(1) Immunohistochemical methods and three antibodies (against actin, desmin and smooth muscle actin) were used to demonstrate the myoid cells in the domestic fowl testis and its excurrent ducts. (2) A positive reaction to actin, smooth muscle actin and desmin was found in the myoid cells of peritubular tissue of the testis and in rete testis, ductuli efferentes and ductus epididymidis. (3) In the testis myoid-reactive cells form a single layer. In the rete testis, ductuli efferentes and the ductus epididymidis reactive myoid cells form a main component of the stroma. (4) Positive reaction to actin, smooth muscle actin and desmin was also observed in the myoid cells of the tunica albuginea and in the wall of blood vessels in the testis and epididymis, indicating a contractile function for the testicular capsule.
The present study demonstrates histological and immunohistochemical changes in the peritubular testicular tissue of rat testis after application of cadmium chloride. After 5-day cadmium exposure, advanced deterioration of the boundary testicular tissue, mainly oedema, disarrangement of collagen fibres and peritubular cells, dilatation and thrombosis of blood vessels were observed. Changes in the boundary tissue were accompanied with desquamation of the germinal epithelium. Immunohistochemically, positive reaction for alpha-smooth muscle actin and desmin in tunica media of large testicular blood vessels basically was not affected. No reaction for vimentin was seen in endothelial cells of blood capillaries, whereas positive reaction presented only these cells in large blood vessels. The myofibroblasts positively reacting for desmin and alpha-smooth muscle actin form a single incomplete layer in the lamina propria of seminiferous tubules. Vimentin reactivity in the myofibroblasts and in the supporting Sertoli cells as well as Leydig cells in damaged testicular tissue was not observed. An increase in fibroblasts and free inflammatory cells positive for vimentin in the peritubular space on the peripheric area of the testis was observed.
In human and animals, it has been reported that Cd was linked with a number of health problems including marked damage of testes and fertility reduction. As for the sensitivity of fowl testes to Cd the results published so far differ from those reported in mammalian species. In this experiment, the effect of Cd with and without Se on spermatogenesis and semen quality in the rooster was studied after dietary Cd uptake. Cadmium (Cd) as Cd chloride (CdCl 2 ) and Se (Se) as sodium selenite (Na 2 SeO 3 ) were added to the feed at dosages: group 0control, group 1 -20 mg kg -1 Cd, group 2 -30 mg kg -1 Cd + 4 mg kg -1 Se. The cocks were exposed to Cd for 8 weeks. The structure of seminiferous tubules and boundary tissue, volume of semen, motility, concentration of spermatozoa and total sperm count were evaluated. In groups with 20 mg kg -1 Cd, the disarrangement of germinal epithelium, diminution of spermiocytes, detachment and presence of developing cells in the lumen of seminiferous tubules was observed. Analysis of the semen showed a significant decrease of volume of semen, the total sperm count and motility of spermatozoa (P<0.05). In the group with 30 mg kg -1 Cd and Se supplementation, seminiferous tubules displayed all the developing spermatogenic cells. Local disarrangement and accumulation of germ cells in the luminal space was observed. In semen, a significant increase of volume of semen, motility and total sperm count (P<0.05) was observed. A beneficial effect of Se on the development of spermatogenic cells and on semen quality was observed.
Immunohistochemical localization of S-100 protein was studied in anterior, intermediate and posterior lobe of the pig pituitary gland. Two immunopositive cells for S-100 protein were identified: the folliculo-stellate cells (FSc) in the glandular lobes and the pituicytes in the neural lobe. In the anterior lobe, immunoreactive folliculo-stellate cells were scattered among secretory cells. In the area where the secretory cells form strands and follicle-like groups the positive cells were concentrated in groups. In the intermediate lobe, S-100 protein-positive cells were located sparsely among secretory cells and next to secretory follicles and the pituitary cleft. These FSc were more voluminous and displayed fewer cytoplasmic processes. In the neurohypophysis, positive reaction for S-100 protein was seen in the pituicytes. These cells were distributed singly or concentrated in groups. The distribution, and morphologic characteristics of the FSc in the glandular lobes and the pituicytes in the neural lobe in the pig indicate different origin of both S-100 protein-positive cells.
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