Poul Henckel

Prediction of water-holding capacity and composition of porcine meat by comparative spectroscopy

Four spectroscopic instruments, a fibre optical probe (FOP), a visual (VIS) and near infrared (NIR) reflectance spectrophotometer, a reflectance spectrofluorometer and a low-field (1)H nuclear magnetic resonance (LF-NMR) instrument were used to perform measurements on two muscles (longissimus dorsi and semitendinosous) from 39 pigs, 18 of which were carriers of the Halothane gene. Water-holding capacity (drip loss and filter paper wetness) and chemical composition (intramuscular fat and water) of the muscle samples were determined for spectroscopic calibration. Prediction models were established by partial least squares regression to evaluate the potential of using the spectroscopic techniques in an on-line slaughterhouse system. VIS data gave good prediction models, indicating that current industrial colour systems can be advanced into more specific meat evaluation systems by including the entire visible spectral range. The FOP and fluorescence measurements were less successful, and suffered from sampling problems since they measure only a small area. The best regression models were obtained from LF-NMR data for all reference quality measures and yielded a correlation coefficient of 0.75 with drip loss. LF-NMR proved able to distinguish between the two muscles and the results for their longitudinal relaxation times, T(21), were proportional to their average myofibrillar cross-sectional areas reported in the literature.

Histo- and biochemical characteristics of the Longissimus dorsi muscle in pigs and their relationships to performance and meat quality

Histo- and biochemical characteristics of the longissimus dorsi muscle at 65-70 kg body weight and their relationships to performance and meat quality at 100 kg were examined in Danish Landrace and Danish Large White female and castrated male pigs. Breed differences were observed for feed conversion rate, and a number of histochemical and biochemical traits. The organoleptic traits, flavour (13%), tenderness (15%) and overall acceptability (13%) were rated higher in Large White pigs. Significant correlations between histological and biochemical traits of the live muscle on the one side and performance, meat quality and organoleptic traits on the other side, could be demonstrated. However, these correlations were generally low (r < 0.35), and can thus only explain a small part of the variation in the measured quality traits. Consequently live muscle traits measured at 65-70 kg are poor predictors of meat quality characteristics after slaughter at 100 kg.

Metabolic conditions in Porcine longissimus muscle immediately pre-slaughter and its influence on peri- and post mortem energy metabolism.

To clarify the physiological prerequisites for the course of energy metabolism post mortem, 80 pigs consisting of four females from each of 20 litters of crossbreeds (Duroc as sireline and Danish Landrace×Danish Large White as dam line) were within litter allocated to four different treatments (A, B, C and D) to provide a large variation in the concentration of the key metabolites glycogen, ATP and creatine phosphate at the time of stunning. (A) no stress before stunning, (B) physical stress consisting of treadmill running (3.8 km/h for 10 min) immediately before stunning, (C) intermediate reduction of glycogen at stunning achieved by application of adrenaline (0.2 mg/kg live weight 15-18 h before stunning), and (D) maximal reduction of glycogen achieved by application of adrenaline (0.3 mg/kg live weight 15-18 h before stunning) and treadmill running (3.8 km/h for 5 min). Compared with resting values (measured in samples taken in the pen the day before slaughter by needle biopsy), longissimus muscle glycogen (16, 13, 57 and 66% for A, B, C and D, respectively), creatine phosphate (17, 22, 12 and 9% for A, B, C and D, respectively) and ATP levels (10, 15, 38 and 31% for A, B, C and D, respectively) measured immediately before stunning were all reduced by the treatments. Stunning caused a rather uniform reduction in creatine phosphate level in all the models. Glycogen concentrations were also further reduced in treatments A, C and D, but not in B, and although ATP levels increased in all the models during stunning, this was only significant for the B model. Consequently, the effect of CO(2) stunning on glycogen and ATP levels depends on pre-slaughter handling. It was also shown that an inverse relationship between ultimate pH and glycogen concentration at the time of stunning existed only when glycogen levels at stunning were below 53 mmol/kg (r=0.88, P<0.001). The validity of this threshold value is discussed. Furthermore, the possibility to standardise the physiological prerequisites of the post mortem pH decreases represents a potent tool to investigate metabolic causes of variations in meat quality characteristics.

The effect of stress during lairage and stunning on muscle metabolism and drip loss in Danish pork

