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.2019 Dec 26;116(52):26210-26216.
doi: 10.1073/pnas.1902278116. Epub 2019 Dec 23.

Nonhuman primate models of hippocampal development and dysfunction

Affiliations

Nonhuman primate models of hippocampal development and dysfunction

Jocelyne Bachevalier. Proc Natl Acad Sci U S A..

Abstract

Nonhuman primates provide highly valuable animal models that have significantly advanced our understanding of numerous behavioral and biological phenomena in humans. Here, we reviewed a series of developmental neuropsychological studies that informed us on the timing of development of the hippocampus and of hippocampal-dependent cognitive functions in primates. Data indicate that, in primates, the emergence of adult-like proficiency on behavioral tasks sensitive to hippocampal dysfunction is a stepwise process and reflects the gradual maturation of different hippocampal circuits and their connections with other neural structures. Profound and persistent memory loss resulting from insult to the hippocampus in infancy was absent in early infancy but became evident later in childhood and persisted in adulthood, indicating very little sparing or recovery of function. Finally, the early hippocampal insult resulted in both adaptive and maladaptive neuroplasticity: i.e., sparing contextual memory, but affecting working memory processes as well as emotional reactivity and hypothalamic-pituitary-adrenal (HPA) axis functioning. The results provide significant information on the emergence of hippocampal-dependent functions in humans, on the time course of memory impairment in human cases with early hippocampal insult, and on the clinical implication of the hippocampus in developmental neuropsychiatric disorders.

Keywords: developmental amnesia; recognition memory; schizophrenia; spatial memory; working memory.

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Conflict of interest statement

The author declares no conflict of interest.

Figures

Fig. 1.
Fig. 1.
Thionin-stained section through the midbody of the hippocampus of rhesus monkeys. Arrows represent the flow of information through the trisynaptic circuits: i.e., Erh to DG to CA3 to CA2 to CA1 to Sub and back to ERh (continuous white arrow) and a more direct pathway (dashed white arrow). For both pathways, information from medial temporal cortical areas is relayed within the entorhinal cortex (black arrows). CA3, CA2, CA1, fields of the hippocampus proper; DG, dentate gyrus; ERh, entorhinal cortex; PHG, parahippocampal cortical areas; PRh, perirhinal cortex; Sub, subiculum.
Fig. 2.
Fig. 2.
Exemplars of stimuli used in each of the 3 VPC tasks. New stimuli were used for each trial of a task and across all 3 tasks. For the Object-VPC, the comparison was between a single familiar object and novel objects, and delays between familiarization and recognition test varied between 10 s and 120 s. For the Location-VPC, the comparison was between a single object in a location of the screen and the same object in a new location. For the Object-in-Place VPC, the comparison was between an array of 5 objects and the same objects with permuted locations of 3 of the objects. For the last 2 spatial VPC tasks, the delays between familiarization and recognition test were set at 5 s.
See this image and copyright information in PMC

References

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