Evidence against the non-enzymatic calcium theory of tenderization

The objective of the present study was to determine whether variation in the tenderization of lamb longissimus could be attributed to variations in the rise in free calcium postmortem and sarcomere lengthening post rigor. The longissimus muscle of 10 crossbred lambs (Romney×Coopworth) was sampled at 1 and 7 days postmortem for determination of MIRINZ shear force, myofibrillar fragmentation index (MFI), sarcomere length, free calcium, and proteolysis of troponin-T. Despite considerable variation in tenderness and tenderization of the muscles, sarcomere lengthening was not observed. The concentration of free calcium at 7 days postmortem correlated significantly with the MFI (r=0.640; P<0.05) and tended to correlate with the shear force (r=−0.596; P<0.1) and degradation of troponin-T (r=0.625; P<0.1). Degradation of troponin-T was significantly correlated with tenderization (r=0.664; P<0.05). Troponin-T is a calpain substrate, but reportedly is not degraded through a direct effect from calcium. The present results, therefore, suggest that the variation in free calcium in postmortem muscle affects tenderization through an effect on the calpain system and not through a direct effect of calcium on myofibrillar proteins. Consequently, the results of this study do not support the (calcium) theory that calcium directly affects tenderization.     

Carcass traits, muscle characteristics, and palatability attributes of lambs expressing the callipyge phenotype

Dorset×Suffolk crossbred wethers expressing a normal phenotype (normal, n=10) and callipyge phenotype (CLPG, n=9) were fed individually and slaughtered upon reaching maximum growth potential. Carcass weight did not differ (P>0.05), but fat thickness was lower (0.30 vs. 0.56 cm), ribeye area was greater (24.4 vs. 16.6 cm²), and USDA yield grade was improved (1.6 vs. 2.6) for CLPG carcasses (P < 0.05). Carcasses from CLPG demonstrated higher cutability and a more desirable muscle to bone ratio, with less fat and more lean as a percentage of total side weight (P<0.05). Biceps femoris (BF), semitendinosus (ST), semimembranosus (SM), longissimus thoracis et lumborum (LTL), and triceps brachii (TB) were used to compare muscle characteristics of both phenotypes. Muscle from normal lambs had lower calpastatin activity, higher fat percentages and lower moisture percentages (P<0.05). Total amount and solubility of collagen were not affected by phenotype nor was sarcomere length. Shear force and trained sensory attributes were evaluated for BF and LTL only. Shear force values did not differ between normal and CLPG BF while CLPG LTL had higher (P< 0.05) shear force values than normal LTL. Biceps femoris did not differ between phenotypes in trained sensory panel ratings. However, CLPG LTL received the lowest sensory ratings for connective tissue amount and myofibrillar and overall tenderness (6.11, 4.97, and 4.95, respectively) and the normal LTL received the highest ratings (P < 0.05; 7.10, 7.00, and 6.90, respectively). The CLPG phenotype had a positive influence on carcass characteristics but had a negative influence on tenderness of some muscles, possibly through the myofibrillar component of the muscle.     

High voltage electrical stimulation enhances muscle tenderness, increases aging response, and improves muscle color from cabrito carcasses

Our study examined high and low voltage electrical stimulation and postmortem storage as strategies to improve tenderness and lean color in cabrito carcasses. Boer cross (n=60) kids were assigned to either high (550 V), low (20 V), or no electrical stimulation treatments. No differences in muscle temperature were observed between treatments at any time measured. Muscle pH declined fastest in high voltage treated carcasses. High voltage electrical stimulation slightly increased (P<0.05) b^* and a^* in the M. gluteus medius and tended to increase L^* and b^* (P=0.06 and 0.11, respectively) values in the M. longissimus thoracis. Electrical stimulation had no effect on myofibril fragmentation at 1-, 3-, or 14-d postmortem or sarcomere length. High voltage electrical stimulation increased (P<0.05) tenderness at 1- and 3-d postmortem, but not at 14-d postmortem. Aging for 3 d did not affect tenderness regardless of stimulation treatment, but aging time for 14 d improved (P<0.05) tenderness. These data indicate that high voltage electrical stimulation and 14 d aging were effective in improving the tenderness of meat from cabrito carcasses.     

