Agricultural and Food Science, Vol. 18 (2009): 27-34 A G R I C U L T U R A L A N D F O O D S C I E N C E Vol. 18 (2009): 27–34. 27 © Agricultural and Food Science Manuscript received May 2008 Effects of L-carnitine and iron diet supplementations on growth performance, carcass characteristics and blood metabolites in fattening pigs Arkadiusz Pietruszka*, Eugenia Jacyno, Anita Kołodziej, Maria Kawęcka, Czesław Elzanowski and Beata Matysiak Department of Pig Breeding, Agricultural University of Szczecin, Doktora Judyma 10 st., 71-460 Szczecin, Poland *e-mail: Arkadiusz.Pietruszka@biot.ar.szczecin.pl The aim of this study was to evaluate the effect of dietary L-carnitine supplementation either with or without extra Fe supplementation from Fe-amino acid (Fe-AA) complex on body weight gain, feed conversion, carcass characteristics and blood metabolite concentrations in fattening pigs. The study was carried out with 75 fatteners (30–100 kg body weight), divided into three groups, of 25 pigs each. The control group was given a basal diet that contained 85 mg/kg of Fe from premix. A L-carnitine group was given a basal diet supplemented with 100 mg/kg of L-carnitine, and a L-carnitine+Fe group was given a basal diet supplemented with 100 mg/kg of L-carnitine and 60 mg/kg of Fe from a Fe-AA complex. The supplement of L-carnitine to the diets did not have any effects on the growth performance and carcass traits. The L-carnitine supplement decreased the concentration of triglycerides (p≤0.05), cholesterol (p ≤0.05) and low-density lipoproteins (p ≤0.01) in the blood serum of pigs, while it increased (p≤0.01) the concentration of high-density lipoproteins. The combination of L-carnitine+Fe increased the growth performance of growing pigs (p ≤0.05) and the lean percentage and fatless ham weight in carcass and also increased (p ≤0.05) the Fe content in the blood serum and the longissimus dorsi muscle of pigs. The results suggest the more effective outcomes can be reached when L-carnitine+Fe rather than only L-carnitine is used in diets. Key-words: L-carnitine, iron, fatteners, growth performance, blood metabolites A G R I C U L T U R A L A N D F O O D S C I E N C E Pietruszka, A. et al. Effects of L-carnitine and iron on pig’s traits 28 A G R I C U L T U R A L A N D F O O D S C I E N C E Vol. 18 (2009): 27–34. 29 Introduction L-carnitine is a vitamin-like compound that is necessary for the transportation of long-chain fatty acids across the inner mitochondrial membrane for β-oxidation (Hoppel 2003). It can be synthesized in the body from protein-bound lysine and methionine. In addition, several cofactors are involved such as iron (Fe+2), ascorbate, niacyn and vitamin B6 (Vaz and Wanders 2002). The synthesis of L-carnitine in mammal or- ganisms is insufficient, thus its requirement should be supplemented by feed ration. The amount of L-carnitine in plant feeds is small (5–29 mg/kg), while much larger quantities (at about 150 mg/kg) are found in feeds of animal ori- gin (Jacobs 2002). At present, pig diets are based first of all on plant components, thus the demand of pigs for L-carnitine might not be covered, and L-carnitine supplementation could be necessary. Studies have demonstrated the beneficial effects of L-carnitine supplementation on the reproduc- tive performance of breeding sows and weaning of piglets (Eder et al. 2001, Ramanau et al. 2004) and the quality of boar semen (Währner et al. 2004, Jacyno et al. 2007). In the studies on the effect of L-carnitine on the growth rate, feed conversion and the quality of pig carcasses, no clear results have been found (Owen et al. 2001a, 2001b, Rekiel and Zackiewicz 2004, Han and Thacker 2006). L-carnitine has a role in the metabolism of lipids, carbohydrates and some amino acids and thus can modify the concentration of metabolites in blood (Grela et al. 2005). One of the most important functions of iron (Fe) is to stimulate the blood-producing system to synthesize hemoglobin and myoglobin, as well as to participate