Closed traumatic brain injury (CTBI) leads to increase mortality rates in developing countries. However, a sustainable therapeutic approach has not been established yet. Therefore, the present study was designed to evaluate the impact of normabaric hyperoxia treatment (NBOT) on striatum associated Locomotor Activity (LA) in IntelliCage after Fluid-Percussion Injury (FPI). Animals were divided in four groups: Group I control (n=24), Group II sham (n=24), Group III FPI (n=24) and Group IV FPI with NBOT (n=24). Animals were habituated in IntelliCage for 4 days following transponder implanted in mice neck region on day 5. Then the LA of all groups was assessed 6hr daily for 5 days before inducing FPI. On day 6, cannula was implanted on the striatum, on day 7 FPI was performed in Group III (kept in normal environment) and IV (immediately exposed to NBOT for 3 hr). LA (in terms of number of visits in all four corners) was assessed 6 hr at days 1, 7, 14, 21 and 28 following FPI. After the animals were sacrificed to study the neuronal damage, dopamine receptors and transporters expression in striatum. The results suggested that the LA of FPI impaired mice as compared to the control and sham showed less number of visits in all four corners in IntelliCage. Morphological results revealed that FPI induced neuronal damage as compared to sham and control. Dopamine receptors and transporters were down regulated in the FPI group as compared to the control. Immediate exposure to NBOT improved LA in terms of increased number of visits in all four corners, reduced number of cell death and improved receptor expression as compared to FPI. In conclusion, NBOT exposure could improve the LA of mice following FPI through prevention of neuronal damage, improved dopamine receptors and transporters.

In brief: Numerous studies have examined the impact of 2.45 GHz Wi-Fi exposure on the testes, highlighting concerns about its potential effects on male fertility. This study extends the investigation beyond the testes to include the epididymis, seminal vesicle and coagulating gland, providing a more comprehensive understanding of how 2.45 GHz Wi-Fi influences the male reproductive system. Numerous studies have documented the effect of 2.45 GHz Wi-Fi exposure on the testes and sperm quality. Nevertheless, detailed histological alterations of other male reproductive organs are underexplored. Therefore, this study aimed to evaluate detailed histological alterations of the testes, epididymis, seminal vesicle, coagulating organ and sperm parameters following 2.45 GHz Wi-Fi exposure. Eighteen adult male Sprague Dawley rats ( n = 18) were equally divided into three groups ( n = 6): control, 4 h and 24 h groups. The groups were exposed to an active router daily for 4 or 24 h, respectively. The control group was sham-exposed using an inactive router. The exposure lasted for 8 weeks at a 20 cm distance, with a power density of 0.141 W/m ² and a specific absorption rate of 0.41 W/Kg. Histological findings revealed vacuolation in the testes and the corpus epididymis of the 4 and 24 h groups. The seminal vesicle in both exposed groups exhibited multifocal atypical hyperplasia. Besides, the seminiferous tubule diameter decreased gradually in both exposed groups, with a substantial decrease in the 24 h group. The spermatogenesis index in 4 and 24 h groups also reduced significantly. The latter result was reflected in the sperm concentration, where both groups showed a significant reduction compared to the control group. Sperm motility also decreased significantly in the 4 h groups. Interestingly, there was a substantial increase in sperm viability in the 24 h group. These findings indicate that 2.45 GHz Wi-Fi exposure causes changes in the histology and histomorphometry measurement and impairs important sperm parameters. This highlights the consequences following Wi-Fi exposure on male reproductive health.

Background/Objectives: The rapid rollout of 5G has renewed interest in potential reproductive effects of mid-band (3.5 GHz) and millimeter-wave (24 GHz) radiofrequency electromagnetic fields (RF-EMF). We examined frequency- and duration-dependent changes in testicular cytokines, apoptosis-related genes, and sperm quality in rats. Methods: Male Sprague Dawley rats (n = 6 per group) were exposed for 60 days to 3.5 GHz or 24 GHz RF-EMF for 1 h/day or 7 h/day. The sham controls were housed identically. Testicular expressions of IL-10, IL-6, IL-1β, and TNF-α were quantified; Tp53, Bax, Bcl2, and Casp3 mRNA expressions were measured; and sperm concentration, viability, and motility were evaluated. Results: IL-10 was significantly reduced in the 24 GHz group at both 1-h and 7-h exposure duration. At 7 h, TNF-α was also lower at 24 GHz. Casp3 expression was higher and Tp53 was lower at 3.5 GHz at 1-h exposure duration. Sperm concentration and viability were reduced after 24 GHz exposure at 7 h, while sperm motility was reduced after 3.5 GHz exposure at both durations. Conclusions: Exposure to RF-EMF 3.5 GHz primarily impacts sperm motility via extrinsic pro-apoptotic pathways, while exposure to 24 GHz impacts sperm concentration and viability potentially through immune–apoptotic mechanisms, with all negative effects amplified by 7-h daily exposure.

