BACKGROUND: Myocardial bridge (MB) is generally defined as a superfacial muscular band that forms sporadic or multiple across the coronary artery in dog, cat, sheep, and human. OBJECTIVES: From the view of embryology MB is a preformatted structure with coronary artery during  forming. The type of study in human is during sonography and angiography examination, but in veterinary science the study on MB is  done after death examination. METHODS: This study was performed on over 50 sheep hearts that were prepared from slaughterhouse of Shahr e kord. First, pericardium was opened and the heart brought out of the pericardial cavity and then the hearts were studied with concentrated light and lens on both sides. After the M B recognition,  their length and width were measured by a ruler. In both sides of the heart,the MB was  divided into 1/3 proximal, 1/3 middle and 1/3 distal. In all of the studied hearts, only 10 samples (20%) had M B. RESULTS: The average length of recognised MBs was 1.55±1.17 (SD) cm and  with width of 1.09±.092 (SD) cm. The positive samples were transferred to histology laboratory for preparation of cross section of heart and were stained with  H&E staining.CONCLUSIONS: The longitudinal section showed the long fibers of myocardium with continual narrow fibers and intercalated discs were located between them.

BACKGROUND: Probiotics have more functional effects and less survival  under hard acidic-bile circumstances of digestive system, and foodstuff products situation has persuaded investigators to find techniques to resolve this problem. Microencapsulation as a useful method has a perceptible effect in this regard. Objectives: The aim of this study was to assess the protective role of double coated beads of calcium alginate-chitosan-eudragit S100 achieved from microencapsulation of Lactobacillus acidophilus as a predominant flora of human and animals gut. Methods: Following activation of starter culture of L.acidophilus in MRS-broth medium,  centrifuge (at aspeed of 5000 rpm for 10 minutes) was used to purify bacteria. Extrusion technique was used for Microencapsulation of probiotic bacterium. The survey of beads solidity was carried out for 12 hours and the study of survival of microencapsulated bacteria was done for 120 minutes inside hydrochloric acid, phosphate buffer and digestive powder solution.  MRS-Salicin-agar and pour plate method and incubation at 37oC for 48 h was done for cultivation. Data were analyzed by means of an independent t-test. Results: Shape and size of beads were shown by optical microscope. The consequences demonstrated that survivability of microencapsulated bacteria in the mentioned conditions, in both situation with and without mechanical tensions, is significantly more than free bacteria (p<0/05). Conclusions: Microencapsulation with calcium alginate- chitosan-eudragit S100 plays a significant role  in increasing the rate of L. acidophilus viability.

BACKGROUND: Lactoperoxidase is an enzyme of the oxidoreductase family. Lactoperoxidase is an important antimicrobial agent. Applications of lactoperoxidase are being found as a preservative in food and cosmetics. Immobilized LPO provides several significant benefits such as: easily separated from the reaction products, reducing production costs by efficient recycling and control of the process. Objectives: Purification and immobilization of lactoperoxidase extracted from camel milk using sodium alginate polymer. Methods: The lactoperoxidase was purified from camel milk by using sephadex G-100 gel filtration CM and sephadex C-50 ion-exchange chromatography. Encapsulation was carried out by using LPO, sodium alginate, glycerol and Tween 80. Afterward, the microcapsules were stablized by calcium ion (1%). Efficiency of encapsulation was calculated. The particle size and distribution were measured with particle size analyzer. Morphology and formation of the particles were studied  using Scanning Electron Microscope (SEM). Stability of encapsulated and uncapsulated  LPO was studied at 4 °C during 70 days. Results: After purification and purity measurement by SD-SPAGE, concentration of 0/28 micrograms per liter for each of the fractions was obtained. Microencapsulation efficiency was 84% and microcapsules  less than 200 nm were formed. Observation by SEM confirmed the formation of microparticles. Microcapsules have a relatively smooth surface, spherical with low tenacity as well. Stability of encapsulated enzyme at 70 days was obtained 81%. Conclusions: Immobilization of Lactoperoxidase extracted from camel milk  using sodium alginate is a good method to increase performance of the enzyme.