The effect on meat quality of a low stress handling system (LSS) compared with a traditional handling system (TS) was investigated in Duroc×(Landrace×Yorkshire; n=117) and (Hampshire×Duroc)×(Landrace×Yorkshire) pigs (n=110) under commercial conditions. In the low-stress handling system the pigs were kept in groups of 15 during lairage and movement up to the stunner. Before the stunner the groups were divided into three groups of five pigs for the CO(2)-stunning in a specially designed set-up. The pH and temperature were determined in m. longissimus dorsi (LD) and m. biceps femoris (BF) at various times post mortem. Immediately after exsanguination a biopsy was taken from the LD and analysed for the concentration of glycogen, lactate and creatine phosphate. The day after slaughter the pH was determined in the LD, BF, m. semimembranosus (SM) and m. semispinalis capitis (SC). The temperature was determined in the LD and BF, the internal reflectance was determined in the LD, SM and BF, the colour was determined in LD, the drip loss was determined in LD and BF, and the amount of blood splashing/bruising was evaluated in LD. There was a tendency for a higher concentration of creatine phosphate in the LSS-group (P=0.06). The pH in both the LD and BF on the day of slaughter decreased more slowly from 5 min post mortem to 40 min post mortem in the LSS-group than in the TS-group (P<0.001). From 40 min to 6 h post mortem the rate of the pH decline was similar in the two groups producing the lowest pH-level in the TS group. The day after slaughter the pH was similar in the two groups in the LD and SC, whereas in the BF and SM it was lower in the LSS-group than in the TS-group. The drip loss was lower in the LSS-group in both LD (P<0.01) and BF (P<0.05) whereas the internal reflectance was only different in LD with the lowest value in the LSS-group (P<0.001). The lightness (L*) was higher in the LSS-group (P<0.05). There was no effect of stunning system on the amount of blood splashing/bruishing in the LD. The study showed that by using a low stress stunning system it is possible to decrease drip loss, possibly by increasing the concentration of creatine phosphate and thereby delaying the acceleration of pH fall in muscles after death.

Control of post mortem pH decrease in pig muscles: experimental design and testing of animal models

From a series of experiments aimed at manipulating and relating the resting levels of glycogen and creatine phosphate (CP) in the live muscle four models were selected to induce different rates and extents of pH decrease post mortem in pig muscle. Model A served as the control, animals being slaughtered under minimal stress, in model B animals were subjected to 10 min treadmill exercise at 3.8 km/h immediately prior to stunning, in model C, animals were given 0.2 mg adrenaline/kg live weight 16 h prior to slaughter, and in model D they were given 0.3 mg adrenaline/kg live weight 16 h before slaughter and subjected to 5 min of treadmill exercise immediately before stunning. After slaughter, the decline in pH and temperature post mortem was recorded in M. longissimus dorsi (LD), M. biceps femoris (BF), M. semimembranosus (SM) and M. psoas major (PM) from 1 min to 24 h after bleeding. Significant differences in ultimate pH and the time course of pH decrease were observed, both as an effect of model as well as type of muscle. No differences in ultimate pH between model A and model B were observed in any of the muscles. Ultimate pH in the C and the D models were significantly higher than in A and B. In the B model lower pH values were observed from 1 min to 6 h post bleeding compared to the other three models. No differences in rate of pH decrease were observed between the A and the B models in any of the muscles. Within the A model no differences in ultimate pH between muscles were seen, indicating that the frequently observed differences in ultimate pH are caused by environmental factors rather than by differences in physiological and morphological characteristics. The exercise bouts caused elevated temperatures during the first hour after bleeding (model B and D). The BF muscle in all the models displayed the fastest rate of pH decrease and SM the slowest; a slower rate of temperature decline occurred in the BF than in the SM.

Effect of pre-slaughter physiological conditions on the oxidative stability of colour and lipid during chill storage of pork.

The physiological condition of the live animal was found to significantly affect colour, lipid oxidation and water holding capacity of chill stored pork chops (M. Longissimus dorsi) in a study, where various pre-slaughter conditions were achieved by the following four treatments: (A) control; (B) subjected to treadmill exercise immediately prior to stunning; (C) given epinephrine injection 15 h prior to slaughter; and (D) given epinephrine injection 15 h before slaughter and further subjected to treadmill exercise immediately before stunning. The treatments resulted in variations in energy metabolites (glycogen, lactate, creatine phosphate, ATP) and ultimate pH (pH(u)), with the lowest pH(u) in chops from treatments A and B, and in significantly different tristimulus colour L(∗)-, a(∗)- and b(∗)-parameters, although the effect of treatment on colour was not consistent during the chill storage period of 6 days. Overall, chops from treatments A and B had significantly higher L(∗)- and b(∗)-values (were paler and less blue) than chops from C and D during storage under conditions typical for retail trade. The initial a(∗)-values were higher (redder) in chops from treatments A and B, but the colour, as judged by the a(∗)-values, was less stable in meat from these treatments compared with treatments C and D. Lipid oxidation, evaluated by thiobarbituric acid reactive substances (TBARS) in the fresh meat, and drip loss, measured after 6 days of storage, were both significantly higher in chops from treatments A and B compared to chops obtained from treatments C and D. Statistical analysis relating the pH and the level of various energy metabolites post-mortem in the individual animals to the measured quality parameters, revealed that pH(u) was the most important factor affecting product quality. In conclusion, over all product quality depends on obtaining a pH(u) in the narrow range where both meat quality parameters such as colour, lipid oxidation and drip loss as well as microbiological aspects have to be considered.

Oxidative stability of chilled pork chops following long term freeze storage.