Influence of ultimate pH on bovine meat tenderness during ageing

The aim of this work was to evaluate the influence of ultimate pH and ageing at 2±2°C on the tenderness of beef. The m.longissimus thoracis et lumborum from 23 young bulls excised at 28 h post mortem were grouped into: Normal (pH 5.5 to 5.8) moderate DFD (mod DFD) (5.8p<0.05) lower in the DFD group than in the Normal one and a significant (p<0.001) linear relationship was found between ultimate pH and tenderness as evaluated by both methods. The myofibrillar protein solubility (MPS) at pH 7.0 was significantly higher in the DFD group at all post mortem times whereas for myofibrillar fragmentation index (MFI) higher values (p<0.05) were only found in the DFD group at day 1. In all three groups toughness decreased (p<0.05) from 1 to 6 days, with no further decrease to 13 days. This decrease in toughness was associated with an increase of MFI in all pH groups. Collagen solubility in all three groups was not affected by ageing. No significant (p>0.05) differences in soluble collagen and myofibrillar protein solubility (MPS) at pH 5.5 were found between the pH groups at any time. The tenderness evaluated by both methods was significantly (p<0.05) related to MFI, MPS at pH 7.0, cooking loss and juiciness. Total and soluble collagen, sarcomere length, intramuscular fat and MPS at pH 5.5 were not significantly (p>0.05) related with tenderness.     

Contribution of postmortem muscle biochemistry to the delivery of consistent meat quality with particular focus on the calpain system

Tenderness has been repeatedly reported as the most important quality aspect of meat. However, a number of studies have shown that a significant portion of retail meat can be considered tough. As a consequence, a significant consumer segment is willing to pay a premium for guaranteed tender meat. However, apart from measuring the shear force, there is no reliable method to predict tenderness. Most of the branded meat programs therefore attempt to ensure eating quality by controlling some of the factors that affect tenderness. Meat tenderness is determined by the amount and solubility of connective tissue, sarcomere shortening during rigor development, and postmortem proteolysis of myofibrillar and myofibrillar-associated proteins. Given the effect of postmortem proteolysis on the muscle ultrastructure, titin and desmin are likely key substrates that determine meat tenderness. A large number of studies have shown that the calpain proteolytic system plays a central role in postmortem proteolysis and tenderization. In skeletal muscle, the calpain system consists of at least three proteases, μ-calpain, m-calpain and calpain 3, and an inhibitor of μ- and m-calpain, calpastatin. When activated by calcium, the calpains not only degrade subtrates, but also autolyze, leading to loss of activity. m-Calpain does not autolyze in postmortem muscle and is therefore not involved in postmortem tenderization. Results from a number of studies, including a study on calpain 3 knockout mice, have shown that calpain 3 is also not involved in postmortem proteolysis. However, a large number of studies, including a study on μ-calpain knockout mice, have shown that μ-calpain is largely, if not solely, responsible for postmortem tenderization. Research efforts in this area should, therefore, focus on elucidation of regulation of μ-calpain activity in postmortem muscle. Discovering the mechanisms of μ-calpain activity regulation and methods to promote μ-calpain activity should have a dramatic effect on the ability of researchers to develop reliable methods to predict meat tenderness and on the meat industry to produce a consistently tender product.     

