Maternal exposure during organogenesis to chlorpyrifos insecticide induce apoptosis process.

OBJECTIVE: Nowadays, one of the issues that matter in infertility is abortion or teratogenicity of embryos, followed by environmental pollution. Additionally, the continuous use of pesticides as the requirements of modern agriculture can increase the number of released radicals, which ultimately affects cell membranes and cell death via apoptosis pathway. MATERIALS AND METHODS: NMRI mice were divided into 3 groups: (1) Chlorpyrifos received group, (2) DMSO received as the sham group, (3) Control group. The mice were mated and euthanized 10 days post gestation. The number of embryos, progesterone and estradiol hormones and the liver enzymes levels of mouse mothers were evaluated in each group. The apoptosis pathway genes (Bax and Bcl2) and protein expressions (Caspase3 and Caspase9) were evaluated in the embryos of each group by qPCR and immunohistochemistry staining, respectively. RESULTS: The number of embryos in the experimental group was significantly lower than from the other groups. The liver enzymes and hormone levels were higher in CPF induced mice in comparison to the others. The mRNA expression of Bax in the embryos was significantly higher in the CPF group compared to sham and control groups. Caspase3 and Caspase9 protein expression revealed a higher rate of apoptosis in CPF group embryos. CONCLUSIONS: Continuous use of Chlorpyrifos can be regarded as having a negative effect on pregnancy as well as raising the mechanism of apoptosis in the development of embryos that may contribute to abortion or the birth of teratogenic disorders embryos.

Expression and localization of Septin 14 gene and protein in infertile men testis.

An increasing body of data implicates the Septin family in the pathology of several diseases, including male fertility. The objective of this study was to evaluate the gene and protein expression pattern of Septin 14 in the testis tissue of azoospermic men. In addition, Septin 14 localization was also assessed in the sperm. Testicular tissues were obtained from biopsies of non-obstrutive azoospermic men who underwent diagnostic testicular biopsy in Royan institute and were divided into two groups: TESE + with positive result in testicular sperm extraction (with hypospermatogenesis pathology) and TESE- with negative result (included patients with Sertoli cell only syndrome and maturation arrest pathologies). Total RNA and protein was extracted using trizol reagent. Septin 14 gene and protein expression level were assessed by real-time reverse transcription polymerase chain reaction (RT-PCR) and Western blot techniques, respectively. The localization of Septin 14 protein was also studied by Immunocytochemistry. The expression of Septin 14 was significantly lower (p < 0. 05) in TESE- group than TESE + in both mRNA and protein levels. The localization of Septin 14 protein was detected in the head to tail of normal sperms with high localization in front of the acrosome and the neck. This is a novel localization report on Septin 14 in sperm. Regarding the presence of this protein in the sperm acrosome and neck, it can be concluded that decreasing of Septin 14 protein expression may be associated with the pathogenesis of male infertility and therefore Septin 14 expression level maybe critical for human spermatogenesis.