BACKGROUND: The histogenetic study is a useful and practical laboratory method for obtaining basic and effective information in order to reveal the process of histogenesis and development of organs in different stages during the embryonic period. This applied method helps us to understand the formation time of each organ and its tissue structure. OBJECTIVES: The aim of the present study was to study the histogenesis and histochemistry of the pheasant liver during the embryonic period. METHODS: Sixty fertile eggs were placed in the incubator and sampling was performed from day 5 to the end of incubation period. The liver samples were fixed in 10% Buffered Formalin and the slides were stained with Hematoxylin and Eosin (H&E), Periodic Acid Schiff (PAS) and Masson Trichrome (MT). RESULTS: In this study, liver parenchyma, changes in the hepatocytes and their glycogen storage, as well as the appearance time of canaliculi, biliary ducts, central veins and port spaces were investigated. CONCLUSIONS: Differences in the time of the formation of the organs and structures in various birds relate to different incubation period or species variations. In this research, as the first study on the liver histogenesis of the pheasant, the formation of this organ from the fifth day to the end of the fetal period was examined and it was observed that the evolution and tissue development of the liver is completed until the eighteenth day of incubation period.

BACKGROUND: Skin is the first line of defense against the external environment and and it is possible to maintain the natural physiological functions in the body. The mucus layer on the surface of the fish body contains anti-microbial combination that provides the first layer of defense against pathogens. The mucus is released by some of the epidermis cells which are called goblet cells and it mostly contains the mucin and other glycoproteins. OBJECTIVES: Histomorphometrical, Histochemical and Electron Microscopic Studies of Goblet Mucous Cells in Different Regions of Argyrosomus Hololepidotus Epidermis. METHODS: In this study, six Argyrosomus hololepidotus are used and the structure of the fish’s skin was studied. For doing this microscopic study, the sampling was done on dorsal Regions of fish with a thickness of 0.5µ then they were stained with H & E, PAS, AB (PH = 2.5) and AB (PH = 2.5)-PAS. For electron microscopic study, the samples after primary and post-fixation were dehydrated and were embedded in resin. Then, thin sections 50 μm were prepared and stained with uranyl acetate. RESULTS: Argyrosomus hololepidotus fish has maximum goblet cells in ventral and dorsal skin and minimum numbers of goblet cells were seen in tail skin in 100 µm length of epidermis. There were goblet mucous cells containing mucous in the Argyrosomus Hololepidotus epidermal that thier numbers were different in difference areas but mucus components were similar in different areas and they reacted positively to PAS and AB dyes with PH = 2.5.The electron microscopic results of this study were showed that goblet cells immigrate in thickness of epidermis and they include mucosal drops. CONCLUSIONS: There are goblet mucus cells in all parts of Argyrosomus Hololepidotus Epidermis and they have similar mucus nature.

BACKGROUND: The trachea is the main air passages which is important for taxonomic reasons. The structure of trachea varies considerably in different avian species. OBJECTIVES: This study has been carried out in order to determine the histological and histochemical structure of the trachea in ostriches. METHODS: Sixteen tracheas of 8 female and 8 male nine-month-old healthy blue-necked African ostriches in slaughterhouse of Isfahan were selected. Each trachea divided into cranial, middle and caudal portions and fixed in 10% neutral buffered formalin. Tissues sections were stained with H&E and special stains included Masson’s trichrome, Verhoeff’s, Foot’s, Van Gieson’s, Periodic acid-Schiff, and Alcian blue. RESULTS: The trachea of blue-neck ostriches was composed of tunica mucosa-submucosa, cartilaginous, muscular and serosa. The epithelium was ciliated pseudostratified columnar contained simple alveolar goblet mucous glands. These glands reacted negatively to Periodic acid-Schiff but positively to Alcian blue. The propria-submucosa was composed of dense connective tissue. The muscularis mucosa was absent. Tunica cartilaginous and muscular was made up of sternotrachealis muscle and cartilaginous rings. The rings were only composed of hyaline cartilage. There is no osseous tissue in the tracheal rings. Tunica serosa was composed of loose tissue contained parasympathetic ganglia, adipose tissues, vessels, and all the connective fibers. Three final cartilage rings were shaped tympanum of the syrinx. The histological structure of the trachea showed no significant differences between the male and female ostriches. Except for the decreased number of mucous glands in caudal portion of the trachea, the histological structures of the trachea showed no considerably differences among various portions. CONCLUSIONS: Based on this study, it can be concluded that although the histological and histochemical structure of the trachea in ostrich was similar to those of some other species, but that there were also some differences.

