Authors:
Supitcha Kaewma Bio-Innovation Research Center, Tokushima University, Tokushima, Japan
Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand
Faculty of Veterinary Science, Prince of Songkla University, Songkhla, Thailand

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Zhao Namula Bio-Innovation Research Center, Tokushima University, Tokushima, Japan
College of Coastal Agricultural Sciences, Guangdong Ocean University, Zhanjiang China

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Suong Thi Nguyen Joint Graduate School of Veterinary Sciences, Yamaguchi University, Yamaguchi, Japan

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Qingyi Lin Bio-Innovation Research Center, Tokushima University, Tokushima, Japan
Faculty of Bioscience and Bioindustry, Tokushima University, Tokushima, Japan

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Nanaka Torigoe Bio-Innovation Research Center, Tokushima University, Tokushima, Japan
Faculty of Bioscience and Bioindustry, Tokushima University, Tokushima, Japan

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Bin Liu Bio-Innovation Research Center, Tokushima University, Tokushima, Japan
Faculty of Bioscience and Bioindustry, Tokushima University, Tokushima, Japan

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Megumi Nagahara Bio-Innovation Research Center, Tokushima University, Tokushima, Japan
Faculty of Bioscience and Bioindustry, Tokushima University, Tokushima, Japan

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Masahiro Nii Tokushima Prefectural Livestock Research Institute, Tokushima, Japan

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Masayasu Taniguchi Joint Graduate School of Veterinary Sciences, Yamaguchi University, Yamaguchi, Japan

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Takeshige Otoi Bio-Innovation Research Center, Tokushima University, Tokushima, Japan
Faculty of Bioscience and Bioindustry, Tokushima University, Tokushima, Japan

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Abstract

This study examined the effects of ergothioneine (EGT) supplementation as an antioxidant on the quality of boar spermatozoa when using liquid and frozen preservation methods. In the first experiment, boar semen was preserved in an extender supplemented with 0, 50, 100 and 200 µM EGT, at 15 °C, part of the samples for one and another part for three weeks. In comparison with the control (without EGT), EGT supplementation at 100 µM significantly increased the percentage of total motility of spermatozoa that were preserved as a liquid both for one and three weeks (P < 0.05). EGT supplementation did not affect the quality of preserved spermatozoa, irrespective of the EGT concentration. In the second experiment, semen was frozen and thawed in the freezing extender supplemented with 0, 50, 100 and 200 µM EGT. In comparison with the control, the 100 µM EGT supplementation significantly increased the percentages of total and progressive motility of frozen-thawed spermatozoa (P < 0.05). EGT (100 µM) supplementation did not affect the viability, the plasma membrane integrity, or the acrosomal integrity of frozen-thawed spermatozoa. These findings indicate that supplementing extenders with 100 µM EGT may improve the motility of boar sperm in both liquid and freezing preservation methods.

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Senior editors

Editor-in-Chief: Ferenc BASKA

Editorial assistant: Szilvia PÁLINKÁS

 

Editorial Board

  • Mária BENKŐ (Acta Veterinaria Hungarica, Budapest, Hungary)
  • Gábor BODÓ (University of Veterinary Medicine, Budapest, Hungary)
  • Béla DÉNES (University of Veterinary Medicine, Budapest Hungary)
  • Edit ESZTERBAUER (Veterinary Medical Research Institute, Budapest, Hungary)
  • Hedvig FÉBEL (University of Veterinary Medicine, Budapest, Hungary)
  • László FODOR (University of Veterinary Medicine, Budapest, Hungary)
  • János GÁL (University of Veterinary Medicine, Budapest, Hungary)
  • Balázs HARRACH (Veterinary Medical Research Institute, Budapest, Hungary)
  • Peter MASSÁNYI (Slovak University of Agriculture in Nitra, Nitra, Slovak Republic)
  • Béla NAGY (Veterinary Medical Research Institute, Budapest, Hungary)
  • Tibor NÉMETH (University of Veterinary Medicine, Budapest, Hungary)
  • Zsuzsanna NEOGRÁDY (University of Veterinary Medicine, Budapest, Hungary)
  • Dušan PALIĆ (Ludwig Maximilian University, Munich, Germany)
  • Alessandra PELAGALLI (University of Naples Federico II, Naples, Italy)
  • Kurt PFISTER (Ludwig-Maximilians-University of Munich, Munich, Germany)
  • László SOLTI (University of Veterinary Medicine, Budapest, Hungary)
  • József SZABÓ (University of Veterinary Medicine, Budapest, Hungary)
  • Péter VAJDOVICH (University of Veterinary Medicine, Budapest, Hungary)
  • János VARGA (University of Veterinary Medicine, Budapest, Hungary)
  • Štefan VILČEK (University of Veterinary Medicine in Kosice, Kosice, Slovak Republic)
  • Károly VÖRÖS (University of Veterinary Medicine, Budapest, Hungary)
  • Herbert WEISSENBÖCK (University of Veterinary Medicine, Vienna, Austria)
  • Attila ZSARNOVSZKY (Szent István University, Gödöllő, Hungary)

ACTA VETERINARIA HUNGARICA

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E-mail: acta.veterinaria@univet.hu (ed.-in-chief)

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Acta Veterinaria Hungarica
Language English
Size A4
Year of
Foundation
1951
Volumes
per Year
1
Issues
per Year
4
Founder Magyar Tudományos Akadémia
Founder's
Address
H-1051 Budapest, Hungary, Széchenyi István tér 9.
Publisher Akadémiai Kiadó
Publisher's
Address
H-1117 Budapest, Hungary 1516 Budapest, PO Box 245.
Responsible
Publisher
Chief Executive Officer, Akadémiai Kiadó
ISSN 0236-6290 (Print)
ISSN 1588-2705 (Online)

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