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Annals of Warsaw University of Life Sciences – SGGW. Animal ...

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26 J. Gajewska et al.<br />

effect, e.g. L-carnitine used most <strong>of</strong>ten<br />

in flocks <strong>of</strong> breeding poultry, improving<br />

sperm concentration, hatchability and<br />

affecting production results (Zhai, 2008;<br />

Keralapurath et al., 2010; Shafey et al.,<br />

2010). Application <strong>of</strong> 20 to 100 mg per<br />

kg feed, L-carnitine in the nutrition <strong>of</strong><br />

poultry for slaughter allows for a reduction<br />

<strong>of</strong> fat content in carcass (Rabie et al.,<br />

1997a, b; Arslan et al., 2004). There are<br />

however, no reports on the effects <strong>of</strong> L-<br />

-carnitine on the composition <strong>of</strong> intestinal<br />

micr<strong>of</strong>lora <strong>of</strong> broiler chickens therefore<br />

Aminokarnifarm was used to because<br />

(43.68% <strong>of</strong> L-carnitine) to determine<br />

the composition <strong>of</strong> the micr<strong>of</strong>lora in the<br />

small intestine <strong>of</strong> chickens.<br />

MATERIALS AND METHODS<br />

The experiment was conducted in poultry<br />

farm <strong>of</strong> Experimental Station (RZD)<br />

Wilanów-Obory on 640 broiler chickens<br />

<strong>of</strong> COBB 500. One-day chicks were at<br />

random allocated to 2 groups: control<br />

and experimental (Aminokarnifarm), each<br />

<strong>of</strong> them in four repetitions. The birds<br />

were kept on the litter, according to the<br />

standards for management <strong>of</strong> broilers, as<br />

recommended by Cobb company. The<br />

differentiating factor was the administration<br />

<strong>of</strong> the group Aminokarnifarm<br />

to water for the experimental group <strong>of</strong><br />

chickens.<br />

Aminokarnifarm is a preparation<br />

amino acid vitamin, which a combination<br />

<strong>of</strong> vitamins and amino acids with taurine<br />

(13.33%) and L-carnitine (43.68%) has<br />

a very strong anabolic effects, improving<br />

production results. The preparation<br />

ensures the proper metabolism <strong>of</strong> fatty<br />

acids and amino acids, sufficient production<br />

<strong>of</strong> energy from ketones, regulation<br />

<strong>of</strong> concentration <strong>of</strong> ammonia in the<br />

blood, stimulation the immune system,<br />

the process <strong>of</strong> respiration and active<br />

transport <strong>of</strong> ATP at the cellular level.<br />

Composition <strong>of</strong> the preparation has a significant<br />

impact on the proper functioning<br />

<strong>of</strong> all systems in the body, in particular<br />

neurohormonal system, digestive, circulatory<br />

and reproductive. The presence <strong>of</strong><br />

L-carnitine determines the capacity <strong>of</strong><br />

the body, muscle strength, cardiac activity,<br />

in combination with the metabolism<br />

<strong>of</strong> amino acids enhances the whole body<br />

and neutralizes the negative effects <strong>of</strong><br />

various types <strong>of</strong> stress factors (Bi<strong>of</strong>aktor<br />

<strong>–</strong> producer information).<br />

Aminokarnifarm was added in drinking<br />

water in quantities <strong>of</strong> 100 g <strong>of</strong> the<br />

preparation <strong>of</strong> 160 liters <strong>of</strong> water, rearing<br />

on the following dates: 1<strong>–</strong>7 days, 21<strong>–</strong>28<br />

days, 35<strong>–</strong>42 days. During the rearing<br />

<strong>of</strong> chickens from the control group and<br />

experimental (Aminokarnifarm) were fed<br />

compound having the following nutritional<br />

value: Starter from 1 to 14 day<br />

(22.1% crude protein and 13.7 MJ <strong>of</strong><br />

EM). Grower from 15 to 35 day (20.4%<br />

crude protein and 14.1 MJ <strong>of</strong> EM).<br />

Finisher from 36 to 42 day (19.1%<br />

crude protein and 14.3 MJ EM, without<br />

coccidiostatic). On 42 day, from 9 males<br />

and 9 females, parts <strong>of</strong> intestinal were taken<br />

after slaughter. The aim was to determinations<br />

quantitative and qualitative factors<br />

<strong>of</strong> intestinal micr<strong>of</strong>lora in small intestine<br />

content <strong>of</strong> chicken broilers.<br />

Quantitative determination <strong>of</strong> small<br />

intestine content, received from two<br />

feeding groups, were done by standat<br />

Koch’s plate method, with surface sowing<br />

(Salyers, Whitt, 2003).<br />

The following microbiological rates<br />

were determined:

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