ObjectiveTo evaluate varicocele effects on conventional semen parameters: sperm DNA
fragmentation, chromatin packaging, mitochondrial membrane potential (MMP)
and sperm apoptosis.MethodsA cross-sectional study was carried out with semen samples from 2,399 men of
couples who attended an infertility clinic. A total of 16.3% (391/2399) of
the men were diagnosed with varicocele by a urologist.ResultsA regression analysis revealed that the percentages of sperm with DNA
fragmentation, abnormal chromatin packaging, and abnormal MMP were
significantly increased in individuals with varicocele, when compared to men
without varicocele. Apoptosis was not influenced by varicocele. Conventional
semen parameters were significantly worse in individuals with the disease.
On the other hand, in men with varicocele, Spearman's correlation
demonstrated that early apoptosis and abnormal MMP showed a positive and
significant correlation with sperm DNA fragmentation.ConclusionMen with varicocele had worse semen parameters, including increased levels of
sperm DNA fragmentation, inactive mitochondria, and abnormal chromatin
packaging. These changes are possible causes of infertility in individuals
with varicocele.
The phytoalexin Resveratrol (3,5,4′-trihydroxystilbene; RSV) has been related to numerous beneficial effects on health by its cytoprotection and chemoprevention activities. Liver fibrosis is characterized by the extracellular matrix accumulation after hepatic injury and can lead to cirrhosis. Hepatic stellate cells (HSC) play a crucial role during fibrogenesis and liver wound healing by changing their quiescent phenotype to an activated phenotype for protecting healthy areas from damaged areas. Strategies on promoting the activated HSC death, the quiescence return or the cellular activation stimuli decrease play an important role on reducing liver fibrosis. Here, we evaluated the RSV effects on some markers of activation in GRX, an HSC model. We further evaluated the RSV influence in the ability of GRX on releasing inflammatory mediators. RSV at 1 and 10 µM did not alter the protein content of α-SMA, collagen I and GFAP; but 50 µM increased the content of these activation-related proteins. Also, RSV did not change the myofibroblast-like morphology of GRX. Interestingly, RSV at 10 and 50 µM decreased the GRX migration and collagen-I gel contraction. Finally, we showed that RSV triggered the increase in the TNF-α and IL-10 content in culture media of GRX while the opposite occurred for the IL-6 content. Altogether, these results suggested that RSV did not decrease the activation state of GRX and oppositely, triggered a pro-activation effect at the 50 µM concentration. However, despite the increase of TNF-α in culture media, these results on IL-6 and IL-10 secretion were in accordance with the anti-inflammatory role of RSV in our model.
Fructose‐1,6‐bisphosphate (F1,6BP), an intermediate of the glycolytic pathway, has been found to play a promising anticancer effect; nevertheless, the mechanisms involved remain poorly understood. The present study aimed to evaluate the effect and mechanisms of F1,6BP in a human endometrial cancer cell line (Ishikawa). F1,6BP showed an antiproliferative and non‐cytotoxic effect on endometrial cancer cells. These effects are related to the increase in reactive oxygen species (ROS) levels and mitochondrial membrane potential (ΔΨm). These harmful stimuli trigger the upregulation of the expression of pro‐apoptotic genes (p53 and Bax), leading to the reduction of cell proliferation through inducing programmed cell death by apoptosis. Furthermore, F1,6BP‐treated cells had the formation of autophagosomes induced, as well as a decrease in their proliferative capacity after withdrawing the treatment. Our results demonstrate that F1,6BP acts as an anticancer agent through the generation of mitochondrial instability, loss of cell function, and p53‐dependent cell death. Thus, F1,6BP proves to be a potential molecule for use in the treatment against endometrial cancer.
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