Objective: This study was conducted to assess the effect of dietary Moringa oleifera leaf (MOL) feed supplementation on serum biochemical parameters of broilers challenged with very virulent infectious bursal disease virus (vvIBDV). Materials and methods: Two hundred and forty day-old Ross 308 hybrid broiler chicks were randomly assigned into four groups (A, B, C and D) of 60 chicks each and raised in deep litter housing. Broiler starter (BS) and broiler finisher (BF) mash were formulated each with 5% MOL included as part of the feed ingredient for broilers in groups A and B while BS and BF for broilers in groups C and D were formulated without MOL. Broilers in groups A, B and C were challenged intraocularly at 35 days of age with with 0.05 mL of a live vvIBDV, while those in group D served as control. Blood was collected from 10 broilers in each group via the wing vein at 35, 38 and 42 days of age to determine their serum biochemical profile.Results: The level of melondialdehyde (MDA) was observed to significantly decrease in groups A and C. There was a significant decrease in the level of AST in group A, B, C and D. The values of ALT significantly decreased in group A, B, C and D. Conclusion: Supplementing broilers feed with MOL neither protect the liver from damage nor prevent lipid peroxidation. [J Adv Vet Anim Res 2018; 5(2.000): 155-165]

Objective: The objective of this study was to evaluate some hematological parameters in commercial layers inoculated with two virulent Pasteurella multocida serotypes.Materials and Methods: A total of 84 twenty-week-old black Harco layers were randomly assigned to seven groups (A, B, C, D, E, F and G) with 12 birds per group. 1mLof live attenuated fowl cholera (FC) vaccine was administered subcutaneously at 24 weeks of age to groups A and B, emulsified inactivated (killed) FC vaccine was administered dosed at 0.5 mL per bird subcutaneously at 24 weeks of age to groups C and D, groups E and F were not vaccinated, while group G served as control. Groups A, C and E were inoculated with P. multocida serotype A:1 and groups B, D and F were inoculated with P. multocida serotype A:3. Using McFarland Standard, each bird received a dose of 0.5 mL (0.1 mL intranasally and 0.4 mL intramuscularly) containing 4.5 x 108 cfu/bird. Results: For PCV (P≤0.2692 and P≤0.7643) and HB (P≤0.2806 and P≤0.7266) on day 2 and 10 post inoculation, there was no significant difference between the vaccinated, non-vaccinated groups and control group G. However, there was a highly significant difference P≤0.05 in the mean concentrations of ALP between the control group G (67.67±1.453 u/l) vaccinated groups A (80.33±4.98 u/l), B (81.33±2.60 u/l), C (75±6.35 u/l), and D (84±5.132 u/l) and unvaccinated groups E (104±1.528 u/l ), and F (78 ±3.512 u/l) post inoculation.Conclusion The PCV significantly decrease P≤0.05 in layers vaccinated and inoculated with P. multocida but increase in unvaccinated layers inoculated P. multocida. The mean serum ALP concentration significantly increase P≤0.05 in unvaccinated layers inoculated with P. multocida when compared to layers vaccinated and inoculated with P. multocida. [J Adv Vet Anim Res 2017; 4(3.000): 234-240]

This study was carried out to find whether phenidone (1-phenyl-3-pyrazolidinone), a cyclooxygenase as well as a lipoxygenase inhibitor, exhibits the preventive effect on carbon tetrachloride (CCl₄)-induced acute liver injury in rats. Rats were pretreated with phenidone at a dose of 50 or 200 mg/kg (p.o.) once daily for 3 consecutive days before CCl₄ administration. Serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were measured. Malondialdehyde (MDA) production was determined as an index of lipid peroxidation in the liver and serum. The histopathological changes in the liver were also examined in each group. The reduction in body weights was significantly inhibited in the phenidone-treated group than in the CCl₄ control group. Significant increase in the relative liver weights of the phenidone-treated groups was observed compared with either the vehicle or CCl₄ groups. Elevation of serum AST and ALT activities occurred after CCl₄ treatment was significantly attenuated by the pretreatment with phenidone. The elevation of MDA levels in liver and serum were completely inhibited in phenidone-treated groups. The protective effects on phenidone-treated groups were confirmed histopathologically. These results suggest that phenidone may be a useful protector through modulation of hepatic inflammation in CCl₄-induced acute liver injury.

