapy and Experimental Psychiatry · doi:10.1016/j.jbtep.2004.11.005 · Cited by 60 · see citing works
REM sleep enhancement induced by different procedures improves memory retention in rats
Wetzel, W., Wagner, T., & Balschun, D. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02890.x · Cited by 58 · see citing works
Anterior medial temporal lobe in human cognition: Memory for fear and the unexpected
Strange, B. A., & Dolan, R. J. (2006) · Cognitive Neuropsychiatry · doi:10.1080/13546800500305096 · Cited by 60 · see citing works
Power, A. E., & McGaugh, J. L. (2002) · Neurobiology of Learning and Memory · doi:10.1006/nlme.2001.4030 · Cited by 57 · see citing works
Self-citationYiannakas, A., & Rosenblum, K. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00335 · Cited by 69 · see citing works
“Indeed neural substrates for feeling states initially formed subcortically are sufficient for retrieval, despite their long-term storage in the cortex (Cahill and MacGaugh, 1996).”
BackgroundRoesler, R., Vianna, M., de-Paris, F., & Quevedo, J. (1999) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1999.3910 · Cited by 56 · see citing works
c-Jun N-terminal kinases in memory and synaptic plasticity
Sherrin, T., Blank, T., & Todorovic, C. (2011) · Reviews in the Neurosciences · doi:10.1515/rns.2011.032 · Cited by 56 · see citing works
A test to identify judgement bias in mice
Boleij, H., Klooster, J. G. L. T., Lavrijsen, M., Kirchhoff, S., Arndt, S. S., & Ohl, F. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.04.039 · Cited by 53 · see citing works
Roles of β-adrenergic receptors in Alzheimer's disease: Implications for novel therapeutics
Yu, J., Wang, N., Ma, T., Jiang, H. F., Guan, J., & Tan, L. (2010) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2010.11.004 · Cited by 50 · see citing works
Holahan, M., & White, N. (2002) · Neurobiology of Learning and Memory · doi:10.1006/nlme.2001.4012 · Cited by 55 · see citing works
Effect of the Estrous Cycle on Water Maze Acquisition Depends on the Temperature of the Water.
Rubinow, M. J., Arseneau, L. M., Beverly, J. L., & Juraska, J. M. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.4.863 · Cited by 50 · see citing works
Finsterwald, C., Steinmetz, A. B., Travaglia, A., & Alberini, C. M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0771-15.2015 · Cited by 48 · see citing works
“…or stress are beneficial for strengthening memory up to an optimal level, after which, however, an additional rise in stress leads to a decrease or loss of memory (Cahill and McGaugh, 1996; Diamond et al., 2007; Sandi and PineloReceived Feb. 25, 2015; revised Sept. 22, 2015; accepted Oct. 22, 2015.”
BackgroundThe biochemistry of memory formation and its regulation by hormones and neuromodulators
Izquierdo, I., & Medina, J. (1997) · Psychobiology · doi:10.3758/bf03327022 · Cited by 53 · see citing works
“Some data suggest that the main role of the amygdala would be to actually modulate memories laid down in the hippocampus and other places, particularly the caudate nucleus (Cahill & McGaugh, 1996; McGaugh et ai., 1995).”
BackgroundInfluentialDa Silva, W. C., Cardoso, G., Bonini, J. S., Benetti, F., & Izquierdo, I. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1302356110 · Cited by 52 · see citing works
“M maintenance or persistence depends on the degree of emotional arousal present at the time of consolidation (1, 2), and apparently on several different biochemical and behavioral variables over the next several hours or days (3–9), especially in the hippocampus, which is widely recognized as the region in charge of c…”
Barros, D., Ramirez, M., & Izquierdo, I. (2005) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2004.10.001 · Cited by 52 · see citing works
“Inhibitory avoidance is strongly modulated by the basolateral amygdala (BLA) in the Wrst few minutes of consolidation (Bianchin, Mello e Souza, Medina, & Izquierdo, 1999; Cahill & McGaugh, 1996).”
Background
- Authors
- Cahill, L., & McGaugh, J. L.
- Affiliations
- University of California, Irvine (US)
- Corresponding author
- Cahill, Larry
- McGaugh, James L
- Venue
- Current Opinion in Neurobiology
- Publisher
- Elsevier BV
- Published
- 1996-04
- Volume
- 6
- Issue
- 2
- Pages
- 237-242
- ISSN
- 0959-4388 (ISSN-L)
- OpenAlex
- W2022694793
- Cited by
- 301
- References
- 66
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 6 · 2023: 6 · 2022: 4 · 2021: 10 · 2020: 9 · 2019: 5 · 2018: 4 · 2017: 8 · 2016: 13 · 2015: 8 · 2014: 10 · 2013: 9 · 2012: 14
- FWCI
- 2.29
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Current Opinion in Neurobiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Mental Health (MH12526)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Keywords
- memory modulation, memory storage, emotional memory, stress hormones, sympathoadrenal system, adrenal cortex hormones, hypothalamic-pituitary-adrenal axis, amygdala, emotional arousal
- MeSH terms
- Adrenal Cortex Hormones, Amygdala, Animals, Brain, Catecholamines, Glucose, Humans, Memory, Peripheral Nerves
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