OBJECTIVE To determine whether an enrofloxacin–silver sulfadiazine emulsion (ESS) labeled for treatment of otitis externa in dogs has ototoxic effects in rabbits following myringotomy. ANIMALS 6 healthy adult New Zealand White rabbits. PROCEDURES Rabbits were anesthetized for brainstem auditory-evoked response (BAER) tests on day 0. Myringotomy was performed, and BAER testing was repeated. Saline (0.9% NaCl) solution and ESS were then instilled in the left and right middle ears, respectively, and BAER testing was repeated prior to recovery of rabbits from anesthesia. Application of assigned treatments was continued every 12 hours for 7 days, and rabbits were anesthetized for BAER testing on day 8. Rabbits were euthanized, and samples were collected for histologic (6 ears/treatment) and scanning electron microscopic (1 ear/treatment) examination. RESULTS Most hearing thresholds (11/12 ears) were subjectively increased after myringotomy, with BAER measurements ranging from 30 to 85 dB in both ears. All day 8 hearing thresholds exceeded baseline (premyringotomy) values; results ranged from 30 to 85 dB and 80 to > 95 dB (the upper test limit) in saline solution–treated and ESS-treated ears, respectively. All ESS-treated ears had heterophilic otitis externa, epithelial hyperplasia of the external ear canal, various degrees of mucoperiosteal edema, and periosteal new bone formation on histologic examination. Scanning electron microscopy revealed that most outer hair cells in the ESS-treated ear lacked stereocilia or were absent. CONCLUSIONS AND CLINICAL RELEVANCE Results supported that ESS has ototoxic effects in the middle ear of rabbits. Further research is needed to confirm these findings. Myringotomized laboratory rabbits may be useful to study ototoxicity of drugs used in human medicine.

OBJECTIVE To evaluate glomerular filtration rate (GFR) estimation by means of plasma clearance of iohexol (IOX) in domestic rabbits and to assess accuracy of limited-sampling models for GFR estimation. ANIMALS 6 healthy domestic rabbits (Oryctolagus cuniculus). PROCEDURES Each rabbit received IOX (64.7 mg/kg [0.1 mL/kg], IV), and blood samples were collected at predetermined times before and after administration. Plasma IOX concentration was determined by high-performance liquid chromatography. The pharmacokinetics of IOX was determined by a noncompartmental method. For each rabbit, plasma clearance of IOX was determined by dividing the total IOX dose administered by the area under the concentration-time curve indexed to the subject's body weight. The GFR estimated from the plasma IOX concentration at 6 sampling times (referent model) was compared with that estimated from the plasma IOX concentration at 5 (model A), 4 (model B), and 3 (models C, D, and E) sampling times (limited-sampling models). RESULTS Mean ± SD GFR was 4.41 ± 1.10 mL/min/kg for the referent model and did not differ significantly from the GFR estimated by any of the limited-sampling models. The GFR bias magnitude relative to the referent model was smallest for model D in which GFR was estimated from plasma IOX concentrations at 5, 15, and 90 minutes after IOX administration. CONCLUSIONS AND CLINICAL RELEVANCE Results suggested that plasma clearance of IOX was a safe, reliable, accurate, and clinically feasible method to estimate GFR in domestic rabbits. Further research is necessary to refine the method.

OBJECTIVE To determine the pharmacokinetics and adverse effects of maropitant citrate after IV and SC administration to New Zealand White rabbits (Oryctolagus cuniculus). ANIMALS 11 sexually intact (3 males and 8 females) adult rabbits. PROCEDURES Each rabbit received maropitant citrate (1 mg/kg) IV or SC. Blood samples were collected at 9 (SC) or 10 (IV) time points over 48 hours. After a 2-week washout period, rabbits received maropitant by the alternate administration route. Pharmacokinetic parameters were calculated. Body weight, food and water consumption, injection site, mentation, and urine and fecal output were monitored. RESULTS Mean ± SD maximum concentration after SC administration was 14.4 ± 10.9 ng/mL and was detected at 1.25 ± 0.89 hours. Terminal half-life after IV and SC administration was 10.4 ± 1.6 hours and 13.1 ± 2.44 hours, respectively. Bioavailability after SC administration was 58.9 ± 13.3%. Plasma concentration at 24 hours was 2.87 ± 1.69 ng/mL after IV administration and 3.4 ± 1.2 ng/mL after SC administration. Four rabbits developed local dermal reactions at the injection site after SC injection. Increased fecal production was detected on the day of treatment and 1 day after treatment. CONCLUSIONS AND CLINICAL RELEVANCE Plasma concentrations of rabbits 24 hours after SC and IV administration of maropitant citrate (1 mg/kg) were similar to those of dogs at 24 hours. Reactions at the SC injection site were the most common adverse effect detected. Increased fecal output may suggest an effect on gastrointestinal motility. Additional pharmacodynamic and multidose studies are needed.

