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ANIMAL PRODUCTION |

* Department of Animal Sciences, University of Illinois, Urbana 61801 and
and
Elanco Animal Health, Greenfield, IN 46140
| Abstract |
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Key Words: Acid-Base Balance Handling Live Weight Stressor
| Introduction |
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| Materials and Methods |
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The study was carried out as a randomized block design with treatments in a 2 x 2 x 2 factorial arrangement: 1) live weight (light [104 kg] vs. heavy [128 kg]), 2) handling intensity (low vs. high), and 3) gender (barrows vs. gilts). The protocol for this study was approved by the Institutional Animal Care and Use Committee, University of Illinois.
Animals.
A total of 80 pigs (progeny of Line 337 sires mated to C22 dams; PIC U.S.A., Franklin, KY) consisting of equal numbers of barrows and gilts was used in the study. The study was carried out in four blocks over time with 20 animals in each block. Within a block, pigs were randomly allotted to treatments on the basis of sex, weight, and sire.
Housing and Feeding.
For a 28-d period before the handling test, pigs were housed in a mechanically ventilated building at the University of Illinois Swine Research Center that had part-solid, part-slotted floors. Animals were kept in pens of five pigs at a floor space allowance of 0.94 m2/pig, and had ad libitum access to a standard corn/soybean meal finisher diet (as fed; 16.0% CP, 0.83% lysine, and 3,176 kcal ME/kg) from a single-space feeder, and to water from a nipple waterer in each pen.
Handling Test.
At 0600 on the day of the handling test, rectal temperature was taken and a venous blood sample was collected to establish baseline measurements. Rectal temperature was recorded (to 0.1°C) with an M500HPDT digital thermometer (GLA Agricultural Electronics, San Luis Obispo, CA). Venous blood samples were collected via jugular venipuncture into 3-mL sodium lithium heparinized vacuum tubes (Becton Dickinson, Franklin Lakes, NJ). Animals were restrained using a snout snare during the blood collection process. Care was taken to collect only venous blood. Within 10 min of sampling, blood was assayed for pH, PCO2, partial pressure of oxygen (PO2), saturated oxygen (SO2), total carbon dioxide (TCO2), bicarbonate (HCO3), base excess, and lactate using an i-STAT Clinical Analyzer and CG4+ cartridges (i-STAT Corp., Princeton, NJ). Following the collection of baseline measurements, pigs were weighed and moved into clean pens. Each pen of pigs was given 2 h to recover from the process of collecting baseline measures before being subjected to the handling test. Measurements of rectal temperature and other blood variables were repeated at 0 and 2 h posthandling as previously described.
Individual pigs were moved from the pen to the handling course and then through the course for a total of eight laps. The handling course was 12.2 m long x 0.91 m wide, with solid walls and an area for the pigs to turn at each end. One lap was defined as the pig passing once in each direction through the course. Pigs subjected to the high-intensity handling treatment were moved through the handling course using an electric goad and a moving panel. Each pig was subjected to a single short-duration shock (approximately 0.5 s) from the goad at the beginning of each pass through the model, for a total of 16 shocks (two per lap). Pigs on the low-intensity treatment were moved using a paddle and a moving panel and each pig was allowed to move at their own pace. If the pig stopped moving it was gently tapped with the paddle or bumped with the panel to reinitiate movement.
Statistical Analysis.
The PROC MIXED procedure of SAS (SAS Inst., Inc., Cary, NC) was used to analyze data, with the individual pig as the experimental unit. The model used included the effects of live weight, handling intensity, gender, replicate, block, and two- and three-way interactions. Least squares means were evaluated using the PDIFF and STDERR options of SAS.
| Results and Discussion |
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There were no effects of live weight or gender on baseline measurements (Table 1
). Hamilton also reported no effects of gender on baseline blood acid-base levels. Furthermore, baseline values for lactate, pH, HCO3, and base excess in this study were similar to the values obtained in other studies that collected blood samples from pigs using either indwelling jugular catheters (van der Wal et al., 1986
; Bickhardt and Wirtz, 1987
) or jugular venipuncture (Haydon et al., 1990
; Bertol et al., 2002a
,b
). This suggests that jugular venipuncture produces blood acid-base values that are similar to those of other sampling methods.
