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Platelet-rich plasma (PRP) has a potential effect on tissue repair through proliferation and differentiation of tissue progenitor cells. The aim of this study was to evaluate the effect of PRP on the testis structure and function in infertile rat model by stereological method. Thirty-two male rats were divided into four groups. Infertility was induced by the administration of busulfan (BUS) (10mg/kg, I.P., single dose). PRP (80μl, testis local injected, single dose) was administered for the subjects. After 48 days, semen analysis was performed and blood samples were taken from the heart to measure the testosterone. Then, the left testis was removed, fixed, embedded, sectioned, and stained by H&E; after that the testes were analyzed. The results showed that BUS can decrease the sperm count, motility, normal morphology, length of the spermatozoon tail, volume of the testis, seminiferous tubules, germinal epithelium height, and the number of spermatogenesis lineage cells in comparison with the control group (p < 0.01). PRP increased the number of spermatogenic stem cell, count, motility and tail length of the sperm and testosterone level in BUS-treated animal significantly, but it did not have any effect on the volume of the testis, germinal epithelium height, Sertoli and Leydig cells number, and seminiferous tubules length. It concluded that PRP can improve the structural and functional impairment of the testis in treatment by BUS. [ABSTRACT FROM AUTHOR]

Chronic Sleep Restriction (CSR) is known as a risk factor for cardiovascular diseases. However, the structural changes of Sinoatrial (SA) node cells have received less attention. This study aimed to evaluate the effects of CSR on SA node in an animal model using stereological methods. Adult male Sprague-Dawley rats were randomly divided into CSR, grid-floor, and control groups. The CSR procedure was designed such a way that the animals had a full cycle of sleep (6 hours) per day, while they were unable to have a Rapid Eye Movement (REM) sleep during the remaining 18 hours. This was induced by a multiplatform box containing water. The grid-floor animals were placed in the same multiplatform box with a grid-floor covering to prevent falling in water. After 21 days, the right atria were dissected out. Then, the location of the SA node was determined and evaluated by stereological techniques. The total volume of the SA node, the total volume of the main node cells, the volume of the connective tissue, and mean volume of the node cells were respectively enlarged by 60%, 47%, 68%, and 51% in the CSR animals compared to the grid-floor rats (p < 0.05). However, no significant changes were detected in these parameters in the control and grid-floor animals. The population of the main node cells remained constant in all animal groups. In addition, the three-dimensional reconstruction of the SA node in the CSR group showed a hypertrophied appearance. In conclusion, CSR induced hypertrophic changes in the rats' SA node structures without alteration in the number of main node cells. [ABSTRACT FROM AUTHOR]

Objectives Sodium metabisulfite as a food preservative can affect the central nervous system. Curcumin, the main ingredient of turmeric has neuroprotective activity. This study was designed to evaluate the effects of sulfite and curcumin on the medial prefrontal cortex (mPFC) using stereological methods. Methods Thirty rats were randomly divided into five groups. The rats in groups I–V received distilled water, olive oil, curcumin (100 mg/kg/day), sodium metabisulfite (25 mg/kg/day), and sulfite + curcumin, respectively, for 8 weeks. The brains were subjected to the stereological methods. Cavalieri and optical disector techniques were used to estimate the total volume of mPFC and the number of neurons and glial cells. Intersections counting were applied on the thick vertical uniform random sections to estimate the dendrites length, and classify the spines. Non-parametric tests were used to analyze the data. Results The mean mPFC volume, neurons number, glia number, dendritic length, and total spines per neuron were 3.7 mm3, 365 000, 180 000, 1820 µm, and 1700 in distilled water group, respectively. A reduction was observed in the volume of mPFC (∼8%), number of neurons (∼15%), and number of glia (∼14%) in mPFC of the sulfite group compared to the control groups (P < 0.005). Beside, dendritic length per neuron (∼10%) and the total spines per neuron (mainly mushroom spines) (∼25%) were reduced in the sulfite group (P < 0.005). Discussion The sulfite-induced structural changes in mPFC and curcumin had a protective role against the changes in the rats. [ABSTRACT FROM AUTHOR]

Objective. Spermatic cord torsion is a true urological emergency. Significant subfertility exists in patients following unilateral testicular torsion. Several studies have tested several agents such as vasodilators and antioxidants to inhibit or temper testicular damage. Material and methods. Sprague–Dawley rats were divided into five groups; in group 1 (control) no operation or drug injection was done. In groups 2–5 the left testis was subjected to 270 torsions. Two hours after induced torsion, drugs were injected intraperitoneally. Rats in group 2 received no drug, whereas those in groups 3, 4 and 5 were administered a single dose of papaverine (35 mg/kg), lidocaine (4 mg/kg) and verapamil (0.1 mg/kg), respectively. Thirty minutes after drug injection (2.5 h after torsion), testis detorsion was performed in all groups. The drug injections continued for 1 week. After 20 days, bilateral orchiectomy was carried out and semen from both testes was evaluated. Results. In animals treated with verapamil, left testis sperm count and the percentage of motile sperm were increased significantly in comparison with the sham-operated animals. Sperm morphology in all groups was in the normal range. Mean sperm count and motility in the right testes were not significantly different in different groups. Conclusions. Verapamil can induce beneficial effects on semen analysis parameters after testicular torsion in rats. [ABSTRACT FROM AUTHOR]