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XII - 12th International Symposium - Digestive Physiology of Pigs

XII - 12th International Symposium - Digestive Physiology of Pigs

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<strong>Digestive</strong><br />

<strong>Physiology</strong><br />

<strong>of</strong> <strong>Pigs</strong><br />

cell hemogloblin concentration (MCHC, P = 0.05) was<br />

lower and platelet count tended to be lower (P = 0.07) on<br />

d 110 <strong>of</strong> gestation in Bt maize-fed sows; however, MCHC<br />

tended to be higher in their <strong>of</strong>fspring at birth (P = 0.08).<br />

Feeding Bt maize did not affect piglet organ weight at birth.<br />

The differences in sow serum biochemistry observed in<br />

response to feeding Bt maize were not indicative <strong>of</strong> organ<br />

dysfunction. Haematological differences are thought to be<br />

due to numerically higher litter size in Bt maize-fed sows<br />

and appear to be unrelated to Bt maize exposure. Although<br />

some differences in <strong>of</strong>fspring serum biochemistry and<br />

hematology were observed at birth in response to maternal<br />

feeding <strong>of</strong> Bt maize, they are not believed to be <strong>of</strong> biological<br />

importance. Sows fed Bt maize were heavier on d 56 <strong>of</strong><br />

gestation but their <strong>of</strong>fspring tended to be lighter at weaning<br />

compared with the isogenic treatment.<br />

Key words: cry1Ab, safety, maize<br />

3011 zinc oxide at low supplementation level<br />

improves productive performance and health status <strong>of</strong><br />

piglets. J. Morales 1 , G. Cordero 1 , C. Pineiro 1 , and S. Durosoy*<br />

2 , 1 PigCHAMP Pro Europa SL, Segovia, Spain, 2 ANI-<br />

MINE, Sillingy, France.<br />

Use <strong>of</strong> Zinc oxide (ZnO) at high doses (3000 ppm) for<br />

diarrhea prophylaxis in piglets is widely extended in postweaning<br />

Spanish diets, in compliance with the national<br />

veterinary regulation. However, European feed legislation<br />

limits total dietary Zn to a maximum <strong>of</strong> 150 mg/kg <strong>of</strong><br />

complete feed. The objective <strong>of</strong> this study was to compare<br />

a new potentiated form <strong>of</strong> zinc oxide (HiZox, Animine) at<br />

nutritional level (150 ppm) with pharmacological dosage<br />

(3000 ppm) <strong>of</strong> regular ZnO in starter diets on the productive<br />

performance and health status <strong>of</strong> piglets in a mediumlow<br />

health status farm. A total <strong>of</strong> 144 pigs at weaning (28<br />

d <strong>of</strong> age) were distributed in 6 piglets/pen and 12 pens/<br />

treatment. In the prestarter phase (28–42 d <strong>of</strong> age), all pigs<br />

received the same commercial feed, including 3000 ppm<br />

ZnO. In the starter phase (42–63 d <strong>of</strong> age) T1 included 3000<br />

ppm <strong>of</strong> regular ZnO, and T2 was supplemented with 110<br />

ppm Zn from potentiated zinc oxide (HiZox). Feed intake<br />

(FI), average daily weight gain (ADWG), feed conversion<br />

ratio (FCR) and PigMAP serum concentration, an acute<br />

phase-protein commonly used as unspecific biomarker <strong>of</strong><br />

disease or other acute phase reactions, were measured at<br />

42 and 63 d <strong>of</strong> life. Pen <strong>of</strong> 6 piglets was the experimental<br />

