Abstract

Simple SummaryReactive oxygen species that accumulate during liquid storage of boar semen lead to oxidative stress to sperm. In this study, we found that proline significantly improved boar sperm quality and protected sperm against oxidative damages during liquid storage at 17 °C. Using the model of artificially induced oxidative stress, we found that proline exerted an antioxidative role by modulating redox homeostasis in boar sperm. The secondary amine structure of proline and proline dehydrogenase-mediated metabolism are involved in the antioxidative role. We suggest that addition of proline to the extender would be beneficial to improve boar sperm quality.Proline was reported to improve sperm quality in rams, stallions, cynomolgus monkeys, donkeys, and canines during cryopreservation. However, the underlying mechanism remains unclear. The aim of this study was to investigate the effect of proline on boar semen during liquid storage at 17 °C and explore the underlying mechanism. Freshly ejaculated boar semen was supplemented with different concentrations of proline (0, 25, 50, 75, 100, 125 mM) and stored at 17 °C for nine days. Sperm motility patterns, membrane integrity, ATP (adenosine triphosphate), reactive oxygen species (ROS), and GSH (glutathione) levels, and the activities of catalase (CAT) and superoxide dismutase (SOD) were evaluated after storage for up to five days. It was observed that boar sperm quality gradually decreased with the extension of storage time, while the ROS levels increased. Addition of 75 mM proline not only significantly improved sperm membrane integrity, motility, and ATP levels but also maintained the redox homeostasis via increasing the GSH levels and activities of CAT and SOD. When hydrogen peroxide (H2O2) was used to induce oxidative stress, addition of proline significantly improved sperm quality and reduced ROS levels. Moreover, addition of proline also improved sperm quality during the rapid cooling process. Notably, addition of DL-PCA (DL-pipecolinic acid) rescued the reduction of progressive motility and total motility caused by H2O2, and THFA (tetrahydro-2-furoic acid) failed to provide protection. Furthermore, addition of proline at 75 mM increased the activity of proline dehydrogenase (PRODH) and attenuated the H2O2-induced reduction in progressive motility. These data demonstrate that proline protects sperm against oxidative stress through the secondary amine structure and proline dehydrogenase-mediated metabolism.

Highlights

  • Artificial insemination is widely used in pig industry for improving the fertility and spreading genetic progress [1,2]

  • In the absence of H O2, the addition of tetrahydro-2-furoic acid (THFA) did not cause alteration in the progressive motility when compared to the 2group in the absence of THFA. These results motility when compared to the group in the absence of THFA. These results indicated that inhibition of the activity of proline dehydrogenase (PRODH) abolished the antioxidant function of proline

  • Accumulation of reactive oxygen species (ROS) occurs during liquid storage of boar semen, which results in oxidative stress to sperm when it overwhelms the antioxidant defense [9]

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Summary

Introduction

Artificial insemination is widely used in pig industry for improving the fertility and spreading genetic progress [1,2]. The addition of antioxidants protects sperm from oxidative damages and extends the lifespan [21,22]. Proline has been reported to protect plant cells, Saccharomyces cerevisiae, and mammalian cells against oxidative stress [23,24,25]. Reported that treatment of melanoma cells with exogenous proline significantly increased cell viability and diminished oxidative damage under ROS stress. Addition of proline to semen extender significantly improved donkey sperm motility after cold storage at 5 ◦ C for three days [30]. Supplementation of proline to the freezing extender improved motility [31,32,33,34,35,36] and decreased lipid peroxidation damage in ram sperm [31] during the cryopreservation process. The aim of the present study was to investigate whether the addition of the proline could improve boar sperm quality, and, if so, to elucidate the underling mechanism

Animals and Semen Collection
Experiment I
Semen Storage
Motility Analysis
Integrity of Membrane and Acrosome
Measurement of ATP Levels
Mitochondrial Membrane Potentials
Experiment II
Reactive Oxygen Species
Lipid Peroxidation
Measurement of Glutathione Levels
Analysis of Catalase and Superoxide Dismutase Activity
Experiment III
Experiment IV
Experiment V
Western Blotting
Immunofluorescence Staining of PRODH in Boar Sperm
Analysis of Proline Dehydrogenase Activity
Statistical Analysis
Proline Improves Sperm Motility
Proline Improves the Integrity of the Membrane and Acrosome
Proline Increases the Mitochondrial Membrane Potential and ATP Levels
Effect
Discussion
Conclusions
Full Text
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