The aim of this study was to investigate the effects of quercetin (QUE) on the testicular architecture as well as markers of oxidative, inflammatory, and apoptotic profile of male gonads in Zucker diabetic fatty (ZDF) rats suffering from Type 2 diabetes mellitus in the absence or presence of obesity. QUE was administered orally at a dose of 20 mg/kg/day for 6 weeks. Morphometric analysis revealed that QUE treatment led to an improvement in testicular appearance, particularly in the case of Obese ZDF rats. Furthermore, a significant stabilization of the antioxidant capacity (p < 0.05), superoxide dismutase and catalase activity (p < 0.01), with a concomitant decrease in lipid peroxidation (p < 0.05) were observed in Obese ZDF animals exposed to QUE. Our data also indicate a significant decline in the levels of interleukin (IL)-1 (p < 0.05), IL-6 (p < 0.01) and tumor necrosis factor alpha (p < 0.001) following QUE supplementation to Obese ZDF rats in comparison with their respective control. Finally, a significant down-regulation of the pro-apoptotic BAX protein (p < 0.0001) was observed in Obese ZDF rats administered with QUE, while a significant Bcl-2 protein overexpression (p < 0.0001) was recorded in Lean ZDF animals when compared to their untreated control. As such, our results suggest that QUE is a potentially beneficial agent to reduce testicular damage in ZDF rats with Type 2 diabetes mellitus by decreasing oxidative stress, chronic inflammation, and excessive cell loss through apoptosis.

The study focused on the effect of microwave radiation at a dose which commonly does not lead to tissue heating, however, in the rat testes it resulted in accumulation of heat. Adult rats were exposed to whole body pulse radiation at a frequency of 2.45 GHz and mean power density of 28 W/m ² , for 3 h a day for the duration of 3 weeks. Immediately after each irradiation, the body temperature and the testicular temperature were measured in the control and experimental animals. Samples for histological and immunohistochemical analysis were taken after the last irradiation and processed for light and transmission electron microscopy. An evaluation of spermatozoa motility was performed using computer-assisted sperm analysis. Although the body temperature of the rats was not elevated after the irradiations, the testicular temperature was significantly increased ( P < 0.004). Testes of the experimental animals had considerably dilated and congested blood vessels and the seminiferous epithelium showed degenerative changes. The Leydig cells showed no obvious structural abnormalities. Transmission electron microscopy revealed ultrastructural changes in developing sex cells, Sertoli cells, and endothelial cells. An intensified immunoreactivity to superoxide dismutase 1 was found in spermatogonia and Leydig cells in the experimental animals. Results of the present study revealed a distinctly adverse effect of microwave radiation on the thermoregulatory capability and histological structure of rat testes as well as an oxidative damage of the tissue. The scientific knowledge confirming or denying the thermal effect of microwave radiation on living tissue is scarce and thus the present study may be regarded as unique and helpful to clarify the issue.

This study was conducted to investigate the influence of whole-body electromagnetic radiation (EMR) on testicular parenchyma of Wistar rats. Sexually mature rats were subjected to pulsed electromagnetic field at frequency of 2.45 GHz and mean power density 2.8 mW/cm² by 3-h daily applications for 3 wk. Tissue samples were obtained 3 h after the last irradiation and processed by histological techniques for light and transmission electron microscopy. Testes showed apparent degenerative changes of seminiferous epithelium. The seminiferous tubules were mostly irregular in shape, and seminiferous epithelium contained a number of empty spaces of different size. Subsequently, groups of sloughed epithelial cells were often found inside the lumina of tubules. Except for relatively unchanged Sertoli cells, some locations of basal compartment of seminiferous epithelium contained shriveled Sertoli cells with dark cytoplasm. These areas showed degenerative features including necrotizing and shriveled spermatogonia surrounded by empty irregular spaces, and undulating basement membrane. The intertubular spaces were enlarged but interstitial Leydig cells did not show any marked morphological changes. Evidence demonstrates the adverse effects of EMR on testicular parenchyma in rats.