Association of polymorphisms in the calpain I, calpain II and growth hormone genes with tenderness in bovine M. longissimus dorsi

The objective of this study was to determine if there is an association between tenderness in bovine M. longisimus dorsi (LD) and polymorphisms in the bovine calpain I (exons 9 & 14), calpain II (regulatory subunit) or growth hormone (intron 3) genes. Genomic DNA was isolated from bovine LD (n = 281) on which quality attributes (Warner Bratzler shear force (WBSF), sarcomere length and composition) were also characterised. DNA polymorphisms were analysed using polymerase chain reaction (PCR) and restriction fragment length polymorphism analysis. Association analyses were performed between genotypes at the four polymorphic loci and day 14 WBSF values. It was found that the calpain 1 exon 9 genotypes had an association with WBSF such that animals with the GA genotype exhibited decreased WBSF and increased tenderness when compared to animals with the GG genotype (P < 0.05). This observation concurs with that of earlier studies, suggesting that this polymorphism is a functional marker for beef tenderness.     

Effect of dietary ractopamine on tenderness and postmortem protein degradation of pork muscle

Twenty-four finishing pigs with a mean starting weight of 82 kg were assigned to two dietary regimens: (1) a corn–soybean meal basal diet (control; n = 12), and (2) the basal diet supplemented with 20 ppm ractopamine HCl (RAC; n = 12). After 28–30 days on the feeding trial, pigs were slaughtered, and the growth and carcass characteristics were measured. Furthermore, the 3rd–13th rib section of longissimus muscle was excised at 48 h postmortem, sliced into 19-mm thick chops, vacuum packaged, stored at 2 °C, and subjected to Warner–Bratzler shear force (WBSF) and electrophoretic tests after 2, 4, 7, 10, 14, and 21 days (postmortem). RAC feeding increased (P < 0.01) pig carcass weight and percent lean, but it also increased the day-2 muscle WBSF by 20% (P < 0.01). The shear force difference between control and RAC pig muscles gradually decreased and vanished by day 10 (P > 0.05) when both muscle groups became more tender. The muscle from RAC-fed pigs exhibited a slower protein degradation rate than muscle from the control animals, notably for proteins in the 15–45 kDa range. The results suggested that the tenderness difference between ractopamine-treated and control pig muscles was related to the proteolysis rate, and could be diminished with adequate postmortem ageing.     

Effect of Duroc content, sex and ageing period on meat and eating quality attributes of pork loin

This study was conducted to determine the effect of percentage Duroc content of entire male and female pigs and ageing period on meat and eating quality attributes of pork loin (M. longissimus thoracis et lumborum). A total of 84 pigs [entire males (n=42) and female (n=42)] of 0% Duroc (100% Large White), 50% Duroc (Duroc×Large White) or 100% Duroc (n=14 pigs per sex×genotype combination) were slaughtered at a liveweight of 100 kg. Steaks from the M. longissimus lumborum of female pigs were aged for either 2 or 7 days post-slaughter and evaluated using a consumer taste panel. Eating quality attributes of tenderness, flavour and overall liking of pork loin steaks from female pigs were not (P>0.05) influenced by Duroc content. Pork from 100% Duroc pigs was juicier (P=0.05) and had a higher (1.84%, P=0.05) intramuscular fat content than pork from 0 and 50% Duroc pigs (1.40 and 1.25%, respectively). Pork from entire male pigs had a lower (P<0.001) intramuscular fat content, was darker (P<0.01) in colour and recorded higher (P<0.01) Warner Bratzler shear force values compared with pork from female carcasses. Ageing pork loin steaks in vacuum bags for 7 days improved tenderness (P<0.01), flavour (P<0.05) and overall liking (P<0.05) compared with steaks aged for 2 days post-slaughter. Ageing of pork steaks for 7 days post-slaughter improved eating quality attributes far more effectively than increasing percentage Duroc content of pigs, which only influenced consumer scores for juiciness.     

