XII - 12th International Symposium - Digestive Physiology of Pigs
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.