BACKGROUND: Staphylococcus aureus (S. aureus) possess a variety of virulence genes that are involved in the pathogenesis of infections caused by this agent. OBJECTIVES: The aim of this study was to evaluate the prevalence of the genes encoding collagen binding (cna) and fibronectin binding (fnb) adhesion factors in Staphylococcus aureus isolates from food and clinical specimens. METHODS: During the time period 2010-2013, a total of 38 isolates of Staphylococcus aureus from clinical specimens and 32 isolates from food samples were collected. All isolates were identified biochemically and subjected to DNA extraction. The accuracy of DNA extraction from each isolate was confirmed by PCR amplification of aroA gene and then the presence of cna and fnb genes in the extracted DNAs was assessed by PCR, using the specific primers. RESULTS: The results showed that among 38 isolates from clinical specimens, 15 (39.5%) &amp; 32 (84.2%) and among 32 isolates of food origin 10 (31/2%) and 16 (50%) isolates had cna and fnb genes respectively. Thirteen clinical (34.21%) and 6 food isolates (18.7%) were positive for both fnb and cna genes and 4 clinical (10.5%) and 12 food isolates (37.5%) were lacking both genes. CONCLUSIONS: According to the results, it is concluded that, although these adhesion genes are not present in all Staphylococcus aureus clinical isolates, but their prevalence is high and using the products of these genes in vaccines may be effective in protecting against infections caused by this bacterium.

BACKGROUND: Babesiosis and Thosis are parasitic tick-borne diseases that cause a lot of economic loss in livestock Industry. Objectives: The purpose of the present study was to detect Babesia and Theileria infection in goats and and vector ticks in goats in Mashhad. Methods: One hundred blood samples of goats and 246 ticks were collected from some suspected flocks with history of piroplasmosis. The samples were transported to laboratory under cold condition. Blood smears were prepared and stained by Geimsa method and examined with a light microscope at ×1000 magnitude. The collected ticks were separated into tick pools of five according to their species and sex. The blood, salivary gland and ovaries of tick samples were examined using specific primers of Babesia.spp and Theileria.spp by semi nested-PCR. Results: Piroplasm bodies were not observed in any blood samples of goat in Mashhad. In a total of 246 collected ticks, seven species were identified as follows: R. turanicus 127(51.6%), D. marginatus 67 (27.2%), Hy. marginatum 44 (17.9%), R. sangunincus 4(1.6%), Hy. anatolicum 2(0.8%), Hy. asiaticum 1(0.4%) and Heam. sulcata 1(0.4%). Dominant tick species of goats in Mashhad suburb were R. turanicus and D. marginatus. The results of PCR showed that none of the blood samples were infected with Babesia spp. and Theileria spp. Also, Theileria infectoin was detected in a sample salivary glands  of Hy. marginatum. ConclusionS: Based on microscopic and molecular results, no  Theileria spp. and Babesia spp. infection were detected in goats. R.turanicus was the dominat tick species and Theileria spp. infection was detected in one sample of Hy.marginatum.

BACKGROUND: No study has been conducted on iron requirements of broiler breeder hens until now. OBJECTIVES: The purpose of the present study was to determine the iron requirement of broiler breeder hens using nonlinear models. METHODS: Forty eight (Cobb 500) broiler breeder hens were individually placed in galvanized wire cages. In order to depletion of hens iron reserved, hens were offered a semi purified iron deficient diet for 3 weeks. At 62 week of age, Hens  were  randomly  allocated  to  4  dietary  treatments  (37, 52, 67, 82 ppm of diet iron) with 4 replicates. Body weight gain, egg production and egg weight were measured during 6 weeks experimental period. RESULTS: The results showed that the estimated iron requirement for egg production(H.H), egg weight, iron content of the liver, blood serum, bone marrow, spleen and egg yolk were 65, 62, 54, 72, 57, 63, 64 ppm respectively. The logistic model was fitted to iron content of liver, spleen, serum and bone marrow, suggested that iron requirement were equal to 66, 53, 129, 58 ppm respectively. Fitted exponential model estimated iron requirement for egg weight, iron content of liver, spleen, serum and bone marrow were 62, 96, 70, 73, 111 ppm respectively. Also based on the quadratic equation models, estimated iron requirement for egg production(H.H), egg weight, iron content of the liver, blood serum, bone marrow, spleen and egg yolk were 65, 66, 71, 220, 51, 70, 62 ppm respectively. Among the four models used, the broken line model is more accurate in estimating the required iron than other models due to the low variance between estimated requirements. CONCLUSIONS: Results indicated that value recommended by primary breeder (Cobb 500 management guide, 55 ppm) is lower than values obtained in present study.