Mycotoxins are considered hidden dangers that threaten the poultry industry globally because they suppress the immunity of birds, reduce their production, and increase their chance of being infected with diseases, which exposes the poultry industry to enormous economic losses. Therefore, this investigation aimed to assess the effectiveness of VemoZyme Detox®, a novel enzymatic detoxifier, in mitigating the detrimental consequences of mycotoxin contamination in broiler chickens. The experiment involved 10,000-day-old, Cobb 500 broiler chicks, which were allotted into two groups of 5000 birds each as follows: T1: received a control basal diet; and T2: birds were provided with a basal diet supplemented with VemoZyme Detox®. The birds underwent comprehensive monitoring, including evaluations of growth performance, blood parameters, mycotoxin levels, hepatic histopathological alterations, and litter bacteriological counts. Broilers receiving dietary VemoZyme Detox® exhibited significant improvements in various aspects, including growth performance, reduced mortality rates, and more favorable feed conversion ratios. Moreover, the enzymatic supplement played a protective role in maintaining hepatic and renal health, as evidenced by reductions in blood aspartate aminotransferase (AST), alanine aminotransferase (ALT), uric acid, and creatinine. Importantly, although there was no significant difference in mycotoxin levels (zearalenone, fumonisin B1, ochratoxin A, aflatoxin B1) within the feed, VemoZyme Detox® had a significant impact on decreasing mycotoxin levels, particularly those of zearalenone and fumonisin B1. Hepatic histological examinations also revealed healthier conditions in T2, and positive impacts extended to litter samples, as indicated by reduced counts of Clostridium perfringens (C. perfringens) and Escherichia coli (E. coli) counts. In conclusion, the use of an enzymatic detoxifier is a promising method for counteracting the negative impacts of mycotoxin contamination in broilers. The results underscore the substantial potential of enzymatic detoxifiers for ensuring the health and productivity of broilers, opening new avenues for safer poultry production.

The research was carried out to study the effects of dietary supplementation of Tulasi (Ocimum sanctum) and selenium on ALT and AST enzyme levels in broiler chicken. A total of forty-two broiler chicks of day old divided into six groups of seven each were used for this study. Ocimum sanctum leaf powder (0.25% and 0.5%), organic selenium (0.3 ppm) and their combinations were added to the basal diet. Body weight and feed consumption were recorded at weekly intervals. Blood samples were taken at the end of 6th week for enzymological assay from each treatment. The enzymes assayed were alanine transaminase (ALT) and aspartate transaminase (AST). Dietary supplementation of Ocimum sanctum leaf powder at 0.25%, 0.5% levels and its combination (0.5% level) with selenium (0.3 ppm) reduced the levels of ALT and AST significantly (P<0.05). It was concluded that Tulasi (Ocimum sanctum) has hepato-protective properties.

