Semen collection by urethral catheterization and electro-ejaculation with different voltages, and the effect of holding temperature and cooling rate before cryopreservation on semen quality in the Japanese macaque (Macaca fuscata)
In the Japanese macaque, semen has been collected by electro-ejaculation (EE), using the higher voltage stimuli compared to other species including genus Macaca. Semen coagulates immediately after ejaculation, which makes difficult to produce high-quality semen for artificial insemination. Recently,...
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Published in | Journal of Veterinary Medical Science Vol. 84; no. 3; pp. 429 - 438 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Japan
JAPANESE SOCIETY OF VETERINARY SCIENCE
2022
The Japanese Society of Veterinary Science |
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Abstract | In the Japanese macaque, semen has been collected by electro-ejaculation (EE), using the higher voltage stimuli compared to other species including genus Macaca. Semen coagulates immediately after ejaculation, which makes difficult to produce high-quality semen for artificial insemination. Recently, semen collection using urethral catheterization (UC) has been reported in carnivore and this technique may allow semen collection without coagulation in a less invasive manner. Further, the temporal preservation temperature and cooling rate of semen during cryopreservation affect post thawing sperm quality. In this study, to improve semen quality and quantity, as well as the animal welfare, semen collection was performed by EE with high (5–15 V) or low (3–6 V) voltage, UC and a combination of the two (EE-UC). It has been suggested that a high voltage is necessary for semen collection, but 10 V stimulation was effective enough and 15 V is for additional sperm collection. Also, liquid semen was collected by EE-UC and this could increase the total number of sperm. Further, to improve the post thawing sperm motility, semen was kept at four temperatures (4, 15, 25 and 37°C) for 60 min, and processed with two cooling procedures (slow cooling before second dilution and fast cooling after second dilution). Holding semen at 25°C and fast cooling after the second dilution maintained progressive motile sperm rate. The present results will contribute to the improvement of semen collection and animal welfare of Japanese macaques. |
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AbstractList | In the Japanese macaque, semen has been collected by electro-ejaculation (EE), using the higher voltage stimuli compared to other species including genus Macaca. Semen coagulates immediately after ejaculation, which makes difficult to produce high-quality semen for artificial insemination. Recently, semen collection using urethral catheterization (UC) has been reported in carnivore and this technique may allow semen collection without coagulation in a less invasive manner. Further, the temporal preservation temperature and cooling rate of semen during cryopreservation affect post thawing sperm quality. In this study, to improve semen quality and quantity, as well as the animal welfare, semen collection was performed by EE with high (5–15 V) or low (3–6 V) voltage, UC and a combination of the two (EE-UC). It has been suggested that a high voltage is necessary for semen collection, but 10 V stimulation was effective enough and 15 V is for additional sperm collection. Also, liquid semen was collected by EE-UC and this could increase the total number of sperm. Further, to improve the post thawing sperm motility, semen was kept at four temperatures (4, 15, 25 and 37°C) for 60 min, and processed with two cooling procedures (slow cooling before second dilution and fast cooling after second dilution). Holding semen at 25°C and fast cooling after the second dilution maintained progressive motile sperm rate. The present results will contribute to the improvement of semen collection and animal welfare of Japanese macaques. In the Japanese macaque, semen has been collected by electro-ejaculation (EE), using the higher voltage stimuli compared to other species including genus Macaca. Semen coagulates immediately after ejaculation, which makes difficult to produce high-quality semen for artificial insemination. Recently, semen collection using urethral catheterization (UC) has been reported in carnivore and this technique may allow semen collection without coagulation in a less invasive manner. Further, the temporal preservation temperature and cooling rate of semen during cryopreservation affect post thawing sperm quality. In this study, to improve semen quality and quantity, as well as the animal welfare, semen collection was performed by EE with high (5-15 V) or low (3-6 V) voltage, UC and a combination of the two (EE-UC). It has been suggested that a high voltage is necessary for semen collection, but 10 V stimulation was effective enough and 15 V is for additional sperm collection. Also, liquid semen was collected by EE-UC and this could increase the total number of sperm. Further, to improve the post thawing sperm motility, semen was kept at four temperatures (4, 15, 25 and 37°C) for 60 min, and processed with two cooling procedures (slow cooling before second dilution and fast cooling after second dilution). Holding semen at 25°C and fast cooling after the second dilution maintained progressive motile sperm rate. The present results will contribute to the improvement of semen collection and animal welfare of Japanese macaques.In the Japanese macaque, semen has been collected by electro-ejaculation (EE), using the higher voltage stimuli compared to other species including genus Macaca. Semen coagulates immediately after ejaculation, which makes difficult to produce high-quality semen for artificial insemination. Recently, semen collection using urethral catheterization (UC) has been reported in