1. Introduction
Fat addition to diets is important for growing-finishing pigs because of the high-energy value of the diet. In addition, supplementing 1 to 2% fat in the diet will reduce dust in feed and wear of mixing equipment and augurs [
1]. For pig diets, there is a wide range of fat sources available. Animal fats, such as beef tallow and lard, are less expensive than vegetable oils, and thus are widely used. However, animal fat has higher saturated fatty acids (SFAs) than vegetable oils.
Consumer preference has increased for products with higher levels of unsaturated fatty acids (UFAs). Because research has confirmed that the increased intake of n-3 fatty acids (FAs) can decrease the risk of heart disease and vascular disorders and can improve the clinical features of some autoimmune and inflammatory disorders [
2]. Sakuma and Yamaguchi [
3] and Wong et al. [
4] recommended that an adequate intake of n-3 polyunsaturated fatty acids (PUFAs) is 1.6 g/day for men and 1.1 g/day for women. The n-6/n-3 PUFA ratio should be less than 5 [
5,
6]. The most important n-3 FAs are α-linolenic acid (ALA), eicosapentaenoic (EPA), and docosahexaenoic (DHA) acids. These acids can be accreted in animal tissue directly from the feed. The EPA and DHA can be synthesized from precursor α-linolenic acid [
7].
The fatty acid profile of pork directly reflects the FA profile of the pig diet [
8]. Vegetable oils such as soybean or rapeseed oil contain high levels of UFAs and may lead to healthier products for consumers [
9]. On the other hand, the incorporation of PUFAs into the diet is restricted by the resulting decrease in lipid oxidative stability [
10], which influences taste, flavour, colour [
11], and shelf life [
12]. Moreover, feed with a high level of vegetable oil that is rich in UFAs affects the fat consistency (soft and sticky), and thus decreases the quality of meat products [
13].
The aim of this study was to evaluate the effect of two sources of fat, and the duration of supplementing the pig diet on physical characteristics, FA profile, and lipid oxidative stability of backfat.
2. Materials and Methods
2.1. Animals and Experimental Design
The study was conducted in the pig breeding test station at the Czech University of Life Sciences Prague (Czech Republic). The experiment was approved by the Ethics Committee of the Central Commission for Animal Welfare at the Ministry of Agriculture of the Czech Republic (Prague, Czech Republic) and was carried out in accordance with Directive 2010/63/EU for animal experiments. All procedures described in this study were conducted after obtaining the approval by the Local Ethics Commission, case number 08/2015; the experiment was conducted in CZ21038206.
A total of sixty 70-day-old final hybrid DanBred genotype pigs (
n = 10; 1:1 gilt and barrow) at an average live weight of 29.2 kg were included in the experiment. The placing and housing of pigs was performed according to methodology described by Stupka et al. [
14]. The pigs were housed in pens (two pigs of the same sex per pen) and fed with the complete feed mixture, which contained wheat, barley, soybean meal, and premix. Feed mixture was mixed separately for each pen according to the methodology described by Stupka et al. [
14].
The pigs were divided into 6 experimental groups according to the addition of rapeseed or soybean oil and duration of supplying either oil in the pig diet (
n = 10). The pigs were fed the P1 feed mixture without added oil from the beginning of the experiment until 110 days of age. Then, for 2, 4 or 6 weeks before slaughter the pigs were fed the P3 feed mixture with rapeseed (40 g/kg) or soybean oil (40 g/kg). The groups receiving feed supplemented with oils for 2 or 4 weeks before slaughter were fed the P2 diet until old enough to receive the supplemented P3 diet. The composition and nutritional values of each feed is shown in
Table 1 and
Table 2. The pigs from all groups were fed ad libitum throughout the experiment.
2.2. Carcass Value and Sampling
For the determination of qualitative and quantitative carcass value traits, a carcass analysis of all 60 pigs according to Scheper and Scholz [
15] was carried out. For the physical characteristics, fatty acid composition and oxidative stability of backfat, samples from the section between the 1st and 3rd cervical vertebrae were taken. Backfat for fatty acid analysis and oxidative stability was frozen and stored at −80 °C (Jouan HX450S, Trigon-plus, Říčany, Czech Republic) until the analysis.
2.3. Physical Characteristics
The colour parameters of lightness (L*; 0 = black, 100 = white), redness (a*; −100 = green, 100 = red), and yellowness (b*; −100 = blue, 100 = yellow) of backfat were measured using a Minolta CM-700d spectrophotometer (Minolta Ltd., Osaka, Japan) 24 h post mortem. The perforation of the upper (between skin and 1st fascia) and lower (under the 1st fascia) part of backfat was detected 24 h post mortem using an Instron Model 3342 (Instron, Norwood, MA, USA) with the injection probe. Each sample was perforated with 6 injections above and 6 under the fascia. The crosshead speed was 200 mm/min with a pressure elongation of 22 mm and sampling rate of 20 mm/s. The maximum perforation (N) was detected.
2.4. Fatty Acid Analysis
The methyl esters of fatty acids after the extraction of total lipids were detected according to the methodology of Folch et al. [
16]. Methanolysis was carried out in the presence of KOH and extraction of the acids in the form of methyl esters into heptane. Isolated methyl esters were detected by a flame ionization detector (FID) using the split regime of the chromatography Master GC (Dani Instruments, S.P.A., Milano, Italy) equipped with the Famewax column with polyethylene glycol (Famewax; 30 m × 0.32 mm × 0.25 μm) as the stationary phase. Helium was used as the carrier gas at a constant flow of 5 mL/min, and the split ratio was 1:9. The peaks were identified using Clarity 5.2 and quantified based on known retention times of standards for the Food Industry FAME Mix (Restek Corporation Company, Bellefonte, PA, USA). Atherogenic index (AI) was calculated from monounsaturated fatty acids (MUFA) and PUFA ratio in accordance with the methodology of Chillard et al. [
17] as follows: AI = (C12:0 + 4 × C14:0 + C16:0)/(MUFA + PUFA). The thrombogenic index (TI) was calculated according to Ulbright and Southgate [
18] as follows: TI = (C14:0 + C16:0 + C18:0)/(0.5 × MUFA + 0.5 × n-6 PUFA + 3 × n-3 PUFA + n-3/n-6 PUFA).
2.5. Oxidative Stability
The lipid oxidative stability of backfat was measured immediately after defrosting (0) and the 3rd and 5th days of storage in the fridge at 5 °C. For the extraction, the samples of backfat were homogenized, weighed, and distilled using hydrochloric acid. The results were expressed as thiobarbituric acid reactive substances (TBARS) in mg malondialdehyde (MDA) per kg of backfat. For measuring the absorbance of the colour complex, a Genesys 10vis spectrophotometer (Thermo Fisher Scientific, Madison, Wisconsin, USA) was used at lambda 538 nm against the standard calibration curve 1,1,3,3-tetramethoxypropane.
2.6. Statistical Analysis
The experiment was conducted using a 2 × 3 full factorial design. The main effects were the source of oil (rapeseed or soybean oil), the duration of oil feeding (2, 4 or 6 weeks before slaughter) and the interaction between these two factors. The pen was considered as a random effect. The experimental unit was the pen. The data were evaluated by two-way analysis of variance (ANOVA) with the general linear models (GLM) procedure in the SAS 9.4 software (SAS Institute Inc., Cary, NC, USA). The results are presented as the mean and standard error of the mean (SEM). The differences between traits were considered significant when p ≤ 0.05.
4. Discussion
From the results of the present study, it is evident that the values of backfat perforation significantly decreased after six weeks supplementing the diet with vegetable fats. The negative effect on backfat consistency of feeding with vegetable oils is explained by higher UFA levels in these fat sources [
13]. Consistent with our results, Benz et al. [
19] stated that increasing feeding duration of soybean oil increased the amount of UFAs leading to softer carcass fat. In addition, Gläser et al. [
20] showed that only approximately 30% of the variation in firmness of native backfat could be explained by the fatty acid composition. The amount of superficial fat and therefore thickness of backfat seemed to be more important for firmness of native backfat than its composition. Moreover, there is a strong inverse correlation between the amount of fat and the concentration of PUFAs [
21]. Koczanowski et al. [
22] found that with the increasing thickness of backfat (from 12 to 16 mm), the concentration of SFAs increased (from 37.7 to 40.4%), while the concentration of PUFAs decreased (from 16.1 to 12.9%).
Rapeseed oil is rich in MUFA and has higher levels of n-3 PUFAs while soybean oil has a high C18:2 content and moderate levels of C18:1 and C18:3. In pigs, dietary FAs are absorbed unchanged from the intestine and incorporated into tissue lipids [
23]. Hence, dietary fat influences the FA profile of the adipose tissue [
24]. These data correspond with our findings that dietary rapeseed oil increased n-3 FAs and decreased the n-6/n-3 ratio to 4.5:1, whereas soybean oil increased n-6 FAs in backfat. In accordance with our results, Park et al. [
25], in a study testing soybean oil as a lipid source for pig diets, showed that the content of PUFA, especially n-3 FAs, in the carcass can be linearly increased depending on the length of the feeding period of a diet supplemented with soybean oil. Similar findings were obtained by Stephenson et al. [
26] who stated that increasing the duration of feeding with soybean oil lowered MUFA and increased PUFA concentrations for all fat depots. When pigs are fed diets with n-3 fatty acids, pork and pork products could be recognized as functional foods with new health-promoting properties [
27]. This would change the view of pork, which is considered less healthy because the n-6/n-3 PUFA ratio in the meat from pigs fed a commercial feed exceeds the 5:1 recommended by the World Health Organization for meat with health-promoting properties.
Moreover, rapeseed oil is a rich source of oleic acid (54.5% compared to 21.9% in soybean oil in the present study), which has similar effects as the n-3 FAs. It was demonstrated that oleic acid leads to a reduction in cholesterol levels, risk of atherogenesis and high blood pressure [
28]. In addition, oleic acid induces beneficial anti-inflammatory effects on autoimmune diseases [
29], a protective effect on breast cancer and improvement of immune system function [
30]. In the present experiment, we tested two indicators related to human health, the atherogenic and thrombogenic indices. These indices reflect the probability of an increase in pathogenic phenomena, such as atheroma and thrombus formation. The values of the atherogenic and thrombogenic indices were significantly reduced as the rapeseed or soybean oil feeding period increased. In the case of the thrombogenic index, rapeseed oil was more efficient than soybean oil.
Lipid peroxidation is a complex process that is affected by several factors including the degree of saturation. Lipid sources that contain high concentrations of PUFA are highly susceptible to peroxidation [
12]. Both soybean oil and backfat of pigs fed soybean oil showed a higher percentage of PUFAs in comparison with rapeseed oil. In this study, however, the malondialdehyde content was not influenced by oil source in fresh backfat nor in backfat stored for three or five days. This was probably because these two vegetable oils are not contrasting fats. A surprising finding was that the feeding of vegetable oils for six weeks decreased malondialdehyde content in backfat stored for five days. This can be explained by the higher oleic acid content in these vegetable oils, especially in rapeseed oil, which can reduce lipid oxidation. In addition, soybean oil used in the feed industry is rich in choline, phospholipids, antioxidants and vitamin E, which prevent oxidation [
31]. Similar results were obtained with pork in the study conducted by Alonso et al. [
32].