Protective Effects and Potential Mechanisms of D-Aspartate on Testicular Damage Induced by Polystyrene Microplastics
Sara Falvo1, Giulia Grillo1, Imed Messaoudi2
1Dipartimento di Scienze e Tecnologie Ambientali, Biologiche e Farmaceutiche, Università degli Studi della Campania 'Luigi Vanvitelli', Via Vivaldi, 43, 81100 Caserta, Italy.
Abstract:
Polystyrene Microplastics (PS-MPs) affect testicular activity, as evidenced by increased oxidative stress, apoptosis, and autophagy activation, impairing steroidogenesis and spermatogenesis. The present study investigates, for the first time in vivo, the potential protective effect of D-aspartate (D-Asp) against PS-MPs-induced damage on the testicular function of adult rats. D-Asp, well-known stimulator of testosterone biosynthesis and spermatogenesis progression, possesses pharmacological properties, including antioxidant and anti-apoptotic ones. The results showed that PS-MP's adverse effects on testicular activity were reversed by D-Asp treatment. Mechanistically, D-Asp inhibited testicular oxidative stress by modulating the protein levels of CAT, SOD1, SOD2, and 4-HNE; affecting TBARS levels; and reducing apoptosis, as suggested by CYT C analysis and a TUNEL assay. Furthermore, D-Asp administration mitigated PS-MPs-induced autophagy activation by modulating the expression of LC3BI, LC3BII, and p62 proteins. Finally, the amino acid counteracts PS-MPs damage on steroidogenesis and spermatogenesis by restoring normal levels of steroidogenic (StAR, 3β-HSD, and 17β-HSD) and spermatogenic (PCNA and SYCP3) markers. This study encourages further research to understand the potential value of the amino acid in improving human testicular health and male fertility.
Insights
D-aspartate (D-Asp) protects against testicular damage caused by polystyrene microplastics (PS-MPs). D-Asp treatment reversed PS-MP-induced oxidative stress, apoptosis, and autophagy, improving male reproductive health.
Area of Science:
- Environmental Toxicology
- Reproductive Biology
- Biochemistry
Background:
- Polystyrene microplastics (PS-MPs) exposure is linked to testicular dysfunction, including oxidative stress, apoptosis, and impaired steroidogenesis and spermatogenesis.
- D-aspartate (D-Asp) is known to stimulate testosterone biosynthesis and spermatogenesis and possesses antioxidant and anti-apoptotic properties.
Purpose of the Study:
- To investigate the protective effects of D-aspartate (D-Asp) against PS-MPs-induced testicular damage in vivo.
- To elucidate the mechanisms underlying D-Asp's protective action against PS-MP toxicity.
Main Methods:
- Adult rats were exposed to PS-MPs, with some receiving D-Asp treatment.
- Assessment of testicular oxidative stress markers (CAT, SOD1, SOD2, 4-HNE, TBARS).
- Evaluation of apoptosis (CYT C, TUNEL assay) and autophagy (LC3BI, LC3BII, p62).
- Analysis of steroidogenic (StAR, 3β-HSD, 17β-HSD) and spermatogenic (PCNA, SYCP3) markers.
Main Results:
- D-Asp treatment reversed PS-MP-induced increases in oxidative stress and apoptosis.
- D-Asp mitigated PS-MP-induced autophagy activation.
- D-Asp restored normal levels of key steroidogenic and spermatogenic markers, counteracting PS-MP damage.
Conclusions:
- D-aspartate demonstrates significant protective effects against PS-microplastic-induced testicular damage in rats.
- D-Asp ameliorates testicular dysfunction by inhibiting oxidative stress, apoptosis, and autophagy, and restoring steroidogenesis and spermatogenesis.
- These findings suggest D-Asp's potential therapeutic value for male reproductive health impacted by microplastic pollution.
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