Abstract

BackgroundThis study observes changes in levels of seminal nitric oxide (NO), nitric oxide synthase (NOS), macrophage migration inhibitory factor (MIF), sperm DNA integrity, chromatin condensation and Caspase-3in adult healthy men after scrotal heat stress (SHS).MethodsExposure of the scrotum of 25 healthy male volunteers locally at 40–43°C SHS belt warming 40 min each day for successive 2 d per week. The course of SHS was continuously 3 months. Routine semen analysis, hypo-osmotic swelling (HOS) test, Aniline blue (AB) staining, HOS/AB and terminal deoxynucleotidyl transferase-mediated d UDP nick-end labeling (TUNEL) were carried out before, during and after SHS. Seminal NO and NOS contents were determined by nitrate reduction method. The activated Caspase-3 levels of spermatozoa and MIF in seminal plasma were measured by the enzyme-linked immunosorbent assay (ELISA) method. Statistical significance between mean values was determined using statistical ANOVA tests.ResultsThe mean parameters of sperm concentration, motile and progressive motile sperm and normal morphological sperm were significantly decreased in groups during SHS 1, 2 and 3 months compared with those in groups of pre-SHS (P<0.001). Statistically significant differences of sperm DNA fragmentation, normal sperm membrane, and Caspase-3 activity as well as the level of NO, NOS and MIF in semen were observed between the groups before SHS and after SHS 3 months and the groups during SHS 1, 2 and 3 months (P<0.001). After three months of the SHS, various parameters recovered to the level before SHS. WBC in semen showed a positively significant correlation with the levels of NO, NOS, MIF and Caspase-3 activity. The percentage of abnormal sperm by using the test of HOS showed a positively significant correlation with that of HOS/AB.ConclusionsThe continuously constant SHS can impact the semen quality and sperm DNA and chromatin, which may be contributed to the high level of NO, NOS, MIF and Caspase-3 by SHS.

Highlights

  • In most mammals, male germ cells should be maintained below body temperature for proper development

  • The continuously constant scrotal heat stress (SHS) can impact the semen quality and sperm DNA and chromatin, which may be contributed to the high level of nitric oxide (NO), nitric oxide synthase (NOS), migration inhibitory factor (MIF) and Caspase-3 by SHS

  • Previous studies on azoospermia or oligozoospermia induced by SHS mainly focused on germ cell apoptosis [5,6,7]; no data regarding their possible effect on nitric oxide (NO), nitric oxide synthase (NOS) and macrophage migration inhibitory factor (MIF) in semen are available

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Summary

Introduction

Male germ cells should be maintained below body temperature for proper development. Previous studies on azoospermia or oligozoospermia induced by SHS mainly focused on germ cell apoptosis [5,6,7]; no data regarding their possible effect on nitric oxide (NO), nitric oxide synthase (NOS) and macrophage migration inhibitory factor (MIF) in semen are available. MIF secreted in the epididymis and correlated with sperm maturation and stability [14,15] It is unknown how MIF influences sperm function and apoptosis after scrotal heat stress. The effect of NO, NOS and MIF on human sperm concentration, motility, morphology and DNA stability has not been elucidated clearly. This study observes changes in levels of seminal nitric oxide (NO), nitric oxide synthase (NOS), macrophage migration inhibitory factor (MIF), sperm DNA integrity, chromatin condensation and Caspase-3in adult healthy men after scrotal heat stress (SHS)

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