RESUMO
Abstract Introduction: In this study, Anzer propolis, which can only be obtained from the Eastern Black Sea region in Turkey, is studied for its effect on spinal cord ischemia/reperfusion injury. Methods: A total of 12 healthy male New Zealand White rabbits with an average weight of 3.0 to 3.5 kg were separated into two blind and randomized groups: the ischemia/reperfusion group (n=6) and the treatment group (n=6). Each rabbit in the treatment group was given a dose of 100 mg/kg of ethanol-dissolved Anzer propolis orally 1 hour before surgery. Blood samples were examined at the 0th hour and postoperatively at the 24th and 48th hours. Tissue samples were taken at the 48th hour during the sacrification. Results: There was a statistically significant difference between the two groups in terms of postoperative Tarlov scoring (P=0.012). There was a difference between the two groups in terms of the blood levels of interleukin-6 (IL-6) and tumor necrosis factor-alpha (TNF-α) at the 48th hour, myeloperoxidase (MPO) at the 24th and 48th hours, ischemia-modified albumin (IMA) at the 24th hour, and intercellular adhesion molecule-1 (ICAM-1) and total oxidant status (TOS) at the 48th hour (P<0.005). There was also a difference between the two groups in terms of apoptotic index data obtained with the terminal deoxynucleotidyl transferase (TdT)‐mediated dUTP nick‐end labelling (TUNEL) method in the histopathological examination (P=0.001). In the transmission electron microscopic (TEM) analysis, while ischemia/reperfusion group generally had axon-myelin separation, axoplasmic dissolution and myelin separation, the propolis treatment group had normal myelin sequencing. Discussion: In our study, after biochemical, histopathological, ultrastructural and neurological functional examination, it was demonstrated that Anzer propolis has sufficient neuroprotective effect on spinal cord ischemia/reperfusion injury in rabbits.
RESUMO
Mammalian reproductive axis is regulated by the combination of three fundamental tissues of neuroendocrine system including hypothalamus, hypophysis and gonads. In recent years, pineal gland has been included in this axis. The aim of the present study was to investigate the effect of 12L (Light):12D (Dark) photoperiod and melatonin administration (0.5 mg/kg/day; subcutaneously) on testicular volume and cellular parameters of testis at the pinealectomized (PE) rats. For this aim, twelve adult rats were firstly pinealectomized and then divided into two groups as GI and GII randomly. The GI rats served as control group and received only normal saline, whereas GII rats were the melatonin administered group. It was found that the total testicular volume, diameter and epithelial height of seminiferous tubules and number and nuclear diameter of the interstitial cells of the testes were increased in the GII. However, increase in the interstitial cell number was not found statistically significant among groups. In conclusion, it was observed that the 12L:12D photoperiod and doses of melatonin given increased the investigated parameters in PE rats.
El eje reproductivo de los mamíferos está regulado por la combinación de tres tejidos fundamentales del sistema neuroendocrino, incluyendo el hipotálamo, hipófisis y las gónadas. En los últimos años, la glándula pineal se ha incluido en este eje. El objetivo fue investigar el efecto del fotoperíodo 12L (Luz):12O (oscuridad) y la administración de melatonina (0,5 mg/kg/día, vía subcutánea) sobre el volumen testicular y los parámetros celulares del testículo en ratas pinealectomizadas (RP). Doce ratas adultas fueron pinealectomizadas y divididas en dos grupos, GI y GII de manera aleatoria. Las ratas del GI sirvieron como grupo de control y recibieron sólo solución salina normal, mientras que a las ratas del GII se les administró melatonina. Se encontró que el volumen total, diámetro y altura del epitelio de los túbulos seminíferos de los testículos, y el número y diámetro nuclear de las células intersticiales se incrementaron en el GII. Sin embargo, el aumento en el número de las células intersticiales no fue significativo entre los grupos. En conclusión, se observó que el fotoperíodo 12L:12O y la dosis administrada de melatonina aumentan los parámetros investigados en RP.