scholarly journals Dissociating retrieval success from incidental encoding activity during emotional memory retrieval, in the medial temporal lobe

Author(s):  
Andrea T. Shafer ◽  
Florin Dolcos
Neurocase ◽  
2013 ◽  
Vol 21 (1) ◽  
pp. 23-32 ◽  
Author(s):  
Silke Lux ◽  
Valeska N. Bindrich ◽  
Hans J. Markowitsch ◽  
Gereon R. Fink

2015 ◽  
Vol 8 (2) ◽  
pp. 355 ◽  
Author(s):  
M.B. Merkow ◽  
J.F. Burke ◽  
A.R. Ramayya ◽  
A. Sharan ◽  
M.J. Kahana ◽  
...  

2008 ◽  
Vol 15 (9) ◽  
pp. 611-617 ◽  
Author(s):  
I. Tendolkar ◽  
J. Arnold ◽  
K. M. Petersson ◽  
S. Weis ◽  
A. Brockhaus-Dumke ◽  
...  

2007 ◽  
Vol 2007 ◽  
pp. 1-14 ◽  
Author(s):  
Lynn Nadel ◽  
Jenna Campbell ◽  
Lee Ryan

Multiple trace theory (MTT) predicts that hippocampal memory traces expand and strengthen as a function of repeated memory retrievals. We tested this hypothesis utilizing fMRI, comparing the effect of memory retrieval versus the mere passage of time on hippocampal activation. While undergoing fMRI scanning, participants retrieved remote autobiographical memories that had been previously retrieved either one month earlier, two days earlier, or multiple times during the preceding month. Behavioral analyses revealed that the number and consistency of memory details retrieved increased with multiple retrievals but not with the passage of time. While all three retrieval conditions activated a similar set of brain regions normally associated with autobiographical memory retrieval including medial temporal lobe structures, hippocampal activation did not change as a function of either multiple retrievals or the passage of time. However, activation in other brain regions, including the precuneus, lateral prefrontal cortex, parietal cortex, lateral temporal lobe, and perirhinal cortex increased after multiple retrievals, but was not influenced by the passage of time. These results have important implications for existing theories of long-term memory consolidation.


2014 ◽  
Vol 84 (1) ◽  
pp. 90-96 ◽  
Author(s):  
José María López-Frutos ◽  
Claudia Poch ◽  
Irene García-Morales ◽  
José María Ruiz-Vargas ◽  
Pablo Campo

NeuroImage ◽  
2001 ◽  
Vol 14 (5) ◽  
pp. 995-1003 ◽  
Author(s):  
Sophie Dupont ◽  
Yves Samson ◽  
Pierre-François Van de Moortele ◽  
Séverine Samson ◽  
Jean-Baptiste Poline ◽  
...  

2021 ◽  
Vol 15 ◽  
pp. 100383
Author(s):  
Hendrik Heinbockel ◽  
Conny W.E.M. Quaedflieg ◽  
Till R. Schneider ◽  
Andreas K. Engel ◽  
Lars Schwabe

2021 ◽  
Author(s):  
Heidrun Schultz ◽  
Jungsun Yoo ◽  
Dar Meshi ◽  
Hauke R. Heekeren

AbstractForming new memories is a fundamental part of human life, and the medial temporal lobe (MTL) is central to memory formation. Recent research suggests that within MTL, the perirhinal and parahippocampal cortices (PRC, PHC) process object and scene memory, respectively, whereas the hippocampus (HC) is agnostic to stimulus category. It is unclear, however, whether MTL category specificity extends to item encoding. Furthermore, MTL does not act in isolation: Reward-related memories are formed in interplay with the dopaminergic midbrain (substantia nigra/ventral tegmental area, SNVTA) and amygdala (AMY), but it is unclear whether reward modulates neural item encoding in a category-specific way. To address these questions, we had 39 healthy volunteers (27 for all memory-based analyses) undergo functional magnetic resonance imaging while they solved an incidental encoding task, which paired objects or scenes with high or low reward, followed by a next-day surprise recognition test. Behaviourally, high reward preferably enhanced object memory. Importantly, neural activity in PRC and PHC reflected item encoding of objects and scenes, respectively. Moreover, AMY encoding effects were selective for high-reward objects, with a similar pattern in PRC. SNVTA and HC showed no clear evidence of item encoding. The behavioural and neural asymmetry of reward-related encoding effects may be conveyed through an anterior-temporal memory system, including AMY and PRC, potentially in interplay with the ventromedial prefrontal cortex (vmPFC).


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