behavior/neurological
N |
• mutant mice displayed normal working memory in a Y maize test, and exhibited no significant alteration in the open-field test or the elevated plus maize test relative to wild-type
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• mutants exhibited significantly increased mobility in the forced swim test, suggesting a state of hyperactivity and increased vigilance to stress
• mutants showed no adaptation to inescapable stress, indicating a sustained stress-induced hyperactivity
• notably, mutants did not display increased locomotion in the open field test
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homeostasis/metabolism
N |
• mutant mice displayed normal concentrations of 5-HT, 5-hydroxy-3-indole-acetic acid (5-HIAA), dopamine (DA), dihydroxyphenylacetic acid (DOPAC), homovanillic acid (HVA), 3-methoxytyramine (3-MT), norepinephrine (NE) and 3-methoxy-4-hydroxy-phenylglycol (MHPG) in various brain regions relative to wild-type
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• MPTP neurotoxicity resulted in the depletion of DA, DOPAC and possibly HVA in wild-type mice; in contrast, mutants suffered no apparent MPTP toxicity of dopaminergic terminals in the striatum
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• urinary beta-phenylethylamine (PEA) excretion showed an 8-fold increase in mutant mice relative to wild-type; notably, brain levels of PEA were also increased ~8-fold
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renal/urinary system
• urinary beta-phenylethylamine (PEA) excretion showed an 8-fold increase in mutant mice relative to wild-type; notably, brain levels of PEA were also increased ~8-fold
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nervous system
• MPTP neurotoxicity resulted in the depletion of DA, DOPAC and possibly HVA in wild-type mice; in contrast, mutants suffered no apparent MPTP toxicity of dopaminergic terminals in the striatum
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cellular
• MPTP neurotoxicity resulted in the depletion of DA, DOPAC and possibly HVA in wild-type mice; in contrast, mutants suffered no apparent MPTP toxicity of dopaminergic terminals in the striatum
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