fig8

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

Figure 8. Spinal GFAP mRNA levels are reduced following BIRT377 in both males and females. mRNA was extracted from tissues behaviorally verified in Figure 2B. (A-B) Astrocyte activation marker, GFAP, mRNA levels were increased on both sides of the spinal cord, in all mice with CCI (ipsilateral: F1,1 = 41.91, P < 0.0001; contralateral: F1,1 = 16.68, P = 0.0002). BIRT377 treatment reduced spinal GFAP mRNA levels in mice with CCI (ipsilateral: F1,1 = 5.533, P = 0.023; contralateral: F1,1 = 12.28, P = 0.001). In the contralateral side, CCI-induced GFAP mRNA levels were greater in females than in males (F1,1 = 9.9, P = 0.003). (C-D) Microglial proliferation marker, TMEM119, mRNA levels were increased following CCI (ipsilateral: F1,1 = 40.49, P < 0.0001; contralateral: F1,1 = 7.66, P = 0.008). Neuropathic females displayed significantly greater contralateral TMEM119 expression than neuropathic males (P = 0.015), as a main effect of sex (F1,1 = 4.16, P = 0.048) was observed. TMEM119 mRNA levels were comparable between BIRT377 or vehicle treated neuropathic males or females bilaterally. No significant difference was detected between male or female Sham + Veh. and Sham + BIRT group. *P values from post hoc comparisons ranges from P = 0.04 to P < 0.0001. n = 6 per group

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

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