A macroanatomical and histological study of the uropygial gland in the white stork (Ciconia cicionia) / Un estudio macroanatómico e histológicos de la glándula uropigial de la cigüeña blanca (Ciconia cicionia)

The present study was aimed at the macroanatomical and histological investigation and the demonstration of the structural characteristics of the uropygial gland in the white stork. The uropygial gland of two adult male white storks constituted the material of the study. It was determined that the gland was situated subcutaneously in between the caudal aspect of the lumbosacral bone and the first coccygeal vertebrae. The gland was composed of two lobes, which displayed an oval appearance when viewed from above and resembled a water drop when observed medially. Tuft of feathers were present on the caudal margin of each lobe. The present study revealed that the uropygial gland of the white stork is a simple tubular gland, which discharges its secretion into the lumen by a holocrine mode. Each lobe, possessed centrally located large cavities and a main excretory duct and displayed the presence of externally situated "peripheral tubules" and interiorly situated "central tubules". These secretory tubules, which composed the parenchyma, were separated by connective tissue septa referred to as "trabeculae", and released their secretion into a centrally located lumen. The wall of the secretory tubules was comprised of four layers, referred to as the germinative, intermediary, secretory and degenerative layers. The silver-staining procedure demonstrated that the stroma of the uropygial gland did not contain reticulum fibres. The anatomy and histology of the gland has been examined in few avian species. Up to date, this study is the first to describe the histological and anatomical peculiarities of the uropygial gland in white stork. The results acquired hereby will surely contribute to further studies to be conducted on the related area.

El estudio tuvo como objetivo la investigación anatómica e histológica de la glándula uropigial de la cigüeña blanca, junto con demostrar las características estructurales de ella. El material del estudio estuvo constituido por glándula uropigial de dos cigüeñas blancas adultas macho. Se determinó que la glándula se encuentra vía subcutánea entre la parte caudal del hueso lumbosacro y las primeras vértebras coccígeas. La glándula se compone de dos lóbulos que muestran un aspecto ovalado, vista desde arriba y se asemejan a una gota de agua cuando se observa en sentido medial. Un penacho de plumas estaba presente en el margen caudal de cada lóbulo. El presente estudio reveló que la glándula uropigial de la cigüeña blanca es una glándula tubular simple, que descarga su secreción al lumen de un modo holocrino. Cada lóbulo posee una gran cavidad de ubicación céntrica y un conducto excretor principal, además muestra la presencia de "túbulos periféricos" situados exteriormente y "túbulos centrales "situados interiormente. Estos túbulos secretores que componen el parénquima, estaban separados por tabiques de tejido conectivo denominado "trabéculas", y liberan su secreción en una luz central. La pared de los túbulos secretores se componen de cuatro capas: germinativa, intermedia, secretora y degenerativa. La tinción de plata demostró que el estroma de la glándula uropigial no contienen fibras reticulares. La anatomía e histología de esta glándula se ha examinado en algunas especies de aves. Hasta la fecha, este es el primer estudio en describir las particularidades histológicas y anatómicas de la glándula uropigial de la cigüeña blanca. Los resultados obtenidos contribuirán a llevar a cabo nuevos estudios relacionados en el área.

A comparative study on the histological structure of the spleen in the ostrich (Struthio camelus), the kestrel (Falco tinnunculus) and the osprey (Pandion haliaetus).

The spleen structurally and functionally belongs to the hematopoietic organs and is also an important component of the reticuloendothelial system, which is known to play a major role in host defense. The histological structure of the spleen was investigated in the ostrich, a non-flying bird, the kestrel, a raptor, and the osprey, a fish-eating bird of prey (fish eagle). For this purpose, Mallory's modified triple stain, methyl green-pyronin and silver stain were used. Germinal centers were not present in the spleen of the osprey. In the spleen of the kestrel, penicillar arterioles and the surrounding lymphoid tissue were markedly dense. Compared to the other two birds, the red and white pulps were clearly distinguishable in the spleen of the ostrich.

