Prolactin treatment reduces kainic acid-induced gliosis in the hippocampus of ovariectomized female rats.

Neuroinflammation involves a set of responses occurring as a result of brain damage including astro- and microgliosis. In previous studies, we showed that treatment with prolactin (PRL) decreased neuronal loss induced by kainic acid (KA) in the hippocampus of female rats. This effect correlated with a decrease in astrogliosis. Here, we investigate whether treatment with PRL decreases astro- and microgliosis in the dorsal hippocampus, and how it modulates the expression of some important inflammatory factors such as TNFα, iNOS, IL-6, IL-10 and IL-4 after an excitotoxic lesion. For this, ovariectomized female rats were treated chronically with PRL (0.1 mg / day for 4 days, SC). On the third day of treatment, they received a KA injection (7.5 mg / kg, IP) and were sacrificed 24 or 48 h later. Chronic treatment with PRL reduced the astro- and micro-gliosis in CA4, CA3, and CA1 hippocampal subfields induced by KA. Morphometric analysis in CA4 showed that PRL reduced microglial activation. The analysis for anti- and pro-inflammatory cytokines revealed an increase of IL-10 and IL-4 in neurons due to treatment with PRL, accompanied by a decrease in the expression of TNFα and iNOS in lesioned rats. These results indicate that PRL has anti-inflammatory actions in the hippocampus, both by decreasing the astrogliosis and microglial activation and by reducing the level of pro-inflammatory cytokines probably through the upregulation of neuronal IL-10 and IL-4.