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Oxidative stress markers in seminal plasma of idiopathic infertile men may be associated with glutathione S‐transferase M1 and T1 null genotypes
Author(s) -
Barati Erfaneh,
Karimian Mohammad,
Nikzad Hossein
Publication year - 2020
Publication title -
andrologia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.633
H-Index - 59
eISSN - 1439-0272
pISSN - 0303-4569
DOI - 10.1111/and.13703
Subject(s) - asthenozoospermia , male infertility , genotype , tbars , biology , andrology , oxidative stress , glutathione s transferase , medicine , infertility , glutathione , endocrinology , genetics , gene , lipid peroxidation , biochemistry , pregnancy , enzyme
This study aimed to investigate the association between glutathione S‐transferase (GST) M1 and T1 null genotypes and thiobarbituric acid reactive substances (TBARS), total antioxidant capacity (TAC) and nitric oxide (NO) levels in male infertility. For this purpose, semen samples were collected from fertile and infertile subjects, and then they were genotyped for GSTT1 and GSTM1 genes using multiplex‐PCR. The TBARS, TAC and NO levels in seminal plasma were then measured via the ferric‐reducing ability of plasma (FRAP). A significant association was observed between GSTT1 null genotype and oligozoospermia, asthenozoospermia and teratozoospermia. But, the GSTM1 null genotype was merely associated with teratozoospermia. Moreover, the GSTT1 −/ GSTM1 + combined genotype was associated with all subgroups of male infertility. Besides, an association was observed between GSTT1 −/ GSTM1 − genotype and asthenozoospermia and teratozoospermia. Further analysis showed that the GSTT1 null genotype was associated with increased NO in asthenozoospermia. Also, the GSTT1 null genotype was associated with increased TBARS in oligozoospermia and asthenozoospermia. As well, GSTM1 null genotype was associated with decreased TAC and increased NO in asthenozoospermia respectively. As a preliminary conclusion, the GSTM1 and GSTT1 null genotypes could be considered as genetic risk factors for male infertility, interfering with some oxidative stress markers in infertile men.