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AB185. Semen pH effects sperm motility and capacitation by influencing Na/K-ATPase activity and Ca concentration in spermoplasm

BACKGROUND: The pH of semen is one of the important elements for maintaining spermatic normal functions. Variation of semen pH could lead to male infertility, but the mechanism of which is still unknown. METHODS: The healthy human spermatozoa cultured in sperm nutrition solution with pH 5.2, 6.2, 7....

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Autores principales: Chen, Li, Ge, Yifeng, Liang, Yuanjiao, Yao, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4708466/
http://dx.doi.org/10.3978/j.issn.2223-4683.2014.s185
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author Chen, Li
Ge, Yifeng
Liang, Yuanjiao
Yao, Bing
author_facet Chen, Li
Ge, Yifeng
Liang, Yuanjiao
Yao, Bing
author_sort Chen, Li
collection PubMed
description BACKGROUND: The pH of semen is one of the important elements for maintaining spermatic normal functions. Variation of semen pH could lead to male infertility, but the mechanism of which is still unknown. METHODS: The healthy human spermatozoa cultured in sperm nutrition solution with pH 5.2, 6.2, 7.2, 8.2, 9.2 and 10.2 respectively were analyzed for sperm motility, vitality, hypoosmotic swelling rate, Na/K-ATPase activity and the intracellular Caconcentration. RESULTS: The results showed that sperm motility, vitality, hypoosmotic swelling rate were all on the peak in pH 7.2 sperm nutrition solution, and decreased in different degree in pH 5.2, 6.2, 8.2, 9.2 and 10.2. Furthermore, the hypoosmotic swelling rate had a positive correlation with the sperm motility and viability. Sperm penetration meter test was displayed that in compared with pH 7.2, the sperm ascending altitude in sperm nutrition solution with pH 5.2, 6.2, 8.2, 9.2 and 10.2 were significantly declined. In addition, sperm Na/K-ATPase activity in sperm nutrition solution with different pHs was detected and the enzyme activity were significantly lower in pH 5.2, 6.2, 8.2, 9.2 and 10.2 medium compared to pH 7.2. Using flow cytometry and laser confocal scanning microscope to contrast the intracellular Ca concentration of sperm cultured in pH 5.2, 6.2, 7.2, 8.2, 9.2 and 10.2 sperm capacitation solution. Taking pH 7.2 group as a control, the mean fluorescence intensity of sperm in pH 5.2, 6.2 and 10.2 medium were decreased significantly, while pH 8.2 and 9.2 group had no differences with control. CONCLUSIONS: All the results suggested that hydrogen-ion concentration outside spermatozoa could affect sperm motility and capacitation by influencing sperm Na/K-ATPase activity and spermoplasm Ca concentration revealing one of the mechanisms of male infertility.
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spelling pubmed-47084662016-01-26 AB185. Semen pH effects sperm motility and capacitation by influencing Na/K-ATPase activity and Ca concentration in spermoplasm Chen, Li Ge, Yifeng Liang, Yuanjiao Yao, Bing Transl Androl Urol Abstract Publication Basic Research BACKGROUND: The pH of semen is one of the important elements for maintaining spermatic normal functions. Variation of semen pH could lead to male infertility, but the mechanism of which is still unknown. METHODS: The healthy human spermatozoa cultured in sperm nutrition solution with pH 5.2, 6.2, 7.2, 8.2, 9.2 and 10.2 respectively were analyzed for sperm motility, vitality, hypoosmotic swelling rate, Na/K-ATPase activity and the intracellular Caconcentration. RESULTS: The results showed that sperm motility, vitality, hypoosmotic swelling rate were all on the peak in pH 7.2 sperm nutrition solution, and decreased in different degree in pH 5.2, 6.2, 8.2, 9.2 and 10.2. Furthermore, the hypoosmotic swelling rate had a positive correlation with the sperm motility and viability. Sperm penetration meter test was displayed that in compared with pH 7.2, the sperm ascending altitude in sperm nutrition solution with pH 5.2, 6.2, 8.2, 9.2 and 10.2 were significantly declined. In addition, sperm Na/K-ATPase activity in sperm nutrition solution with different pHs was detected and the enzyme activity were significantly lower in pH 5.2, 6.2, 8.2, 9.2 and 10.2 medium compared to pH 7.2. Using flow cytometry and laser confocal scanning microscope to contrast the intracellular Ca concentration of sperm cultured in pH 5.2, 6.2, 7.2, 8.2, 9.2 and 10.2 sperm capacitation solution. Taking pH 7.2 group as a control, the mean fluorescence intensity of sperm in pH 5.2, 6.2 and 10.2 medium were decreased significantly, while pH 8.2 and 9.2 group had no differences with control. CONCLUSIONS: All the results suggested that hydrogen-ion concentration outside spermatozoa could affect sperm motility and capacitation by influencing sperm Na/K-ATPase activity and spermoplasm Ca concentration revealing one of the mechanisms of male infertility. AME Publishing Company 2014-09 /pmc/articles/PMC4708466/ http://dx.doi.org/10.3978/j.issn.2223-4683.2014.s185 Text en 2014 Translational Andrology and Urology. All rights reserved.
spellingShingle Abstract Publication Basic Research
Chen, Li
Ge, Yifeng
Liang, Yuanjiao
Yao, Bing
AB185. Semen pH effects sperm motility and capacitation by influencing Na/K-ATPase activity and Ca concentration in spermoplasm
title AB185. Semen pH effects sperm motility and capacitation by influencing Na/K-ATPase activity and Ca concentration in spermoplasm
title_full AB185. Semen pH effects sperm motility and capacitation by influencing Na/K-ATPase activity and Ca concentration in spermoplasm
title_fullStr AB185. Semen pH effects sperm motility and capacitation by influencing Na/K-ATPase activity and Ca concentration in spermoplasm
title_full_unstemmed AB185. Semen pH effects sperm motility and capacitation by influencing Na/K-ATPase activity and Ca concentration in spermoplasm
title_short AB185. Semen pH effects sperm motility and capacitation by influencing Na/K-ATPase activity and Ca concentration in spermoplasm
title_sort ab185. semen ph effects sperm motility and capacitation by influencing na/k-atpase activity and ca concentration in spermoplasm
topic Abstract Publication Basic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4708466/
http://dx.doi.org/10.3978/j.issn.2223-4683.2014.s185
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