The expansion of fifth-generation (5G) wireless networks has increased environmental exposure to mid-band and millimeter-wave radiofrequency electromagnetic fields (RF-EMF), but their molecular effects on male reproductive tissues remain insufficiently understood. This study evaluated whether repeated exposure to 3.5 GHz and 24 GHz RF-EMF alters testicular stress-associated molecular responses by integrating electromagnetic dosimetry with an in vivo rat model. Whole-body specific absorption rate (SAR) and 10 g peak SAR were estimated using a rat voxel model and scaled to the 20 cm antenna-to-cage geometry used during exposure. Thirty-six adult male Sprague Dawley rats were allocated to sham, 3.5 GHz, or 24 GHz groups and exposed for 1 h/day or 7 h/day over 60 days. Testes were examined histologically and assessed for HSP27, HSP70, and HSP90 protein expression. SAR values were low overall, although absorption was higher at 3.5 GHz than at 24 GHz. Histological evaluation showed preserved seminiferous tubule architecture without consistent structural injury. In contrast, molecular analysis demonstrated frequency- and duration-dependent modulation of heat shock proteins, including early HSP70 downregulation at both frequencies, followed by HSP90 upregulation at 3.5 GHz and HSP27 upregulation at 24 GHz. These findings indicate that low-level 5G-relevant RF-EMF exposure can modify molecular stress responses in testicular tissue even in the absence of overt histological damage.

The brain and testes are connected via the hypothalamic–pituitary–gonadal (HPG) axis. Both are vulnerable to radiofrequency electromagnetic radiation (RF-EMR). However, no comprehensive study had evaluated the effects of RF-EMR on key hormones along this axis. Hereby, this study evaluated the effect of RF-EMR on the hormonal changes along the axis, including the neuropeptide kisspeptin. A total of 18 (N = 18) adult Sprague–Dawley rats were divided into three groups (n = 6): Control, 4 h, and 24 h. The Control group was sham-exposed to an inactive router. The exposed groups were subjected to 2.45 GHz RF-EMR for 4 and 24 h daily, for 60 days at a 20 cm distance. The power density was 0.141 W/m² with a whole-body specific absorption rate (SAR) of 0.41 W/kg. No significant changes were observed in hypothalamic Kiss1 gene expression or serum kisspeptin levels. GnRH levels increased significantly in both exposed groups, while FSH and LH remained unchanged. Testicular testosterone was significantly reduced in the 24 h group, while serum testosterone was elevated in the 24 h group compared to the 4 h group. In conclusion, prolonged 2.45 GHz RF-EMR exposure caused selective changes in components of the HPG axis, particularly involving GnRH and testosterone, suggesting potential endocrine effects on male reproductive regulation.

The rapid expansion of 5G technology has increased exposure to high-frequency radiofrequency electromagnetic fields (RF-EMF), raising concerns about male reproductive health. This study investigated the effects of 5G frequencies at 3.5 GHz and 24 GHz on male libido, reproductive hormones, the testosterone-to-oestrogen (T/E) ratio, and androgen receptor expression in rats. Eighteen male Sprague–Dawley rats were randomly assigned to Control, 3.5 GHz, and 24 GHz (n = 6/group). Exposed groups received 7 h/day RF-EMF exposure for 60 consecutive days, while the Control underwent sham exposure. During the final week of exposure, mating behaviours were assessed using mount frequency, mount latency, intromission frequency, ejaculation latency, and post-ejaculatory interval. Serum testosterone and oestrogen levels, the T/E ratio and androgen receptor expression in the testis and hypothalamus were evaluated. The 3.5 GHz group demonstrated statistically significantly prolonged ejaculation latency (3480 ± 1576.956, p < 0.01, Hedges’ g = 1.03) compared with the Control group. In contrast, 24 GHz exposure statistically significantly reduced mount frequency (4.80 ± 0.837, p < 0.01, Hedges’ g = −0.65) and prolonged the post-ejaculatory interval (588.83 ± 206.41 s, p < 0.01, Hedges’ g = 1.63) compared with the Control group. Hormonal analysis revealed statistically significant elevation of testosterone levels in the 3.5 GHz group, whereas the 24 GHz group showed statistically significant reductions in testosterone and oestrogen. Androgen receptor expression was unchanged. These findings suggest frequency-dependent effects of 5G RF-EMF on male libido and endocrine balance.