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For grip strength test, the mice were placed with their forelimbs on a narrow bar and the amount of time taken for the mouse to fall was assessed.
The time taken for the mouse to fall off the Rotarod was measured in seconds.
The amount of time for each mouse to fall from the rod was recorded for each trial.
The time it took for the mouse to fall was measured, up to a criterion time of 60 seconds.
The time it took for the mouse to fall was measured, up to a criterion of 60 s.
The time taken for the mouse to fall from the apparatus was recorded and the maximum time on the rotarod was set at 400 seconds.
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The latency times for the mice to fall from the rod were recorded automatically by the apparatus.
In our recently published study [ 16], we showed that in a rotarod function test, the latency of MIPKO mice to fall off the rotating rod was decreased.
The extract caused no significant effect on the time taken by mice to fall off the rotarod compared to the control at all the doses used (P > 0.05 at 30 300 mg kg−1).
Although the Pitx1 transgenic mice tended to fall off the rotarod cylinders sooner than the control mice (Fig. 4B), the difference between the groups was not statistically significant.
In EAU mice the numbers of recirculating monocytes in both CD62L and CD44 mAb treated EAU mice continued to fall and remained profoundly reduced compared with controls (P <.01 in both groups), showing that the depletion of circulating monocytes observed in EAU mice was inflammation specific.
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Justyna Jupowicz-Kozak
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