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Incubating frozen-thawed buffalo sperm with olive fruit extracts counteracts thawing-induced oxidative stress and improves semen quality

Title: Incubating frozen-thawed buffalo sperm with olive fruit extracts counteracts thawing-induced oxidative stress and improves semen quality
Authors: Benitez Mora M. P.; Del Prete C.; Longobardi V.; Cocchia N.; Esposito R.; Piscopo F.; Sicari A.; Vinale F.; Carbonari A.; Gasparrini B.
Contributors: Benitez Mora, M. P.; Del Prete, C.; Longobardi, V.; Cocchia, N.; Esposito, R.; Piscopo, F.; Sicari, A.; Vinale, F.; Carbonari, A.; Gasparrini, B.
Publication Year: 2024
Collection: IRIS Università degli Studi di Napoli Federico II
Subject Terms: Antioxidant; Hydroxytyrosol; Reactive oxygen specie; Semen quality; Spermatozoa
Description: Freezing-thawing procedures and semen manipulation for in vitro fertilization induce oxidative stress, which in turn leads to impaired sperm quality. The aim of this study was to evaluate whether incubation of frozen-thawed buffalo semen with olive fruit extracts (OFE), known to contain a high concentration of phenolic antioxidants, would improve semen quality by reducing oxidative stress. Frozen sperm (4 ejaculates/4 bulls/3 replicates) were thawed and diluted to 30 × 106/mL in IVF medium with 0, 72, 143, and 214 μL/mL of OFE, corresponding to 0 (D0-control), 50 (D50), 100 (D100), and 150 (D150) μM hydroxytyrosol. Sperm viability, acrosome integrity, membrane functionality, motility, and sperm kinetics were evaluated immediately after thawing (T0) and after 1 (T1) and 2 h (T2) of incubation at 38.7 °C. Based on the results, sperm biological antioxidant potential (BAP) and ROS levels (ROMs) were assessed in D0 and D100 groups at T1 and T2. To assess the effect of OFE on fertilizing ability, heterologous penetration rates were also evaluated, using bovine abattoir-derived oocytes. The treatment with OFE at all concentrations tested increased (P < 0.05) the percentage of acrosome intact spermatozoa compared to the D0-control at T1, but the effect was more evident (P < 0.01) with D100 (54.5 ± 3.0, 60.5 ± 1.5, 65.2 ± 3.3, and 62.5 ± 1.7, with D0, D50, D100, and D150 OFE, respectively). Total motility, progressive motility, rapid velocity, and progressive velocity decreased (P < 0.05) at T2 only in the D0-control group. The percentage of rapidly progressive sperm and the progressive motility tended to increase (P < 0.10) at T1 and T2, respectively, in D100 compared to D0 (24.7 ± 4.1 vs 16.4 ± 1.6 and 22.8 ± 2.7 vs 17.0 ± 1.2, respectively). The treatment with D100 OFE of frozen-thawed sperm increased (P < 0.05) some kinetic parameters (VAP and WOB). Spermatozoa incubated with D100 OFE exhibited higher (P < 0.01) total and normospermic oocyte penetration rates compared to D0 (86.5 ± 1.4 vs 78.5 ± ...
Document Type: article in journal/newspaper
Language: English
Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:001302150500001; volume:229; firstpage:118; lastpage:126; numberofpages:9; journal:THERIOGENOLOGY; https://hdl.handle.net/11588/970243
DOI: 10.1016/j.theriogenology.2024.08.024
Availability: https://hdl.handle.net/11588/970243; https://doi.org/10.1016/j.theriogenology.2024.08.024
Rights: info:eu-repo/semantics/openAccess ; license:Copyright dell'editore ; license uri:publisher
Accession Number: edsbas.6346A398
Database: BASE