behavior/neurological
N |
• animals do not exhibit any signs of self-mutilation or taste response deficits
• animals have normal mechanosensory responses following nerve ligation or sensitization by inflammation; responses in assays for touch and pinch assays are identical to controls
• rotarod results are normal, indicating no loss of proprioceptive function
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• responses to capsaicin and mustard oil in eye wipe and paw injection paradigms are eliminated
• animals display no 'wet-dog shakes' in response to icilin injection which gives perception of cooling, whereas controls show robust characteristic responses
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• mice are insensitive to noxious heat compared to controls (animals do not display protective thermosensory responses in hot plate paw withdrawal or tail-flick assays)
• mice show no reaction to a cold plate assay or preference in a 2-temperature choice test (30 C vs 5 C)
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nervous system
N |
• distribution and arrangement of dorsal horn interneurons is not significantly different from wild-type animals
• recordings from sciatic nerve in response to stimulation of the foot (by brush, von Frey microfilaments, or vibration) are not different than in controls
• rotarod results are normal, indicating no loss of proprioceptive function
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• mutants have reduced numbers of TRPV2-containing sensory neurons
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homeostasis/metabolism
• in response to IP injection of capsaicin, mice do not exhibit the profound hypothermia that is shown by treated controls
• mutants are unable to maintain their body temperature than wild-type controls when the environmental temperature is changed
• animals exhibit a greater hypothermic response than wild-type upon antigen injection, with slower re-establishment of normal resting temperature
• animals show a greater temperature change in response to mild fever induced by Il-1beta injection relative to wild-type
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immune system
• responses to ATP, prostaglandins, bradykinin, histamine and serotonin are lost in mutants; significant loss of neurogenic inflammation is observed, and significantly less inflammation occurs in response to carageenan challenge
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integument
• mutants display complete loss of behavioral responses to injection of pruritogenic compounds
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