in oxygen transportation by erythro- cytes. The effect of iron on the growth rate, feed conversion and pig carcass quality is ambiguous. Dove and Haydon (1991) and Saddoris et al. (2003) found that pig diet supplementation with iron did not have any effect on the fattening results. In other studies, the positive effect of iron was observed on the daily gain in piglets (Rincker et al. 2004) and fatteners (Liao et al. 2005). Some studies also show that the supplementation of fatteners diet with Fe increases its content in meat and blood as well as positively affecting meat sensory quality (O’Sullivan et al. 2003, Liao et al. 2005, Apple et al. 2007). Iron requirements have not been precisely established for pigs. According to the National Research Council (1998), iron requirements of growing pigs range between 40 and 100 mg/kg. In the European Union, a differential level of iron in the feed for fatteners is used: 80–150 for grow- ing pigs, 65–110 mg/kg for finishing pigs (Lipiński 2007). According to Commission Regulation (No 1334/2003/EC) the maximum content of iron can not exceed 750 (totally) mg/kg of the complete feeding stuff. The aim of this study was to determine the ef- fect of L-carnitine and L-carnitine and iron sup- plementation of fattening pig diets on body weight gain, feed conversion, carcass characteristics and concentration of blood metabolites. Material and methods Animals and feeding The study was carried out at production farm with 75 fatteners, hybrids after Polish Large White × Polish Landrace sows and Pietrain × Duroc and Pietrain × Hampshire boars. The same number of pigs with different sex, genotype and body weight were allotted to three treatments. There were 25 pigs in each treatment group. The animals were housed with litter in pens of five pigs. Feed was provided ad libitum and water was provided by nipple waterers. The pigs were given grower base diets during the fattening period of 30–60 kg body weight and finisher types during the fattening period of 60–100 kg body weight. The basal diet met or exceeded NRC (1998) recommendations for nutrients (Table 1). The basal diets contained a supplement of 85 mg/kg Fe (from premix). The factor distinguishing A G R I C U L T U R A L A N D F O O D S C I E N C E Pietruszka, A. et al. Effects of L-carnitine and iron on pig’s traits 28 A G R I C U L T U R A L A N D F O O D S C I E N C E Vol. 18 (2009): 27–34. 29 respective groups was the content of L-carnitine (Carniking®; Lonza, Ltd, Basel, Switzerland) and Fe (from Fe-AA complex, Polfa Kutno, Ltd, Kutno, Poland) in the diets. Pig fattening was carried out from 30 to 100 kg body weight. During this period, they were weighed three times: at the beginning of fattening, at a body weight of about 60 kg, and before slaugh- ter (at about 100 kg). Average daily gain (ADG), average daily feed intake (ADFI), feed conver- sion (feed:gain ratio) were determined for all pigs throughout the experimented period. Slaughter value All pigs were slaughtered at 100 kg body weight. Carcasses were weighed immediately following slaughter, then chilled at 4 °C for 24 h, and the right side was dissected. Carcass evaluation was conducted according to the Polish Pig Testing Sta- tions methodology. Grower Finisher Ingredients (g/kg) Barley 350 150 Triticale 226 427.5 Wheat 150 150 Wheat bran 50 100 Soybean meal 120 53.5 Rapeseed meal 60 90 Soybean oil 15 - Mineral, vitamin and amino acid premixa 29 29 Nutrients Metabolisable energy (MJ/kg) 12.8 12.6 Crude protein (g/kg) 177 156 Crude fibre (g/kg) 32.0 32.9 Crude fat (g/kg) 32.4 21.4 Crude ash (g/kg) 53.4 38.6 Lysine (g/kg) 9.4 7.7 Methionine + cystine (g/kg) 6.1 5.1 Threonine (g/kg) 6.6 5.4 Ca (g/kg ) 7.3 5.3 P (g/kg) 5.9 4.5 Na (g/kg) 1.3 1.1 Fe from premix (mg/kg) 85 85 a The premix supplied the following per kg diet: Mn, 60 mg; Zn, 130 mg; Cu, 25 mg; I, 0.5 mg; Se, 0.3 mg; Fe, 85 mg (analyzed); vitamin A, 9000 IU; vitamin D3, 1000 IU; vitamin E, 87.5 mg; vitamin K, 2 mg; vitamin B12, 25 μg; biotin, 25 μg; niacin, 20 mg; folic acid, 1 mg; choline chloride, 125 mg; pantothenic acid, 20 mg; lysine, 2.4 mg; me- thionine, 0.6 mg; threonine, 1.1 mg. Table1. Composition and nutritive value of basal grower and finisher diets. A G R I C U L T U R A L A N D F O O D S C I E N C E Pietruszka, A. et al. Effects of L-carnitine and iron on pig’s traits 30 A G R I C U L T U R A L A N D F O O D S C I E N C E Vol. 18 (2009): 27–34. 