behavior/neurological
• mice exhibit impaired egocentric spatial memory acquisition compared with control mice
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• impaired visual discrimination learning
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• impaired
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• impaired in a Morris water maze
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• impaired in a Morris water maze and appetitive, elevated Y maze
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• impaired in a discrete trial, spontaneous alternation paradigm in an enclosed T maze or a reward alternation on an elevated T maze
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• more so than in Grin2btm1Mony/Grin2btm1Mony Tg(Camk2a-Grin2c/itTA)12Rps Tg(tetO-cre)LC1Bjd mice
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• improved performance on a rotarod
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• more so than in Grin2btm1Mony/Grin2btm1Mony Tg(Camk2a-Grin2c/itTA)12Rps Tg(tetO-cre)LC1Bjd mice
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nervous system
N |
• mice exhibit normal cortical layer 4 whisker barrel structures and paired-pilse facilitation
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• ifenprodil-treated mice fail to exhibit an acceleration of NMDAR-mediated excitatory postsynaptic currents compared with wild-type mice
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• at high stimulation frequency, mice exhibit smaller maximal depolarization of the excitatory postsynaptic potentiation (EPSP) envelop and EPSP integral compared with control mice
• however, mice exhibit normal input resistance, action potential threshold, firing pattern and maximal firing frequency
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• mice fail to exhibit a reduction in NMDA currents in response to the Grin2b antagonist ifenprodil unlike control mice
• mice exhibit a faster deactivation kinetics (weighted tau) compared with control mice
• ifenprodil-treated mice fail to exhibit an acceleration of NMDAR-mediated excitatory postsynaptic currents compared with wild-type mice
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• low-frequency synaptic stimulation long term potentiation is reduced compared to in control mice
• during long term potentiation induction, charge transfer is reduced compared to in control mice
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• miniature excitatory postsynaptic current amplitudes 50 ms are attenuated after onset unlike in control mice
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growth/size/body
• slightly
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