CONTEXT:Effects of zinc on male sexual competence are poorly understood.AIM:To study the effects of different doses of zinc on the sexual competence of males using a rat model.MATERIALS AND METHODS:Three subsets (eight in each subset) of sexually experienced adult male rats were supplemented with three different oral doses of zinc sulphate (a daily dose of 1 mg, 5 mg and 10 mg respectively) for two weeks. A subset of eight animals without zinc supplementation was used as the control group Sexual behavior was observed by placing them individually in cages with receptive females.STATISTICAL ANALYSIS:Data analysis was done using SPSS v10 for windows computer software.RESULTS:Supplementation of 5 mg of zinc/day for two weeks led to a prolongation of ejaculatory latency; 711.6 sec. (SEM 85.47) vs. 489.50 sec. (SEM 67.66), P < 0.05 and an increase in number of penile thrusting; 52.80 (SEM 11.28) vs. 26.50 (SEM 6.17), P < 0.05, compared to controls. The same group had elevated prolactin (PRL) and testosterone (T) levels compared to controls at the end of treatment period; PRL- 7.22 ng/dl (SEM 3.68) vs. 2.90 ng/dl (SEM 0.34) and T- 8.21 ng/ml (SEM 6.09) vs. 2.39 ng/ml (SEM 1.79), P < 0.05. In contrast, reduction of libido was evident in the same group, but this effect was not statistically significant (P > 0.05). However, partner preference index was positive and 5 mg zinc supplementation did not exert a significant adverse effect on the muscle strength and co-ordination. The subset of rats supplemented with 1 mg/day did not show a difference from the control group while supplementation with 10 mg/day led to a reduction of the libido index, number of mounts and intromissions.CONCLUSIONS:Zinc therapy improves sexual competence of male rats; the effect is dose dependent. Increase in the T levels is beneficial in this regard. However, increase in PRL is responsible for the reduced libido index. Further studies on pigs and monkeys are needed to evaluate the therapeutic use of zinc in sexual dysfunction.

RATIONALE:Current knowledge on the relationship between seminal zinc levels and different parameters of human semen is inconsistent.OBJECTIVES:To assess the relationship between seminal plasma zinc and semen quality using two markers; zinc concentration (Zn-C) and total zinc per ejaculate (Zn-T).DESIGN:The study was carried out as a cross-sectional study.SUBJECTS AND METHODS:Semen parameters of 152 healthy men undergoing evaluation for subfertility were assessed. Seminal plasma zinc levels were determined using flame atomic absorption spectrometry. Zn-C, expressed as μg/mL, was multiplied by ejaculated volume to calculate Zn-T. Mann Whitney U test and Chi-square test were used to compare the zinc levels between different seminal groups when appropriate. Correlations were observed with Pearson’s correlation of coefficient. Analysis was carried out using SPSS 10.0 for windows software.RESULTS:Zn-C was low in 23 (15%) samples, while in 32 (21%) of the samples Zn-T was abnormal. The number of subnormal samples was high in the low-zinc groups compared with the normal-zinc groups, 15 vs. 8 (P > 0.05) for Zn-C and 28 vs. 4 (P < 0.001) for Zn-T. Zn-C was significantly high in the asthenozoospermics compared with the normal motile group; 138.11 μg/mL (83.92) vs. 110.69 11 μg/mL (54.59) (P < 0.05). Zn-T was significantly low in samples with hyperviscosity compared with samples with normal viscosity; 220.06 μg (144.09) vs. 336.34 μg (236.33) (P < 0.05). Conversely, Zn-T was high in samples with low viability compared with those with normal viability; 437.67 μg (283.88) vs. 305.15 μg (221.19) (P < 0.05). Weak correlations were found between Zn and some semen parameters. However, the correlation was negative between pH and Zn-C (r = –0.193, P < 0.05) as well as Zn-T (r = –0.280, P < 0.01). On the other hand, correlations were positive between Zn-T and sperm count (r = 0.211, P < 0.05).CONCLUSION:Count, motility, viability, pH and viscosity are affected by variations of seminal plasma zinc. Seminal plasma Zn-T is the better marker for assessing the relationship between zinc and semen quality.