Ellipsometry across isolated muscle fibres indicates a refractive contribution to paleness in pork

Muscle fibres isolated from pork were mounted in a microscope chamber and pH was controlled with 0.2 M phosphate buffer. Optical path differences between ordinary and extraordinary rays were measured by ellipsometry while a scanning stage moved the fibre across the optical axis of the microscope. The depth of fibre in the optical axis was estimated from the lateral diameter of fibres. Path differences increased as fibre depth increased. Static ellipsometry of unmounted fibre fragments showed maximum path differences at pH 5.5 were higher than at pH 7.0, but variance was high and the difference was not significant (64.4±15.1 nm at pH 5.5 versus 58.9±15.2 nm at pH 7.0, P>0.05, n=40). However, the mean depth of fibre fragments at pH 5.5 was less than at pH 7.0 (53.9±15.1 μm at pH 5.5 versus 70.6±16.1 μm at pH 7.0, P<0.005, n=40). Thus, path differences per micrometre of fibre depth were greater at pH 5.5 than at pH 7.0 (1.25±0.37 nm^{−1 μm} at pH 5.5 versus 0.87±0.31 nm^{−1 μm} at pH 7.0, P<0.0005, n=40). As pH decreases, therefore, muscle fibre diameter decreases while birefringence increases. Refraction through muscle fibres may contribute to pork paleness.     

Calpains from thaw rigor muscle

Pre-rigor beef M. Longissimus lumborum and diaphragma were frozen at −70 °C and thawed at different temperatures and the activities of extracted calpains and the toughness of heated meat compared with those in chilled muscle.

Fresh muscle contained about 14 μg of μ-calpain/g and was unaffected by freezing, but was reduced after thawing. Rapid thawing at 30 °C for 20 min reduced the μ-calpain to 14%. When cooked from the frozen state, extensive shortening occurred and tender meat was obtained.

By storing at −3 °C for 1 day, thaw-shortening was prevented, but tougher meat obtained. The μ-calpain decreased to 70% whilst the m-calpain was unaffected. Toughness decreased after further storage at −3 °C, as did the μ-calpain. The latter changes were similar to those during development of rigor mortis and ageing of non-shortened meat stored at 4 °C. Variation in calpain activity, rather than in sarcomere length, are likely to be the cause of toughness variation in thaw rigor muscle.     

Stability of catalase and its potential role in lipid oxidation in meat

The activity of catalase in microbial growth-controlled and uncontrolled ground beef muscle (semimembranosus, SM) did not change (P>0.05) during 6-day storage at 4°C. Likewise, catalase activity in ground, beef SM and longissimus dorsi (LD), pork LD, and chicken breast (B) and thigh (T) muscles was not affected (P>0.05) by 2-month storage at −20°C, with or without mid-month thawing/refreezing. When sodium azide (a catalase inhibitor) was added to ground beef SM, lipid oxidation (as measured by peroxide values) during 4-day refrigeration was higher (P<0.05) in treated samples — 43 and 55% higher at day 2 and day 4, respectively — than in the controls. It was concluded that catalase would be stable during meat storage/distribution and contribute significantly to the antioxidative process in raw meat products.     

Augmented postmortem glycolysis does not occur early postmortem in AMPKγ3-mutated porcine muscle of halothane positive pigs

