Ontogeny of contextual fear memory formation, specificity, and persistence in mice

被引:60
作者
Akers, Katherine G. [1 ]
Arruda-Carvalho, Maithe [1 ,2 ]
Josselyn, Sheena A. [1 ,2 ,3 ]
Frankland, Paul W. [1 ,2 ,3 ]
机构
[1] Hosp Sick Children, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Inst Med Sci, Toronto, ON M5S 1A8, Canada
[3] Univ Toronto, Dept Physiol, Toronto, ON M5S 1A8, Canada
基金
加拿大健康研究院;
关键词
AGE-OF-ONSET; PRENATAL ALCOHOL EXPOSURE; INFANTILE AMNESIA; POSTNATAL-DEVELOPMENT; HIPPOCAMPAL DAMAGE; RETROGRADE-AMNESIA; DORSAL HIPPOCAMPUS; SYSTEM-DEVELOPMENT; MENTAL-DISORDERS; ETHANOL EXPOSURE;
D O I
10.1101/lm.027581.112
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Pinpointing the precise age when young animals begin to form memories of aversive events is valuable for understanding the onset of anxiety and mood disorders and for detecting early cognitive impairment in models of childhood-onset disorders. Although these disorders are most commonly modeled in mice, we know little regarding the development of learning and memory in this species because most previous studies have been restricted to rats. Therefore, in the present study, we constructed an ontogenetic timeline of contextual fear memory ranging from infancy to adulthood in mice. We found that the ability of mice to form long-term context-shock associations emerged similar to 13-14 d of age, which is several days earlier than previously reported for rats. Although the ability to form contextual fear memories remained stable from infancy into adulthood, infant mice had shorter-lasting memories than adolescent and adult mice. Furthermore, we found that mice subjected to fetal alcohol exposure showed a delay in the developmental emergence of contextual fear memory, illustrating the utility of this ontogenetic approach in detecting developmental delays in cognitive function stemming from maladaptive early life experience.
引用
收藏
页码:598 / 604
页数:7
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