mortality/aging
• following intraperitoneal water infusion to induce water intoxication most wild-type mice become uncoordinated within 10 minutes, rapidly progress to paralysis and by 60 minutes 92% are dead compared to homozygotes which develop only mild lethargy with 76% surviving after 60 minutes
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hearing/vestibular/ear
• at 4-5 weeks, the amplitudes of wave I are significantly decreased at click intensities of 70, 60, and 50 dB relative to wild-type; however, the organ of Corti remains intact with clearly demarcated hair cells and supportive cells
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• at 4-5 weeks of age, homozygotes exhibit a significantly increased ABR threshold by >12 db relative to wild-type mice
(J:71154)
• at 12 weeks of age, homozygotes of a predominantly CD-1 background exhibit a >2.5-fold elevation in average ABR thresholds to both broadband and tone-specific stimuli relative to wild-type mice (37 dB SPL vs 14 dB SPL, respectively)
(J:79863)
• however, no significant differences in the latency period for all major peaks are observed in response to tone specific stimuli, indicating normal neural conduction times
(J:79863)
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• Background Sensitivity: hearing loss is less severe than in mice on a coisogenic C57BL/6 background which are almost all deaf
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• unlike wild-type mice, homozygotes show a significantly higher inter-ear variability or bilateral asymmetry, as assessed by ABR thresholds
• 2 of 7 homozygotes exhibit extreme bilateral asymmetry in auditory function, with one ear displaying an ABR threshold of 15 dB (i.e. intact hearing), while the other ear displays a threshold of 50 dB (auditory dysfunction)
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homeostasis/metabolism
N |
• serum gastrin levels are similar to wild-type
(J:63987)
• serum sodium concentration and osmolality are similar to wild-type
(J:111923)
|
• following intraperitoneal water infusion to induce water intoxication pericapillary astrocytic foot process swelling in the brain is reduced and the increase in brain water content is decreased compared to wild-type mice
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• following middle cerebral artery occlusion mortality rate, neurological deficit scores, brain edema, and infarct volume are all decreased compared to wild-type mice
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nervous system
N |
• no gross abnormalities are seen in brain morphology and the blood-brain barrier is intact
|
• following middle cerebral artery occlusion mortality rate, neurological deficit scores, brain edema, and infarct volume are all decreased compared to wild-type mice
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digestive/alimentary system
N |
• gastric pit morphology and gastric acid output are similar to wild-type
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vision/eye
N |
• basal and pilocarpine-stimulated tear production and chloride concentration are similar to wild-type
(J:62579)
• Background Sensitivity: b-wave amplitude and oscillatory potentials are reduced in mice on a C57BL/6 background but not in mice on a mixed CD-1 and C57BL/6 background
(J:109783)
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• ischemia-induced impairment of b wave and oscillatory potential amplitudes is reduced compared to wild-type mice
• ischemia-induced decreases in retinal thickness and cellularity are reduced compared to wild-type mice; however, prior to ischemia no differences in retinal morphology are seen
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behavior/neurological
N |
• no behavioral, motor sensory, or coordination abnormalities are detected
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cardiovascular system
N |
• morphology of the posterior, anterior and middle cerebral arteries is similar to wild-type
|