31 Meat content was estimated as follow: y = 1.745x1 + 0.836x2 + 0.157x3 – 1.884 where: y – weight of meat in right carcass side (kg), x1 – weight of fatless ham (kg), x2 – weight of longissimus muscle (kg), x3 – double width + height of the longissimus muscle (cm). For determining the content of Fe, samples of the longissimus dorsi muscle were collected from the section between lumbar vertebra 2 and 4. Also blood samples were collected from the pigs during slaughter for biochemical analyses. Chemical analysis Basic nutrients in feeds were determined by standard methods (AOAC, 1995), while amino acids with a Beckman automatic analyser. Phosphorus (P) was assayed by the vanadium-molybdenum photocalori- metric method, whereas calcium (Ca) and sodium (Na) through an emission spectrometry method on a BUCK Scientific spectrophotometer. The content of Fe in premix, Fe-AA complex and the longis- simus dorsi muscle was determined by the emis- sion spectrometry method in inductively coupled argon plasma (ICP-OES) on an Optima 2000 DV spectrophotometer (PerkinElmer Instruments INC, Waltham, USA). Metabolites in the blood serum: glucose, total protein, triglycerides, total cholesterol, high-density lipoproteins, low-density lipoproteins, as well as iron were determined by spectrophoto- metric methods with a PRO-Bio spectrophotometer (Marcel) using Alpha Diagnostics reagents. Statistical analysis The obtained data was analysed statistically by means of the STATISTICA 6.0 PL computer software using one-way analysis of variance. The significance of differences between the feeding groups was evaluated with the Duncan test. Results In the fattening period 30–60 kg, pigs fed a diet supplemented with L-carnitine and Fe from Fe-AA complex had higher (p≤0.05) AGD than the fatten- ers of other two groups, whereas, feed conversion was 0.32 kg less (p≤0.05) than control group and 0.21 kg less than the group of L-carnitine (Table 2). In the fattening period 60–100 kg, as well as in the whole fattening period (30–100 kg), ADG, ADFI and feed:gain ratio in all feeding groups were similar. Carcass characteristics of fatteners are present- ed in Table 3. The pigs obtaining a L-carnitine+Fe (as Fe-AA complex) supplement, when compared to the control group and L-carnitine, were char- acterised by a better meatiness (p≤0.05) and a higher weight of fatless ham, respectively at 4.5% (p≤0.05) and 3.4%. The pigs of L-carnitine+Fe group also had a slightly larger area of longissimus dorsi muscle and a slightly thinner backfat. The pigs fed a diet with L-carnitine+Fe had increased Fe concentration in the longissimus dorsi muscle of these animals (p≤0.05). The carcass traits of pigs obtaining 100 mg L-carnitine in 1 kg feed did not differ significantly when compared with the control group. The effect of the applied supplements on me- tabolites in the blood serum is presented in Table 4. The supplementation of diet with L-carnitine and L-carnitine+Fe decreased the concentration of triglycerides (by 10.9%, p≤0.05, and 15.6%, p≤0.05, respectively), total cholesterol (by 10.3%, p≤0.05, and 7.0%, respectively), low-density lipo- proteins (by 18.8%, p≤0.01, and 16.3%, p≤0.01, respectively) and glucose (by 3.9 and 12.3%, re- spectively; non-significant differences). On the other hand, the concentration of high-density lipo- proteins in the blood serum of pigs fed L-carnitine and L-carnitine+Fe diets was higher (p≤0.01) by 24.7 and 26.0%, respectively when compared to the control group. The combination of L-carnitine+Fe supplementations increased the Fe concentration in the blood serum of these animals (p≤0.05). A G R I C U L T U R A L A N D F O O D S C I E N C E Pietruszka, A. et al. Effects of L-carnitine and iron on pig’s traits 30 A G R I C U L T U R A L A N D F O O D S C I E N C E Vol. 18 (2009): 27–34. 