The study investigated the effects of kaempferol on growth performance in two weeks old broilers challenged with Eimeria tenella. Sixty, one-day old broiler chicks were randomly allotted into six groups (I-VI) of ten broiler chicks each and brooded for two weeks with commercial broiler feed (vital feed®) and provided water ad libitum. At two weeks of age, broilers in group 1 were neither infected nor treated. Broilers in groups II- VI were infected 4 with Eimeria tenella sporulated oocyst (10 /mL) via oral inoculation. After infection was established, broilers in groups II-IVwere treated Per os with 1 mg/kg, 1.5 mg/kg and 2 mg/kg of kaempferol respectively. Broilers in group V were treated for five days with amprolium, 1.25 g/L in drinking water and those in group VI were administered normal saline, 5 mL/kg per os for five days. The experimental birds were examined daily for feed intake (FI), weight gain (WG) and feed conversion ratio (FCR). Data obtained were analyzed using pad prism version 5.0. There was a statistically significant (p<00.5) increase in the mean values of WG, FI and FCR in groups II, III and IV in a dose dependent fashion when compared to VI. There was also statistically significant (p<00.5) reduction in the mean values of WG in Group II and III than in Groups IV and V. Mean WG of Groups IV and V did not differ statistically, but there were statistically higher WG in Group V than in group IV. There were consequent high FCR values of 7.3, 5.71, 5.67, 6.19 and 7.08 for groups I, II, III, IV and V respectively compared to 4.9 for Group VI. Thus, the treatment with kaempferol in two weeks old broilers had ameliorated the effects of Eimeria tenella on WG, FI and FCR in this study.
The present study was carried out to investigate some biochemical alterations in layers experimentally infected with Pasteurella multocida. A total of 20 eighteen-week old ISA Brown layers were used in the experiment. The birds were randomly assigned to two groups (infected and control) of 10 layers each. To establish infection, each bird in the infected group was challenged by intra nasal (0.1 ml) and intramuscular (0.4 ml) administration of P. multocida inoculum containing 4.5 × 10 8 CFU/ml. Meanwhile, birds in the control group were given clean drinking water and fed standard commercial layers mash ad libidum. All the experimental birds were monitored closely for clinical signs of fowl cholera. Blood samples were collected from both groups at day zero (Day 0), 2, 4, 7, 14, 21, 28, 35, 42, post-infection (pi) and used to assay some biochemical parameters. By day 5 post-inoculation (pi), all birds in the infected group manifested clinical signs typical of fowl cholera; weakness, ruffled feathers, sneezing, greenish-yellowish diarrhoea, decrease in feed and water consumption, weight loss, drop in egg production and mortality rate of (20%). However, there were significant increase in the plasma activities of aspartate amino transferase, alanine aminotransferase, alkaline phosphatase, and level of uric acid and significant hypoproteinaemia. The experimental P. multocida infection initiated hepatic, intestinal and renal dysfunctions.
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