Abstract
Quercetin (QUE) is a natural flavonol-type flavonoid with antibacterial, anti-inflammatory and anti-aggregatory properties. It is also a powerful reactive oxygen species (ROS) scavenger and chelating agent. The aim of this study was to assess the effectiveness of QUE to reverse ROS-mediated alterations to the motility, viability and intracellular antioxidant profile of bovine spermatozoa. Spermatozoa were washed out of fresh bovine semen, suspended in 2.9% sodium citrate and subjected to QUE treatment (7.5, 25, 50 and 100μmol/l) in the presence or absence of a pro-oxidant, that is ferrous ascorbate (FeAA; 150μmol/l FeSO4 and 750μmol/l ascorbic acid) during a 6-h invitro culture. Spermatozoa motion characteristics were assessed using the SpermVision computer-aided sperm analysis (CASA) system. Cell viability was examined with the metabolic activity (MTT) assay, ROS generation was quantified via luminometry, and the nitroblue tetrazolium (NBT) test was applied to quantify the intracellular superoxide formation. Cell lysates were prepared at the end of the invitro culture to investigate the intracellular activity of superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx) as well as the concentrations of glutathione (GSH) and malondialdehyde (MDA). FeAA treatment led to a reduced sperm motility (p<0.001), viability (p<0.001) and decreased the antioxidant parameters of the sperm samples (p<0.001) but increased the ROS generation (p<0.001), superoxide production (p<0.001) and lipid peroxidation (p<0.001). QUE administration resulted in a preservation of the spermatozoa vitality and antioxidant characteristics (p<0.01 with respect to the enzymatic antioxidants, p<0.001 in relation to GSH) with a concentration range of 50-100μmol/l QUE revealing to be the most effective. Our results suggest that QUE exhibits significant ROS-scavenging and metal-chelating properties which may prevent spermatozoa alterations caused by ROS, and preserve the functionality of male reproductive cells.
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