The objective of this study was to determine the effects of the halothane (HAL) and Rendement Napole (RN) genes on the rate-limiting reactions of glycolysis and their relationship to pork quality development. Samples were collected from the longissimus muscle at 0, 30, 60, and 120 min and 24 h postmortem from homozygous HAL and RN pigs (NN/rn⁺rn⁺, NN/RN⁻RN⁻, nn/rn⁺rn⁺, nn/RN⁻RN⁻). Muscle pH was recorded at 0, 15, and 45 min, and 24 h postmortem. HAL mutants, compared with HAL normal, had lower (P < 0.05) ATP concentrations at 0 and 30 min, lower (P < 0.05) pH at 45 min, and hastened glycogen degradation and lactate accumulation in the first 120 min postmortem (HAL × time, P < 0.0001). RN mutants had greater (P < 0.0001) glycolytic potentials than RN normal, and lower (P < 0.05) 24 h pH compared with the normal genotype, but not the HAL mutant genotype. The HAL mutation negatively affected (P < 0.05) L*, b* and color scores whereas both HAL and RN mutations independently decreased (P < 0.05) firmness, marbling and water holding capacity. RN mutant genotypes had higher (P < 0.0001) phosphocreatine concentrations than other genotypes at 0 min. Compared with HAL normal, HAL mutants had elevated (P < 0.05) muscle glucose concentrations at 30, 60, and 120 min, and 24 h. RN mutants had higher (P < 0.05) glucose levels than RN normal after 60 min. Glucose-6-phosphate (G6P) concentrations decreased (P < 0.05) during the first hour postmortem except in HAL/RN mutants, which had higher (P < 0.01) G6P concentrations than all other genotypes at 30 min. From 60 min to 24 h postmortem, G6P increased (P < 0.05) in HAL normal genotypes. Altogether, these data show that elevated muscle glycogen content does not further aggravate rapid early postmortem metabolism.     

Determination of potential inherent variability when measuring beef quality

Probes, which can be used on-line to rapidly and efficiently detect beef quality attributes (colour and tenderness), are currently being considered to predict ultimate beef quality. The contribution of the inherent sampling variability (due to factors such as muscle location) needs to be evaluated in order to optimise the sampling procedure for these measurements. The main objective of this trial was to monitor some sampling factors which may contribute to variation in pH and various quality attributes in bovine M. longissimus thoracis et lumborum (LTL). Location along the muscle did not impact on colour measurements (P0.05). Location had no effect on cook loss, Warner Bratzler shear force (WBSF) and sarcomere length values (P0.05). The moisture and intramuscular fat contents did vary (P0.05); however, as the differences were very small this may not be of practical significance. Different models of pH meters/probes had a significant influence (P0.01) on recorded pH values. However pH did not differ significantly (P0.05) along the length of the LTL. The type of meter used also had a significant impact on colour readings and 1 h ‘blooming’ time was observed as optimal for measuring colour on beef.     

Impact of muscle type and sodium chloride concentration on the quality, sensory, and instrumental color characteristics of solution enhanced whole-muscle beef

Beef biceps femoris (n = 10; muscle sections, n = 20; BF), infraspinatus (n = 10; muscle sections, n = 20; IS), and longissimus (n = 10; muscle sections, n = 20; LM) muscles were utilized to evaluate the effect of enhancement with phosphate and varying levels of sodium chloride in beef muscles differing in composition and palatability. Muscles were untreated or solution enhanced to 112% of raw product weight with sodium tripolyphosphate at 0.4% of product weight (STPP), or STPP and sodium chloride (NaCl) at 0.5%, 1.0% or 1.5% of product weight. There was a quadratic relationship (P = 0.04) for percent free water to decrease and a linear relationship (P < 0.01) for cook yield to increase as the level of NaCl increased. The IS steaks required less (P < 0.05) shear force than either the BF or LM, with the BF and LM having similar (P > 0.05) shear force values. There was a linear relationship (P < 0.01) for shear force values to decrease with increasing salt concentration. Steaks from all four enhancement treatments had lower (P < 0.05) shear force values than untreated steaks. Sensory overall tenderness ratings revealed that the IS and LM were similar (P > 0.05) and superior (P < 0.05) to the BF in tenderness. Steaks enhanced with STPP and 0.5%, 1.0%, or 1.5% NaCl all were rated more tender (P < 0.05) than untreated or STPP-only treated steaks. The BF exhibited the lowest (P < 0.05) L* (lightness) and a* (redness) values, as well as decreased (P < 0.05) vividness. The LM generally exhibited superior color to the other two muscle types. There was a linear relationship (P < 0.01) for L*, a*, b* (yellowness) values, and vividness to decline with increasing salt concentration, but steaks enhanced with STPP and 0.5% NaCl were similar (P > 0.05) in a* values and vividness to untreated steaks. These results suggest that across three different muscles varying in composition and palatability, enhancement with 0.4% STPP and 0.5% NaCl allowed for improvements in palatability while minimizing the color deterioration associated with phosphate/salt enhancement.     

