» Articles » PMID: 10097158

Segregating the Functions of Human Hippocampus

Overview
Specialty Science
Date 1999 Mar 31
PMID 10097158
Citations 123
Authors
Affiliations
Soon will be listed here.
Abstract

It is now accepted that hippocampal lesions impair episodic memory. However, the precise functional role of the hippocampus in episodic memory remains elusive. Recent functional imaging data implicate the hippocampus in processing novelty, a finding supported by human in vivo recordings and event-related potential studies. Here we measure hippocampal responses to novelty, using functional MRI (fMRI), during an item-learning paradigm generated from an artificial grammar system. During learning, two distinct types of novelty were periodically introduced: perceptual novelty, pertaining to the physical characteristics of stimuli (in this case visual characteristics), and exemplar novelty, reflecting semantic characteristics of stimuli (in this case grammatical status within a rule system). We demonstrate a left anterior hippocampal response to both types of novelty and adaptation of these responses with stimulus familiarity. By contrast to these novelty effects, we also show bilateral posterior hippocampal responses with increasing exemplar familiarity. These results suggest a functional dissociation within the hippocampus with respect to the relative familiarity of study items. Neural responses in anterior hippocampus index generic novelty, whereas posterior hippocampal responses index familiarity to stimuli that have behavioral relevance (i.e., only exemplar familiarity). These findings add to recent evidence for functional segregation within the human hippocampus during learning.

Citing Articles

Meta-analytic connectivity perturbation analysis (MACPA): a new method for enhanced precision in fMRI connectivity analysis.

Cauda F, Manuello J, Crocetta A, Duca S, Costa T, Liloia D Brain Struct Funct. 2024; 230(1):17.

PMID: 39718568 DOI: 10.1007/s00429-024-02867-4.


Social and nonsocial environmental loss have differential effects on ventral hippocampus-dependent behavior and inhibitory synaptic markers in adult male mice.

Gore I, Brown C, Waters R, Gould E Learn Mem. 2024; 31(12).

PMID: 39681456 PMC: 11662144. DOI: 10.1101/lm.053968.124.


Neural Mechanisms of Learning and Consolidation of Morphologically Derived Words in a Novel Language: Evidence From Hebrew Speakers.

Nathaniel U, Eidelsztein S, Geskin K, Yamasaki B, Nir B, Dronjic V Neurobiol Lang (Camb). 2024; 5(4):864-900.

PMID: 39301207 PMC: 11410356. DOI: 10.1162/nol_a_00150.


Connecting to the long axis.

Strange B Elife. 2022; 11.

PMID: 36346216 PMC: 9643000. DOI: 10.7554/eLife.83718.


Relations between physical activity and hippocampal functional connectivity: Modulating role of mind wandering.

Shi D, Geng F, Hao X, Huang K, Hu Y Front Hum Neurosci. 2022; 16:950893.

PMID: 36262959 PMC: 9573939. DOI: 10.3389/fnhum.2022.950893.


References
1.
Schacter D, Alpert N, Savage C, Rauch S, Albert M . Conscious recollection and the human hippocampal formation: evidence from positron emission tomography. Proc Natl Acad Sci U S A. 1996; 93(1):321-5. PMC: 40230. DOI: 10.1073/pnas.93.1.321. View

2.
Lepage M, Habib R, Tulving E . Hippocampal PET activations of memory encoding and retrieval: the HIPER model. Hippocampus. 1998; 8(4):313-22. DOI: 10.1002/(SICI)1098-1063(1998)8:4<313::AID-HIPO1>3.0.CO;2-I. View

3.
Martin A, Wiggs C, Weisberg J . Modulation of human medial temporal lobe activity by form, meaning, and experience. Hippocampus. 1997; 7(6):587-93. DOI: 10.1002/(SICI)1098-1063(1997)7:6<587::AID-HIPO1>3.0.CO;2-C. View

4.
Elger C, Grunwald T, Lehnertz K, Kutas M, Helmstaedter C, Brockhaus A . Human temporal lobe potentials in verbal learning and memory processes. Neuropsychologia. 1997; 35(5):657-67. DOI: 10.1016/s0028-3932(96)00110-8. View

5.
Knight R . Contribution of human hippocampal region to novelty detection. Nature. 1996; 383(6597):256-9. DOI: 10.1038/383256a0. View