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: PRP (Platelet-Rich Plasma) is a biological product that has shown significant therapeutic results compared to synthetic drugs and some traditional methods. The advantages of this method include: PRP, compared to other biological materials, is easily prepared in clinic and the safety is high as well. OBJECTIVES: We aimed to investigate the evaluation of histomorphometric properties after injection of plasma. METHODS: Thirty rats were divided randomly into three groups: control group (normal saline), PRP and PPP (Platelet-Poor Plasma) groups. In order to prepare PRP and PPP, blood samples (1cc) were collected through cardiac puncture and were centrifuged. The upper layer consisted of PPP and lower layer consisted of PRP. The 2% calcium gluconate solution (100 µl) was added to platelet-rich plasma (200 µl) layer to activate platelet. After seven days, the dorsal skin samples were collected. They are cut into 5 to 6 μm thickness sections using paraffin embedding method and were stained by hematoxylin, eosin and Masson’s trichrome. The epidermis, dermis and hypodermis layers of skin, the epithelial thickness of hair root sheath, maximum depth of hair follicles, the thickness of the whole skin, the number of sebaceous glands and hair follicles in the specified scale, finally the number of fibroblast cells and the percent distribution of connective tissue fibers were investigated in histometric structure of the skin and skin appendages. RESULTS: The results of this study indicated that systematic and controlled PRP may have beneficial effects on the reconstruction and rehabilitation of the skin and its appendages. CONCLUSIONS: The present study showed that growth factors in plasma especially PRP, could be stimulated connective tissue fibroblast of dermal layer in the skin.

Transcutaneous oxygen (PO2.TC) monitoring is commonly used in human medicine for evaluating skin viability. The application of transcutaneous monitoring for evaluating skin viability in dogs was investigated. The changes in PO2-TC values were measured from 16 avascular skin flaps created along the lateral hemithoraces of 4 dogs. Transcutaneous oxygen values were serially recorded from the vascular base and avascular apex of each flap for 12 hours after surgery. A single transcutaneous measurement was obtained from each flap base and apex 24 hours after surgery. Serial arterial blood gas analyses were obtained to compare central oxygen values with PO2-TC values. Full-thickness skin biopsy specimens were harvested from the base and apex of each flap 24 hours after surgery. The flaps were observed for 4 days and then excised for histologic examination. A subjective grading scale was used to assess histologic changes. Throughout the 12-hour period and at 24 hours, a statistically significant difference was found between the PO2-TC values for apices and bases of the flaps. The mean PO2-TC for all bases was 90.9 mm of Hg +/- 3.3 SEM, and the mean PO2-TC for all apices was 21.2 mm of Hg +/- 1.8 SEM. The mean regional perfusion index (apex PO2.TC/base PO2-TC) was 0.23 +/- 0.02. The subjective numbers assigned to the biopsy specimens were statistically evaluated by using a paired Student's t test and a Wilcoxon signed-rank test. A significant difference was found between the numbers for the collective bases and apices with both tests. A statistically significant difference was found between the numbers for the apex biopsy specimens taken 24 hours after creation of the skin flap and those taken when the flap was excised, whereas no difference was found between the numbers for the base biopsy specimens. On the basis of our findings, PO2-TC monitoring is a useful technique for assessing skin viability in dogs.

A study was undertaken to determine the pressor and toxic effects of etoposide, an antineoplastic agent, when administered IV in 0.9% sodium chloride solution (0.4 mg of etoposide/ml) over a 30-minute period to dogs at a dosage of 40 mg/m2 of body surface. On day 1, 6 adult German Shorthaired Pointers were anesthetized with halothane, and blood pressures were measured via a femoral artery catheter before, during, and after the etoposide was administered. Systolic, diastolic, and mean blood pressures of each dog increased significantly (P less than 0.01) within 30 minutes after initiation of etoposide infusion. On day 3, when the dogs were not anesthetized, etoposide was again administered to each dog, using the same dosage. Each dog developed a moderate to severe cutaneous reaction characterized by moderate to severe pruritus, urticaria, and swelling of the head and extremities that began during the second infusion of etoposide. These same cutaneous reactions were seen on day 30, when etoposide was administered to 3 of the previously treated dogs and 2 previously untreated Beagles. We concluded that the administration of the commercial preparation of etoposide is likely to cause a significant reduction in blood pressure of anesthetized dogs, and that the drug is likely to induce a moderate to severe cutaneous reaction when administered to unanesthetized dogs.

