To assess the influence of diclofenac sodium (DIC) treatment on tilmicosin (TIL) prompted cardiotoxicity, forty albino rats were randomly divided into four equal groups: control, TIL group (single subcutaneous injection of 75 mg/kg BW tilmicosin phosphate 30%), TIL + DIC group (single subcutaneous injection of tilmicosin phosphate 30% and then injection intramuscularly of 13.5 mg/kg BW/day for 6 days diclofenac sodium) and DIC group (intramuscular injection of 13.5 mg/kg BW/day diclofenac sodium for 6 days). Creatine kinase-MB, lactate dehydrogenase, aspartate aminotransferase, alanine aminotransferase, urea and creatinine significantly elevated in all treated groups, but markedly in TIL + DIC group serum. Lipid peroxidation significantly increased, and reduced glutathione significantly decreased in tissues of all groups. Several histopathological alterations were noticed in heart, liver, kidneys and lungs of all treated groups, particularly TIL + DIC group. Ultrastructurally, myocardium of TIL and TIL + DIC groups showed characteristic changes for myocardial apoptosis and degeneration. Significant differences were detected in area percentage of caspase-3 protein expression and bcl-2 immunoreactivity in cardiomyocytes, particularly in TIL + DIC group. This study is the first to indicate that one of the possible mechanisms of TIL cardiotoxicity is myocardial apoptosis. DIC amplifies TIL-induced cardiotoxicity besides its hepato-nephrotoxicity.

Tonsils form Waldeyer's ring which guards all body orifices. They form the first line of defense against foreign antigens and play a key role in initiating immune responses. The lingual tonsils react to ingested antigen and are replication sites of some pathogens. The data about the lingual tonsils of buffalo are lacking, therefore the present work studied the lingual tonsils of 5 buffalo calves (40-60 days). Fresh lingual tonsils were examined macroscopically and used for microscopic and ultrastructural investigations. The lingual tonsils were formed from several elevated macroscopic spherical masses on the dorso-lateral surface of the tongue with central crypt. The surface and crypt was covered with stratified squamous non-keratinized epithelium. An incomplete capsule encloses all the tonsils except at the crypt. The parenchyma was formed mainly from lymphoid follicles and interfollicular diffused lymphocytes. The lymphoid follicles arranged as one layer around the crypts. The interfollicular regions were formed from diffused lymphocytes supported with reticular fibers. High endothelial venules were present among these lymphocytes. Groups of mucous secreting units were distributed among the tonsilar units enclosed within the connective tissue capsule.

The ostrich foot has four toepads, two on the 3rd digit, one on the 4th digit and one at metatarso-phalangeal joint. Previous studies have not detailed the histo-morphological structure of these toepads. In this study, we have described the macroscopic and microscopic structures of the toepad of ostrich (Struthio camelus). Numerous papillae with different direction, length and thickness have been observed grossly on the ventral surface of each toepad. Histological examinations have revealed that the epidermis of the ostrich toepad, similar to other digitigrades, consists of an outer stratum corneum and an inner stratum germinativum (which is subdivided into basal, intermediate and transitional layers). The stratum corneum has several layers of flattened horny cells. The nuclei of basal cells have several mitotic figures. The cytoplasm of the stratum germinativum cells has multiple lipid droplets and multigranular bodies (in transitional cells only). Scanning electron microscopic examination revealed presence of collagen fibers in mid and deep dermis of each toepad. These fibers run parallel and connect to each other by very thin fibrils which are branched, crossed with each other in an oblique direction. Such arrangement of these collagen fibers, thin fibrils and presence of digital cushion are likely to be responsible for the protection of the underlying soft tissues and absorption of concussion.

The feeding habits and habitat of different fish species influence the morphology and functions of their gill rakers. This study used gross anatomy and scanning electron microscopy to investigate the morphological features of the gill rakers in Siganus luridus, Boops boops, and Pagrus pagrus. The gill rakers appeared as medial and lateral rows in all studied fishes. Except for Pagrus pagrus, which had a unique gill rakers arrangement in which the medial row of the 4th gill arch had the most gill rakers, the longest and most gill rakers were on the 1st gill arch in all studied fishes. The gill rakers of Siganus luridus were smooth, with various spine-like shapes, such as spine-like gill rakers, which were bifid or trifid spines, or duck toe-shaped gill rakers. According to SEM of the Siganus luridus' gill rakers, the trifid end gill rakers resembled caterpillars, and the duck toe-like gill rakers had three or four finger-like spines connected by inter-spine tissue. The Boops boops had long conical gill rakers with pointed ends on the lateral sides of the 1st gill arch, and the remaining rows had short gill rakers. According to SEM of the Boops boops' gill rakers, the long gill rakers were semi-conical and only had needle-like spines on the medial surface. The short gill rakers were projected as a boat and had three different shapes based on spine distributions. Gill rakers include those with a median crest and long spine laterals, those with only lateral spines, those with usually dorsal spines, and those with long wedge-shaped spines. Pagrus pagrus’ gill rakers were short, with fine-needle spines covering their tops. By SEM of the Pagrus pagrus' gill rakers, they appeared as a cylindrical elevation with spines on top. The spines were conical in shape with pointed curved or straight ends. The maximum value of the gill rakers’ lengths was discovered in the lateral row of the 1st gill arch, while the minimum value was in the medial row of the 4th gill arch. As a result, this is the first study of the three fish species' gill rakers. In the studied fishes, the morphological characteristics of gill rakers demonstrated unique structural specifications in feeding behavior.

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The footpad of ostrich El-Gendy et al.,

The current study aimed to investigate the ultrastructure of the retinal photoreceptors of the African catfish and to demonstrate their adaptation to nocturnal or diurnal visions or by the two ways. The eyes of eight adult catfish were collected during the daytime, and the retinae were separated and examined by light and transmission electron microscopy. The photoreceptors' layer appeared in contact with the retina's pigmented epithelium. Two photoreceptors were detected in cones and hidden rods.Cones predominate in light-adapted retinae. The outer segments of cones appeared between the retinal pigmented epithelium protrusions, which indicates the movement of melanosomes away from the photoreceptors as a retinomotor response of the catfish. The two types of retinal tapetum were in between cones. The first type, the cored granules, were large, spherical, and had black peripheral parts and central lucent parts, and contained some granules. The second type was Guanine crystallites of tapetum lucidum, which were small electron-lucent, and their shape varied from spherical to rectangular. Melanosomes vary in shape from spherical to elliptical. The Müller cells were darkly stained elongated cells that measured about 5.5-8.5 μm in length and 2.2-2.5 μm in width, and their microvilli appeared between the inner segments of the rods and cones. Müller cell processes were extended from the photoreceptor layer to the inner limiting membrane. Zonula occludentes appeared between the Müller cell processes and the internal segment of the rods and cones. African catfish have eyes which are adapted not only for nocturnal but also for daytime light.

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