Sunday, June 9, 2019
The effect of nitric oxide and cGMP on follecogenises Essay
The effect of nitric oxide and cGMP on follecogenises - Essay Exampleto female disorders, 20% of male origin, 27% resulting from abnormalities in both man and woman, while 15% of the cases could not be attributed to either partner (de Kretser, 1997). According to Evers (2002), five types of disorders mavening to infertility have been recognised. They are summarised in Table 1.Ovulation disturbances are a rough-cut cause of subfertility in women (Snick et al., 1997). Ovulation problems due to disturbances in reproductive hormones present themselves as irregular or absent menstrual periods viz., oligomenorrhoea or amenorrhoea (Hamilton-Fairley and Taylor, 2003). Hormonal proportionateness governing the ovarian cycle is a critical instrument in female fertility. Several factors including stressful lifestyles, extremes in body weight, diet, certain hormonal diseases (e.g., pituitary gland tumours) and endocrine disrupting chemicals, such as PCBs and some pesticides can impact a woma ns hormonal balance and, thereby, the ovulatory pattern (Farr et al., 2004). Age is another important factor that influences female fertility (Maheshwari et al., 2008) which starts to decline around the mean age of 37.5 years (Hourvitz, 2009). Fecundity of a woman declines with age because of the loss of follicles from the ovary. Advancing age could lead to infertility in a woman on tarradiddle of poor oocyte quality related to a higher number of chromosomal aberrations and cytoplasmic mal arrangements in the oocytes (Laufer et al., 2004). Furthermore, advancing maternal age could adversely influence the capacity of the oocyte to sustain early embryo development vis-a-vis biochemical and molecular processes promoting fertilisation, embryo formation and successful development to term (Gilchrist et al., 2008)Male infertility resulting in the reduced ability of the female partner to become pregnant is usually on account of low sperm counts, obstructive azoospermia or primary spermatog enic failure including reduced motility and/or abnormal morphology of sperm (Snick et al., 1997)
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