31 Treatment1 Control L-carnitine L-carnitine+Fe SEM.c N 25 25 25 Grower phase (30 to 60 kg) Body weight (kg) 30.0 30.0 30.0 0.262 ADG (kg) 0.64 b 0.66b 0.72a 0.046 ADFI (kg) 1.96 1.97 1.96 0.186 Feed:gain 3.14b 3.03ab 2.82a 0.025 Finisher phase (60 to100 kg) Body weight (kg) 60.0 60.0 60.0 0.311 ADG (kg) 0.76 0.76 0.71 0.062 ADFI (kg) 2.66 2.72 2.53 0.228 Feed:gain 3.54 3.62 3.67 0.023 Overall (30 to 100 kg) ADG (kg) 0.70 0.71 0.71 0.053 ADFI (kg) 2.31 2.35 2.24 0.242 Feed:gain 3.34 3.30 3.20 0.028 1 In each treatment, basal diet contained 85 mg/kg of Fe from mineral premix. L-carnitine supplementation was 100 mg/kg, and Fe sup- plementation 60 mg/kg from Fe-amino acid complex. a,b means marked with different small letters are significantly different, p≤0.05 c Standard error of the mean Table 2. Growth performance of pigs fed diets supplemented L-carnitine or L-carnitine and iron. Treatment Control L-carnitine L-carnitine+Fe SEMc N 25 25 25 Slaughter weight (kg) Carcass length (cm) Dressing percentage Meat in right carcass side (kg) Fatless ham weight (kg) Longissimus muscle weight (kg) Longissimus muscle area (cm2) Backfat thickness (cm) - above shoulder blade - on the back Percentage lean Fe in longissimus muscle (mg/kg) 100 82.8 78.3 21.12 8.73b 4.30 53.2 3.40 2.02 56.0b 5.72b 100 81.4 80.4 21.17 8.92ab 4.13 51.4 3.33 1.87 56.8b 5.81b 100 85.0 78.7 21.93 9.12a 4.00 54.9 3.28 1.91 58.5a 6.44a 0.34 0.85 0.37 0.193 0.094 0.054 0.99 0.132 0.057 0.66 0.112 a,b means marked with different small letters are significantly different, p≤0.05 c Standard error of the mean Table 3. Carcass characteristics of pigs fed diets supplemented L-carnitine or L-carnitine and iron. A G R I C U L T U R A L A N D F O O D S C I E N C E Pietruszka, A. et al. Effects of L-carnitine and iron on pig’s traits 32 A G R I C U L T U R A L A N D F O O D S C I E N C E Vol. 18 (2009): 27–34. 33 Discussion In piglets and growing pigs, L-carnitine supplemen- tation led to a reduction in body fat and an increase in body protein (Heo et al. 2000, Owen et al. 2001a, 2001b). This effect is due to an enhanced rate of β-oxidation of long-chain fatty acids. On the other hand, Owen et al. (2001a, 2001b) failed to detect an effect of supplementing 50 or 125 ppm L-carnitine on growth performance of growing pigs. In other studies it was shown that pigs fed a diet supple- mented with 50 ppm L-carnitine had a higher daily gain, better feed conversion, better carcass meatiness and thinner backfat (Rekiel and Zackiewicz 2004). However, in our study, a supplement of 100 mg/kg L-carnitine to the pigs’ diet did not have any effect both on the daily gains and feed conversion and the carcass traits. Similar results were obtained by Han and Thacker (2006) who used a 50 ppm L-carnitine supplement to the diet of finishing pigs. In our study the supplementation of L-carnitine had no effect on the quality of pork carcasses (non-significant statistical differences), however the pig carcasses of fatteners from the L-carnitine group characterised slightly thinner backfat (8%) and slightly higher meatiness in comparison with control groups. L-carnitine supplementation, by promoting β-oxidation of fatty acids, lowered the synthesis of very low-density lipoproteins and decreased the concentrations of triglycerides and total cholesterol (Maccari et al. 1987). In the presented study, and in those of Grela et al. (2005), it was also shown that L-carnitine decreased the concentration of trig- lycerides, cholesterol and low-density lipoproteins, while it increased that of high-density lipoproteins in the blood serum. On the other hand, it was found in other studies that L-carnitine did not differentiate the concentration of triglycerides and cholesterol in the blood plasma of piglets and pregnant