Oxidative status in testis and epididymal sperm parameters after acute and chronic stress by cold-water immersion in the adult rat

• Published in: Systems biology in reproductive medicine Vol. 61; no. 3; pp. 150 - 160
• Main Authors: García-Díaz, Erika Cecilia, Gómez-Quiroz, Luis Enrique, Arenas-Ríos, Edith, Aragón-Martínez, Andrés, Ibarra-Arias, Juan Antonio, Retana-Márquez, María del Socorro I.
• Format: Journal Article
• Language: English
• Published: England Informa Healthcare USA, Inc 01.06.2015; Informa Healthcare
• Subjects: Acute Disease; Animals; Antioxidant enzymes; Chromatography, High Pressure Liquid; Chronic Disease; Cold Temperature; Corticosterone - blood; Epididymis - cytology; Epididymis - metabolism; lipid peroxidation; Male; Oxidative Stress; Rats; Rats, Wistar; redox state; sperm parameters; stress; Stress, Physiological; Testis - cytology; Testis - metabolism; Testosterone - blood; Water; stress; redox state; lipid peroxidation; Antioxidant enzymes; oxidative stress; sperm parameters
• ISSN: 1939-6368; 1939-6376
• DOI: 10.3109/19396368.2015.1008071

Abstract Stress is associated with detrimental effects on male reproductive function. It is known that stress increases reactive oxygen species (ROS) generation in the male reproductive tract. High ROS levels may be linked to low sperm quality and male infertility. However, it is still not clear if ROS are generated by stress in the testis. The objective of this study was to characterize the role of oxidative stress induced by cold-water immersion stress in the testis of adult male rats and its relation with alterations in cauda epididymal sperm. Adult male rats were exposed to acute stress or chronic stress by cold-water immersion. Rats were sacrificed at 0, 6, 12, and 24 hours immediately following acute stress exposure, and after 20, 40, and 50 days of chronic stress. ROS production increased only at 6 hours post-stress, while the activity and expression of antioxidant enzymes, lipid peroxidation (LPO), and sperm parameters were not modified in the testis. Corticosterone increased immediately after acute stress, whereas testosterone was not modified. After chronic stress, testicular absolute weight decreased; in addition, ROS production and LPO increased at 20, 40, and 50 days. The activity of superoxide dismutase (SOD) and glutathione peroxidase (GPx) decreased throughout the duration of chronic stress and the activity of catalase (CAT) decreased at 40 and 50 days, and increased at 20 days. The expression of copper/zinc superoxide dismutase (SOD1) and CAT were not modified, but the expression of phospholipid hydroperoxide glutathione peroxidase (GPx-4) decreased at 20 days. Motility, viability, and sperm count decreased, while abnormal sperm increased with chronic stress. These results suggest that during acute stress there is a redox state regulation in the testis since no deleterious effect was observed. In contrast, equilibrium redox is lost during chronic stress, with low enzyme activity but without modifying their expression. In addition, corticosterone increased while testosterone decreased, this decrease is related to the negative effects seen in sperm.