BACKGROUND: Today the use of natural substances plays a major role in improving the growth and immunity of aquatic organisms. OBJECTIVES: The purpose of the present study was to evaluate the effects of Iron nanoparticles with Lactobacillus casei as a probiotic on growth parameters and probiotic counts in rainbow trout intestine. METHODS: Seven hundred and twenty fish with 12±0.49 g initial weight were prepared and after acclimatized to the laboratory conditions divided randomly into six groups. First group was selected as control, other groups were fed with a commercial diet supplemented with 108 CFU/g Lactobacillus casei (group 2), 50 µg/kg Iron nanoparticles (group 3), 100 µg/kg Iron nanoparticles (group 4), 50 µg/kg Iron nanoparticles with 108 CFU/g Lactobacillus casei (group 5) and 100 µg/kg Iron nanoparticles with 108 CFU/g Lactobacillus casei (group 6), respectively. Biometry and intestine bacteriologic examination were carried out at days 0 and 60. RESULTS: Results showed that growth parameters (weight gain, body weight gain, specific growth rate, daily growth rate, and condition factor and food conversion rate) were significantly higher in group 5 compared with the other groups. Also, intestine bacterial counts increased by using Iron nanoparticles in combination with Lactobacillus casei. The fish that received 100 µg/kg Iron nanoparticles and probiotic had significantly higher bacterial counts in their intestine compared with the other groups. CONCLUSSIONS: Based on the obtained results we conclude that diet supplementation with Iron nanoparticles and Lactobacillus casei as a probiotic could significantly improve growth parameters in rainbow trout. However, these results would warrant further study on the clinical application of these agents.

BACKGROUND: Zeolites containing silver ion, in combination with synthetic fibers, show antibacterial activity. OBJECTIVES: The purpose of this study was to use silver zeolite indirectly as antimicrobial agents to control Streptococcus iniae infection which recently has caused disease in some of rainbow trout farms in Iran. METHODES: In this context polyurethane foams containing silver zeolite (10 and 20%) were used in water filtration of semi circulation culture system of rainbow trout fry. After addition of Streptococcus iniae (105 Cell/ml) to water in culture systems, the filters were evaluated for efficacy in inhibiting bacteria through measuring bacterial loading in water, monitoring disease symptom and culture of bacteria from kidney and spleen. RESULTS: The results indicated that filters containing silver compounds could significantly reduce load of bacteria from the water to 102 (p<0.05) compared to the control. Filter with 10% silver zeolite had higher efficiency among others. CONCLUSIONS: According to the results of this study, it seems that silver zeolite in combination with polyurethane foams has the sufficient potential to control bacterial infection and disease prevention in semi circulation system of Rainbow trout. Development of these filters and their application in control of aquatic animal diseases can result in reduction of using chemical drugs.

BACKGROUND: Oxidative stress reflects an imbalance between the reactive oxygen species (ROS) and a biological system's ability to readily detoxify the oxidative agents. Disturbances in the normal redox state of cells can cause toxic effects through production of peroxides and free radicals that damage all components of the cell, including proteins, lipids, and DNA. ObjectiveS: The purpose of this study was to evaluate the oxidative status in calves within 3 days of birth. Methods: Twenty calves from Zagros dairy farm were selected. Blood samples were collected from the jugular vein at 0 (before administration of colostrum), 24, 48 and 72 hours after birth for measurement of serum levels of TBARS, Superoxide dismutase and catalase. Results: The results indicated higher levels of serum malondialdehyde concentration at birth that subsequently decreased at 24 and 48 hours after birth (p<0.05). There were lower levels of serum concentration of catalase at birth that followed by increasing in it at 24 and 48 hours after birth (p<0.05). Also, the concentration of superoxide dismutase was lower at the birth that subsequently increased at 24 hours after birth (p<0.05). Conclusions: Based on this study, it seems that antioxidant capacity of calves has been increased within 3 days of birth. Improvement of oxidative status in calves could be due to gradual increasing of their antioxidative capacity and also beneficial effects of colostrum.

BACKGROUND: Medical plants have been recently used to treat diabetes. Osteoporosis is one of diabetes side effects and increases the risk of bone fracture in diabetic patient. OBJECTIVES: The purpose of the present study was to investigate the potential bone protective effects of O.persica ethanolic extract in streptozotocin-induced diabetic rats. METHODS: Forty male rats were randomly divided into five equal groups and treated as follows: group 1 (control); group 2 (STZ group): received STZ 50 mg/kg by a single IP injection; groups 3, 4 and 5 treated with STZ as above+ 200 mg/kg, 300 mg/kg and 450 mg/kg of O. persica extract per day by oral gavage, respectively. On day 29, serum taken for glucose level measurement and left femoral and tibio-fibular bones were dissected for histomorphometric study, while L4 vertebrate were removed for determination of ash weight. RESULTS: 300mg/kg of extract reduced serum glucose levels. Epiphyseal and metaphyseal Trabecular thickness as well as epiphyseal bone area/tissue area significantly decreased in STZ group. O. persica extract at the dosage of 200 mg/kg reversed all these parameters to the control level. No significant difference observed in osteoid thickness among different groups. Ash weight of L4 vertebrate in rats treated with 300 and 450 mg/kg of extract was significantly lower than other groups. CONCLUSIONS: The results show that ethanolic extract of O. persica has bone protective effects in STZ-treated rats.