The aim of this study was to determine the serum activities of enzymes aspartate aminotransferase, creatine kinase and lactate dehydrogenase in Arabian horses submitted to exercise on high-speed equine treadmill. Eleven mature Arabian horse were training and submitted to Standard Incremental Exercise Test on high-speed equine treadmill. Venous blood samples were taken before exercise, immediately and 30 min, 60min, 3h, 6h, 24h, 3 days and 5 days after exercise. The serum activity aspartate aminotransferase, creatine kinase and lactate dehydrogenase were determined. The serum activies of AST, CK and LDH increase immediately and returned to baseline value 30 minutes after exercise. The AST enzyme activity increased at 12 hours and 24 hours, CK at 3 hours and 6 hours, and LDH at 24 hours after Standard Incremental Exercise Test. | Objetivou-se determinar a atividade sérica das enzimas aspartato aminotransferase (AST), creatina quinase (CK) e lactato desidrogenase (LDH) de cavalos da raça Árabe submetidos a exercício em esteira de alta velocidade. Onze eqüinos adultos da raça Árabe foram condicionados e submetidos ao Teste Padrão de Exercício Progressivo em esteira. Antes, imediatamente após o término do exercício, e nos momentos pós-exercício, 30min, 60min, 3h, 6h, 12h, 24h, 3 dias e 5 dias, foram coletadas amostras de sangue venoso para as determinações séricas das enzimas aspartato aminotransferase (AST), creatina quinase (CK) e lactato desidrogenase (LDH). As concentrações séricas da AST, da CK e da LDH elevam-se imediatamente e retornam a valores semelhantes ao de repouso 30 minutos após o término do Teste Padrão de Exercício Progressivo. A atividade enzimática da aspartato aminotransferase (AST) eleva-se de 12 horas a 24 horas, da creatina quinase (CK) de 3 horas a 6 horas e da lactato desidrogenase (LDH) 24 horas após o término do Teste Padrão de Exercício Progressivo.

<p>O objetivo do trabalho foi avaliar a influência do exercício físico (provas de marcha) sobre os valores séricos de AST e CK e valores plasmáticos de lactato em equinos da raça Mangalarga Marchador criados no estado do Espírito Santo. Amostras de soro e plasma foram obtidas de 15 equinos em quarto diferentes momentos: repouso (T0) e com 5 minutos (T1), 30 minutos (T2) e 2 horas (T3) após o término do exercício. Foram registrados valores de lactato plasmático de 1,02 ± 0,41 mmol/L, 2,73 ± 2,43 mmol/L, 1,89 ± 1,24 mmol/L e 1,31 ± 0,60 mmol/L, respectivamente nos momentos T0, T1, T2 e T3. Na análise de AST, os resultados registrados nos momentos T0, T1, T2 e T3 foram, respectivamente, de 189,3 ± 56,0 UI/L, 223,9 ± 53,5 UI/L, 186,8 ± 25,8 UI/L e 193,9 ± 44,7 UI/L. Finalmente, os valores séricos de CK foram de 113,4 ± 56,3 UI/l, 144.1 ± 70,9 UI/L, 143,0 ± 81,0 UI/L e 173,1 ± 128,0 UI/L, respectivamente nos momentos T0, T1, T2 and T3. A análise dos resultados demonstrou que a marcha influenciou de forma significativa o lactato plasmático, porém não influenciou a atividade sérica de AST e CK, sugerindo que os equinos usados encontravam-se condicionados ao exercício físico imposto.</p> | <p>The aim of this study was evaluate the influence of physical exercise (marcha gait) on serum values of CK and AST and plasmatic values of lactate in Mangalarga Marchador horses trained in Espirito Santo, Brazil. Serum and plasma samples were obtained from 15 horses in four different moments: rest (T0), 5 minutes (T1), 30 minutes (T2) and 2 hours (T3) after the exercise. Lactate analysis revealed values of 1.02 ± 0.41 mmol/L, 2.73 ± 2.43 mmol/L, 1.89 ± 1.24 mmol/L and 1.31 ± 0.60 mmol/L, respectively at T0, T1, T2 and T3. When evaluating AST, the results recorded in T0, T1, T2 and T3 were, respectively, 189.3 ± 56.0 UI/L, 223.9 ± 53.5 UI/L, 186.8 ± 25.8 UI/L and 193.9 ± 44.7 UI/L. Finally, the CK at moments T0, T1, T2 and T3 were, respectively, 113.4 ± 56.3 UI/l, 144.1 ± 70.9 UI/L, 143.0 ± 81.0 UI/L and 173.1 ± 128.0 UI/L. The results showed that marcha gait leaded to significantly increased in plasma lactate and did not alter serum AST and CK, suggesting that the equines used were conditioned to the physical exercised imposed.</p>