Colour stability and development of lipid oxidation were followed during chill storage for 6 days of chops from M. Longissimus dorsi produced from pigs with high (6.3) and low (5.5) ultimate pH (pH(u)). The chops from the same individual pigs were either chill stored at 2 days post-mortem or after frozen storage for 30 months (pre-frozen). Initial redness, measured as tristimulus parameter a(*), was lower for pre-frozen chops than for fresh chops. Chops with the high pH(u) had a stable a(*)-value during chill storage, while chops with the low pH(u) showed a rapidly decreasing a(*)-value both for fresh and pre-frozen chops. In contrast, initial lipid oxidation, measured as TBARS, was similar for pre-frozen and fresh chops prior to chill storage for both the high and the low pH(u) meat but developed most significantly in pre-frozen, low pH(u) meat. Individual differences in colour stability and development of lipid oxidation between pigs were notable for pre-frozen low pH(u) meat and need to be considered in quality control since meat from single pigs otherwise might give problems.

Influence of dietary conjugated linoleic acid (CLA) and age at slaughtering on performance, slaughter- and meat quality, lipoproteins, and tissue deposition of CLA in barrows

To assess the effects of dietary conjugated linoleic acid (CLA) on performance, slaughter and meat quality, 100 Danish barrows were fed diets containing 0.5% sunflower oil (control) and 0.5% CLA from 40 kg live weight until slaughter at either 100 or 130 kg live weight. Plasma total cholesterol (P=0.006) and HDL-cholesterol (P=0.021) was reduced, and plasma FFA-concentration increased (P=0.06) in pigs fed CLA. CLA supplementation improved (P=0.01) the feed utilisation by 4.7% and 4.3% for pigs slaughtered at 100 and 130 kg, respectively. Daily gain tended (P=0.06) to increase with the CLA-treatment (1.236 versus 1.194 kg for CLA- and control, respectively). Dietary treatments had no effects on slaughter- (meat percentage and backfat thickness) and meat quality responses (pH, temperature and water holding capacity). CLA tended (P=0.09) to reduce the intramuscular cholesterol, but had no influence on the total content of intramuscular fat.

Significance of early postmortem temperature and pH decline on colour characteristics of pork loin from different crossbreeds

The significance of early postmortem (pm) temperature and pH decline and the level of the muscle metabolites creatine phosphate (CP) and adenosine triphosphate (ATP) on the colour of porcine M. longissimus dorsi was studied in a factorially designed experiment. Two stress levels peri mortem (minimal stress vs treadmill exercise and electrical stunning of the pigs) and four genotypes (Duroc boars crossed with Landrace-Yorkshire sows vs. Hampshire-Duroc boars crossed with Landrace-Yorkshire sows, including carriers and non-carriers of the halothane and RN(-) genes, respectively) were included. Early pm muscle temperature and the accompanying pH decline had a significant influence on the pork colour independent of genotype. The combination of high temperature and low pH early pm increased lightness and yellowness, which is ascribed to inactivation of oxygen-consuming enzymes and protein denaturation. The effect of early pm temperature and pH on pork redness was more complex. It appears to be closely related to the extent of heat generation, CP and ATP levels and pH immediately pm in the muscle, which influence the activity of oxygen-consuming enzymes.

A within litter comparison of muscle fibre characteristics and growth of halothane carrier and halothane free crossbreed pigs

The influence of the halothane gene on performance, carcass composition, chemical composition of carcass fractions, and muscle fibre characteristics of M. semitendinosus (ST) was examined in 14 litters of two pigs of either NN (halothane free) or Nn genotype (heterozygous for the halothane gene) (within litter comparison). The pigs were offspring of Duroc×Pietran boars (Nn) mated to Landrace×Yorkshire females (NN). The feed intake of Nn pigs was 8% (P<0.05) lower compared with NN pigs. Based on the carcass composition, deposition rates of muscle tissue and bones did not differ between genotypes, while the deposition rate of fat tissue was lower in Nn compared with NN pigs (P<0.01). This resulted in increased meat content of the carcass (2.6% units, P<0.001). The cross-sectional area of type I and type II fibres was 22% (P<0.05) and 12% (P<0.04) larger in Nn pigs, respectively. The estimated fibre number was 9% (P<0.05) lower in Nn compared with NN pigs due to both a reduction in the number of primary (24%, P<0.05) and secondary fibres (8%, P<0.1). The estimated amount of DNA and RNA per fibre was elevated in Nn pigs compared with NN pigs suggesting a higher rate of satellite cell proliferation and capacity for protein synthesis per fibre. There was no difference in the rate of proliferation of C2C12 myoblasts and the rate of protein turnover of C2C12 myotubes when sera from the two genotypes were compared. The present results indicate that fewer fibres accomplish muscle growth of heterozygous carrier of the halothane gene with a higher growth rate due to an increased rate of satellite cell proliferation and capacity for protein synthesis. Results on cell cultures indicate that the higher rate of muscle fibre growth in Nn pigs was due to muscle intrinsic factors, i.e., changes in muscle sensitivity and/or responsiveness to growth factors.