Hyperactive behaviour in the mouse model of mucopolysaccharidosis IIIB in the open field and home cage environments

A Langford‐Smith, M Malinowska… - Genes, Brain and …, 2011 - Wiley Online Library
A Langford‐Smith, M Malinowska, KJ Langford‐Smith, G Wegrzyn, S Jones, R Wynn…
Genes, Brain and Behavior, 2011Wiley Online Library
Mucopolysaccharidosis IIIB (MPS IIIB) is a lysosomal storage disorder characterized by
severe behavioural disturbances and progressive loss of cognitive and motor function.
There is no effective treatment, but behavioural testing is a valuable tool to assess
neurodegeneration and the effect of novel therapies in mouse models of disease. Several
groups have evaluated behaviour in this model, but the data are inconsistent, often
conflicting with patient natural history. We hypothesize that this discrepancy could be due to …
Mucopolysaccharidosis IIIB (MPS IIIB) is a lysosomal storage disorder characterized by severe behavioural disturbances and progressive loss of cognitive and motor function. There is no effective treatment, but behavioural testing is a valuable tool to assess neurodegeneration and the effect of novel therapies in mouse models of disease. Several groups have evaluated behaviour in this model, but the data are inconsistent, often conflicting with patient natural history. We hypothesize that this discrepancy could be due to differences in open field habituation and home cage behaviour. Eight‐month‐old wild‐type and MPS IIIB mice were tested in a 1‐h open field test, performed 1.5 h after lights on, and a 24‐h home cage behaviour test performed after 24 h of acclimatization. In the 1‐h test, MPS IIIB mice were hyperactive, with increased rapid exploratory behaviour and reduced immobility time. No differences in anxiety were seen. Over the course of the test, differences became more pronounced with maximal effects at 1 h. The 24‐hour home cage test was less reliable. There was evidence of increased hyperactivity in MPS IIIB mice, however, immobility was also increased, suggesting a level of inconsistency in this test. Performance of open field analysis within 1–2 h after lights on is probably critical to achieving maximal success as MPS IIIB mice have a peak in activity around this time. The open field test effectively identifies hyperactive behaviour in MPS IIIB mice and is a significant tool for evaluating effects of therapy on neurodegeneration.
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