Complete Sperm Suppression in Rats With Dienogest Plus Testosterone Undecanoate Is Facilitated Through Apoptosis in Testicular Cells
Dienogest plus testosterone undecanoate completely suppressed sperm production in rats via germ cell and interstitial cell apoptosis, regulated by both intrinsic and extrinsic apoptotic pathways.
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The study evaluated whether complete sperm suppression in rats treated every 45 days with dienogest plus testosterone undecanoate is accompanied by testicular apoptosis, using high-level assessments of sperm production and apoptosis markers. Across treatment, there was a significant increase in germ cell apoptosis along with simultaneous upregulation of caspase 3 activity/expression, and increased caspase 8 and caspase 9 activities corresponded with overexpression of upstream proteins from both extrinsic (Fas, FasL, caspase 8) and intrinsic (Bax, Bcl2, caspase 9) apoptosis pathways. The authors also observed apoptosis in interstitial cells and a decline in the number of functional Leydig cells, concluding that sperm suppression was mainly driven by removal of precursor germ cells through apoptosis. This paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.
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Cites (3)
- Extended intervention time and evaluation of sperm suppression by dienogest plus testosterone undecanoate in male rat 2011
- Trials for development of once-a-month injectable, hormonal male contraceptive using dienogest plus testosterone undecanoate: dose standardization, efficacy and reversibility studies in rats 2009
- Complete sperm suppression induced by dienogest plus testosterone undecanoate is associated with down-regulation in the expression of upstream steroidogenic enzyme genes in rat testis 2012
References (37)
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