scholarly journals Spontaneous Object Recognition in the Göttingen Minipig

2002 ◽  
Vol 9 (4) ◽  
pp. 255-259 ◽  
Author(s):  
Anette Moustgaard ◽  
Nanna Marie Lind ◽  
Ralf Hemmingsen ◽  
Axel Kornerup Hansen

Göttingen minipigs were tested in an object recognition procedure based on spontaneous exploration. Eight pigs were exposed to two similar objects in a sample trial and after a one-hour delay exposed to two objects, one familiar and one novel, in a test trial. The pigs explored the novel object significantly more than the familiar object in the test trial (p<0.05), thereby showing recognition of the familiar object. Furthermore, habituation of exploration of the familiar object between the sample trial and the test trial was found (p<0.05). The procedure can be useful for testing of spontaneous trial-unique memory in pigs.

2021 ◽  
Vol 15 ◽  
Author(s):  
Cesar Sierra ◽  
Ilario De Toma ◽  
Lorenzo Lo Cascio ◽  
Esteban Vegas ◽  
Mara Dierssen

The use of mouse models has revolutionized the field of Down syndrome (DS), increasing our knowledge about neuropathology and helping to propose new therapies for cognitive impairment. However, concerns about the reproducibility of results in mice and their translatability to humans have become a major issue, and controlling for moderators of behavior is essential. Social and environmental factors, the experience of the researcher, and the sex and strain of the animals can all have effects on behavior, and their impact on DS mouse models has not been explored. Here we analyzed the influence of a number of social and environmental factors, usually not taken into consideration, on the behavior of male and female wild-type and trisomic mice (the Ts65Dn model) in one of the most used tests for proving drug effects on memory, the novel object recognition (NOR) test. Using principal component analysis and correlation matrices, we show that the ratio of trisomic mice in the cage, the experience of the experimenter, and the timing of the test have a differential impact on male and female and on wild-type and trisomic behavior. We conclude that although the NOR test is quite robust and less susceptible to environmental influences than expected, to obtain useful results, the phenotype expression must be contrasted against the influences of social and environmental factors.


2018 ◽  
Author(s):  
Damien Marechal ◽  
Véronique Brault ◽  
Alice Leon ◽  
Dehren Martin ◽  
Patricia Lopes Pereira ◽  
...  

ABSTRACTIdentifying dosage sensitive genes is a key to understand the mechanisms underlying intellectual disability in Down syndrome (DS). The Dp(17Abcg1-Cbs)1Yah DS mouse model (Dp1Yah) show cognitive phenotype and needs to be investigated to identify the main genetic driver. Here, we report that, in the Dp1Yah mice, 3 copies of the Cystathionine-beta-synthase gene (Cbs)are necessary to observe a deficit in the novel object recognition (NOR) paradigm. Moreover, the overexpression ofCbsalone is sufficient to induce NOR deficit. Accordingly targeting the overexpression of human CBS, specifically in Camk2a-expressing neurons, leads to impaired objects discrimination. Altogether this shows thatCbsoverdosage is involved in DS learning and memory phenotypes. In order to go further, we identified compounds that interfere with the phenotypical consequence of CBS overdosage in yeast. Pharmacological intervention in the Tg(CBS) with one selected compound restored memory in the novel object recognition. In addition, using a genetic approach, we demonstrated an epistatic interaction betweenCbsandDyrk1a, another human chromosome 21 gene encoding the dual-specificity tyrosine phosphorylation-regulated kinase 1a and an already known target for DS therapeutic intervention. Further analysis using proteomic approaches highlighted several pathways, including synaptic transmission, cell projection morphogenesis, and actin cytoskeleton, that are affected by DYRK1A and CBS overexpression. Overall we demonstrated that CBS overdosage underpins the DS-related recognition memory deficit and that bothCBSandDYRK1Ainteract to control accurate memory processes in DS. In addition, our study establishes CBS as an intervention point for treating intellectual deficiencies linked to DS.SIGNIFICANT STATEMENTHere, we investigated a region homologous to Hsa21 and located on mouse chromosome 17. We demonstrated using three independent genetic approaches that the overdosage of the Cystathionine-beta-synthase gene (Cbs) gene, encoded in the segment, is necessary and sufficient to induce deficit in novel object recognition (NR).In addition, we identified compounds that interfere with the phenotypical consequence of CBS overdosage in yeast and in mouse transgenic lines. Then we analyzed the relation between Cbs overdosage and the consequence of DYRK1a overexpression, a main driver of another region homologous to Hsa21 and we demonstrated that an epistatic interaction exist betweenCbsandDyrk1aaffecting different pathways, including synaptic transmission, cell projection morphogenesis, and actin cytoskeleton.


2019 ◽  
Author(s):  
Jorge M Ferreira ◽  
Ana M Valentim

AbstractConcerns have been raised about how deeply patients are anaesthetized, and the effects that different depths of anaesthesia may have after recovery. In order to study the anaesthetic drugs per se, and to eliminate the effect of clinical variables, several animal studies have been published. Isoflurane induced transient deficits on spatial memory at low concentrations, affecting the hippocampus. However, the influence of different concentrations of isoflurane on non-spatial memory still needs clarification. Thus, our aim was to study the effects of different depths of anaesthesia (1% and 2% isoflurane) on a non-spatial memory task, the object recognition test, in C57BL/6 adult mice.Twenty-eight 2-month-old C57BL/6 male mice were habituated to the test arena of the object recognition test for 10 min each day over 2 days before anaesthesia. Mice were then randomly allocated in different treatment groups: 1% or 2%, anaesthetized with 1% or 2% of isoflurane, respectively, for 1 h or the control group, which was not anaesthetised. Twenty-four hours after anaesthesia, the animals were placed in an arena with two identical objects and allowed to explore for 10 min-Sample Trial. One hour later, mice were allowed to explore the arena for 10 min in the presence of one of the objects presented in the previous trial (familiar object) and a novel object - Choice Trial. The time spent exploring each object was evaluated by a blinded analysis. The recognition of one object as familiar was detected based on a higher level of exploration of the novel object.Animals that were anaesthetized previously with 2% isoflurane performed at control levels, indicating the recognition of a familiar object in the object recognition task; this contrasted with the results of the group that was anaesthetized with 1% isoflurane.Lighter (1%) rather than deeper (2%) isoflurane anaesthesia may affect non-spatial memory in C57BL/6 male mice. Our results raise awareness of the need for careful consideration of the depth of anaesthesia used, especially the use of light isoflurane anaesthesia, which is often chosen to provide animal immobilization during non-invasive procedures.


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