Textural assessment of clenbuterol treatment in beef

Eight Charolais heifers (ca. 300 kg) were fed a diet containing either 0 (control) or 1 ppm clenbuterol during 5 weeks. Daily live weight gain was higher (p<0.01), by about 34%, in treated animals. They were slaughtered after a week of withdrawal. Activity of μ-calpain of meat from clenbuterol-fed heifers was lower (p<0.01) immediately post mortem, while activity of calpastatin was higher (p<0.05) than in meat from controls. According to sensory and instrumental data, meat from clenbuterol-fed heifers did not tenderise during aging, and was tougher (p<0.05) than control meat at 8th day post mortem. Both principal component analysis and multivariate discriminant analysis of a pool of data of the textural profile showed differences due to clenbuterol treatment at 24 h. The slope after yield (calculated from the Warner–Bratzler shearing force–deformation curve), was the only textural parameter affected (p<0.05) at 24 h by the treatment.     

Relationship of texture profile analysis and Warner-Bratzler shear force with sensory characteristics of beef rib steaks

Cyclical texture profile analysis (TPA) parameters measured using a star-shaped probe with two cycles of 80% penetration and Warner-Bratzler shear force (WBS) were compared as predictors of objective tenderness and subjective sensory characteristics of rib steaks from 52 beef loins. The TPA parameters of hardness, cohesiveness and chewiness were negatively correlated (P<0.05) with trained panel sensory characteristics of initial tenderness (r=−0.64, −0.41, −0.62, respectively), amount of connective tissue (r=−0.57, −0.27, −0.55, respectively), overall tenderness (r=−0.68, −0.39, −0.64, respectively) and overall palatability (r=−0.56, −0.37, −0.53, respectively). These sensory characteristics were also negatively correlated (P<0.05) with WBS (r=−0.61, −0.49, −0.60, −0.56, respectively). Stepwise regression analysis generated prediction equations that included the TPA parameters of hardness and adhesiveness, which accounted for 47, 36, 51 and 38% of the variation in initial tenderness, amount of connective tissue, overall tenderness and overall palatability, respectively. Prediction equations using WBS accounted for 37, 24, 36 and 31% of the variation in initial tenderness, amount of connective tissue, overall tenderness and overall palatability, respectively. Hence, TPA explained more of the variation in subjective sensory tenderness of the rib steaks than WBS.     

Evaluation of feedlot cattle working chute behavior relative to temperament,tenderness, and postmortem proteolysis

The objective was to investigate if the association between working chute behavior and beef tenderness found in our previous study is related to protein degradation and calpain system activity. Crossbred steers (n = 183) allotted to 16 pens were weighed every 28 d. Temperament was evaluated as exit velocity (EV), chute score (CS), and catch score (CAPS). Between 14 and 16 mo of age (606 ± 52 kg), steers were harvested. Strip steaks were collected and aged for 14 d. Subsamples were collected at 36 h and 7 d postmortem and analyzed for calpastatin activity, μ-calpain autolysis, and troponin-T degradation. Shear force (WBSF) was correlated (P < 0.05) with calpastatin activity and measurements of troponin-T. Calpastatin activity, μ-calpain autolysis, and troponin-T measurements did not correlate with the measurements of EV, CS, and CAPS. Therefore, activation of the calpain system or differences in protein degradation did not appear to influence the differences in tenderness that are correlated with working chute behavior.     

