2006
DOI: 10.1515/cclm.2006.154
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Fluorimetric determination of activity and isoenzyme composition of N-acetyl-β-D-hexosaminidase in seminal plasma of fertile men and infertile patients with secretory azoospermia

Abstract: Our findings show that the isoenzyme composition of N-acetyl-beta-D-hexosaminidase in seminal plasma from patients with secretory azoospermia is significantly different from controls, but this difference does not represent a useful marker of secretory azoospermia. The fluorimetric assays are simple and rapid methods for evaluating the isoenzyme composition.

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Cited by 4 publications
(2 citation statements)
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“…Sperm contain the enzyme N-acetyl-beta-D hexosaminidase type B or HEX-B, which cleaves the ZP-glycoproteins of the zona pellucida of the ovum. In vitro employment of ZP-glycoprotein analogues to block HEX-B of rodent and bovine semen had 98% efficacy regarding fertilization failure, 108 while in vivo, the corresponding efficiency rates were approximately 90%, 109 without overt adverse effects and restoration of fertility one week after discontinuation of treatment.…”
Section: Disruption Of Sperm Transport In the Epididymismentioning
confidence: 99%
“…Sperm contain the enzyme N-acetyl-beta-D hexosaminidase type B or HEX-B, which cleaves the ZP-glycoproteins of the zona pellucida of the ovum. In vitro employment of ZP-glycoprotein analogues to block HEX-B of rodent and bovine semen had 98% efficacy regarding fertilization failure, 108 while in vivo, the corresponding efficiency rates were approximately 90%, 109 without overt adverse effects and restoration of fertility one week after discontinuation of treatment.…”
Section: Disruption Of Sperm Transport In the Epididymismentioning
confidence: 99%
“…[17][18][19] Different and expensive techniques have been carried out for the evaluation of NAG isoenzymes in urine. [17][18][19][20][21][22][23] Noteworthy, all NAG isoenzymes have activity toward 4-methylumbelliferyl-2-acetamido-2-deoxy-β-D-glucopyranoside (MUG) substrate. The presence of α subunit enables NAG A to hydrolyze the GM2 ganglioside and the fluorogenic substrate 4-methylumbelliferyl-2-acetamido-2-deoxy-β-Dglucopyranoside-6-sulfate (MUGS) while NAG B isoform does not hydrolyze the MUGS substrate.…”
Section: Introductionmentioning
confidence: 99%