, FIGUEROA VILLALOBOS, ELIAS GUSTAVO, VALDEBENITO ISLER, NEMESIO IVAN, Villalobos, Elías Figueroa, Lee-Estevez, Manuel, Valdebenito, Iván, Watanabe, Ii Sei, Pinheiro de Souza Oliveira, Ricardo Pinheiro S., Romero, Jaime, Castillo, Rodrigo L., Farias, Jorge G.

The development of cryopreservation techniques has led to important changes in animal reproductive biotechnology. However, these techniques are associated with cellular and molecular damage, affecting the mitochondrial function and quality of spermatozoa; moreover studies in fish are limited. In this work, the effects of cryopreservation on ultrastructure, mitochondrial function and antioxidant defences in Atlantic salmon (Salmo salar) spermatozoa were assessed, along with intracellular calcium (Ca2+)i, mitochondrial DNA sequence and sperm function (motility and fertilization rate). Significant ultrastructure alterations of the middle piece and mitochondria were observed in cryopreserved spermatozoa as compared to controls. Oxygen consumption and ATP were also significantly different in cryopreserved spermatozoa, and in spermatozoa incubated with electron transport chain (ETC) uncouplers and inhibitors. Mitochondrial membrane potential, motility, fertilization rate and Ca2+ i in cryopreserved spermatozoa displayed significant reductions compared to fresh spermatozoa. Mitochondrial potential correlated significantly with motility and fertilization rate. A redox imbalance was observed in frozen spermatozoa due to increased lipid peroxidation and superoxide anion production as compared to fresh spermatozoa. Likewise, increased activity of glutathione peroxidase and total glutathione (GSH/GSSG), as well as reduced catalase activity, were observed in comparison with fresh spermatozoa. Our results contribute to a better understanding of cryodamage to mitochondrial functions in fish spermatozoa, and enabled us to establish potential quality assessment indicators. The data suggest that cryopreservation induces a reduction in overall sperm quality and functionality through disruption of the mitochondrial ultrastructure and function, leading to energy depletion and increased oxidative stress. This knowledge may also lead to the identification of a potential biotechnological tool for improving reproductive efficiency in species of commercial and biological interest. © 2019 Elsevier B.V., All rights reserved.

, FIGUEROA VILLALOBOS, ELIAS GUSTAVO, VALDEBENITO ISLER, NEMESIO IVAN, Dumorné, Kelly, Valdebenito, Iván, Risopatron, Jennie, Villalobos, Elías Figueroa, Díaz, Rommy, Farias, Jorge G.

In this study, the morphology and ultrastructure of Genypterus blacodes spermatozoa were characterized through scanning and transmission electron microscopy. Findings revealed that the G. blacodes spermatozoa can be differentiated into three major parts: a spherical head without an acrosome (typical for externally fertilizing fish), a short mid-piece, and a long flagellum. The mean length of the spermatozoa was 57.6 ± 6.08 ?m, with flagella accounting for 56.2 ± 7.2 ?m. The head was 1.47 ± 0.2 ?m long, and 0.89 ± 0.06 ?m wide. The mid-piece had a total dimension of 0.72 ± 0.16 ?m, and was 0.31 ± 0.02 ?m in length and 0.6 ± 0.05 ?m in width. It was located lateral to the nucleus and contained 4 or 5 spherical mitochondria. The mitochondria were separated from the axoneme by a cytoplasmic canal. The main piece of the flagellum had short irregular side-fins, and the axoneme was composed of the typical 9 + 2 microtubular doublet structure enclosed by a cell membrane. The present study reveals that G. blacodes sperm can be categorized as a primitive type. This study is the first to provide comprehensive details on the morphology and ultrastructure of spermatozoa in G. blacodes. © 2018 Elsevier B.V., All rights reserved.