Inhibitory effects of human seminal plasma on an ELISA used to detect anti-sperm antibodies: Implications for the determination of sperm quality

2000 ◽  
Vol 47 (1) ◽  
pp. 33-40 ◽  
Author(s):  
Nian Qing Lu ◽  
Shu Wei Zha
Andrology ◽  
2019 ◽  
Vol 7 (6) ◽  
pp. 859-866 ◽  
Author(s):  
M. Rao ◽  
Z. Wu ◽  
Y. Wen ◽  
R. Wang ◽  
S. Zhao ◽  
...  

1988 ◽  
Vol 34 (8) ◽  
pp. 1605-1607 ◽  
Author(s):  
M Gavella

Abstract I describe an automated assay for zinc and acid phosphatase in seminal plasma. These, which are markers of the function of the prostate, were assayed bichromatically with an Abbott ABA-100 analyzer. As many as 25 samples of human seminal plasma can be analyzed sequentially with CVs of 3.1% for zinc and 1.5% for acid phosphatase. The sensitivity, specificity, and speed of this assay system make it practicable for use in investigation of male infertility.


1997 ◽  
Vol 11 (3) ◽  
pp. 182-184 ◽  
Author(s):  
P. Apostoli ◽  
S. Porru ◽  
C. Morandi ◽  
A. Menditto

2006 ◽  
Vol 29 (2) ◽  
pp. 331-338 ◽  
Author(s):  
LENA CARLSSON ◽  
GUNNAR RONQUIST ◽  
RUNE ELIASSON ◽  
NILS EGBERG ◽  
ANDERS LARSSON

2010 ◽  
Vol 22 (5) ◽  
pp. 886 ◽  
Author(s):  
H. Bertelsmann ◽  
S. Keppler ◽  
M. Höltershinken ◽  
H. Bollwein ◽  
D. Behne ◽  
...  

The essential trace element selenium is indispensable for male fertility in mammals. Until now, little data existed regarding the relationship between selenium and sperm quality in the stallion. Selenium, or selenium-dependent glutathione peroxidase activity, was determined in red blood cells, semen, seminal plasma and spermatozoa, and the percentages of spermatozoa with progressive motility (PMS), intact membranes (PMI), altered (positive) acrosomal status (PAS) and detectable DNA damage, determined by the sperm chromatin structure assay, were evaluated in 41 healthy stallions (three samples each). The pregnancy rate per oestrus cycle (PRC) served as an estimation of fertility. An adverse effect on stallion fertility caused by low dietary selenium intake was excluded, as all stallions had sufficient selenium levels in their blood. Interestingly, no significant correlations (P > 0.05) between the selenium level in blood and the selenium level in seminal plasma or spermatozoa were found, suggesting that the selenium level in blood is no indicator of an adequate selenium supply for spermatogenesis. The selenium level in spermatozoa (nmol billion–1) was correlated with PMI, PMS and PAS (r = 0.40, r = 0.31 and r = –0.42, respectively; P ≤ 0.05), and the selenium concentration in spermatozoa (nmol g–1) was correlated with PRC (r = 0.40, P < 0.03). The results of the present study show that the determination of an adequate selenium status for the male equine reproduction requires the analysis of selenium in spermatozoa. Furthermore, selenium is associated with improved sperm quality and fertility in the stallion.


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