unit and data were analyzed using the GLM procedure <strong>of</strong><br />

SAS v9.0. Piglets fed with T2-HiZox had improved ADWG<br />

and FCR (P < 0.001) compared with piglets fed with T1-<br />

ZnO. In addition, at 63 d <strong>of</strong> age, T2 group has a lower<br />

PigMAP serum concentration than T1 group (1.71 vs 0.95<br />

μg/ml; P < 0.05), indicating higher health status in T2 group.<br />

In conclusion, in low-medium sanitary conditions and in<br />

compliance with European regulation, HiZox significantly<br />

increased piglet growth compared with pharmacological<br />

dosage <strong>of</strong> regular ZnO in the starter phase. This can be<br />

explained by a better health <strong>of</strong> pigs expressed by a lower<br />

level <strong>of</strong> inflammatory protein PigMAP.<br />

Key words: zinc oxide, PigMAP, piglets<br />

<strong>XII</strong> INTERNATIONAL SYMPOSIUM ON<br />

DIGESTIVE PHYSIOLOGY OF PIGS<br />

120<br />

Session V<br />

3012 Brain development is dependent on colostrum<br />

intake in newborn piglets. G. Skibo* 1 , T. Kovalenko 1 , I.<br />

Osadchenko 1 , K. Goncharova 1 , G. Ushakova 2 , J. Wolinski 3 ,<br />

P. Ochniewicz 3 , M. Slupecka 3 , K. Szwiec 4 , O. Prykhodko 4 , O.<br />

Fedkiv 4 , D. Gruijc 4 , B. Westrom 4 , and S. G. Pierzynowski 4,5 ,<br />

1 Bogomoletz Inst <strong>of</strong> <strong>Physiology</strong>, Kiev, Ukraine, 2 Department<br />

<strong>of</strong> Biophysics & Biochemistry, Dnepropetrovsk National<br />

Univ, Ukraine, 3 The Kielanowski Inst <strong>of</strong> Animal <strong>Physiology</strong><br />

& Nutrition, Jablonna, Poland, 4 Departmet <strong>of</strong> Biology, Lund<br />

Univ, Sweden, 5 Inst <strong>of</strong> Rural Health, Lublin, Poland.<br />

Colostrum is an indispensable source <strong>of</strong> antibodies (IgG)<br />

protecting the newborn pig against infection. In addition,<br />

it has been observed that the behavior <strong>of</strong> colostrumdeprived<br />

piglets is different from ones that suckle. This<br />

study was designed to evaluate the role <strong>of</strong> colostrum in<br />

brain development in newborn pigs. Shortly after birth,<br />

piglets were divided into 5 groups: unsuckled (A), suckled<br />

(B), and fed: colostrum (C), elemental diet (ED), and ED<br />

+ IgG (purified serum IgG) via a stomach tube, 10 mL/kg<br />

during first 24 h. From 24 to 72 h all pigs were fed with ED<br />

after which they were killed and the brain was dissected.<br />

The hippocampal neurons, astrocytes and microglial cells<br />

were identified by specific antibodies and analyzed with<br />

confocal microscope. Neuron-specific protein (NeuN),<br />

used as a marker <strong>of</strong> post-mitotic cells, labeled both<br />

mature and newly generated neurons in the hippocampal<br />

CA1 area. The number <strong>of</strong> newly generated neurons was<br />

diminished in C, ED and ED+IgG groups compared with<br />

group A (for ED+IgG group, P < 0.01). Active migration <strong>of</strong><br />

microglial cells and astrocytes from the proliferative areas<br />

and their significant increase was observed only in the<br />

hippocampus <strong>of</strong> suckling piglets (B). In the group ED we<br />

observed a 52% decrease in microglial cells by at 72h (P<br />

< 0.01) as compared with group C. In group ED+IgG the<br />

microglial cell numbers was decreased only by 12% at 72h<br />

and was different from group ED (P < 0.01). In conclusion,<br />

piglets deprived <strong>of</strong> colostrum in this study had a reduction<br />

in postnatal hippocampal neuro and gliogenesis. Feeding<br />

with ED, instead <strong>of</strong> colostrum, didn’t help physiological<br />

postnatal brain development. Addition <strong>of</strong> IgG to ED<br />

improved the neurogenesis and supported immune status<br />

<strong>of</strong> the brain.<br />

Key words: colostrum, brain, development<br />

3013 Behavioral changes in response to feeding<br />

pancreatic-like enzymes to exocrine pancreatic insufficient<br />

(EPI) pigs. S. G. Pierzynowski 1,2 , P. Swieboda 1 , K.<br />

Szwiec 1 , D. Gruijc 1 , J. Botermans 3 , J. Svendsen 3 , J. L. Valverde<br />

Piedra 4 , O. Prykhodko 1 , G. Skibo 5 , T. Kovalenko 5 , K.<br />

Goncharova 5 , G. Ushakova 6 , D. Kruszewska 2,7 , R. Filip 2,8 ,<br />

and B. Westrom* 1 , 1 Department <strong>of</strong> Biology, Lund Univ,<br />

Sweden, 2 Inst <strong>of</strong> Rural Health, Lublin, Poland, 3 Department<br />

<strong>of</strong> Rural Buildings, Swedish Univ Agricultural Sciences,<br />

Alnarp, Sweden, 4 Department Biochemistry & Animal<br />

<strong>Physiology</strong>, Univ Life Scienecs, Lublin, Poland, 5 Bogomoletz<br />

Inst <strong>of</strong> <strong>Physiology</strong>, Kiev, Ukraine, 6 Department <strong>of</strong><br />

Biophysics & Biochemistry, Dnepropetrovsk National University,<br />

Ukraine, 7 The John Paul II Catholic Univ, Lublin,<br />

Poland, 8 Warsaw University <strong>of</strong> Life Sciences, Poland.

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