BACKGROUND: The Eustachian tube is an osteocartilaginous channel connecting the tympanic cavity with the nasopharynx. There is no anatomical and histological research performed on this organ in buffalo. OBJECTIVES: Anatomical and histological study of Eustachian tube in buffalo will be useful for basic knowledge of this organ. METHODS: For this study 8 adult male and female buffalo's head were provided from slaughter house and their Eustachian tube were studied anatomically, then tissue samples were obtained and paraffin sections were prepared for using of staining methods such as H&E (for general study), Verhoff (for elastic fibers), PAS (for carbohydrates) and Masson's Trichrome Stainning Kit (for collagen fibers). RESULTS: Anatomical results showed Eustachian tube was white and funnel- like tube, no curve and structurally supported by cartilage and in both sexes they had the same structure. Histological and Histochemical results showed the epithelium of Eustachian tube in buffalo is pseudostratified ciliated columnar and in some regions of the Eustachian tube epithelium was stratified squamous. In the first portion of Eustachian tube cartilage was elastic and then eustachian tube cartilage was hyaline. The glands of Eustachian tube in buffalo were mucous and non folicular tubal tonsil could be found around the pharyngeal opening with obviously lymphoid tissue. CONCLUSIONS:. The results of this research can be used as the basic anatomical and Histological knowledge in buffalo..

Red hot pepper, in the science of botany is a plant belonging to the Solanaceae family and known as Capsicum annuum. Capsaicin is the active ingredient in cayenne pepper. Mast cells are cells with intracytoplasmic granules in the connective tissue, showing metachromasia under appropriate conditions. The aim of the study is to observe mast cell localization and tryptase and chymase expression in ovaries of rats administered subcutaneous capsaicin at 1 mg / kg dose during postnatal development periods. Sixty female Spraque-Dawley rats (21 d old) were used.  The rats were randomly divided into 3 groups (n=20 each) as pubertal, post pubertal and adult.  Each group was subdivided into two groups.  The first subgroup (control) was given no injections.  The second subgroup (experiment) received subcutaneous injection of equal volume of capsaicin (1 mg/kg/d) for 7 weeks. Mast cells were observed in the cortex and medulla regions of the ovary during three different developmental periods, giving rise to tryptase and chymase positive reactions. In conclusion, low dose long-term capsaicin administration does not inactivate the presence of mast cells in the ovarian tissue, and the observation of fewer tryptase and chymase immunoreactive cells in the capsaicin-treated experimental groups led us to the conclusion that capsaicin positively affected mast cell heterogeneity in gonads.

The brain samples were collected from 10 calves and 10 adult Indian buffaloes. Routine histological and histochemical processing and sectioning were done. The hippocampus was a curved elevation, lying immediately ventral to the splenium of the thalamus. Longitudinal section showed the ependyma, the alveus, the stratum oriens, the stratum pyramidale, the stratum radiatum, the stratum lacunosum and the stratum moleculare from above downwards. The prominent layer was the stratum pyramidale, composed of pyramidal cells in 2-3 rows. The four fields of the cornu ammonis, (CA1, CA2, CA3 and CA4) were identified based on the sizes of the pyramidal cells and their dendritic arborizations, both in the calf and in the adult. The presence of mucopolysaccharides was recorded. 

The brain samples were collected from 10 calves and 10 adult Indian buffaloes. Routine histological and histochemical processing and sectioning were done. The hippocampus was a curved elevation, lying immediately ventral to the splenium of the thalamus. Longitudinal section showed the ependyma, the alveus, the stratum oriens, the stratum pyramidale, the stratum radiatum, the stratum lacunosum and the stratum moleculare from above downwards. The prominent layer was the stratum pyramidale, composed of pyramidal cells in 2-3 rows. The four fields of the cornu ammonis, (CA1, CA2, CA3 and CA4) were identified based on the sizes of the pyramidal cells and their dendritic arborizations, both in the calf and in the adult. The presence of mucopolysaccharides was recorded. 

