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Effects of nitric oxide on reproductive organs and related physiological processes
Authors: Ayoob Rostamzadeh, Reza Ahmadi, Mahdi Heydari, Amir Raoofi
Number of views: 203
Nitric oxide (NO), a member of the reactive nitrogen species
family, plays a role in several physiologic processes, including
vasculogenesis and angiogenesis, growth and puberty, and
senescence and apoptosis. NO plays an important role in the
production of ovarian steroids, ovulation, and follicular apoptosis.
In other words, increased activity of nitric oxide synthase (NOS)
leads to an increased amount of NO, which triggers production
of prostaglandins and inflammatory cascades which facilitate
follicular rupture and atresia. NO concentration elevation inhibits
steroid synthesis in luteal and granulosa cells. Since NO is a
major paracrine mediator of various biological processes, as
well as a key factor in both the reproductive cycle and embryo
implantation, oversynthesis of NO in the uterus results in toxicity
and inflammation in epithelial cells and immunorejection of
implantation. In the male physiological system, NO synthesized by
NOS plays a major role in erectile function and androgen secretion,
as well as semen parameters, and oocyte junction to the sperm.
Furthermore, this supposedly simple molecule is involved in a
number of other functions, such as germ cell evolution, connections
between sertoli cells and germ cells in the blood-testis barrier,
homodynamic contraction, and germ cell apoptosis. Moreover, NO
is considered a key factor in male fertility due to its widespread
distribution in both normal and diseased testis tissue. The difference
of expression level of NOS in normal and pathological states is a
probable cause of fertility destructive processes.