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. Author manuscript; available in PMC: 2019 Jul 1.
Published in final edited form as: Exp Neurol. 2018 Apr 9;305:97–107. doi: 10.1016/j.expneurol.2018.04.002

Figure 3. SNIRKO mice do not display sensorimotor deficits characteristic of PDN in murine models.

Figure 3

It was hypothesized that the reduction in sensory neuron insulin signaling despite euglycemia would produce a phenotype similar to PDN in mouse models. Similar patterns were observed across males and females between groups and data presented here is combined from males and females. No significant difference between IRlox/lox and SNIRKO was observed in mechanical sensitivity (A). For thermal sensitivity, there was no significant difference of group between IRlox/lox and SNIRKO mice upon analysis with 2-way repeated measures ANOVA (B). However, Bonferroni’s post-hoc does show a significant difference between IRlox/lox and SNIRKO mice at 13 weeks of age. Of note, the thermal threshold for SNIRKO mice appears to remain relatively constant throughout the period tested, yet IRlox/lox mice show an increase in threshold at 13 weeks. No significant difference between IRlox/lox and SNIRKO mice was observed in beamwalk (C) or rotorod (D). Mechanical sensitivity, thermal sensitivity, and beamwalk were analyzed with a repeated measures 2-way ANOVA and Bonferroni’s post-hoc. Rotorod was analyzed with a student’s t-test. n=24 IRlox/lox and n=23 SNIRKO. *=p<0.05.