Neural mechanisms of sexual imprinting

2003 ◽  
Vol 53 (2) ◽  
pp. 89-112 ◽  
Author(s):  
Hans-Joachim Bischof

Abstract Sexual imprinting is an early learning process by which a young animal acquires information which will help in choosing a sexual partner. It consists of two separate phases, an acquisition phase where features of the social environment are learnt, and a stabilisation phase in which, guided by the previously acquired social information, a preference for a sexual partner is established and stabilised, such that it cannot be altered subsequently. The stabilisation process is short and can be controlled experimentally. This review summarises research on the neural events accompanying consolidation in those brain areas which have previously been identified as important for imprinting. It shows that the period during which consolidation can occur can be shifted only within a certain time window, and demonstrates the fast adjustment of spine densities within the imprinting areas after consolidation has started. It further suggests that long term potentiation (LTP) and long term depression (LTD)-like mechanisms may be involved in this learning process, and that the immediate early genes ZENK and c-fos are expressed within the relevant imprinting areas in the course of consolidation. Evidence is presented for a prominent role of the lateral neostriatum in the imprinting process, and also for the involvement of the hippocampus in this type of early learning.

2004 ◽  
Vol 96 (2) ◽  
pp. 188-198 ◽  
Author(s):  
Hiroshi Otani ◽  
Subrina Jesmin ◽  
Hiroko Togashi ◽  
Ichiro Sakuma ◽  
Kunihiko Nakai ◽  
...  

2016 ◽  
Vol 2016 ◽  
pp. 1-13 ◽  
Author(s):  
Pablo Muñoz ◽  
Carolina Estay ◽  
Paula Díaz ◽  
Claudio Elgueta ◽  
Álvaro O. Ardiles ◽  
...  

Although the importance of DNA methylation-dependent gene expression to neuronal plasticity is well established, the dynamics of methylation and demethylation during the induction and expression of synaptic plasticity have not been explored. Here, we combined electrophysiological, pharmacological, molecular, and immunohistochemical approaches to examine the contribution of DNA methylation and the phosphorylation of Methyl-CpG-binding protein 2 (MeCP2) to synaptic plasticity. We found that, at twenty minutes after theta burst stimulation (TBS), the DNA methylation inhibitor 5-aza-2-deoxycytidine (5AZA) impaired hippocampal long-term potentiation (LTP). Surprisingly, after two hours of TBS, when LTP had become a transcription-dependent process, 5AZA treatment had no effect. By comparing these results to those in naive slices, we found that, at two hours after TBS, an intergenic region of the RLN gene was hypomethylated and that the phosphorylation of residue S80 of MeCP2 was decreased, while the phosphorylation of residue S421 was increased. As expected, 5AZA affected only the methylation of the RLN gene and exerted no effect on MeCP2 phosphorylation patterns. In summary, our data suggest that tetanic stimulation induces critical changes in synaptic plasticity that affects both DNA methylation and the phosphorylation of MeCP2. These data also suggest that early alterations in DNA methylation are sufficient to impair the full expression of LTP.


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