RATIONALE:Bacterial flora can be isolated from many semen samples of subfertile males. Bacteriospermia can compromise the outcome of intra uterine insemination (IUI) by contaminating the post-processed sperm sample.OBJECTIVES:The objective of the present study is to determine the efficacy of penicillin and streptomycin in eliminating the bacteria from semen samples in the sperm processing procedure, and to assess the effects of antibiotics on sperm motility, survivability, and pregnancy rates.DESIGN AND SETTINGS:A prospectively controlled study was carried out using couples undergoing IUI with their informed consent.INTERVENTION:Sperm processing using the swim-up technique in penicillin and streptomycin supplemented culture medium.SUBJECTS AND METHODS:Couples were consecutively allocated in two groups for sperm processing (a) Group AB+ (antibiotics supplemented culture medium, n = 33) and (b) Group AB− (antibiotic free culture medium, n = 33). Semen culture was performed before and after sperm processing. Sperm motility was assessed immediately after processing and after 24 h of incubation.RESULTS:Bacterial isolates were found in 20 (60.6%) and 22 (66.1%) of samples before processing in Groups AB+ and AB− respectively. Addition of antibiotics resulted in completely eliminating non-specific bacteria from semen samples without affecting sperm motility. In vitro survival rate of sperm enhanced in AB+ group compared with AB− group (motile sperm after 24 h), 62.21% (standard deviation [SD]: 37.27) versus 41.36% (SD: 30.78), P = 0.012. Pregnancy rate, was comparable between two groups (9% in Group AB+ vs. 6% in Group AB−, P = 0.45).CONCLUSION:Penicillin streptomycin combination could completely eliminate non-specific bacteria from semen samples during sperm processing in this population. The types of antibiotics and dosage used did not seem to have any harmful effects on human sperm.

CONTEXT:Artificial reproductive techniques using seminal preparations with bacteria may cause pelvic inflammatory disease and its sequalae.AIMS:To assess efficacy of two sperm preparation techniques to clear bacteria and the effect of bacteriospermia on sperm recovery rates.SETTINGS AND DESIGN:A descriptive cross-sectional study was carried out among males of subfertile couples.SUBJECTS AND METHODS:Semen samples were randomly allocated into swim-up method (group S, n = 68) and density gradient method (group D, n = 50) for sperm preparation. Seminal fluid analysis and bacterial cultures were performed in each sample before and after sperm preparation.STATISTICAL ANALYSIS:McNemar's chi-squared test and independent samples t-test in SPSS version 16.0 were used.RESULTS:Organisms were found in 86 (72.88%) out of 118 samples, before sperm preparation; Streptococcus species (n = 40, 46.51% of which 14 were Group D Streptococcus species), Coagulase negative Staphylococcus species (n = 17, 19.76%), Staphylococcus aureus (n = 13, 15.11%), Coliform species (n = 11, 12.79% of which 09 were Escherichia coli) and Corynebacterium species (n = 5, 5.81%). There was a statistically significant reduction of culture positive samples in raw vs. processed samples; in group S, 49 (72.05%) vs. 16 (23.52%) and in group D, 37 (74%) vs. 18 (36%). In group S and D, mean (SD) recovery rates of culture positive vs. culture negative samples were 39.44% (SD-14.02) vs. 44.22% (SD-22.38), P = 0.39 and 52.50% (SD-37.16) vs. 49.58% (SD-40.32), P = 0.82 respectively.CONCLUSIONS:Both sperm preparation methods significantly reduced bacteria in semen, but total clearance was not achieved. Sperm recovery rate was not affected by bacteriospermia.

