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Ameliorative effects of Helianthus annuus against nephrotoxic, cardiac, and haematological disorders in alloxan-induced hyperglycaemia in albino rats

was not significant. The neutrophil : lymphocyte ratio of GLB-and HLEHA-treated groups were reduced (P < 0.05) when compared with the 5% tween-20–treated group ( Table 2 ). Table 2 Effect of HLEHA treatment on leukocytic profile (mean ±SEM) Treatment 5% tween-20, 5 mL/kg GLB 2 mg/kg HLEHA 150 mg/kg HLEHA 300 mg/kg HLEHA 600 mg/kg WBC (x103/mL) 11.68 ± 0.58 9.73 ± 0.43 10.89 ± 0.36 10.9 ± 0.68 9.85 ± 1.26 Re neutrophil (%) 37.0 ± 2.66 21.4 ± 1.57* 28.0 ± 0.53* 18.0 ± 2.28* 14.67 ± 1.65* Re lymphocyte (%) 60

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Assessment of the Effect of Selected Components of Equine Seminal Plasma on Semen Freezability

://dx.doi.org/10.1016/S0093-691X(02)00744-6 3. Brinsko, S,P, Blanchard, T.L., Varner, D.D., Schumacher, J., Love, C.C., Hinrichs, K., Hartmen, D. (2011). Manual of equine reproduction. 3rd ed. (pp. 19-192). Mosby, Missouri 4. Trein, C.R., Zikler, H., Bustamante-Filho, I.C., Malschitzky, E., Jobim, M.I.M., Sieme, H., Mattos, R.C. (2008). Equine seminal plasma proteins related with semen freezability. Anim Reprod Sci, 107, 252-253. http://dx.doi.org/10.1016/j.anireprosci.2008.05.129 5. Jasko, D.L., Moran, D.L., Farlin, M.E., Squires

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The Influence of Fortification of Dark Chocolate with Sea Buckthorn and Mulberry on the Content of Biologically Active Substances

of Food Sciences, 10 (1), 59-64, doi: 10.5219/551 10. Cerit, İ., Şenkaya, S., Tulukoğlu, B., Kurtuluş, M., Seçilmişoğlu, Ü. R., Demirkol O. (2016). Enrichment of functional properties of white chocolates with cornelian cherry, spinach and pollen powders, GIDA/The Journal of FOOD, 41 (5), 311-316. 11. Singleton, V. L. & Rossi, J. A. (1965). Colorimetry of total phenolics with phosphomolybdicphosphotungstic acid reagents, American Journal of Enology and Agricultural, 16, 144-158. 12. Willett, W. C. (2002). Balancing

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Different Dynamics of Sensory-Motor Development and Behavior During the Transitional Period in Puppies: Preliminary Results

and social experiences in the canine. J Vet Behav: Clin Appl Res. 4(5): 203-210. https://doi.org/10.1016/j.jveb.2009.03.003 20. Gazzano, A., Mariti, C., Notari, L., Sighieri, C., McBride, E.A. (2008). Effects of early gentling and early environment on emotional development of puppies. Appl Anim Behav Sci. 110, 294-304. https://doi.org/10.1016/j.applanim.2007.05.007 21. Fox, M.W. (1968). Methods of animal experimentation. III (2):37-73. Elsevier Inc. 22. Landis, J.R., Koch, G.G. (1975). A review of statistical methods in the analysis of data

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Effects of natural antioxidants on the stability of omega-3 fatty acids in dog food

-capped, teflon-lined culture tube. The first step was adding 1 mL of prepared internal standard-C17:0 (heptadecaenoic acid) in benzene, followed by adding 2 mL of 5% sodium methoxide, 0.5 M solution in methanol. The tubes were capped and lightly vortexed to mix and then incubated in a water bath at 50°C for 5 min. After cooling for 5 min, 3 mL of 5% methanolic HCl was added and then recapped, vortexed, and incubated in a water bath at 80°C for another 10 min. The tubes were cooled for 7 min and then 1 mL of hexane and 7.5 mL of 6% potassium carbonate was slowly added. The

