Fig. 3.
Ketamine is efficacious when administered at the late, but not early, phase of complex regional pain syndrome. Ketamine shows no efficacy in reversing mechanical allodynia when administered at 3 weeks after fracture (A, B). In contrast, ketamine reverses mechanical allodynia on the ipsilateral (ipsi) hind paw when administered at the 7-week timepoint (C, D). No changes were observed in the contralateral (contra) hind paw. *P < 0.05, **P < 0.005, ***P < 0.001 compared with the Fracture + Saline group. #P < 0.05, ##P < 0.005, ###P < 0.001 compared to the Control + Saline group. (A, B) n = 6 mice for Control + Saline, n = 6 mice for Control + Ketamine, n = 8 mice for Fracture + Saline, and n = 11 mice for Fracture + Ketamine. (C, D) n = 8 mice for Control + Saline, n = 8 mice for Control + Ketamine, n = 6 mice for Fracture + Saline, and n = 9 mice for Fracture + Ketamine. The red lines indicate the duration of ketamine administration.

Ketamine is efficacious when administered at the late, but not early, phase of complex regional pain syndrome. Ketamine shows no efficacy in reversing mechanical allodynia when administered at 3 weeks after fracture (A, B). In contrast, ketamine reverses mechanical allodynia on the ipsilateral (ipsi) hind paw when administered at the 7-week timepoint (C, D). No changes were observed in the contralateral (contra) hind paw. *P < 0.05, **P < 0.005, ***P < 0.001 compared with the Fracture + Saline group. #P < 0.05, ##P < 0.005, ###P < 0.001 compared to the Control + Saline group. (A, B) n = 6 mice for Control + Saline, n = 6 mice for Control + Ketamine, n = 8 mice for Fracture + Saline, and n = 11 mice for Fracture + Ketamine. (C, D) n = 8 mice for Control + Saline, n = 8 mice for Control + Ketamine, n = 6 mice for Fracture + Saline, and n = 9 mice for Fracture + Ketamine. The red lines indicate the duration of ketamine administration.

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