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pubmed-article:8105063pubmed:abstractTextThe effects of adenosine and its analogues on human sperm motility were studied using a transmembrane migration method. Specific binding sites for adenosine in human sperm were also investigated. Adenosine and 5'-N-ethylcarboxamidoadenosine (NECA) stimulated human sperm motility with similar efficacies and the maximal amplitudes of motility increases were both about 70%. 3,7-Dimethyl-1-propargylxanthine (DMPX), a potent A2 antagonist, competitively antagonized NECA-induced motility stimulation. Successively higher concentrations of DMPX shifted the dose-response curve of NECA to the right in a nearly parallel fashion. Dipyridamole, an inhibitor of adenosine uptake, does not reduce the ability of adenosine to stimulate human sperm motility. In radioligand-binding studies, adenosine A1 selective analogues, cyclopentyl-1,3-dipropylxanthine and 1-methyl-2-phenylethyl adenosine, have little competitive effect on [3H]NECA binding in human sperm membrane. These results provide evidence that adenosine enhances human sperm motility via adenosine A2 receptors on the surface of sperm membranes.lld:pubmed
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pubmed-article:8105063pubmed:authorpubmed-author:LindenJJlld:pubmed
pubmed-article:8105063pubmed:authorpubmed-author:ChenS SSSlld:pubmed
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pubmed-article:8105063pubmed:authorpubmed-author:ShehM LMLlld:pubmed
pubmed-article:8105063pubmed:authorpubmed-author:ChiangP HPHlld:pubmed
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pubmed-article:8105063pubmed:pagination650-3lld:pubmed
pubmed-article:8105063pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:8105063pubmed:year1993lld:pubmed
pubmed-article:8105063pubmed:articleTitleAdenosine stimulates human sperm motility via A2 receptors.lld:pubmed
pubmed-article:8105063pubmed:affiliationGraduate Institute of Medicine, Kaohsiung Medical College, Taiwan, R.O.C.lld:pubmed
pubmed-article:8105063pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8105063pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:8105063pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed