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Journal ArticleDOI

Different periods of feed restriction before compensatory growth in Belgian Blue bulls: I. animal performance, nitrogen balance, meat characteristics, and fat composition.

01 Jan 1998-Journal of Animal Science (American Society of Animal Science)-Vol. 76, Iss: 1, pp 249-259
TL;DR: Cattle exhibiting compensatory growth had higher redness, yellowness, cooking losses, and drip losses, but had lower Warner-Bratzler peak shear force values and the saturated fatty acid content of the fat decreased with the duration of the LGP.
Abstract: Thirty double-muscled Belgian Blue bulls were maintained at a rate of gain of .5 kg/d during four periods of time, 115 (G2), 239 (G3), or 411 (G4) d (low growth period, LGP), before fattening (rapid growth period, RGP). Ten control animals (CG) were fed a diet rich in energy and protein. The G2, G3, and G4 were fed a diet low in energy and protein and the same diet as CG during RGP. Live weight was recorded biweekly, feed intake (FI) daily, and nitrogen balance at three times for each group. At the slaughterhouse, the 7, 8, and 9th ribs were removed to determine carcass composition, meat quality, and meat and fat composition. Compensatory growth reached a maximum 2 mo after refeeding and then decreased rapidly, leading to a sharp increase in the feed conversion ratio. Nitrogen balance was higher in compensating groups ( P < .05). Compensating animals had higher carcass connective and adipose tissue contents (P < .05) but lower meat fat content (P < .05). Cattle exhibiting compensatory growth had higher redness, yellowness, cooking losses, and drip losses, but had lower Warner-Bratzler peak shear force values. The saturated fatty acid content of the fat decreased with the duration of the LGP. During the first 2 mo after refeeding, compensatory growth in double-muscled bulls was ascribed to one or more of the following mechanisms: higher FI, lower maintenance requirements, or better efficiency of lean meat production. Compensatory growth at the expense of higher FI increased peripheral fat but decreased intramuscular fat deposition.

Summary (2 min read)

Introduction

  • The Belgian Blue breed, double-muscled type, is a large beef breed with early maturity, characterized by high average daily gain, low feed conversion ratio, and high quality of carcass (Clinquart et al., 1991) .
  • Therefore, an experiment was conducted with Belgian Blue bulls in order to study the effects of a restricted growth, lasting for three different durations, on fattening performances.
  • This paper summarizes animal performance, nitrogen balance, and carcass, meat, and fat characteristics.

Animals and Management

  • The Animal Care and Use Council of their institute approved the use and treatment of animals in this study.
  • A total of 40 Belgian Blue bulls, double-muscled type, initial age and weight range of 9.7 mo and 310 ± 38 kg, were divided into four groups of similar live weight.
  • In each group, four animals were randomly penned in individual stalls allowing for collection of urine and feces, and the remaining page -4-six were housed in a stanchion barn with straw as bedding.
  • The concentrate diet was offered during the rapid growth period (RGP) which lasted until the animals were slaughtered.

Measurements

  • Feed intake of the bulls was recorded each day and live weight at 15-d intervals.
  • At the slaughterhouse, abdominal fat was removed from the carcass.
  • Carcass weight was recorded and pH of both Longissimus thoracis muscles were measured (7, 8, 9 ribs) 1, 2, and 4 h postmortem using a Portamess 751 knick pH-meter (Knick page -5-GmbH & Co, Berlin, Germany) with an Ingold "penetration" pH-electrode (Ingold AG, Urdorf, Switzerland).
  • Seven days later, the cut was weighed in order to estimate drip loss, and heated in open plastic bags in a waterbath for 50 min at 75°C.
  • The fatty acid composition of fat samples was determined by gas chromatography.

Statistical Analysis and Mathematical Modelling

  • Data relative to muscle, connective and adipose tissue, page -6-and bone proportions in the carcasses were compared by analysis of covariance, using group as factor of variation and slaughter weight as factor of covariance.
  • Nitrogen balances either performed during LGP, after the transition period or before slaughter were compared at similar live weight using contemporary weight as factor of covariance.
  • Modelled evolution of the ADG over time was presented, assuming a quadratic evolution during the LGP and a cubic evolution during the RGP.
  • The evolution of ADG during compensatory growth was also studied by GLM procedure of SAS (SAS, 1990) , using group and month after the beginning of the compensatory growth as factors of variation.
  • Predicted maxima and minima were obtained from the model of compensatory growth by derivative of the function obtained from analysis.

Results

  • Table 2 summarizes the performance of the four groups during both periods.
  • Total feed consumption (FC) differed to a large extent because length of the LGP was different.
  • During RGP, ADG was higher in all three groups than in CG.

page -8-

  • The change with time of live weight gain, modelled evolution of the ADG determined between weight records, and FC are given in figure 2 .
  • The maximum ADG after realimentation was close to 2 kg/d in G2 and decreased rapidly.
  • Table 4 summarizes the effects of treatment on slaughter characteristics and carcass composition.
  • As the final live weight of animals from G4 was greater than in the other groups, their live weight at the slaughterhouse and carcass weight were higher (447 kg vs almost 400 kg in the other groups, P < .01).
  • The subcutaneous fat was richer in monounsaturated fatty acids (MUFA).

Discussion

  • It was therefore necessary to further reduce feed intake.
  • Lopez Saubidet and Verde (1976) discarded compensatory feed intake as explanation for compensatory growth after long periods of page -12-growth restriction.
  • Neither G2, G3, nor G4 showed improved FCR as compared to CG during the RGP.
  • The authors results have to be related to the higher fat percentage in the carcass of compensatory groups animals.
  • At heavier weights, as found during the fattening period in G4, the capacity for fat deposition is enhanced (Rompala et al., 1985; Simon, 1989) .

Implications

  • The reduction of growth in a growing fattening system with double-muscled bulls may be beneficial under some conditions.
  • An almost complete compensatory growth was observed when the low growth period was relatively short, overcompensation being difficult to obtain.
  • Growth potential seemed to be maintained until advanced age.
  • Meat was leaner and fat richer in unsaturated fatty acids.
  • Further trials need to be conducted with a large size beef breed in order to locate the period of growth restriction in the pattern of overall growth curves.

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page -1-
COMPENSATORY GROWTH IN DOUBLE MUSCLED BULLS
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Different Periods of Feed Restriction Before Compensatory Growth in Belgian Blue Bulls:
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I. Animal Performance, Nitrogen Balance, Meat Characteristics and Fat Composition
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J. L. Hornick
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, C. Van Eenaeme, A. Clinquart, M. Diez, and L. Istasse
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Department of Nutrition, Veterinary Faculty, Sart Tilman
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B43 4000 Liège, Belgium
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Phone: 32-(0)4-3664139
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Fax: 32-(0)4-3664122
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E-mail: HORNICK@.STAT.ULG.FMV.AC.BE.
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The IRSIA (Institut pour l'Encouragement de la Recherche dans l'Industrie et l'Agriculture,
Brussels, Belgium) is gratefully acknowledged for financial help.
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To whom correspondence should be addressed.

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ABSTRACT: Thirty double-muscled Belgian Blue bulls were maintained at a rate of gain of .5 kg/d
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during four length of time, 4 (G2), 8 (G3) or 14 (G4) mo (low growth period, LGP), before fattening
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(rapid growth period, RGP). Ten control animals (CG) were fed a high-energy, high-protein diet. The
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G2, G3, and G4 were fed a low-energy, low-protein diet during LGP and the same diet as CG during
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RGP. Live weight was recorded biweekly, feed consumption (FC) daily, and nitrogen balance at 3
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occasions in each group. At the slaughterhouse, the 7, 8, and 9th ribs were removed to determine
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carcass composition, meat quality, and meat and fat composition. Compensatory growth reached a
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maximum 2 mo after refeeding. The G2 and G4 exhibited compensatory growth ( P < .05) and had
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higher daily FC ( P < .001). Feed conversion ratio (FCR) increased sharply after refeeding. Nitrogen
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balance was higher in compensating groups ( P < .05). Compensating animals had higher carcass
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connective and adipose tissue contents ( P < .05) but lower meat fat content (P < .05). Cattle exhibiting
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compensatory growth had higher redness, yellowness, hue, cooking losses and drip losses, but tended
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to have lower Warner-Bratzler peak shear force (WBPSF) values. The saturated fatty acid (SFA)
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content of the fat decreased with the length of the LGP. Compensatory growth in double-muscled bulls
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at the expense of higher feed intake increased peripheral fat but decreased intramuscular fat deposition.
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Key Words: Belgian Blue Bulls, Compensatory Growth, Animal Performance, Carcass, Meat, Fatty
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Acids
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Introduction
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Compensatory growth is the ability of an animal to exhibit, after disease (Thomas et al., 1978) or
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feed restriction (Wilson and Osborn, 1960), larger growth rates than in unaffected animals of the same
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chronological age. In cattle, compensatory growth is well expressed when feed restriction occurs at a
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relatively late stage of life (Berge, 1991; Berge et al., 1991). Factors contributing to compensation are
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increases in feed intake (Baker et al., 1992), increases in gut-fill weight, or higher efficiency of feed
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utilization (Carstens et al., 1991). The response varies according to the pattern of undernutrition and
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realimentation, and stage of development of the animal (Wilson and Osborne, 1960). The Belgian Blue
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breed, double-muscled type, is a large beef breed with early maturity, characterized by high average
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daily gain, low feed conversion ratio, and high quality of carcass (Clinquart et al., 1991). Currently,
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there is no published work on compensatory growth in Belgian Blue bulls. Therefore, an experiment
12
was conducted with Belgian Blue bulls in order to study the effects of a restricted growth, lasting for
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three different durations, on fattening performances. Results are presented in 2 papers. This paper
14
summarizes animal performance, nitrogen balance, and carcass, meat, and fat characteristics.
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Materials and Methods
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Animals and Management
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The Animal Care and Use Council of our institute approved the use and treatment of animals in
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this study. A total of 40 Belgian Blue bulls, double-muscled type, initial age and weight range of 9.7
21
mo and 310 ± 38 kg, were divided into four groups of similar live weight. In each group, four animals
22
were randomly penned in individual stalls allowing for collection of urine and feces, and the remaining
23

page -4-
six were housed in a stanchion barn with straw as bedding. Each group was randomly assigned to one
1
of the four treatments. The first group (control, CG) was given from the beginning ad libitum access to
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a fattening diet allowing for rapid growth. The fattening diet was based on sugar beet pulp
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complemented with cereals, protein from vegetable origin, and a mineral mixture (Table 1). During
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three periods with different lengths of time, the other groups received a limited quantity of a low-
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energy, low-protein diet calculated to support an ADG of .5 kg daily gain (LGP, low growth period).
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The low growth diet was based on pelleted straw complemented with dried lucerne, cereals, protein
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from vegetable origin, and mineral mixture. The three groups, namely groups 2, 3, and 4 (G2, G3, G4),
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received the low-growth diet for 115, 239, and 411 d, respectively. Subsequently, G2, G3 and G4 were
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adapted to the concentrate fattening diet over a 15-d period of transition. The amount of concentrate
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feed was then progressively increased and animals were allowed to consume their ration on an ad
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libitum basis for about 1 mo after the beginning of the transition period. The concentrate diet was
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offered during the rapid growth period (RGP) which lasted until the animals were slaughtered. The
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animals were fed twice daily at 0600 and 1400 and were slaughtered per group when mean live weight
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reached at least 600 kg and when the average daily gain (ADG) was lower than 1 kg/d at two
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consecutive measurements.
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Measurements
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Feed intake of the bulls was recorded each day and live weight at 15-d intervals. Feed samples
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were withdrawn at regular intervals for chemical analysis. At the slaughterhouse, abdominal fat was
20
removed from the carcass. Carcass weight was recorded and pH of both Longissimus thoracis muscles
21
were measured (7, 8, 9 ribs) 1, 2, and 4 h postmortem using a Portamess 751 knick pH-meter (Knick
22