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Several studies have reported changes similar to ours in blood acid-base parameters and rectal temperature of pigs subjected to an exercise model or a high-intensity handling treatment (Muylle et al., 1968
; van den Hende et al., 1970
; Ivers et al., 2002a
). For example, van den Hende et al. (1970)
used electrical stimulation (alternating current at 200 V for 5 s) to exercise the leg of pigs for 5 min and reported large decreases in venous blood pH (from 7.46 to 6.88) and base excess (from 7.8 to 22.0 mmol/L) with a corresponding increase in lactate (from 7.38 to 40.6 mmol/L). Van der Wal et al. (1986)
evaluated five potential stressors (forced standing, placing the pig in a maxillary sling, fixation of the pig with the maxillary sling, prolonged fixation, and fixation with a sling and electrical stimulation), and reported much smaller changes in blood pH (from 7.33 to 7.23), base excess (from 0.48 to 3.27 mmol/L), and lactate (from 1.45 to 3.84 mmol/L) from resting to poststress. However, other studies that have employed a high-intensity animal handling treatment similar to that used in the current study have reported similar changes in blood pH, lactate, bicarbonate, base excess, PO2, and PCO2 (Bertol et al., 2002a
,b
). Alterations in blood acid-base levels from resting to posthandling have been shown to be proportional to the intensity and duration of the stressful stimulus and normally result in a change to an acidotic state (van der Wal et al., 1986
; Bertol et al., 2002a
). Thus, variation among studies in the extent of changes in blood gasses are likely due to differences in either the intensity and/or the duration of the stressor. Furthermore, Heinze and Mitchell (1989)
showed that physical exertion, in the form of a treadmill exercise, produced a metabolic response in pigs that was similar to that observed in the current study as a result of high-intensity handling. Jorgensen and Hyldgaard-Jensen (1975)
demonstrated that pigs trained and exercised regularly on a treadmill did not show the blood lactate response that untrained pigs produced the first time that they were exercised on the treadmill. Thus, it is evident that physical exercise and conditioning play a role in determining the extent of lactate production during handling. The pigs used in the present research had been regularly handled and moved before the start of the study but had not been exposed to any formal exercise regimen.
There were no effects of live weight or gender on blood acid-base parameters or rectal temperature when measured 2 h posthandling (Table 4
). However, pigs on the high-intensity handling treatment had greater (P < 0.05) blood lactate and correspondingly lower blood TCO2, HCO3, and base excess when compared with pigs on the low-intensity handling treatment (Table 4
). Nonetheless, the differences between the handling treatments at 2 h posthandling were much less than immediately posthandling, and all measures were generally similar (P > 0.05) to the baseline values (Tables 1
and 4
). These results suggest that a 2-h rest after low-intensity handling may be adequate for blood acid-base status to return to normal; however, if pigs are handled more intensely, then more time is required for blood acid-base levels to return to resting values. The results of the current study are similar to those of Bertol et al. (2002a)
, who found that acid-base levels of pigs subjected to high-intensity handling had returned to baseline levels by 2 h posthandling. In addition, Jorgensen and Hyldgaard-Jensen (1975)
showed that blood lactate levels in pigs subjected to exercise on a treadmill had returned to the normal baseline level within 45 min posthandling. Differences between studies in the length of time before blood parameters return to baseline levels after exercise may, in part, be related to the severity and/or duration of the handling procedures, as well as the particular exercise model tested.
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1 Correspondence: 216 ASL, 1207 W. Gregory Dr. (phone: 217-333-6455, fax: 217-333-7861; e-mail: mellis7{at}uiuc.edu).
Received for publication October 23, 2003. Accepted for publication April 13, 2004.
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