Plasma and cerebrospinal fluid interleukin-1β during lipopolysaccharide-induced systemic inflammation in ewes implanted or not with slow-release melatonin

Background: Interleukin-1 beta (IL-1 beta) is important mediator of inflammatory-induced suppression of reproductive axis at the hypothalamic level. At the beginning of inflammation, the main source of cytokines in the cerebrospinal fluid (CSF) is peripheral circulation, while over time, cytokines produced in the brain are more important. Melatonin has been shown to decrease pro-inflammatory cytokines concentration in the brain. In ewes, melatonin is used to advance the onset of a breading season. Little is known about CSF concentration of IL-1 beta in ewes and its correlation with plasma during inflammation as well as melatonin action on the concentration of IL-1 beta in blood plasma and the CSF, and brain barriers permeability in early stage of lipopolysaccharide (LPS)-induced inflammation. Methods: Systemic inflammation was induced through LPS administration in melatonin- and sham-implanted ewes. Blood and CSF samples were collected before and after LPS administration and IL-1 beta and albumin concentration were measured. To assess the functions of brain barriers albumin quotient (QAlb) was used. Expression of IL-1 beta (Il1B) and its receptor type I (Il1r1) and type II (Il1r2) and matrix metalloproteinase (Mmp) 3 and 9 was evaluated in the choroid plexus (CP). Results: Before LPS administration, IL-1 beta was on the level of 62.0 +/- 29.7 pg/mL and 66.4 +/- 32.1 pg/mL in plasma and 26.2 +/- 5.4 pg/mL and 21.3 +/- 8.7 pg/mL in the CSF in sham-and melatonin-implanted group, respectively. Following LPS it increased to 159.3 +/- 53.1 pg/mL and 197.8 +/- 42.8 pg/mL in plasma and 129.8 +/- 54.2 pg/mL and 139.6 +/- 51.5 pg/mL in the CSF. No correlations was found between plasma and CSF IL-1 beta concentration after LPS in both groups. The QAlb calculated before LPS and 6 h after was similar in all groups. Melatonin did not affected mRNA expression of Il1B, Il1r1 and Il1r2 in the CP. The mRNA expression of Mmp3 and Mmp9 was not detected. Conclusions: The lack of correlation between plasma and CSF IL-1 beta concentration indicates that at the beginning of inflammation the local synthesis of IL-1 beta in the CP is an important source of IL-1 beta in the CSF. Melatonin from slow-release implants does not affect IL-1 beta concentration in plasma and CSF in early stage of systemic inflammation.