OBJECTIVE To evaluate repeatability and reproducibility of muscle condition score (MCS) in dogs with various degrees of muscle loss; to compare MCS, muscle ultrasonographic measurements, and quantitative magnetic resonance (QMR) measurements; and to identify cutoff values for ultrasonographic measurements of muscle that can be used to identify dogs with cachexia and sarcopenia. ANIMALS 40 dogs of various age, body condition score (BCS), and MCS. PROCEDURES A prospective cross-sectional study was conducted. Body weight, BCS, QMR measurements, thoracic radiographic measurements, and muscle ultrasonographic measurements were assessed once in each dog. The MCS for each dog was assessed 3 separate times by 4 separate raters. RESULTS For the MCS, overall κ for interrater agreement was 0.50 and overall κ for intrarater agreement ranged from 0.59 to 0.77. For both interrater and intrarater agreement, κ coefficients were higher for dogs with normal muscle mass and severe muscle loss and lower for dogs with mild and moderate muscle loss. The MCS was significantly correlated with age (r = −0.62), vertebral epaxial muscle score (VEMS; r = 0.71), forelimb epaxial muscle score (FLEMS; r = 0.58), and BCS (r = 0.73), and VEMS was significantly correlated (r = 0.84) with FLEMS. Cutoff values for identification of mild muscle loss determined by use of VEMS and FLEMS were 1.124 and 1.666, respectively. CONCLUSIONS AND CLINICAL RELEVANCE MCS had substantial repeatability and moderate reproducibility for assessment of muscle mass in dogs. Prospective studies of MCS, VEMS, and FLEMS for assessment of muscle mass in dogs are warranted.

The oil of Juniperus communis (JC) which is among medicinal plants, has many pharmacological activities. In this study, the effects of JC oil on serum paraoxonase (PON1), pancreatic enzymes levels and lipid levels in experimental diabetic rats were investigated.Thirty-two male Wistar-Albino rats (250-300g) were used. The rats were dividedequally into four groups, control (C), diabetes (D), JC oil (J), and diabetes + JC oil (DJ). D and DJ groups wereintraperitoneally (IP) injected with 45 mg/kg streptozotocin (STZ). JC oil was administered as 200 mg/kg/21days by oral gavage in J and DJ groups.Total cholesterol (TC) and triglyceride (TG) levels were significantly decreased in the J and DJgroups when compared to C and D groups (p≤0.001). There was no difference in TG levels between D andcontrol group (p≥0.05). Lipoprotein levels were not statistically significant between any group (p≥0.05).Comparing to the control group in the diabetes and DJ groups; significant decreased amylase levels andincreased lipase levels (p≤0.001) was observed. Paraoxonase activity in D group was statistically lower thanin the other groups (p≤0.05). There is no significant difference between the C group and the Jgroup (p>0.05).PON1 level has a significant elevation in the DJ in comparison with the D group (p≤0.05). As a result, JC oil caused an increase in antioxidant PON1 enzyme level and a decrease in lipidlevels in diabetes. The data obtained are supportive that JC oil may be a potential protective effect againstdiabetes-associated complications.

This study was carried out on 124 dogs between February 2018 and November 2018 to determine the prevalence of gastrointestinal helminths in stray dogs in Van. Collected stool samples, after macroscopic examination, were examined by native, flotation and sedimentation methods in terms of eggs and larvae. According to the results of the study, 43 (34.68%) of 124 dogs were detected as infected with various types of helminths. The most common species were respectively Toxascaris leonina (16.13%), Toxocara canis (12.90%), Ancylostoma caninum (5.64%), Taenia spp. (4.84%), Dipylidium caninum (3.22%), Uncinaria stenocephala (3.22%), Capillaria spp. (3.22%), Fasciola hepatica (2.70%) and Dicrocoelium dentriticum (1.35%) 35.14% of the female dogs were infected with parasites, while this rate was 34% for males. Statistically, infection status in males and females does not differ significantly by gender (Chi-Square: 0,17 p >0.05). When the distribution by age is examined, it is 0.5-2 years with the highest rate of 45.3%, 2-6 years with 27.7% and 5-9 years with 25%. According to age, infection status does not show a statistically significant difference (Chi-Square: 4.64, p> 0.05). As a result, it was concluded that the subsi substantial presence of zoonotic helminths in straydogs in the province of Van poses a threat to human health and protective measures should be taken againstit.

