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 />
pigs <strong>of</strong> 35-d <strong>of</strong> age housed in pens with 2 4-space feeders<br />
with diets <strong>of</strong>fered in a paired choice as mash (Exp. 3) or<br />
pellets (Exp. 4) for 3 consecutive 7-d periods (3 d non test,<br />
4 d preference). Diets were formulated to equal NE and<br />
SID AA using canola oil and synthetic AA. Feeding up to<br />
20% napus CM to pigs did not affect growth performance.<br />
Increasing inclusion <strong>of</strong> juncea CM linearly reduced (P <<br />
0.001) ADFI, ADG and feed efficiency. In Exp. 3 and 4,<br />
pigs preferred SBM (P < 0.001) over napus and juncea CM<br />
diets, and pigs preferred napus CM (P < 0.001) over juncea<br />
CM diet. Glucosinolates likely reduced feed preference<br />
in juncea CM more than napus CM. The reduced growth<br />
performance <strong>of</strong> pigs fed juncea CM diets was associated<br />
to its higher glucosinolate content, most likely the bitter<br />
gluconapin-type dominant in juncea CM than the proigotrintype<br />
dominant in napus CM. In conclusion, although pigs<br />
clearly preferred the SBM diet over napus or juncea CM<br />
diets, when given no choice, napus CM but not juncea<br />
CM can replace up to 20% SBM in diets for weaned pigs<br />
without affecting growth performance. Finally, the contrast<br />
<strong>of</strong> results between preference and performance studies<br />
feeding CM to pigs indicates that results <strong>of</strong> preference<br />
studies should be interpreted cautiously until validated by<br />
pig growth performance data.<br />
Key words: canola meal, preference, soybean meal<br />
3039 Redox potential <strong>of</strong> cecum content <strong>of</strong> growing<br />
pigs and its relation with ph and VFA concentration.<br />
R. Lizardo* 1 , N. Tous 1 , M. A. Calvo 2 , C. Sampsonis 3 , R.<br />
D’Inca 3 , and J. Brufau 1 , 1 IRTA - Institut de Recerca i Tecnologia<br />
Agroalimentaries, Constantí, Tarragona, Spain, 2 UAB<br />
- Universidad Autónoma de Barcelona, Bellaterra, Barcelona,<br />
Spain, 3 LFA - Lesaffre Feed Additives, Marcq-en-<br />
Baroeul, Lille, France.<br />
<strong>Digestive</strong> micr<strong>of</strong>lora is partly responsible for physiological<br />
gut conditions. Bacteria density in pig cecum exceeds 10 9<br />
logCFU/g <strong>of</strong> digesta suggesting a high fermentation activity.<br />
The cecal milieu is anaerobic which suppose a redox<br />
potential (Eh) markedly negative, reflecting the absence<br />
<strong>of</strong> oxygen and a strong reducing power. Measurements <strong>of</strong><br />
Eh and pH <strong>of</strong> digesta can give a basis for understanding<br />
microbial activity and dynamics <strong>of</strong> fermentation. However,<br />
few studies have assessed the Eh <strong>of</strong> the gastro-intestinal<br />
tract <strong>of</strong> pigs. Twenty-four pigs <strong>of</strong> around 30 kg liveweight<br />
were slaughtered to measure Eh and pH <strong>of</strong> cecum content<br />
in situ and, samples <strong>of</strong> ileum, cecum and colon contents for<br />
VFA determinations were taken. <strong>Pigs</strong> were previously fed<br />
with a non-medicated starter feed for 5 weeks. The cecum<br />
was reached through an incision on the abdomen then a<br />
second small incision (2–2.5 cm) was made to insert Eh and<br />
pH electrodes. Measurements were recorded first at 2 min<br />
and then each 5 min for 35 min to estimate kinetics and the<br />
delay to reach stabilization <strong>of</strong> Eh value. Cecum Eh dropped<br />
rapidly from −115 to −180 mV for 15th min after insertion<br />
<strong>of</strong> electrodes (P < 0.001) and then slowly decreased until<br />
−185 mV at 35 min. Cecal pH starts at 5.74 decreasing<br />
slowly afterward until 5.53 after 35 min (P < 0.01). The<br />
Eh value after stabilization was negatively correlated<br />
with final pH (r = −0.64; P < 0.001). Acetic, propionic<br />