With the purpose to evaluate the breed factor inf1uence on the hepatic function of cattle, 134 blood samples from, 67 Jersey and 67 Holstein cattle in São Paulo, Brazil, were collected . The hepatic function was studied through the determination of proteinogram; activities of the aspartate aminotransferase (AST), gamma glutamyltransferase (GG1) and dosage of total, direct and inditect bilirrubin in sorology .The evaluation of the proteinogram demonstrated the inf1uence of the breed factor: the values of total protein in Jersey (6.37±0.90 g/dl) was lower than in Holstein (6.82±0.97g/dl). The analysis of proteins showed the differences between the Jersey and the Holstein animals resulting of the globulins concentrations presents in serum, the values of globulins in Jersey (3.13±0..81g/dl) were lower than in Holstein (3.73±0.99g/dl). Values of alpha-, beta- and gamma-globulins were obtained through the eletrophoresis. In Jersey the values were lower (0.89±0,14g/dl; 0.71±0.14g/dl, 2.03±0.38g/dl) than in Holstein (1.00±0.16g/dl; 0.76±0.15g/dl; 2.20±0.45g/dl). The evaluation of breed factor inf1uence on the AST and GGT seric enzimatic activity showed this inf1uence in AST, but not in GGT. Values of AST in Jersey (49.27±17.87U/l) were higher than in Holstein (34.76±10.61U/l). Values of GGT did not show differences between the Jersey (19.46±33.11U/l) and Holstein (19.08±33.26U/l). The evaluation of seric bilirrubins concentrations showed differences on the total and indirect bilirrubin. Hygher values of indirect bilirrubin (0.40±0.33mg/dl; total bilirrubin 0.44±0.33mg/dl) were seen in Jersey than in Holstein. | Para avaliar a influência de fatores raciais sobre a função hepática de bovinos foram colhidas 134 amostras de sangue, sendo 67 animais da raça Jersey e 67 da raça Holandesa, criados em São Paulo. No soro sangüíneo realizaram-se as seguintes determinações: proteinograma; atividade enzimática da aspartato aminotransferase (AST), gama glutamiltransferase (GGT), bilirrubinas indireta, direta e total. A avaliação do proteinograma demonstrou a influência dos fatores raciais, pois os valores médios da proteína total dos bovinos da raça Jersey (6,37±0,90 g/dl) foram menores do que os animais da raça Holandesa (6,82±0,97 g/dl).Essas variações foram decorrentes as frações protéicas que correspondem as globulinas, sendo os teores médios obtidos para bovinos da raça Jersey (3,13 ± 0,81g/dl) menores do que os encontrados para bovinos da raça Holandesa (3,73 ± 0,99 g/dl). Os valores das alfa-, beta- e gama-globulinas obtidos nos animais da raça Jersey (iguais a 0,89±0,14 g/dl; 0,71±0,14 g/dl; 2,03±0,38 g/dl) foram menores do que os encontrados para bovinos da raça Holandesa (iguais a 1,00±0,16 g/dl; 0,76±0,15 g/dl; 2,20±0,45 g/dl). A avaliação da atividade enzimática revelou a influência dos fatores raciais nos resultados da AST, sendo os valores dos bovinos Jersey (49,27±17,87 U/l) maiores do que os da raça Holandesa (34,76±10,61 U/l), enquanto para a GGT não foram observadas diferenças significativas entre os resultados da raça Jersey (19,46±33,11 U/l) e da raça Holandesa (19,08±33,26 U/l). A avaliação dos teores séricos de bilirrubinas evidenciou variações sob influência racial para os teores de bilirrubinas indireta e total, sendo os valores obtidos para a raça Jersey (0,40±0,33 mg/dl de bilirrubina indireta e 0,44±0,33 mg/dl de bilirrubina total) maiores do que os observados para a raça Holandesa (0,22±0,19 mg/dl de bilirrubina indireta e 0,25±0,19 mg/dl de bilirrubina total).