fig7

LFA-1 antagonist (BIRT377) similarly reverses peripheral neuropathic pain in male and female mice with underlying sex divergent peripheral immune proinflammatory phenotypes

Figure 7. Ipsilateral dorsal spinal cord mRNA levels reveal BIRT377 treatment reduces CCL2 in sciatic damaged females only, while no sex differences occur in elevated IL-10. Lumbar spinal cord (LSC) tissues from behaviorally verified mice (Figure 2B), were collected and analyzed for pain-relevant cytokines. (A-B) Ipsilateral CCL2 mRNA levels were increased following CCI (F1,1 = 57.38, P < 0.0001). BIRT377 treatment reduced CCL2 mRNA expression in females with CCI (F1,1 = 5.28, P = 0.026). Neuropathic females displayed significantly more CCL2 mRNA levels than in neuropathic males (P = 0.006). Post hoc comparisons revealed significant reduction in contralateral CCL2 mRNA levels in CCI-treated females following BIRT377 treatment. (C-D) Ipsilateral IL-1β mRNA levels were increased following CCI (F1,1 = 32.8, P < 0.0001) that occurred in females to much a greater degree than males (F1,1 = 6.86, P = 0.012). (E-F) While sciatic nerve CCI induced a bilateral elevation in TGF-β1 mRNA levels in both males and females (ipsilateral: F1,1 = 40.95, P < 0.0001; contralateral: F1,1 = 5.23, P = 0.027), the magnitude of TGF-β1 mRNA increase following BIRT377 treatment was greater in ipsilateral LSC from females than males (F1,1 = 6.56, P = 0.014). No differences in TGF-β1 mRNA levels from contralateral LSC were revealed following BIRT377 treatment. (G-H) IL-10 mRNA levels were decreased following CCI (ipsilateral: F1,1 = 52.26, P < 0.0001; contralateral: F1,1 = 9.45, P = 0.004). BIRT377 treatment increased IL-10 mRNA expression levels in mice with CCI (ipsilateral: F1,1 = 6.19, P = 0.017; contralateral: F1,1 = 4.94, P = 0.032). *P values from post hoc comparisons ranges from P = 0.04 to P < 0.0001. n = 5 in male Sham + Veh and CCI + BIRT for IL-10 contralateral data. n = 6 per group unless otherwise indicated

Neuroimmunology and Neuroinflammation
ISSN 2349-6142 (Online) 2347-8659 (Print)

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