Memory and the hippocampus: A synthesis from findings with rats, monkeys, and humans.
Abstract
This article considers the role of the hippocampus in memory function. A central thesis is that work with rats, monkeys, and humans--which has sometimes seemed to proceed independently in 3 separate literatures--is now largely in agreement about the function of the hippocampus and related structures. A biological perspective is presented, which proposes multiple memory systems with different functions and distinct anatomical organizations. The hippocampus (together with anatomically related structures) is essential for a specific kind of memory, here termed declarative memory (similar terms include explicit and relational). Declarative memory is contrasted with a heterogeneous collection of nondeclarative (implicit) memory abilities that do not require the hippocampus (skills and habits, simple conditioning, and the phenomenon of priming). The hippocampus is needed temporarily to bind together distributed sites in neocortex that together represent a whole memory.
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The hippocampus rapidly and automatically binds together disparate cortical representations into a unitary representation that can then be recalled by partial retrieval cues at a later time.
“The hippocampus rapidly and automatically binds together disparate cortical representations into a unitary representation that can then be recalled by partial retrieval cues at a later time+”
From AT THE INTERFACE: DYNAMIC INTERACTIONS OF EXPLICIT AND IMPLICIT LANGUAGE KNOWLEDGE (2005) · cites this paper as Squire, 1992
The hippocampus is a medial temporal lobe region adjacent to the amygdala that is implicated in declarative memory, contextual memory and fear conditioning.
“the hippocampus, a medial temporal lobe region adjacent to the amygdala that is implicated in declarative memory,27 contextual memory28 and fear conditioning,29”
From Altered resting-state amygdala functional connectivity in men with posttraumatic stress disorder (2012) · cites this paper as [27]
The hippocampus is key for recent memory formation.
“The hippocampus, a brain structure deep in the temporal lobe, is key for recent memory formation (13–15).”
From Reduced glucose tolerance is associated with poor memory performance and hippocampal atrophy among normal elderly (2003) · cites this paper as [15]
Both the standard consolidation model and memory transformation accounts predict that HF activity during retrieval should decline with increasing retention intervals, although they assign different explanations to this decline.
“Both the standard consolidation model and memory transformation accounts predict that HF activity during retrieval should decline with increasing retention intervals, although they assign different explanations to this decline.”
From Delay-dependent contributions of medial temporal lobe regions to episodic memory retrieval (2015) · cites this paper as Squire, 1992
SCT argues that initially the hippocampus is involved in processing spatial memories, and that over time representations in neocortical regions are strengthened, reducing the demand on the hippocampus.
“the standard consolidation theory (SCT) argues that initially the hippocampus is involved in processing the spatial memories, and that over time the representations in neocortical regions are strengthened, reducing the demand on the hippocampus (Squire 1992; Squire and Zola-Morgan 1998).”
From Hippocampal and Retrosplenial Goal Distance Coding After Long-term Consolidation of a Real-World Environment (2019) · cites this paper as Squire 1992
Retention of declarative memory critically depends on the integrity of the hippocampus and benefits specifically from early nocturnal sleep, in which SWS predominates and cortisol concentrations are minimal.
“Retention of declarative memory critically depends on the integrity of the hippocampus and has been shown to benefit specifically from early nocturnal sleep, in which SWS predominates and cortisol concentrations are minimal [52, 53].”
From Impact of Sleep and Its Disturbances on Hypothalamo-Pituitary-Adrenal Axis Activity (2010) · cites this paper as [52]
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References 272 · Cited by 5,376
- Authors
- Squire, L. R.
- Affiliations
- Veterans Health Administration (US)
- Corresponding author
- Squire, Larry R.
- ORCID
- Squire, Larry R.
- Venue
- Psychological Review
- Published
- 1992
- Volume
- 99
- Issue
- 2
- Pages
- 195-231
- ISSN
- 0033-295X (ISSN-L)
- 1939-1471
- OpenAlex
- W1984214648
- Semantic Scholar
- 69f6963992e7b82f6c58855af35d661e3fea6036
- Cited by
- 5,376
- References
- 272
- Citations by year
- 2026: 51 · 2025: 90 · 2024: 105 · 2023: 90 · 2022: 94 · 2021: 114 · 2020: 158 · 2019: 174 · 2018: 165 · 2017: 167 · 2016: 185 · 2015: 179 · 2014: 205 · 2013: 194 · 2012: 192
- FWCI
- 86.16
- Type
- journal article
- Language
- en
- Update notices
- correction (2006-07-10)
- Open access
- closed
- Locations
- Psychological Review (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Mental Health (MH24600)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Keywords
- hippocampus, memory systems, declarative memory, relational memory, implicit memory, priming, conditioning, neocortex, memory binding
- MeSH terms
- Animals, Haplorhini, Attention, Brain Mapping, Cerebral Cortex, Hippocampus, Humans, Learning, Memory, Neural Pathways, Rats
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