The area of skin supplied by the afferent fibers in one cutaneous nerve is called the cutaneous area (CA) for that nerve. The CA of peripheral branches of lumbar and sacral spinal nerves responsive to the stimulation of hair follicle mechanoreceptors were mapped in 27 dogs. The amount of overlap among the CA was similar to that found for other CA of the body. The CA of peripheral branches of the sciatic nerve were restricted to the lateral, cranial, and caudal aspects of the pelvic limb distal to the stifle. The CA of the saphenous nerve was located on the medial side of the limb, except for a small area located on the lateral side of the crus. The distal part of the CA of the saphenous nerve was completely overlapped in the hind paw by branches of the superficial peroneal nerve laterally and the medial plantar branch of the tibial nerve medially. The CA for the deep peroneal nerve was located on the dorsal surface of the webbing between digits 2 and 3 and the adjacent skin of these digits. The CA of the plantar branches of the tibial nerve were small in comparison with the diameter of the nerve, suggesting that these branches contained nerve fibers supplying other, deeper structures in the hindpaw and that damage to these nerves would interfere with cutaneous sensation in only a small region on the plantar surface of the hindpaw. Knowledge of the CA of the various branches of the sciatic nerve allows more accurate localization of injury to the sciatic nerve or its branches by using areas of anesthesia.

Cell proliferation kinetic values were established for the epidermis, hair follicle epithelium, and sebaceous glands of 8 Cocker Spaniels with primary idiopathic seborrhea. Values were established by intradermal pulse labeling injections of tritiated thymidine followed by cutaneous biopsy and autoradiography.The epidermal basal cell-labeling index was 4.96 +/- 0.97%, and the epidermal nucleated cell-labeling index was 3.33 +/- 0.71%. Calculated epidermal cell renewal time for the viable layers of the epidermis was 7.85 +/- 1.80 days. The hair follicle infundibulum basal cell-labeling index was 5.48 +/- 2.01%, and the sebaceous gland basal cell-labeling index was 5.94 +/- 4.15%. When compared with previously reported cell kinetic values for Cocker Spaniels and Beagles with healthy skin, these data indicate accelerated cellular proliferation in all 3 cutaneous structures in seborrheic Cocker Spaniels.

Wild rats are known as a major reservoir and intermediate host for several pathogenic microbial species. Thus, theVeterinary Research Institute (VRI) conducted a survey to determine the presence of parasitic pathogens in local rats, such as blood protozoans, gastrointestinal parasites, as well as ectoparasites such as mites and lice. The study was conducted with the collaboration of Kuala Lumpur City Council Pest Control Unit, whereby a total of 105 wild rats were trapped at two urban areas of Kuala Lumpur; namely PasarPudu and Chow Kit. Autopsy was done on the rats to acquire the skin, organ and blood samples..The skin scrapping was performed on skin samples to identify the common species of mites and lice, while the floatationtechnique was conducted on faecal samples to identify helminth eggs. Results showed thatspecies of Tritrichomonas, Strongyloides, Nippostrongylus, Blastocystis, Rodentolepis, Coccidia, Trichuris, Capillaria and Ascarid were found in the faeces while Trypanosoma sp.was found in the blood samples taken from the animals. Taeniataeniformis was obtained from liver samples while theectoparasites found on skin were identified as Radfordia,Polyplax,Linognathus and Hoploplurasp. Control and eradication of rodent pests is crucial in combating emerging and re-emerging diseases which may be zoonotic as rodents are reservoirs to various pathogens.

In this study, we describe a case of epitheliogenesis imperfecta (EI) observed in the fetus of Korean native cattle. The fetus had multifocal areas of skin defect, especially on the distal portions of the four limbs, and the affected areas were bright-red and glistening. Histopathologically, these areas were characterized by complete absence of squamous epithelium, infiltration of inflammatory cells into the dermis, atrophy of hair follicles, sebaceous and sweat glands. To the best of our knowledge, this is the first report of epitheliogenesis imperfecta in Korean native cattle.