This study was designed to explain the anatomy and histology of kidneys and salt glands in Great Flamingos. Eight adult healthy Great Flamingos of both sexes have been used. The results showed that the kidneys in Great Flamingos consist of three separated lobes. The right kidney was longer 8.9±0.3 mm than the left kidney 8.4±0.4mm. The ratio of the kidneys weight to the total body weight was 0.39%. The salt gland was very large crescent shape, and occupied the supraorbital fossa and has 20.8±0.2mm long and 3.9±0.2mm in diameter. The volume of cortex was 60-70% and the medulla was 30-40%. Within the middle region of cortex there were numerous large corpuscles (mammalian type) and few of small corpuscles (reptilian type). There was a variation between the means diameters of mammalian type 59±1µm and reptilian type 42±0.9µm. The proximal and distal convoluted tubules and collecting ducts were lined by simple cuboidal epithelium and their means diameters were 46±0.9, 44±1 and 55.1±0.7µm, respectively. Within medulla the thick and thin segments were arranged at the peripheral zone of medullary cone while the collecting ducts were at the central part of cone and all were lined with simple cuboidal epithelium except thin segments were lined with squamous cells. The salt gland were consisted of lobules surrounded by thick connective tissue capsule and each has mass of branched tubuloacinar secretory unites. The latter were made up by single layer of cuboidal cells. The tubules lead into central duct lined by double layer of cuboidal cells while the main duct lined with stratified cuboidal epithelium. The secretory units of salt gland gave negative reaction to PAS and combined AB (pH 2.5) and PAS stains and this indicate the absence of neutral mucosubstances. The results concluded that the kidneys in great flamingo was small size organ with low relative weight in compare to birds size and the salt glands was active organ.

Twelve samples of mammary glands (6 immature and 6 lactating ewes) were used for this study. Specimens of glands were immediately dissected and fixed in 10% formalin sol. The specimens were processed according to paraffin technique, sectioned at 5-6µm and stained by hematoxylin and eosin, Masson's Trichrom stains. In both immature and lactating ewes the mammary glands were covered by skin. In immature ewes the mammary quarter was composed of few mammary lobes that separated by very thick inter lobar adipose tissue. The lactating quarter was composed of huge mammary lobes and lobules without adipose tissue. In immature the lobe was consisted of few small lobules that composed of few of mammary alveoli while the lactating lobes had large sizes lobules and each had large alveoli which lined by tall cuboidal cells and supported by fibrous tissue and myo epithelial cells. In both immature and lactating ewes, the gland and teat cisternae were showed many of mucosal folds which lined by pseudo stratified columnar epithelium and supported by fibrous connective tissue. The teat cisterna of both immature and lactating was composed three layers; mucosal cisterna, fibro muscular layer and skin. The teat canal was lined by pseudo stratified squamous epithelium and the sub epithelial connective tissue showed well developed venous sinus and fibro muscular. Statistical analysis was revealed significant differences between the values of all parameters of immature and lactating ewes. Apparent surface areas of the lobe in immature and lactating were 122143.063±23.21 µm2 & 992541.188±33.81 µm2 respectively. Surface areas of lobule in immature and lactating were 1042.938±21.02 µm2 & 91565.977±25.60 µm2 respectively. Surface areas of alveoli in immature and lactating were 994.238±11.39 µm2 & 4584.270±19.26 µm2 respectively. Epithelial heights of alveoli in immature and lactating were 10.290±1.01 µm & 23.012±2.81 µm respectively. Thickness of inter lobar tissue in immature and lactating ewes 677.393±23.67 µm and 361.401±10.86 µm respectively. Thickness of inter lobular connective tissue in immature and lactating were 112.969±±11.48 µm and 90.281±9.81 µm respectively.

Aim:This study aimed to investigate the impact of rabbit serum on skin wound healing with the help of histological examination.Materials and Methods:A total of ten indigenous rabbits were used in this study. The animals were divided into two groups: control and serum- treated. The histological assessment was done with a paraffin embedding technique and the histological sections were stained with H&E stain.Results:Severe infiltration of polymorphonuclear leukocytes with severe fibrin deposits were seen in serum treated group at 2 days post-injury; at 7 days post-injury the changes revealed moderate fibroplasia, fibrin deposit and severe infiltration of both mononuclear and polymorphonuclear leukocytes; at 14 days post-injury, there were marked epithelization and dermal deposition of collagen fibers; and at 21 days post-injury, the epidermis completed epithelization and the dermis showed neither fibroplasia nor infiltration of mononuclear and polymorphonuclear leukocytes.Conclusion:The results indicated that rabbit’s serum can prevent wound infection, accelerate epithelialization and cutaneous regeneration with less granulation.

This study aimed to investigate the impacts of the Trigonella foenum-graecum (T. foenum-graecum) seeds on the female gonad. A total of twenty local rabbits were used in this study; were divided into four groups (5 each): first group (G1) was considered as the control group. The second group (G2), third group (G3) and fourth group (G4) were fed daily1.5%, 3%, and 4.5% of T. foenum-graecum seeds respectively for 60 days (twice daily). At the end of the experiment, the animals were euthanized by diethyl ether (C2H52O). Then the abdomen was incised, and the samples of ovaries were collected and fixed by 10% neutral buffered formalin. The histological assessment was done with a paraffin embedding technique and the histological sections were stained with Hematoxylin and Eosin stain. The result showed that the numbers of primary and secondary follicles were significantly P< 0.05 decreased in G3and G4 compared with the control (G1) and G2. The numbers of Graafian follicles were significantly P<0.05 decreased G4 compared with other groups. The diameters of the primary, secondary, and Graafian follicles were significantly lower than the other groups. The thickness of the granulosa cell layer in G3and G4 were significantly lower than the other groups. The histological figures declared that the ovary of G2 was similar to that in G1. The histological sections of G3 and G4 were revealed marked cortical and medullary vascular congestion and focal hemorrhage; there were also marked follicular degeneration and cystic necrosis. The study concluded that the low concentration of T. foenum-graecum (fenugreek) seeds do not have any positive effect in terms of ovarian stimulation

The current study was aimed to investigate the development of testis during prehatching periods to diverse the components of the testis in duck embryo from embryonic day 5 to 19 consequently; fifteen males' of mallard ducks embryos have been used. The results showed that development of testis has divided into two periods: the first one was the period of undifferentiated gonad (genital ridge) while the second period was the development into a testis which showed various stages. The undifferentiated stage has revealed of development a small protruded thickening of germinal epithelium and primordial germ cells on the ventromedial surface of the mesonephros and dorsal mesentery.The development periods has showed three stages: development of rete cords, sexual cords,primary somniferous tubules and Sertoli progenitor cells at the 8-10 th day embryos. During 14 th day old embryo was revealed of development immature somniferous tubule, tunica albuginea and testicular capsule. While the period of 19 th day embryo showed that development of interstitial cells and thin septa from tunica albuginea, .in addition to marked division of spermatogonia cells. Size of left testis was larger than the right one also the epithelial layer of left gonad is thicker than that covering the right gonad.