and butyric acids account for 58.7, 24.0 and 12.8% <strong>of</strong><br />
<strong>XII</strong> INTERNATIONAL SYMPOSIUM ON<br />
DIGESTIVE PHYSIOLOGY OF PIGS<br />
133<br />
Session VI<br />
total VFA production <strong>of</strong> cecum content, respectively. VFA<br />
production <strong>of</strong> ileal content was lower when compared with<br />
cecum or colon (50.8, 142.1 and 130.8μmol/g; P < 0.001)<br />
and a higher proportion <strong>of</strong> formic and lactic acids was<br />
detected (32.3 and 27.0%, respectively). Proportions <strong>of</strong><br />
acetic and propionic acids were correlated negatively (r =<br />
−0.53; P < 0.01) and positively (r = 0.66; P < 0.001) with<br />
Eh, respectively. In conclusion, cecal Eh was not easily<br />
measured, but predicted fermentative activity. So, it can be<br />
considered in future research relating feed additives and<br />
digestive physiology.<br />
Key words: piglet, redox potential, cecum<br />
3040 Blood sampling and hemolysis affect concentrations<br />
<strong>of</strong> plasma nutrients. P. K. Theil* 1 , L. J. Pedersen 1 ,<br />
M. B. Jensen 1 , C. C. Yde 2 , and K. E. Bach Knudsen 1 , 1 Dept.<br />
<strong>of</strong> Animal Science, Aarhus University, Foulum, DK-8830<br />
Tjele, Denmark, 2 Dept. <strong>of</strong> Food Science, Aarhus University,<br />
Kirstinebjergvej 10,, DK-5792 Aarslev, Denmark.<br />
Blood sampling <strong>of</strong> peripheral blood may be collected by<br />
vein puncture or from a catheter. The latter is preferred<br />
because stress <strong>of</strong> the animal and hemolysis <strong>of</strong> collected<br />
plasma is avoided, but most studies use vein puncture.<br />
This study aimed to reveal metabolites sensitive to stress<br />
and/or hemolysis and quantify the effect on metabolite<br />
concentrations. Blood was collected from early and mid<br />
pregnant sows fed one <strong>of</strong> 2 different diets. A total <strong>of</strong> 24<br />
sows were blood sampled using vein puncture during<br />
nose snaring and another 30 sows were blood sampled<br />
via jugular vein catheters. Sows were fed twice daily (08<br />
and 15 h) and blood sampled repeatedly 1, 4, 11 and 23<br />
h after morning feeding. Plasma levels <strong>of</strong> isobutyrate (P<br />
< 0.001), NEFA (P < 0.01), and acetate (P < 0.05) were<br />
lowered, and plasma levels <strong>of</strong> caproate (P < 0.001),<br />
glucose (P < 0.01), lactate, and isovalerate (P < 0.05) were<br />
elevated in samples obtained via vein puncture. Plasma<br />
insulin, propionate and butyrate were not sensitive to the<br />
blood sampling procedure. These findings suggest that<br />
concentrations <strong>of</strong> many plasma metabolites are sensitive to<br />
the blood sampling procedure, likely due to stress imposed<br />
on the animal. Hemolysis is a common problem when blood<br />
is collected by vein puncture and the effect <strong>of</strong> hemolysis<br />
on plasma metabolite concentrations was studied in 48<br />
sows fed 4 different diets (other conditions identical to that<br />
described above). Plasma was categorized according to<br />
no, minor or major hemolysis (clear (n = 218), yellow (n<br />
= 97) or red (n = 37)) upon centrifugation. Plasma NEFA<br />
(P < 0.001) and plasma insulin (P < 0.10) was lower in<br />
hemolyzed samples while plasma propionate, caproate,<br />
isovalerate (P < 0.001), isobutyrate (P < 0.05) and butyrate<br />
(P < 0.10) was higher in hemolyzed samples compared with<br />
clear plasma samples. Plasma glucose and lactate were<br />
the only metabolites studied which were not affected by<br />
hemolysis. No dietary interactions were found (P > 0.05). In<br />
conclusion, blood sampling procedure and hemolysis affect<br />
the measured metabolite concentrations and should be<br />
considered or accounted for when comparing results within<br />
and between experiments.<br />
Key words: analysis interference, blood metabolites, pigs