Effect of low voltage electrical stimulation of pig carcasses and ageing on sensory attributes of fresh pork

The effect of electrically stimulating pig carcasses and ageing on sensory attributes of pork was evaluated in this study. A total of 48 female pigs [Duroc×Large White/Landrace (A; n=24) and Large White/Landrace (B; n=24)] were randomly allocated immediately prior to slaughter to one of two low voltage stimulation treatments; no stimulation or 150 mA applied for 30 s at 2 min post-exsanguination. Each side of the carcass was then randomly allocated to an ageing treatment of either 2 or 7 days post-slaughter. Muscle pH of the M. longissimus lumborum was lower (P<0.001) in electrically stimulated carcasses when measured from 40 min to 8 h post-slaughter compared with non-stimulated carcasses. Percentage drip loss, muscle lightness and PSE incidence were not influenced (P>0.05) by electrical stimulation. Electrical stimulation of pig carcasses and ageing pork for 7 days post-slaughter both improved (P<0.001) consumer scores for tenderness, juiciness, overall liking and quality category, however the interaction term of electrical stimulation and ageing was not significant for any of the sensory attributes. Pork from non-stimulated carcasses that was aged for 2 day post-slaughter was less tender (P<0.01) compared with pork in all other treatments. These results indicate that electrical stimulation (150 mA applied for 30 sec at 2 min post-exsanguination) was effective in improving eating quality attributes of pork, particularly when pork was aged for only 2 days post-slaughter, without detrimentally affecting colour or drip loss.     

The effect of time and type of electrical stimulation on the calpain system and meat tenderness in beef longissimus dorsi muscle

Effects of type and time of electrical stimulation on the calpain system, sensory and objective meat quality in the M. longissimus thoracis et lumborum from 38 pasture-fed carcasses, were investigated under conventional chilling conditions. High voltage stimulation was applied to whole carcasses at 3 min post-mortem (pm) and to sides at either 40 or 60 min pm, whilst low voltage stimulation was applied to whole carcasses at 3 min pm and to sides at 40 min pm. Unstimulated sides served as controls. The levels of extractable μ-calpain and calpastatin decreased during stimulation by 28-44% and 8-17%, respectively. Shear force and adjusted tenderness score showed that stimulation at 3 min, irrespective of type of stimulation, resulted in significantly tougher meat (P<0.05) which was associated with an rapid rate of pH decline, compared to stimulation at 40 min. Higher calpastatin levels soon after stimulation at 3 min (P < 0.05) and lower μ-calpain level at 24 h pm for high voltage stimulation at 3 min (P<0.05) coincided with the tougher meat. On the other hand, high voltage stimulation at 40 and 60 min resulted in similar tenderness and levels of μ-calpain and calpastatin post-stimulation and 24 h pm. Significantly tougher meat from the control sides, with a higher μ-calpain levels at 24 h pm and similar sarcomere length, compared to those from low voltage stimulation at 40 min (P<0.001), appeared to be linked to the later activation of the calpain system. Results from the current study suggest that early application of stimulation may be associated with a very rapid decline in pH and consequently a reduction in meat quality.     

Effects of nutritional level on pork quality and gene expression of μ-calpain and calpastatin in muscle of finishing pigs

The study was designed to investigate the effects of nutritional level (control diet (CD), 14.19% crude protein, 13.81 MJ of DE/kg; low nutritional level diet (LND), 11.08% crude protein, 12.55 MJ of DE/kg) on pork quality and gene expression of μ-calpain and calpastatin in muscle of finishing pigs. The LND treatment increased drip loss (P < 0.05), had a trend to increase intramuscular fat (IMF) content (P = 0.09), decreased Warner–Bratzler shear force (WBSF) of pork (P < 0.05), improved mRNA level of μ-calpain (P < 0.05) in skeletal muscle, but had no effect on gene expression of calpastatin, compared with the CD treatment. These data suggest that a moderately reduced energy and protein diet increased pork tenderness and intramuscular fat. The increase in tenderness by LND treatment may be partly due to increased gene expression of μ-calpain in muscle.