behavior/neurological
• mice show increased susceptibility to pentylenetetrazone (PTZ) induced seizures than wild-type mice, with 92% developing seizures compared to 57% of wild-type mice and with shorter latency to generalized seizure
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• in the hole board test, mice show prolonged latencies to dipping their heads into all holes, whereas the total number of head dips does not differ
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• in the elevated plus maze, mice spend a longer time in the open arms and show more entries into the open arms, however mice do not show reduced anxiety in the light-dark box test, suggesting increased impulsivity rather than reduced anxiety
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• in the hole board test, mice show a lower total time of rearing
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• mice show increased activity in home cages, mainly in the dark phase
• in the forced swimming test, mice show reduced immobility time
• however, mice show normal prepulse inhibition and pain sensitivity
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• in the light-dark box transition test, the total distance travelled and total number of transitions are larger in mutants
• mice show increased total distance traveled in the elevated plus maze and hole board tests
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• mice exhibit epileptic seizures during routine handling
• handling seizures are seen beginning at 11 weeks of age and the percentage of affected mice peaks (at about 80%) at 5 months
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nervous system
• mice show increased susceptibility to pentylenetetrazone (PTZ) induced seizures than wild-type mice, with 92% developing seizures compared to 57% of wild-type mice and with shorter latency to generalized seizure
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• mice exhibit epileptic seizures during routine handling
• handling seizures are seen beginning at 11 weeks of age and the percentage of affected mice peaks (at about 80%) at 5 months
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• small but significant decrease in GluR1a-positive spine density at 4 months of age
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• EEG activity indicates the presence of frequent sharp waves not seen in wild-type mice
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• impaired presynaptic form of plasticity
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• synapses do not show facilitation and the 3rd, 4th, and 5th excitatory postsynaptic currents (EPSCs) are depressed indicating impaired short-term plasticity at excitatory synapses onto oriens lacunosum moleculare neurons
• however, short-term plasticity of synaptic inputs to pyramidal neurons are normal
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• LTP at pyramidal neuron- onto oriens lacunosum moleculare neuron synapses is impaired
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• a brief train of afferent stimulation induces short-term depression rather than short-term facilitation at CA1 pyramidal neuron- onto oriens lacunosum moleculare neuron synapses
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