The aim of this study was to compare the effect of humic acid (HA) obtained by extraction from alginate on the incubation of roes and fry development in African cichlids, Labidochormis caeruleus, as well as their influence on the stabilization of the physicochemical parameters of water in an aquarium during artificial breeding. The roes were obtained by extruding from a female buccal cavity immediately after fertilization. For the experiment, 4 groups of 40 roes were formed in an incubator with an artificial hatchery. Groups 1–3 were exposed to 1%, 5%, and 10% concentrations of HA, respectively. The control group C was not exposed to HA. In all groups, the mortality and size differences of the fry, as well as the temperature, pH, hardness, nitrite, and nitrate levels in the tanks, were determined during a 30-day monitoring period until the resorption of the yolk sac. The results of this study indicated the ability of HA in 5% and 10% concentrations to reduce nitrite and nitrate levels in the aquatic environment, which significantly reduced the mortality of roes and the survivability of the fry. The determination of the morphological measurements of the fry revealed an increased body length in the groups exposed to 5% and 10% HA concentrations compared to the control group by the end of the monitored period. It was also noted that the yolk sac was resorbed two days earlier in the same groups than in the control. Thus, the results showed that HAs are suitable for use in the artificial aquarium incubation of roes and fry development, which are increasingly exposed to adverse environmental factors. The knowledge obtained in this study and its transfer into practice can allow even less experienced aquarists to successfully breed aquarium fish species that could not normally be bred under artificial conditions without the addition of HA.

The aim of the present study was to determine the influence of orally administered insecticide bendiocarb on the structure and ultrastructure of the kidney parenchyma in rabbits. Bendiocarb in the form of capsules (96% Bendiocarb, Bayer), at a dose of 5 mg/kg of body weight was fed daily for 3 days. After sampling, kidney sections of experimental and control animals were evaluated. Under a light and electron microscope the diffuse degenerative changes in kidney cortex and medulla were noted. Light microscopy revealed that the renal corpuscles had normal structure, but other nephron components and the collecting ducts were invariably changed. The epithelial cells inside the proximal and distal tubules and collecting ducts possessed increased quantity of cytoplasmic vacuoles and some tubular sections showed cellular sloughing and necrotization. The cells within the thin limbs of the Henley’s loops had normal histological structure except for sporadic necrotizing cells within some segments. The ultrastructural evaluation showed extensive cytoplasmic vacuolisation and degenerative changes, such as mitochondrial swelling and shortening of basal infoldings within proximal and distal tubules, and microvilli reduction within proximal tubules. Cells of the collecting tubules exhibited a higher number of vacuoles and some cells had apparently reduced organelles. The cells of the thin limbs of the Henle’s loop showed more vacuolised cytoplasm, some tubular sections revealed cellular detachment between the adjacent epithelial cells and rare necrotising epithelial cells were observed. The described findings addressed in the present study indicate an adverse effect of bendiocarb on the kidney parenchyma in rabbits.

Introduction: Canine mammary gland cancer (CMGC) is the most common neoplastic condition in bitches and is often fatal. There are limited treatment options for CMGC. Primary cell cultures from mammary tumours are promising preclinical in vitro models in which to study personalised treatment approaches. This preliminary study aimed to establish primary cell cultures from two canine mammary gland neoplasms: a common solid adenocarcinoma and a rare carcinosarcoma. Material and Methods: Tumour masses were collected from a 13-year-old and a 16-year-old German shepherd. Tumour cells were isolated by mechanical disaggregation and enzymatic digestion of masses with 0.05% type IV collagenase. Primary cell cultures were validated by immunocytochemistry for specific markers including mucin 1 (MUC1), cytokeratin 8 and 18 (CK8/18) and Kiel 67 (Ki-67). Results: Primary cell cultures achieved confluency by day 7 of culture, displaying polygonal cellular morphology. Cultures of both cell types exhibited strong positivity for MUC1 of >99% and high Ki-67 proliferation activity of 43.1% ± 0.5% in the solid adenocarcinoma-derived positive cells and 87.9% ± 2.7% in the carcinosarcoma-derived positive cells. Positivity was observed for CK8/18 of 98.1% ± 0.3% in cells derived from solid adenocarcinoma and 31.6% ± 1.5% in cells derived from carcinosarcoma. Conclusion: With further characterisation, the primary cell cultures established in this study can be expected to show considerable potential as foundational in vitro models for cancer research.