Melatonin modulates Nrf2 activity to protect porcine pre-pubertal Sertoli cells from the abnormal H 2 O 2 generation and reductive stress effects of cadmium.

Melatonin (MLT) is a cytoprotective agent holding potential to prevent cadmium (Cd) toxicity and its impact in testicular function and fertility. Such potential was explored for the first time in porcine pre-pubertal Sertoli cells (SCs). Cd toxicity in SCs resulted in impaired viability and function, abnormal H2 O2 generation and efflux, and induction of reductive stress by the upregulation of Nrf2 expression and activity, of cystine uptake and use in cellular glutathione biosynthesis, and glutathione-S-transferase P (GSTP) expression, whereas protein glutathionylation was reduced. Cd toxicity also stimulated the activity of cellular kinases (MAPK-ERK1/2 and Akt) and NFkB transcription factor, and cJun expression. MLT produced a potent cytoprotective effect when co-administered with Cd to SCs; its efficacy and the molecular mechanism behind its cytoprotective function varied according to Cd concentrations, but a significant restoration of cell viability and function, and of H2 O2 levels, was observed both at 5 μM and 10 μM Cd. Mechanistically, these effects of MLT were associated with a significant reduction of Cd-induced Nrf2 activation and GSTP expression at all Cd concentrations. An upregulation of CAT and MAPK-ERK1/2 activity was associated with these effects at 5 μM Cd, whereas glutathione biosynthesis and efflux were involved at 10 μM Cd together with an increased expression of the cystine transporter xCT and marked upregulation of Akt and NFkB activity, and cJun expression. Melatonin protects SCs from Cd toxicity reducing its H2O2 generation and reductive stress effects. A reduced activity of Nrf2 and the modulation of other molecular players of MLT signaling, provide a mechanistic rational for the cytoprotective effect of this molecule in SCs. This article is protected by copyright. All rights reserved.