1. The aim of the study was to examine the morphology of the tongue and the histochemical features of the lingual salivary glands in this species. 2. The tongue was elongated, terminating in a rather sharp, dagger-like apex. On the surface of the tongue and situated between the body and root of the tongue, two rows of conical papillae, the sharp apices of which pointed towards the posterior part of the tongue, were observed. The keratinised epithelium lining the dorsal surface lacked typical gustatory papillae. However, it was observed that taste buds were present in the epithelium of the lingual body and root. The tongue was supported by a structure composed of hyaline cartilage, the paraglossum, which extended from the lingual root to the apex. Simple branched tubular glands, which were encapsulated by connective tissue, were embedded within the submucosa in the body (anterior salivary glands) and root (posterior salivary glands) of the tongue. It was observed that the secretion of the lingual glands contained neutral mucins, proteoglycans containing carboxylic acid, weak and strong sulphated groups, N-acetylated sialomucins, but lacked glycogen. 3. It was demonstrated that, the general morphological features, papillary distribution of the tongue and the histological structure of the mucosa epithelium and the supportive elements displayed similarity to those of other domestic avian species. It was also determined that, in view of the particular feeding types, in the partridge, the presence of the papillary crest was not correlated with diet.

Morphology of the palatine mucosa and its secretion was described in Chukar partridges, by gross morphology and histochemistry techniques. For this purpose, 10 healthy adults (five male and five female) were sacrificed. After sacrifice, the palatine tissues were extirpated and fixed in 10% formol‐alcohol for 18 h and were embedded longitudinally and transversally in paraffin. The 5‐μm sections were employed histological and histochemical staining techniques. The lateral rims of the caudal part of the choanal cleft were bordered by large conical papillae. In the periphery of the choanal and the infundibular cleft, small papillae were scattered across the palatine mucosa. The palate was lined by keratinized stratified squamous epithelium, which contained conical papillae of varying height. However, the folds of the keratinized stratified squamous epithelial layer covering the choanal and infundibular cleft were nonkeratinized. The rostral aspect of the choanal cleft contained simple branched tubulo‐alveolar glands of both mucous and sero‐mucous characteristic, whilst the caudal aspect included mucous simple branched tubular glands. Furthermore, it was ascertained that the secretion of the palatine glands contained glycoproteins, carboxylated proteoglycans, weakly and strongly sulphated mucins, sialic acid and hyaluronic acid, but lacked glycogen. In conclusion, it was demonstrated that the histological structure of the mucosal epithelium and the supporting elements displayed similarity to those of other domestic avian species.

The aim of our study was to determine the distribution of estrogen receptor α (ERα) and progesterone receptor B (PR-B) in the bovine oviduct during the follicular and luteal phases. Bovine oviducts from 23 animals were obtained from a local slaughterhouse. Blood samples from these animals also were taken before death to measure estrogen and progesterone levels. The serum levels of estradiol-17β and progesterone changed during the estrous cycle. Tissue distribution of ERα and PR-B was examined using immunohistochemical techniques and the results showed that ERα and PR-B were stained in nuclei of cells and could be detected in all compartments along the entire oviduct during both the follicular and luteal phases. During the follicular phase, no significant differences were found between ERα and PR-B distribution (p < 0.05), while significant differences were found between ERα and PR-B during the luteal phase (p < 0.05). We results indicated that the frequency and intensity of ERα and PR-β immunoreactivity in the oviduct of bovines varied according to the oviductal cell types and the phases of the sexual cycle.

The aim of the study was to investigate the ability of a combination of bone marrow mesenchymal stem cells (BM-MSCs) with and without demineralized freeze-dried bone allografts (DFDBAs) to induce bone regeneration in calvarial defects in ovariectomized rats.Critical size defects were filled with a combination of demineralized freeze-dried bone allografts and bone marrow mesenchymal stem cells (BM-MSCs) or BM-MSCs alone. Eight weeks after calvarial surgery, the rats were sacrificed. The samples were analyzed histologically and immunohistochemically. No difference was observed in vascularization between groups C1 (animals with cranial defect only, control group) and O1 (animals with cranial defect only, ovariectomy group). Intramembranous ossification was observed at a limited level in groups C2 (animals with cranial defect with MSCs, control group) and O2 (animals with cranial defect with MSCs, ovariectomy group) compared to C1 and O1. In group C3 (animals with demineralized freeze-dried bone allografts with MSCs, control group), the fibrous structures of the matrix became compact as a result of a bone graft having been placed in the cavity, but in group O3 (animals with demineralized freeze-dried bone allografts with MSCs, ovariectomy group), the fibrous tissue was poorly distributed between the bone grafts for the most parts. We conclude that the insertion of BM-MSCs enhances bone healing; however, the DFDBA/BM-MSC combination has little effect on overcoming impaired bone formation in ovariectomized rats. Key words: bone healing, bone marrow mesenchymal stem cells (BM-MSCs),demineralized freeze-dried bone allografts (DFDBAs), ovariectomy, calvarial defect

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