1995
DOI: 10.1007/bf00929503
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Protective effect of seminal plasma proteins on the degradation of ascorbic acid

Abstract: The objectives of this study were to determine ascorbic acid stability and its effect on antiproteinase activity of seminal plasma in the presence of an oxidant. Effect of seminal plasma, and additives: glutathione, albumin, hydrogen peroxide and Tris buffer, on ascorbic acid degradation was investigated by UV absorbance. Antiproteinase against trypsin amidase activity was measured spectrophotometrically using N-benzoyl-DL-arginine-p-nitroanilide (BAPNA) as substrate. Ascorbic acid was destroyed much more rapi… Show more

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Cited by 23 publications
(7 citation statements)
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“…The crossover point was between 1-2 mM ascorbate according to Rees and Slater (1997) . According to our previous work, inactivated antiproteinase activity of fish seminal plasma was not protected in vitro by exogenous ascorbic acid of 1-8 mM (Liu et al . 1995).…”
Section: Discussionmentioning
confidence: 94%
“…The crossover point was between 1-2 mM ascorbate according to Rees and Slater (1997) . According to our previous work, inactivated antiproteinase activity of fish seminal plasma was not protected in vitro by exogenous ascorbic acid of 1-8 mM (Liu et al . 1995).…”
Section: Discussionmentioning
confidence: 94%
“…Oxidative damage to some blood plasma anti-proteinase inhibitors led to a reduction, over 1000 times, of their inhibitory activity (Patterson 1991 ). We have found recently that seminal plasma anti-trypsin activity can be reduced by in vitro oxidation by hydrogen peroxide (Liu et al 1995). However, no protective effect of AA was found in vitro; ascorbic acid, at concentrations 1-8 mM, had pro-oxidant effect.…”
Section: Osmolality Of Seminal Plasmamentioning
confidence: 90%
“…In seminal plasma and in spermatozoa of teleostei fish there are different types of antioxidants (Liu et al, 1995;Ciereszko et al, 2000;Lahnsteiner et al, 2010a), which are important for the in vivo maintenance of sperm viability, and that could have relevance for the practice of supplementation of the semen storage and cryopre-servation mediums to improve the quality of the spermatozoa. Ascorbic acid Metwally & Fouad, 2009) and Uric acid (Ciereszko et al, 1999) are considered important antioxidants in teleostei semen.…”
Section: Introductionmentioning
confidence: 99%