Quantitative assessment of heavy metal effects on sperm function using computer‐aided sperm analysis and cytotoxicity assays

One known environmental risk factor impacting on human reproduction is heavy metal pollution. Although some metals (e.g., Cu, Se and Zn) have protective effects on the male reproductive system in low doses, heavy metals can accumulate to toxic levels and result in poor semen quality and decreased sperm function. We investigated the effect of CuSO4 and CdCl2 (10, 50, 100 and 250 μg/ml or 500 μg/ml) on human sperm motility and vitality by using computer‐aided sperm analysis (CASA) and two cytotoxicity assays (WST‐1 and XTT). Several sperm motility parameters were significantly reduced after 5 hr of exposure to the highest concentrations of CuSO4 (250 μg/ml) and CdCl2 (500 μg/ml). The WST‐1 assay also revealed significantly lower absorbance values for 50, 100 and 250 μg/ml CuSO4 and for 500 μg/ml CdCl2; however, no significant effect was seen with XTT. The calculated average IC50 value was 50.31± 4.34 μg/ml for CuSO4 and 392.32 ±76.79 μg/ml for CdCl2. The effects of these metals were confirmed with MgCl2, a positive control. This study provides threshold concentrations for the harmful effect of CuSO4 and CdCl2 on human spermatozoa and recommends the use of WST‐1 as vitality assay in future in vitro studies

Statistics and Thermodynamics of Kerr-Newman-Gödel Black Hole

International audienc

Effects of in vitro copper sulphate supplementation on the ejaculated sperm characteristics in water buff aloes ( Bubalus bubalis )

This study was carried out to investigate effects of copper sulphate (CuSO4) additive tosemen extenders on sperm parameters:progressive motility, viability, membrane integrityand DNA damage, after semen dilution and cryopreservation. Semen samples of 5 buffalobulls of 3-5 years old were collected at 5 different occasions during the autumn 2011. A totalnumber of 25 samples were used in each examination. Sperm progressive motility andviability were measured at 0 (T0), 60 (T1) and 120 (T2) min after diluting semen in tris-citricacid extender containing 0 (control), 0.004, 0.008, 0.016, 0.032 and 0.064 mg L-1CuSO4. Later,semen was diluted in a tris-citric acid-egg yolk-glycerol extender containing the sameamounts ofCuSO4, cooled to 4̊C and kept refrigerated for 4 hr to equilibrate, spermprogressive motility, viability, membrane integrity and DNA damage were estimated. Then,semen was packed in 0.5 mL French straws and frozen in liquid nitrogen. Later, the frozensemen was thawed in 37 ̊C water bath for 30 sec, and the same parameters as well as totalantioxidant capacity (TAC) of the frozen-thawed semen were estimated. The results showedthat copper additive at the rate of 0.032 mg L-1gives a better protection of sperms throughthe process of dilution, equilibration and freeze-thawing than that in control and other Cuconcentrations, while 0.064 mg L-1CuSO4had deleterious effect on the sperm

Statistics and Thermodynamics of Two-Charged STU Black Holes

International audienc