Background and Objective: The spathe of phoenix dactylifera contains protein, fatty, fiber, sugar, moisture, furfural, coumarin, organic compounds of camphor family, phytosterols, 1, 2-Di methoxil 1, 4-Di methyl benzene. This study was done to evaluate the effect of alcoholic extract of phoenix dactylifera spathe on seminiferous tubules and spermatogenesis in adult male rats. Methods: In this experimental study, 50 adult male rats were randomly allocated into five groups including: control, sham and expermintal groups 1, 2 and 3. Animals in control group did not receive any treatment. Animals in sham group were received 0.2 ml normal saline intraperitoneally. Animals in experimental group 1, 2 and 3 were received 0.05, 0.1 and 0.2 g/kg/bw of alcoholic extract of phoenix dactylifera spathe intraperitoneally, respectively. After 14 days of study, the testis was removed and the sections of tissue were prepared. Testosterone hormone measured by Gamma counter method. Results: Serum levels of testosterone and the spermatozoa count were significantly reduced in the experimental groups in compared to control and sham groups (P<0.05). The count spermatogonia, primary spermatocyte, spermatid, sertoli and leydig cells and seminiferous tubules structures did not reduce in the experimental groups in compared to control and sham groups. Conclusion: Phoenix dactylifera Spathe alcoholic extract at doses of minimum and medium in adult male rats reduces sera level of testosterone and spermatozoa number.

One of the main spermatogenesis events is the replacement of histones with small proteins called protamines, which leads to chromatin's condensation in the sperm nucleus and protects it against possible damage. Today, tests such as aniline blue (AB), toluidine blue (TB), and chromomycin A3 (CMA3) staining are used based on different characteristics to evaluate sperm chromatin compaction. For the assessment of DNA fragmentation in sperm, several tests such as 8-hydroxy-2-deoxyguanosine (8-OHdG), TUNEL, Comet, sperm chromatin structure assay (SCSA), sperm chromatic dispersion (SCD), and acridine orange have been introduced that directly and indirectly assay DNA damage. The articles in PubMed and Google Scholar, as well as related books, from 2007 to 2022, were collected and reviewed based on keywords 8-OHdG, TUNEL, Comet, SCD, and acridine orange. So far, many studies have been conducted at the treatment level and on sperm chromatin tests, but the number of cases published so far is limited. Various sperm samples have been used in different studies, with different threshold limits in the tests. The sixth edition of the World Health Organization (WHO) book notes that each laboratory has its threshold limit. Therefore, in this review study, common methods of evaluating chromatin packaging and DNA damage are introduced, and the advantages and disadvantages of each test are discussed based on the latest achievements related to infertility.

Background and Objective: Antioxidant apigenin (AP) is a natural, non-mutagenic, and less toxic flavonoid with pharmacological anti-cancer, anti-viral, anti-bacterial, anti-apoptotic, and anti-inflammatory activities. This antioxidant is easily received by the cell, binds to sperm DNA, and forms a DNA-AP complex, thereby protecting sperm DNA. The present study was conducted to determine the antioxidant effect of AP on human sperm quality after freezing-thawing.
Methods: In this descriptive-analytical study, 10 normozoospermic samples underwent freezing-thawing conditions, and sperm functional tests were investigated in different AP concentrations, including 0.4 mM, 0.2 mM, 0.1 mM, and 0.05 mM.
Results: The quality of total sperm parameters and functional tests decreased after freezing compared to before freezing. Among the AP concentrations, only in the 0.2 mM AP concentration, the improvement of the additional histone percentage, protamine deficiency, and sperm DNA health were observed compared to the control; this finding was not statistically significant.
Conclusion: The use of AP with a concentration of 0.2 mM during freezing-thawing culminates in improving sperm functional tests.