Early stages of memory formation in filial imprinting: Fos-like immunoreactivity and behavior in the domestic chick

Neuroscience ◽  
2004 ◽  
Vol 123 (4) ◽  
pp. 847-856 ◽  
Author(s):  
R Suge ◽  
B.J McCabe
1998 ◽  
Vol 6 (3) ◽  
pp. 17-27 ◽  
Author(s):  
Jörg Bock ◽  
Katharina Braun

Auditory filial imprinting induces quantitative changes of synaptic density in the forebrain area mediorostral neostriatum/hyperstriatum ventrale of the domestic chick. The aim of the present study was to examine the time window and the extent and quality of experience that is required for the induction of these synaptic changes. We found that a brief (30 min) experience with the imprinting situation (tone stimulus + mother surrogate) is sufficient to induce spine elimination, which is detectable on postnatal day 7, but not 80 min after the presentation of the imprinting stimuli. This synaptic reorganization requires the association of the acoustic imprinting tone with an emotional reward (mother surrogate); acoustic stimulation alone does not lead to detectable synaptic changes. The results of the present study provide further evidence that juvenile emotional learning events, such as filial imprinting, lead to a selective synaptic reorganization.


2021 ◽  
Vol 12 ◽  
Author(s):  
Maia Meparishvili ◽  
Lela Chitadze ◽  
Vincenzo Lagani ◽  
Brian McCabe ◽  
Revaz Solomonia

Visual imprinting is a learning process whereby young animals come to prefer a visual stimulus after exposure to it (training). The available evidence indicates that the intermediate medial mesopallium (IMM) in the domestic chick forebrain is a site of memory formation during visual imprinting. We have studied the role of Src, an important non-receptor tyrosine kinase, in memory formation. Amounts of total Src (Total-Src) and its two phosphorylated forms, tyrosine-416 (activated, 416P-Src) and tyrosine-527 (inhibited, 527P-Src), were measured 1 and 24 h after training in the IMM and in a control brain region, the posterior pole of nidopallium (PPN). One hour after training, in the left IMM, we observed a positive correlation between the amount of 527P-Src and learning strength that was attributable to learning, and there was also a positive correlation between 416P-Src and learning strength that was attributable to a predisposition to learn readily. Twenty-four hours after training, the amount of Total-Src increased with learning strength in both the left and right IMM, and amount of 527P-Src increased with learning strength only in the left IMM; both correlations were attributable to learning. A further, negative, correlation between learning strength and 416P-Src/Total-Src in the left IMM reflected a predisposition to learn. No learning-related changes were found in the PPN control region. We suggest that there are two pools of Src; one of them in an active state and reflecting a predisposition to learn, and the second one in an inhibited condition, which increases as a result of learning. These two pools may represent two or more signaling pathways, namely, one pathway downstream of Src activated by tyrosine-416 phosphorylation and another upstream of Src, keeping the enzyme in an inactivated state via phosphorylation of tyrosine-527.


Author(s):  
Mirko Zanon ◽  
Bastien S. Lemaire ◽  
Giorgio Vallortigara

AbstractSoon after hatching, the young of precocial species, such as domestic chicks or ducklings, learn to recognize their social partner by simply being exposed to it (imprinting process). Even artificial objects or stimuli displayed on monitor screens can effectively trigger filial imprinting, though learning is canalized by spontaneous preferences for animacy signals, such as certain kinds of motion or a face-like appearance. Imprinting is used as a behavioural paradigm for studies on memory formation, early learning and predispositions, as well as number and space cognition, and brain asymmetries. Here, we present an automatized setup to expose and/or test animals for a variety of imprinting experiments. The setup consists of a cage with two high-frequency screens at the opposite ends where stimuli are shown. Provided with a camera covering the whole space of the cage, the behaviour of the animal is recorded continuously. A graphic user interface implemented in Matlab allows a custom configuration of the experimental protocol, that together with Psychtoolbox drives the presentation of images on the screens, with accurate time scheduling and a highly precise framerate. The setup can be implemented into a complete workflow to analyse behaviour in a fully automatized way by combining Matlab (and Psychtoolbox) to control the monitor screens and stimuli, DeepLabCut to track animals’ behaviour, Python (and R) to extract data and perform statistical analyses. The automated setup allows neuro-behavioural scientists to perform standardized protocols during their experiments, with faster data collection and analyses, and reproducible results.


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