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Spirocercosis in Dogs in Israel

REFERENCES 1. Aroch, I., Markovics, A., Mazaki-tovi, M., Kuzi, S., Harrus, S., Yas, E., et al., 2015: Spirocercosis in dogs in Israel: A retrospective case-control study (2004—2009). Vet. Parasitol. , 211, 234—240. DOI: 10.1016/j.vetpar.2015.05.011. 2. Cabanova, V., Guimaraes, N., Hurnikova, Z., Chovancova, G., Urban, P., Miterpakova, M., 2017: Endoparasites of the grey wolf ( Canis lupus ) in protected areas of Slovakia. Annals of Parasitology , 63, 4, 283—289. DOI: 10.17420/ap6304.114. 3. Chai, O., Yas, E., Brenner, O., Rojas, A

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Use Of Hormonal and Ultrasonographic Examinations to Determine the Fetal Number in Bulgarian Local Goats

sheep. PhD thesis, Stara Zagora. [in Bulgarian] 4. Capezzuto, A., Chelini, M.O.M., Felippe, E.C.G., Olivera, C.A. (2008). Correlation between serum and fecal concentration of reproductive steroids throughout gestation in goats. Anim Reprod Sci. 103, 78-86. https://doi.org/10.1016/j.anireprosci.2006.11.001 PMid:17156948 5. Medan, M.S., Abd El-Aty, A.M. (2010). Advances in ultrasonography and its application in domestic ruminants and other farm animals‘ reproduction. J Adv Res. 1, 123-128. https://doi.org/10.1016/j.jare.2010.03.003 6. Karen, A

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Changes in the activity of ovine blood-derived macrophages stimulated with antimicrobial peptide extract (AMP) or platelet-rich plasma (PRP)

Congress of the Latin American Association of Immunology - 100 Congreso de la Asociación Colombiana de Alergia, Asma e Inmunología. doi: 10.3389/conf.fimmu.2015.05.00015 (2015). 4. Campbell L., Emmerson E., Williams H., Saville C.R., Krust A., Chambon P., Mace K.A., Hardman J.: Estrogen receptor-alpha promotes alternative macrophage activation during cutaneous repair. J Invest Dermatol 2014, 134, 2447–2457. 5. Campbell L., Saville C.R., Murray P.J., Cruickshank S.M., Hardman J.: Local arginase 1 activity is required for cutaneous wound healing. J Invest

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In vitro evaluation of chitosan-DNA plasmid complex encoding Jembrana disease virus Env-TM protein as a vaccine candidate

and a study of their release properties, Nanotechnology 2008, 19, doi: https://doi.org/10.1088/0957-4484/19/05/055302 . 18. Pachuk C.J., McCallus D.E., Weiner, D.B., Satishchandran C.: DNA vaccines challenges in delivery. Current Curr Opin Mol Ther 2000, 2, 188–198. 19. Pearson L.D., Poss M.L., Demartini J.C.: Animal lentivirus vaccines: problems and prospects. Vet Immunol Immunopathol 1989, 20, 183–212. 20. Siegert W., Nitsche A.: Guideline to reference gene selection for quantitative real-time PCR. Biochem Biophys Res Commun 2004, 313, 856

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Phagocytic activity and oxygen metabolism of peripheral blood granulocytes from rabbits experimentally infected with Trichophyton mentagrophytes

using the commercial Phagotest kit (Orpegen Pharma, Germany), according to the manufacturer’s instructions. Heparinised peripheral blood (100 μL) was incubated with 20 μL of FITC-labelled heat-killed E . coli (10 cfu) for 20 min at 37°C, a negative control remained in the ice bath for 20 min. At the end of the incubation, all the samples were placed in the ice bath in order to stop phagocytosis. A volume of 100 μL of ice-cold Quenching Solution was added to each sample. The samples were mixed (by vortex mixer) for 2 min at 25°C. Then, 3 mL of cold washing solution

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