carnivore and this technique may allow semen collection without coagulation in a less invasive manner. Further, the temporal preservation temperature and cooling rate of semen during cryopreservation affect post thawing sperm quality. In this study, to improve semen quality and quantity, as well as the animal welfare, semen collection was performed by EE with high (5-15 V) or low (3-6 V) voltage, UC and a combination of the two (EE-UC). It has been suggested that a high voltage is necessary for semen collection, but 10 V stimulation was effective enough and 15 V is for additional sperm collection. Also, liquid semen was collected by EE-UC and this could increase the total number of sperm. Further, to improve the post thawing sperm motility, semen was kept at four temperatures (4, 15, 25 and 37°C) for 60 min, and processed with two cooling procedures (slow cooling before second dilution and fast cooling after second dilution). Holding semen at 25°C and fast cooling after the second dilution maintained progressive motile sperm rate. The present results will contribute to the improvement of semen collection and animal welfare of Japanese macaques. In the Japanese macaque, semen has been collected by electro-ejaculation (EE), using the higher voltage stimuli compared to other species including genus Macaca . Semen coagulates immediately after ejaculation, which makes difficult to produce high-quality semen for artificial insemination. Recently, semen collection using urethral catheterization (UC) has been reported in carnivore and this technique may allow semen collection without coagulation in a less invasive manner. Further, the temporal preservation temperature and cooling rate of semen during cryopreservation affect post thawing sperm quality. In this study, to improve semen quality and quantity, as well as the animal welfare, semen collection was performed by EE with high (5–15 V) or low (3–6 V) voltage, UC and a combination of the two (EE-UC). It has been suggested that a high voltage is necessary for semen collection, but 10 V stimulation was effective enough and 15 V is for additional sperm collection. Also, liquid semen was collected by EE-UC and this could increase the total number of sperm. Further, to improve the post thawing sperm motility, semen was kept at four temperatures (4, 15, 25 and 37°C) for 60 min, and processed with two cooling procedures (slow cooling before second dilution and fast cooling after second dilution). Holding semen at 25°C and fast cooling after the second dilution maintained progressive motile sperm rate. The present results will contribute to the improvement of semen collection and animal welfare of Japanese macaques. |
ArticleNumber | 21-0590 |
Author | OKAMOTO, Munehiro KATAGIRI, Seiji KANNO, Chihiro IMAI, Hiroo TAKAESU, Noboru SUGIMOTO, Kosuke SASHIKA, Mariko NAGANO, Masashi KANEKO, Akihisa INDO, Yoriko YANAGAWA, Yojiro HIRAI, Hirohisa SHIMOZURU, Michito TSUBOTA, Toshio |
Author_xml | – sequence: 1 fullname: TAKAESU, Noboru organization: Laboratory of Wildlife Biology and Medicine, Faculty of Veterinary Medicine, Hokkaido University, Hokkaido, Japan – sequence: 2 fullname: KANNO, Chihiro organization: Laboratory of Clinical Veterinary Medicine for Large Animal, School of Veterinary Medicine, Kitasato University, Aomori, Japan – sequence: 3 fullname: SUGIMOTO, Kosuke organization: Laboratory of Theriogenology, Faculty of Veterinary Medicine, Hokkaido University, Hokkaido, Japan – sequence: 4 fullname: NAGANO, Masashi organization: Laboratory of Animal Reproduction, School of Veterinary Medicine, Kitasato University, Aomori, Japan – sequence: 5 fullname: KANEKO, Akihisa organization: Primate Research Institute, Kyoto University, Aichi, Japan – sequence: 6 fullname: INDO, Yoriko organization: Primate Research Institute, Kyoto University, Aichi, Japan – sequence: 7 fullname: IMAI, Hiroo organization: Primate Research Institute, Kyoto University, Aichi, Japan – sequence: 8 fullname: HIRAI, Hirohisa organization: Primate Research Institute, Kyoto University, Aichi, Japan – sequence: 9 fullname: OKAMOTO, Munehiro organization: Primate Research Institute, Kyoto University, Aichi, Japan – sequence: 10 fullname: SASHIKA, Mariko organization: Laboratory of Wildlife Biology and Medicine, Faculty of Veterinary Medicine, Hokkaido University, Hokkaido, Japan – sequence: 11 fullname: SHIMOZURU, Michito organization: Laboratory of Wildlife Biology and Medicine, Faculty of Veterinary Medicine, Hokkaido University, Hokkaido, Japan – sequence: 12 fullname: KATAGIRI, Seiji organization: Laboratory of Theriogenology, Faculty of Veterinary Medicine, Hokkaido University, Hokkaido, Japan – sequence: 13 fullname: TSUBOTA, Toshio organization: Laboratory of Wildlife Biology and Medicine, Faculty of Veterinary Medicine, Hokkaido University, Hokkaido, Japan – sequence: 14 fullname: YANAGAWA, Yojiro organization: Laboratory of Theriogenology, Faculty of Veterinary Medicine, Hokkaido University, Hokkaido, Japan |
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Keywords | semen collection electro-ejaculation Japanese macaques cryopreservation urethral catheterization |
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SubjectTerms | Animals cryopreservation Cryopreservation - veterinary Ejaculation electro-ejaculation Japanese macaques Macaca Macaca fuscata Male Semen - physiology Semen Analysis - veterinary semen collection Semen Preservation - methods Semen Preservation - veterinary Sperm Motility - physiology Spermatozoa - physiology Temperature urethral catheterization Urinary Catheterization - veterinary Wildlife Science |
Title | Semen collection by urethral catheterization and electro-ejaculation with different voltages, and the effect of holding temperature and cooling rate before cryopreservation on semen quality in the Japanese macaque (Macaca fuscata) |
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