Histochemical study was conducted on Bursa of Fabricius of 48 normal Japanese quail birds up to four weeks of age, which were divided into four groups of 12 birds each, at the end of first week, second week, third week and fourth week of age, irrespective of sex. In all age groups, moderate to high periodic acid Schiff’s (PAS) activity was observed in the interfollicular connective tissue septa. Weak PAS activity was observed in the cortex in all age group of birds. The surface epithelium showed moderate PAS activity almost in all age group of birds, along with high PAS activity in the apical border of the surface epithelium in group I age of birds which was intense from group II age of birds. High Alcian blue periodic acid Schiff’s (ABPAS) activity was found in the interfollicular connective tissue septa in group I birds which gradually decreased with the advancement of age. High to intense ABPAS activity was observed in the capillaries as well as tunica intima and adventitia of blood vessels in birds of all age groups.

The study was conducted to add information to the database for concentrate on theBrunner's glands of the duodenum in adult local cows. The histological study showedthat Brunner's glands present in the tunica submucosa of the duodenum in local adultcows, the glands were branched tubuloalveolar secreting mucous, extended from theend of the pylorus to the first and middle third of duodenum, and absent at the lastthird of the duodenum. The excretory ducts of Brunner's glands opened at the cryptsof lieberkuhn at the base of intestinal villi penetrating the muscularis mucosa layer.The statistical analysis showed there was a significant variation in the diameter andlumen of Brunner's glands between the first and middle third of duodenum at (P≤0.05). The diameter and lumen of Brunner's glands at the first third of duodenum werelower than that of the middle third of duodenum. The statistical study showed , thatthere was no significant variation of the lining epithelium of Brunner's glands betweenfirst and middle third of duodenum, and there was no significant variation in thethickness of Brunner's glands aggregation between first and middle third of theduodenum.The histochemical study revealed that there were different types of glycoprotein inBrunner's glands and excretory duct in local adult cows, at first third of duodenumBrunner's glands contain a large amount of neutral glycoprotein and little amount ofacidic glycoprotein, while at middle third of duodenum the Brunner's glands containthe same amount of neutral and acidic glycoprotein. At the first third of duodenum,the excretory ducts of Brunner's glands contain neutral glycoprotein more than acidicglycoprotein, while at the middle third of duodenum the excretory ducts of Brunner's glands contain a large amount of acidic glycoprotein and little amount of neutralglycoprotein.

The objectives of this study were to use non-equilibrium gravitational field-flow fractionation (GrFFF), an immunotag-less method of sorting mesenchymal stem cells (MSCs), to sort equine muscle tissue-derived mesenchymal stem cells (MMSCs) and bone marrow-derived mesenchymal stem cells (BMSC) into subpopulations and to carry out assays in order to compare their osteogenic capabilities. Cells from 1 young adult horse were isolated from left semitendinosus muscle tissue and from bone marrow aspirates of the fourth and fifth sternebrae. Aliquots of 800 × 10(3) MSCs from each tissue source were sorted into 5 fractions using non-equilibrium GrFFF (GrFFF proprietary system). Pooled fractions were cultured and expanded for use in osteogenic assays, including flow cytometry, histochemistry, bone nodule assays, and real-time quantitative polymerase chain reaction (qPCR) for gene expression of osteocalcin (OCN), RUNX2, and osterix. Equine MMSCs and BMSCs were consistently sorted into 5 fractions that remained viable for use in further osteogenic assays. Statistical analysis confirmed strongly significant upregulation of OCN, RUNX2, and osterix for the BMSC fraction 4 with P < 0.00001. Flow cytometry revealed different cell size and granularity for BMSC fraction 4 and MMSC fraction 2 compared to unsorted controls and other fractions. Histochemisty and bone nodule assays revealed positive staining nodules without differences in average nodule area, perimeter, or stain intensity between tissues or fractions. As there are different subpopulations of MSCs with different osteogenic capacities within equine muscle- and bone marrow-derived sources, these differences must be taken into account when using equine stem cell therapy to induce bone healing in veterinary medicine.