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    The Effects of Acetylsalicylic Acid on the Phagocytic Function of Bovine Neutrophils in Vitro
    (ECOLE NATIONAL VET TOULOUSE, 1998) Baş, A. L.; Traş, B.; Elmas, M.; Keskin, E.; Yazar, E.
    Acetylsalicylic acid (ASA), a cyclooxygenase inhibitor, has been used for its analgesic and antiinflammatory properties. Its stimulating effect on the immune system has recently been described. In the present study, the effect of ASA on phagocytic and microbicidal activity was investigated in vitro at the concentrations of 50, 100, 150, 250 and 500 mu g/ml in the peripheral blood polymorphonuclear leucocytes (PMNL) of twelve healthy Holstein heifers. The functions of PMNL were evaluated with flourescent microscopy using flourochrome dye, acridine orange. In this study, all the results compared to the controls at the concentrations of 50, 100 and 150 mu g/ml of ASA revealed that phagocytosis increased from 74.25 % to 80.3, 80.5 and 83.7 %, respectively. There was a statistically significant decrease of phagocytic activity of PMNL between the 500 mu g/ml of ASA and control group. In addition to this, the microbicidal activity increased at the dose of 50 mu g/ml of ASA (97.1 %). Whereas there was a decrease at doses of 250 (87.4 %) and 500 mu g/ml of ASA (87.3 %) compared with the control group (92.2 %). The results of the in vitro experiments showed that the function of bovine polymorphonuclear leucocytes was altered by different concentrations of acetylsalicylic acid.
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    Efficacies of Free and Liposome-Encapsulated Enrofloxacin (Baytril (R)) Against Staphylococcus Aureus Infection in Turkish Shepherd Dog Neutrophils in Vitro
    (Ecole National Vet Toulouse, 2000) Baş, A. L.; Elmas, M.; Şimşek, A.; Traş, B.; Yazar, E.; Hadimli, H. H.
    The influence of free and liposome-encapsulated enrofloxacin at concentrations of 1, 2 and 4 mu g/ml was studied on phagocytic and intracellular killing of Staphylococcus aureus, in cultured neutrophils of six healthy Turkish Shepherd Dogs. Enrofloxacin was encapsulated by using reverse-phase evaporation method in multilamellar liposomes composed of 15 mg egg phosphatidylcholine and 35 mg cholesterol. Phagocytic and killing activity of neutrophils were determined by fluorescent microscopic technique. Liposome-encapsulated enrofloxacin significantly enhanced the intraphagocytic killing of bacteria in neutrophils compared to free drug. Phagocytic activity of neutrophils was not significantly different among groups. The results obtained in the present study show that use of enrofloxacin encapsulated in liposomes may improve the antibacterial efficacy of the antibiotic.
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    Investigation of Biochemical and Haematological Side-Effects of Enrofloxacin in Dogs
    (BLACKWELL WISSENSCHAFTS-VERLAG GMBH, 2001) Traş, B.; Maden, M.; Baş, A. L.; Elmas, M.; Yazar, E.; Civelek, T.
    In the present study, effects of enrofloxacin on biochemical, haematological and blood gas parameters were investigated. Changes in laboratory parameters were monitored during the treatment period. Enrofloxacin was administered (5 mg/kg intramuscularly, once daily) to 10 healthy dogs for 14 days. Acidosis and temporary increases in aspartate aminotransferase, indirect bilirubin, sodium, partial pressure of CO2 and mean corpuscular volume levels as well as decreased levels of inorganic phosphorus, ionized calcium, potassium, partial pressure of O-2 and standard bicarbonate were observed. The results of this study suggest that these observed effects of enrofloxacin on blood gas parameters should be taken into consideration in long-term use of the drug.
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    Pharmacokinetics and Oral Bioavailability of Enrofloxacin in Faunated and Defaunated Angora Goats
    (Ecole National Vet Toulouse, 2000) Elmas, M.; Yazar, E.; Traş, B.; Baş, A. L.; Eryavuz, A.
    The pharmacokinetic properties and bioavailability of enrofloxacin were compared after single oral administration of 5 mg/kg bw to faunated and defaunated adult Angora goats. Plasma enrofloxacin concentrations were measured by high performance liquid chromatography. The pharmacokinetic data were best described by a 2-compartment open model and were similar in both groups. The plasma concentrations of enrofloxacin in defaunated group were higher than those of faunated group except for 8, 12 and 24 hours, and C-max in defaunated goats was also higher than other group (p < 0.05). Although the oral bioavailability of the drug in defaunated group (F, 30 %) was higher than that in the faunated group (F, 23 %), this difference was not significant (p > 0.05). In conclusion, oral absorption of enrofloxacin in adult angora goats was slightly affected by defaunation. Despite of low oral bioavailability, once daily oral administration of enrofloxacin at the dose of 5 mg/kg bw may be suitable in treatment of infectious diseases caused by sensitive pathogens in Angora goats.