Abstract

Impairment of procedural memory is a frequent and severe symptom in many neurological and psychiatric diseases as well as during aging. Our aim was to establish an assay in rats in which procedural learning and changes in performance can be studied on the long term. The work was done in the frame of a larger project aiming to establish a complex cognitive animal test battery of high translational value. The equipment was a 190-cm-diameter circular water tank where 12 flower pots were placed upside down in a circle with increasing distances (18–46 cm) between the adjacent ones. Male Lister Hooded and Long-Evans rats were allowed to move on the pots for 3 min. The arena was filled with shallow water to make the rats stay on the pots. Animals were obviously motivated to move around on the pots; however, the distance which required jumping (> 26 cm) meant a barrier for some of them. Development of motor skill was measured by the longest distance successfully spanned. A relatively flat bell-shaped age dependence was observed, with a peak at 13 months of age. A gradual decline in performance could be observed after the age of 20 months which preceded the appearance of overt physical weakness. Long-Evans rats showed more homogeneous performance and higher individual stability than Lister Hooded rats. The method is appropriate to study the development of motor learning and to follow its age-dependent changes. It may also serve as an assay for testing potential drugs for improving motor skills and/or procedural memory.

Highlights

  • The pharmacological treatment of age-related cognitive disorders is currently unsatisfactory

  • Despite the abundance of cognitive enhancer mechanisms identified in basic research, several dozens of pre-clinically promising compounds failed in clinical studies

  • In searching for an appropriate motor learning assay, we developed the so-called pot jumping test, introduced in this paper

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Summary

Introduction

The pharmacological treatment of age-related cognitive disorders is currently unsatisfactory. A major reason may be that the so-called gold-standard animal assays used in fundamental research fail to predict clinical efficacy against complex and robust cognitive defects. The system consists of learning paradigms that model the various human cognitive domains defective in psychiatric and neurodegenerative disorders (Millan et al 2012). One of these is procedural learning and memory, which is impaired in several age-related diseases, most prominently in Parkinson’s disease (Kim et al 2018; Belghali et al 2017), and weakens during natural aging (Voelcker-Rehage 2008). Our objective was to find a translationally valuable rodent model of procedural learning and memory, which is suitable for longitudinal follow-up of the performance

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