Aeromonas hydrophila is a Gram negative, positive oxidase, anaerobic, and opportunistic bacteria that, under certain conditions, become a pathogen (in humans and fish). This bacterium causes toxin and host infection in which different antibiotic resistance in isolated strains has been reported in different regions of the world. The aim of this study was to determine the prevalence of this bacterium and its susceptibility to common antibiotics in Tabriz city.50 samples from 5 Reared Oncorhynchus mykiss farms in Tabriz city (For each farm,10 numbers) were randomly assigned to suspected fish to the disease. By using biochemical tests, 14 samples (28%) from 2 Fish farms (40%) were identified as A.hydrophila. Antibiogram for these specimens showed that the bacterium had the highest resistance tovancomycin (100 %) and clindamycin (92.8%) antibiotics, and has the most sensitivity to the antibiotics ofsultrim, tetracycline and oxytetracycline with 71.4%.Considering the different antibiotic resistance pattern in this study and other similar studies,the necessity of examining the pattern of resistance in each region seems necessary.

The present study aimed to investigate the prevalence of Salmonella and their antibiotic resistance pattern against two commonly used antibiotics: ciprofloxacin and ceftriaxone in marketed live chickens in a live birds market. Materials and methods: The study was conducted on live Sonali chickens (crossbred of Fayoumi female and Rhode Island Red male). Cloacal swabs were collected from 50 randomly selected live birds from 5 retail sellers (10 samples/seller) at Jhawtola live birds’ market, Chattogram, Bangladesh. Culture and biochemical tests were used to identify Salmonella. Positives samples for Salmonella were further tested for antibiogram by disc diffusion method.Salmonella was identified from 28 (56%) of samples by culture and biochemical test. Among the positive isolates, 27 (96.42%) samples exhibited resistant to ceftriaxone, and 20 (71.42%) samples were to ciprofloxacin.The result of this study indicates there is a high prevalence of Salmonella in marketed local chicken and are resistant to ceftriaxone and ciprofloxacin which has economic importance as well as a public health concern. Awareness should be increased to prevent random use of antibiotics and provision of strict biosecurity measures.

Objective: In this study, LMS, zinc and vitamin AD3E were used with enterotoxaemia vaccine in sheep, in order to investigate their immunostimulant activities and also to make a comparison among them regarding their immunostimulatory properties. Material and Methods: In the research 40 sheep were divided into 4 groups, each group consisted of 10 sheep. Group I only vaccinated against enterotoxaemia. In groups II, III and IV besides enterotoxaemia vaccine, LMS, zinc and vitamin AD3E were used, respectively. Blood samples were taken on days 0 and 35 of the experiment. Serum levels of immunoglobulins (IgM, IgG, IgA and IgE) were determined using ELISA kits specific to sheep immunoglobulins. Hematological parameters and serum zinc levels were also determined.Results: Levamisole-treated group showed a significant increase in serum level of IgM, and zinc-treated group demonstrated a significant increase in serum IgG level (P<0.05). In day 35, serum IgM level was the highest in LMS group (group II) based on its levels in groups III and IV (P<0.05) and also IgG level was highest in group II when compared to its levels in groups III and IV (P<0.01). In group II, statistically significant decrease in total WBC and lymphocyte counts and statistically significant increase in thrombocyte counts were determined on day 35 (P<0.05). In group III, statistically significant decrease in total WBC, neutrophil counts and hematocrit values were detected (P<0.05), although, these changes were within physiologically normal limits.Conclusion: In conclusion, LMS stimulated the increase in IgM levels and zinc stimulated the increase in IgG levels without inducing adverse effect and the increase in antibody production resulted in the enhancement of humoral immune response to enterotoxamia vaccine. The use of LMS and zinc as immunostimulant together with vaccination is recommended.

The study was focused to investigate the occurrence of a fatal capture myopathy (CM) after chemical immobilization during translocation in different places and to evaluate serum enzymes of stressed deer and pathologic alteration of vital organs of dead animals due to CM. Materials and Methods: The experimental data was collected from Bangladesh National Zoo, Dhaka and the experiment was conducted at the Department of Surgery and Obstetrics, Bangladesh Agricultural University, Mymensingh. Immediate after capture the animals were allowed to normalize body temperature by pouring sufficient water over the body. Peripheral blood was aspirated from jugular vein for serum biochemical analysis. Once the animals died, vital organs were collected and processed for histology.Data from 2013 to 2018 revealed 178 animals captured through darting and among them 40 animals died due to post-capture myopathy reflecting death rate of 22.47%. We have closely studied on 16 animals captured on different occasions. Serum enzyme analysis were exhibited increased levels of ALT, AST, Bilirubin, Creatinine, BUN, LDH, CK, Troponin, Cholesterol, Triglyceride, HDL and LDL and were highly indicative of stress-linked muscle and organ damage. The macroscopic lesions consisted of muscular and cardiac degeneration, edema, hemorrhage and congestion in lung, adrenal gland and in kidney. Microscopically there were loss of striation and fragmentation of skeletal muscle, formation of contraction band necrosis in myocardial fiber, degenerative changes in renal tubule and formation of central intraluminal eosinophilic casts.The pathological findings were indicative of capture myopathy in spotted deer. This report underlines that mortality from capture is a risk that must be considered during restocking programs.