sows when compared to control animals (Birkenfeld et al. 2006, Doberenz et al. 2006). Woodworth et al. (2002) and Doberenz et al. (2006) showed that dietary carnitine reduced the concentrations of insulin and glucose in blood plasma, suggesting an enhanced glucose tolerance. In our study only a slight decrease was observed (statistically non-significant) in the concentration of glucose in the blood serum of fatteners obtaining the L-carnitine supplement in their diet. Treatment Control L-carnitine L-carnitine+Fe SEMc N 25 25 25 Glucose (mmol/L) Total protein (g/L) Triglycerides (mmol/L) Total cholesterol (mmol/L) High-density lipoproteins (mmol/L) Low-density lipoproteins (mmol/L) Fe (µmol/L) 8.26 75.6 0.64b 3.01b 0.73B 2.02B 15.7b 7.94 76.6 0.57a 2.70a 0.91A 1.64A 14.8b 7.24 78.2 0.54a 2.80ab 0.92A 1.69A 21.5a 0.159 0.49 0.014 0.036 0.016 0.016 0.79 A,Bmeans marked with different big letters are significantly different, p≤0.01; a,bmeans marked with different small letters are significantly different, p≤0.05 c Standard error of the mean Table 4. Serum metabolites of pigs fed diets supplemented L-carnitine or L-carnitine and iron. A G R I C U L T U R A L A N D F O O D S C I E N C E Pietruszka, A. et al. Effects of L-carnitine and iron on pig’s traits 32 A G R I C U L T U R A L A N D F O O D S C I E N C E Vol. 18 (2009): 27–34. 33 The results of the presented study show that a supplement of 85 mg/kg Fe (from premix) to the basal diet (in accordance with NRC, 1998) can be insufficient for growing pigs. An increase of its lev- el by 60 mg/kg Fe in the diet raised daily gains and feed conversion in pigs in the 30–60 kg body weight fattening period, while it did not have any effect on growth performance in the finishing pigs. Rincker et al. (2004) observed a linear increase in ADG as supplemental Fe increased from 0 to 150 ppm in nursery pigs. On the other hand, Dove and Haydon (1991) failed to detect an effect of supplementing 50 to 300 ppm Fe on growth performance of nurs- ery pigs. Daily gains and feed conversion did not depend on 30 to 120 ppm Fe in the pig diet either (Yu et al. 2000, Saddoris et al. 2003). Apple et al. (2007) found that 50 to 150 ppm Fe supplement in the grower and finisher diet increased the daily gains of growing pigs (55–68 kg BW), while not having any effect on growth performance in the finishing pigs. On the other hand, Liao et al. (2005) found a rise of growth performance in 50 to 100 kg BW pigs obtaining the chelated Fe (1 g/kg diet). Very little information is available concerning the effects of dietary Fe on pork carcass charac- teristics. Saddoris et al. (2003) observed that sup- plementing pig diets with 90 ppm Fe did not affect average backfat depth and longissimus muscle area, whereas Apple et al. (2007) observed a lin- ear increase in 10th-rib fat depth as supplemental Fe from 50 to 150 ppm in diets. Our study showed a favourable effect of L-carnitine+Fe (as Fe-AA complex) supplement on the quality of pork car- casses. They were characterised by a higher lean percentage, larger fatless ham weight as well as by slightly thinner backfat when compared to control group pigs that obtained 100 mg/kg L-carnitine in their diet. It was shown that the diet supplement of Fe increased the Fe concentration in the blood serum of nursery pigs (Rincker et al. 2004), while the supplement of chelated iron increased the Fe con- centration in the longissimus dorsi muscle (Liao et al. 2005). Similar results were also shown in our study. Conclusions The results of the presented study show that a sup- plement of 100 ppm L-carnitine to the diet does not have any effect on the growth performance of growing and finishing pigs and the carcass traits, while it decreases the concentration of lipids in blood. The combination of L-carnitine+Fe sup- plementations increased the growth performance of growing pigs and had a favourable effect on the carcass meatiness traits. References AOAC 1995. 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