Regulation of spermatozoa motility in response to cations in Russian sturgeon Acipenser gueldenstaedtii
Language English Country United States Media print-electronic
Document type Evaluation Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
22444559
DOI
10.1016/j.theriogenology.2012.01.025
PII: S0093-691X(12)00060-X
Knihovny.cz E-resources
- MeSH
- Semen Analysis MeSH
- Potassium pharmacology MeSH
- Magnesium pharmacology MeSH
- Cations pharmacology MeSH
- Sperm Motility drug effects MeSH
- Osmolar Concentration MeSH
- Swimming MeSH
- Fishes * physiology MeSH
- Sodium pharmacology MeSH
- Spermatozoa drug effects physiology MeSH
- Calcium pharmacology MeSH
- Aquaculture MeSH
- Dose-Response Relationship, Drug MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Evaluation Study MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Potassium MeSH
- Magnesium MeSH
- Cations MeSH
- Sodium MeSH
- Calcium MeSH
The aim of this study was to investigate the response of Russian sturgeon (Acipenser gueldenstaedtii) sperm to external cations (Na(+), K(+), Ca(2+), and Mg(2+)) and their susceptibility on the induction of motility and swimming behavior. An in vitro spermatozoa motility assay was used by a computer-aided Motion-Analysis system. Sperm motility was inhibited by 60 mM NaCl (~140 mOsm/kg) and 0.7 mM KCl solutions (~ 21.4 mOsm/kg). The Ca(2+) and Mg(2+) ions were not able to inhibit spermatozoa motility. By contrast, Na(+) within a limited concentration range (between 45 and 55 mm) was able to reverse the inhibitory effect of K(+) at the critical concentration (0.7 mM). Ca(2+) and Mg(2+) were also able to reverse the K(+)-mediated spermatozoa motility restriction at concentrations starting at 0.01 and 0.1 mM, respectively. These results provide evidence for the role of K(+) in suppressing spermatozoa motility, and suggest that Ca(2+), Mg(2+), and possibly Na(+) trigger motility in Russian sturgeon sperm.
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