ObjectiveRecapitulation of the spermatogenesis process in vitro is a tool for studying the biology of germ cells, and may lead to promising therapeutic strategies in the future. In this study, we attempted to transdifferentiate Wharton's jelly-derived mesenchymal stem cells (WJ-MSCs) into male germ cells using all-trans retinoic acid and Sertoli cell-conditioned medium.MethodsHuman WJ-MSCs were propagated by the explant culture method, and cells at the second passage were induced with differentiation medium containing all-trans retinoic acid for 2 weeks. Putative germ cells were cultured with Sertoli cell-conditioned medium at 36℃ for 3 more weeks.ResultsThe gene expression profile was consistent with the stage-specific development of germ cells. The expression of Oct4 and Plzf (early germ cell markers) was diminished, while Stra8 (a premeiotic marker), Scp3 (a meiotic marker), and Acr and Prm1 (postmeiotic markers) were upregulated during the induction period. In morphological studies, approximately 5% of the cells were secondary spermatocytes that had completed two stages of acrosome formation (the Golgi phase and the cap phase). A few spermatid-like cells that had undergone the initial stage of tail formation were also noted.ConclusionHuman WJ-MSCs can be transdifferentiated into more advanced stages of germ cells by a simple two-step induction protocol using retinoic acid and Sertoli cell-conditioned medium.

A controlled ill vitro study was carried out to observe the effect of different Zinc (Zn) levels on sperm recovery rate, chromosome integrity, cell membrane integrity and motility in the swim up procedure. Semen samples were obtained from males who underwent seminal fluid analysis at the

Introduction: Chlamydia trachomatis is sexually transmitted and causes infection of the genital tract that leads to many long term complications. Invasive procedures in infected infertile females increase the risk of ascending infection and long term consequences. Though infertile individuals are considered a high risk population prevalence data for our population is not available. Furthermore, the use of risk factor identification in diagnosis is not well established. This study was planned to determine the prevalence of Chlamydia infection and to describe the socioeconomic clinical characteristics that are associated with the presence of infection among a patient population who sought treatment for infertility at a tertiary care facility. Method: A cross sectional study was carried out among patients who sought infertility treatment at the infertility clinic of Colombo North Teaching Hospital, Ragama. Two hundred married couples were included in the study. The socioeconomic data and any symptoms suggestive of genital infections were collected and Chlamydia trachomatis infection was diagnosed with a rapid antigen test using a commercial test kit. Intracervical swabs of the female and first void urine samples of the male were used. Data analysis was done to describe the prevalence of Chlamydia infection in each partner as well as to identify the number of couples where either partner was affected. Associations with recognized risk factors were identified. Results: Presence of symptoms was low in the males while one third of female subjects had one or more symptoms. The Chlamydia test revealed 12(6%) female and 6(3%) male study participants to be positive for current disease. These study participants were from 15 couples giving a prevalence rate of either partner being positive in 7.5% of couples. Of the risk factors identified the duration of marriage or infertility, education level, household income, alcohol use and smoking by the male, and presence of symptoms did not demonstrate a significant association with the presence of the disease. Partners staying away from each other were significantly associated with a positive result. Conclusion: There is 7.5% disease prevalence among infertile couples seeking treatment. Risk assessment and clinical symptoms have a limited value in identification of affected couples. Couples living separately have a high risk of Chlamydia infection. The high disease prevalence warrants either screening or empirical treatment of all infertile female patients undergoing invasive procedures.

The study of culturing spermatogonial stem cells (SSCs) dates back to the 1950s. However, regeneration of complete spermatogenesis process in vitro is still a greater challenge. Studying spermatogenesis in vitro is significant in elucidating germ cell biology, and the knowledge may be useful for genetic manipulations of defective germ cells or producing transgenic animals, fertility preservation, and treatment of infertility. Fertility preservation would be more beneficial for adult and prepubescent patients who develop sterility due to gonadotoxins. Discovering of the stepwise stages in spermatogenesis and various forms of arrests at specific stages would help in the diagnosis of especially, idiopathic infertility and deciding treatment options. Different techniques have been tried to differentiate stem cells into germ cells over decades. A larger number of studies has used genetically manipulated stem cells to achieve differentiated germ cells. In contrast, differentiation of stem cells directly into SSCs bypassing the step into primordial germ cells (PGCs) to minimize time frame and employing techniques involved in least genetic manipulations are other important techniques to increase utilization within a clinical setting. As the use of transfected cell lines disqualifies the putative gametes obtained for clinical applications, trying to generate patient-specific germ cell with least genetic manipulations will be more effective in future applications, especially for patients with pre-pubertal cancer and azoospermic men who desire to become biological fathers.