The purpose of this study was to evaluate the effect of female sexual
hormones on intestinal and serum
cytokines following
traumatic brain injury (TBI). Adult female rats were ovariectomized and distributed among the following 9 groups: (i)
sham trauma, (ii) TBI (Marmarou's method), (iii) vehicle (
dimethylsulfoxide) treated, (iv)
estrogen (E2) treated, (v)
progesterone (P) treated, (vi) treated with E2+P, (vii)
propylpyrazole triol (PPT) treated, (viii)
diarylpropionitrile (
DPN) treated, and (ix) control. PPT and
DPN are
estrogen receptor αand β agonists, respectively. Serum and intestinal levels of
interleukin (IL)-1β were increased by TBI (P < 0.001). The level of intestinal IL-1β was increased in the group treated with E2 (P < 0.001). There was a reduction in serum IL-1β (P < 0.01) and an increase in intestinal IL-1β level (P < 0.001) in the PPT-treated group compared with the vehicle-treated group. TBI reduced serum
IL-6 (P < 0.01) and increased intestinal
IL-6 (P < 0.001). Serum
IL-6 was increased in the group treated with E2 (P < 0.001), P (P < 0.001), E2+P (P < 0.01), and
DPN (P < 0.001) after TBI; however, intestinal
IL-6 was higher in the E2-treated group compared with the vehicle-treated group (P < 0.01). Intestinal
tumor necrosis factor α (TNF-α) was increased by TBI (P < 0.001).
Progesterone decreased serum TNF-α (P < 0.01). Intestinal TNF-α in the E2 (P < 0.01), E2+P (P < 0.001), and PPT (P < 0.001) treatment groups was less than in the vehicle-treated group. In conclusion,
estrogen influences the intestinal levels of proinflammatory
cytokines, in particular TNF-α, mediated through
estrogen receptor α.