Exogenous insulin-like growth factor 2 administration enhances memory consolidation and persistence in a time-dependent manner

被引:22
作者
Lee, Younghwan [1 ,3 ]
Lee, Young Woo [1 ,3 ]
Gao, Qingtao [1 ,3 ]
Lee, Younghwa [1 ,3 ]
Lee, Hyung Eun [1 ,3 ]
Ryu, Jong Hoon [1 ,2 ,3 ]
机构
[1] Kyung Hee Univ, Dept Life & Nanopharmaceut Sci, Seoul 130701, South Korea
[2] Kyung Hee Univ, Coll Pharm, Dept Oriental Pharmaceut Sci, Seoul 130701, South Korea
[3] Kyung Hee Univ, Coll Pharm, Kyung Hee East West Pharmaceut Res Inst, Seoul 130701, South Korea
基金
新加坡国家研究基金会;
关键词
Insulin-like growth factor 2; Memory consolidation; Memory persistence; ADULT HIPPOCAMPAL NEUROGENESIS; NEUROTROPHIC FACTOR; STORAGE; EXPRESSION; BRAIN; IGF2; BDNF; AVOIDANCE; MICE;
D O I
10.1016/j.brainres.2015.07.002
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Memory consolidation is an important process for the formation of long-term memory. We have previously reported that mature brain-derived neurotrophic factor enhances memory consolidation within 9 h after initial learning. Recent studies suggest that insulin-like growth factor 2 (IGF2) significantly enhances memory consolidation and prevents forgetting. Thus, we hypothesized that IGF2 exerts its activity on cognitive performance in a time-dependent manner as observed in our previous study. In the one-trial step-through inhibitory avoidance task, we demonstrate that a bilateral injection of IGF2 into the dorsal hippocampus 6 or 9 h after training significantly enhanced the step-through latencies compared with the vehicle-treated controls in the retention trial, which was conducted 24 h after the acquisition trial. However, 12 h post-training, IGF2 injection did not increase the step-through latencies. Intriguingly, in the retention trial at 21 days after the training, hippocampal IGF2 injection 6, 9 or 12 h after the acquisition trial significantly increased the step-through latencies compared with the vehicle-treated controls. IGF2 administration at 9 h and 12 h after the acquisition trial significantly increased discrimination index and exploration time on the novel-located object in the test trial at 24h and 21 days, respectively, after the acquisition trial in the novel location recognition task. In addition, IGF2-induced an increase in the step-through latencies in the retention trial 24 h or 21 days, respectively, after the initial learning was completely abolished by co-injected anti-IGF2 receptor antibody. These results suggest that IGF2 enhances memory consolidation within 9 h after initial learning, and increased IGF2 within the 12 h after the acquisition trial, which represents a delayed consolidation phase, is also critical for memory persistence. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:466 / 473
页数:8
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