Medial Prefrontal Cortex Supports Recollection, But Not Familiarity, in the Rat

被引:77
作者
Farovik, Anja [1 ]
Dupont, Laura M. [1 ]
Arce, Miguel [1 ]
Eichenbaum, Howard [1 ]
机构
[1] Boston Univ, Ctr Memory & Brain, Boston, MA 02215 USA
关键词
prefrontal cortex; prelimbic; rat; recognition memory; recollection; familiarity;
D O I
10.1523/JNEUROSCI.3662-08.2008
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
There is continuing controversy about the extent to which the rodent medial prefrontal cortical area (mPFC) is functionally homologous to the dorsolateral prefrontal cortex in humans and nonhuman primates. Previous studies have compared the effects of mPFC lesions in rats to those of dorsolateral prefrontal lesions in working memory, strategy switching, and temporal ordering. None, however, has examined the role of the rodent mPFC in recognition memory, wherein, in humans, dorsolateral prefrontal damage results in a deficit in source monitoring resulting in impaired recollection. In the present study, we examined recognition memory in rats with bilateral mPFC lesions (prelimbic/infralimbic regions; ibotenic acid) using a variant of a non-match-to-sample task with manipulations of response bias that allowed for a signal detection analysis that distinguishes recollection and familiarity contributions to recognition memory. Animals with medial prefrontal lesions had a modest overall deficit in recognition with no general change in their tendency to elicit "old" or "new" responses. Signal detection analyses indicated that rats with mPFC damage had a curvilinear and symmetrical receiver operating characteristic (ROC) curve, compared with a curvilinear and asymmetrical ROC curve in control subjects, indicating that mPFC damage severely reduced recollection-based performance, while sparing familiarity. The recollection failure was associated with an impaired ability to reject new items ( increased false alarm rate), whereas the identification of old items ( hit rate) was normal. This pattern of findings is similar to that observed in humans with dorsolateral prefrontal damage and is complementary to the selective deficit in hit rate observed after hippocampal damage.
引用
收藏
页码:13428 / 13434
页数:7
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