page -5-
GmbH & Co, Berlin, Germany) with an Ingold "penetration" pH-electrode (Ingold AG, Urdorf,
1
Switzerland).
2
Two days after slaughter, the 7, 8, and 9th ribs were removed from the carcass. They were
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dissected in order to separate lean meat, fat and connective tissue, and bones. Regressions of Martin
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and Torreele (1962) for double muscled cattle were then used to assess the composition of the carcass.
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Meat quality was determined from one 2.5-cm-thick cut of the longissimus thoracis muscle. Five
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measurements of the final pH were performed on this cut at 48 h postmortem using the technique
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described above. At the same time, the HunterLab Labscan II device was used for objectively
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measuring CIE Lab brightness (L*), redness (a*) and yellowness (b*) on 5 spots 2.5 cm diameter. Hue
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was estimated by a*/b* ratio. Seven days later, the cut was weighed in order to estimate drip loss, and
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heated in open plastic bags in a waterbath for 50 min at 75°C. After heating, they were cooled in cold
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tap water to room temperature, bags were drained, and cuts were mopped gently dry with paper tissue.
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The difference between raw and heated weights was recorded as cooking loss and expressed as a
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percentage of the raw weight. Warner-Bratzler shear force was determined with a Lloyd LR5K
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perpendicular to the fiber direction on 10, 1.25-cm-diameter cores obtained from the heated cuts.
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The dry matter, ash, ether extract, and crude protein concentrations of the diets were determined
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according to official procedures (AOAC, 1975). The lipids from peripheral, intermuscular and
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intramuscular fat samples were extracted and saponified as described by Ter Meulen et al. (1975). The
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fatty acid composition of fat samples was determined by gas chromatography.
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Statistical Analysis and Mathematical Modelling
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Bulls were blocked (n = 10) by group (Figure 1). One-way analysis of variance, using group as a
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factor of variation, was used to analyze data. Data relative to muscle, connective and adipose tissue,
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Abstract: Compensatory growth (CG), an accelerated growth phenomenon which occurs following a period of dietary restriction is exploited worldwide in animal production systems as a method to lower feed costs. However the molecular mechanisms regulated CG expression remain to be elucidated fully. This study aimed to uncover the underlying biology regulating CG in cattle, through an examination of skeletal muscle transcriptional profiles utilising next generation mRNA sequencing technology. Twenty Holstein Friesian bulls were fed either a restricted diet for 125 days, with a target growth rate of 0.6 kg/day (Period 1), following which they were allowed feed ad libitum for a further 55 days (Period 2) or fed ad libitum for the entirety of the trial. M. longissimus dorsi biopsies were harvested from all bulls on days 120 and 15 of periods 1 and 2 respectively and RNAseq analysis was performed. During re-alimentation in Period 2, previously restricted animals displayed CG, growing at 1.8 times the rate of the ad libitum control animals. Compensating animals were also more feed efficient during re-alimentation and compensated for 48% of their previous dietary restriction. 1,430 and 940 genes were identified as significantly differentially expressed (Benjamini Hochberg adjusted P < 0.1) in periods 1 and 2 respectively. Additionally, 2,237 genes were differentially expressed in animals undergoing CG relative to dietary restriction. Dietary restriction in Period 1 was associated with altered expression of genes involved in lipid metabolism and energy production. CG expression in Period 2 occurred in association with greater expression of genes involved in cellular function and organisation. This study highlights some of the molecular mechanisms regulating CG in cattle. Differentially expressed genes identified are potential candidate genes for the identification of biomarkers for CG and feed efficiency, which may be incorporated into future breeding programmes.

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Q1. What contributions have the authors mentioned in the paper "Compensatory growth in double muscled bulls" ?

Hornick et al. this paper investigated different periods of feed restriction before compensatory growth in Belgian Blue Bulls.