Histologic structure of the uropygial gland of the osprey (Pandion haliaetus).

This study was performed to determine the histologic structure of the uropygial gland in an osprey. The gland was composed of two elongated lobes which were enclosed in a capsule of connective tissue. Each lobe of the gland had a large central cavity with one excretory duct. The secretory tubules consisted of four cell types: basal, intermediate, secretory, and degenerative. The intermediate cells in the osprey were few in number and did not form a layer, while secretory and degenerative cells consist of 2-3 strata, indicating a high level of lipogenesis. The membranes and peripheral cytoplasm of degenerative cells located in the base of the lobes revealed calcium (Ca2+) deposition and an intense acidophilic reaction.

The protective effect of erythropoietin and dimethylsulfoxide on ischemia-reperfusion injury in rat ovary.

OBJECTIVES: The aim of this study was to investigate the effects of erythropoietin and dimethylsulfoxide in the recovery from ischemia-reperfusion injury in an experimental rat adnexal torsion model. STUDY DESIGN: Thirty-six Wistar-albino rats were divided into six groups. Except for the sham operation group, all groups were subjected to left unilateral adnexal torsion for 3h. Erythropoietin and dimethylsulfoxide were intraperitoneally administered 30min before the detorsion operation. Malondialdehyde and nitric oxide levels were detected from both the plasma and the tissue samples. The sections of the tissues were evaluated histologically. The results were analyzed by a one-way analysis of the variance (ANOVA) followed by the Duncan test for multiple comparisons using computer software, SPSS Version 15.0 for Windows. RESULTS: This study demonstrated that dimethylsulfoxide and erythropoietin pretreatment attenuated ischemia-reperfusion-induced lipid peroxidation, prevented post-ischemic ovarian injury and helped to maintain the ovarian morphology. Malondialdehyde levels of plasma and ovary were higher in the torsion and detorsion groups than the sham group. This showed that ischemia-reperfusion had caused lipid peroxidation of the ovarian tissue, thus leading to oxidative damage. One of the major findings of this study is that malondialdehyde was significantly decreased in the plasma of rats who were pre-treated with dimethylsulfoxide and erythropoietin before detorsion. This suggests that dimethylsulfoxide and erythropoietin might prevent oxidative damage in ovarian ischemia-reperfusion injury. Histological examination confirmed that reperfusion caused more detrimental effects than only ischemia, which could be at least partially prevented by dimethylsulfoxide and erythropoietin administration prior to detorsion. CONCLUSION: Erythropoietin and dimethylsulfoxide may have beneficial effects in ischemia-reperfusion injury in ovarian torsion.

Effects of erdosteine on acetaminophen-induced hepatotoxicity in rats.

We investigated the effects of erdosteine on acetaminophen (APAP)-induced hepatotoxicity in rats. Superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-Px), AST (aspartate aminotransferase), and ALT (alanine transaminase) activities, and malonyldialdehyde (MDA) and nitric oxide levels as oxidant/antioxidant biochemical parameters were investigated with light microscopic evaluation in adult female Wistar Albino rats. APAP administration produced a decrease in hepatic SOD, CAT, and GSH-Px activities, and coadministration of erdosteine (150 and 300 mg/kg) resulted in increases in the activities. MDA and NO levels increased in the APAP group, and erdosteine treatments prevented these increases. Significant elevations in serum AST and ALT levels were observed in the APAP group, and when erdosteine and APAP were coadministered, their serum levels were close to those in the control group. Light microscopic evaluation of livers showed that there were remarkable centrilobular (zone III) hepatic necrosis and mild to moderate sinusoidal congestion in the APAP group, whereas in the erdosteine group, cellular necrosis was minimal and the hepatocytes maintained a better morphology when compared to the APAP group. Erdosteine prevented APAP-induced liver injury and toxic side effects probably through the antioxidant and radical scavenging effects of erdosteine.