Abstract
Simple Summary
This study evaluated the dietary effects of extruded linseed and oregano on the quality traits and sensory properties of meat obtained from kids of a Lucanian goat population named “Facciuta Lucana”. Thirty-six male kids were divided into three homogeneous groups fed a control feed (C), a diet containing 3% extruded linseed (L), or 3% linseed plus 0.6% oregano (L + O). Meat from the Longissimus lumborum muscle obtained from linseed-fed groups showed a lower content of fat and total saturated fatty acids and, in turn, an increase in monounsaturated and polyunsaturated fatty acids, and conjugated linoleic acid, with benefits for human health. Oregano addition to the linseed diet proved to be effective in preserving meat shelf-life, since it lowered the malondialdehyde concentration after 10 days of storage, and improved meat succulence, tenderness, juiciness, and overall acceptance.
Abstract
Extruded linseed (Linum usitatissimum) in ruminant diets has been investigated as a strategy to improve the nutritional value and healthiness of meat fat; however, increased polyunsaturated fatty acids may limit the shelf-life of meat. Oregano (Origanum vulgare) has a documented antioxidant activity. The aim of the study was to investigate the effects of dietary supplementation with extruded linseed and oregano on goat milk quality and whether the characteristics of goat milk affect the physical and chemical features, fatty acid profile, meat lipid oxidation, and sensory properties of meat from suckling kids. Thirty-six male kids were weaned and divided into three homogeneous groups (n = 12); each group was either fed a control diet (C), or a diet containing 3% extruded linseed with or without the addition of 0.6% oregano (“L + O” and “L”, respectively). The diets containing linseed lowered (p < 0.05) the saturated fatty acid content in meat, and increased (p < 0.05) monounsaturated and polyunsaturated fatty acids and conjugated linoleic acid. Oregano addition to the linseed diet proved to be effective in preserving meat shelf-life, as shown by a significant (p < 0.01) reduction in the malondialdehyde concentration after 10 days of storage, and improved meat succulence, tenderness, juiciness, and overall acceptance.
Keywords: kids, autochthonous breed, Facciuta Lucana, meat quality, fatty acid profile, sensory quality
1. Introduction
In South Italy, goat farming has been very widespread due to the great ability of goats to adapt to harsh marginal areas. However, in the last decades, many local goat populations have experienced a severe reduction in the number of animals. In the Basilicata region, one of these breeds is the so-called “Facciuta Lucana”, also known by other local names that refer to its most striking feature: two white bands on the muzzle. This breed, according to various testimonies, was present both in family farms consisting of few subjects, as well as in herds of medium proportions, generally not larger than 50 animals. Actually, a total of 95 subjects are present in the whole Basilicata Region (Table S1).
In recent years, an intense research program has been conducted aimed at the recovery and enhancement of the autochthonous sheep and goat populations/breeds of the Basilicata region (Val.Bi.Ovi.Cap. Research project). The preservation of local genotypes is important for rural development and the protection of the environment; furthermore, the association between local breeds and their traditional agri-food products (TAP) represents a great opportunity to convert abandoned marginal areas into sites of cultural interest and food tourism [1].
According to the local traditional rearing system in South Italy marginal areas, kids are raised with their mothers and suckle only dam’s milk until weaning, which generally occurs when they are about 45 days old, in order to use the goat milk for cheese-making. At this age, kids may be slaughtered, providing “capretto” meat, which is greatly appreciated for its organoleptic features [1,2].
The low productive performance of these local breeds is the main reason why breeders have turned their interest towards high-production cosmopolitan breeds; therefore, any attempt to rescue local populations must improve the yield and quality of animal products, while respecting local traditions, through effective feeding strategies.
The dietary inclusion of linseed has been widely investigated in livestock animals, showing effects on meat enrichment in unsaturated fatty acids, especially of the n-3 series, such as α-linolenic acid [3,4,5,6]. However, the greater structural instability of unsaturated fatty acids leads meat to increased lipid oxidation, which results in worsened color, flavor, and shelf life [7]. The extent of lipid oxidation may be reduced using natural antioxidants included in the diet, able to delay and limit the occurrence of oxidation processes. Among the natural antioxidants tested in animal feeding, oregano (Origanum vulgare L.) is a common essence present in South Italy pastures, the antioxidant activity of which is mainly attributed to carvacrol and thymol [8]. In previous studies, we found that dietary supplementation with extruded linseed and oregano was able to enhance meat fat oxidative stability in Garganica [9], Grigia di Potenza [10], and Jonica breed kids [11]. On the contrary, in an experiment carried out on Gentile di Puglia lambs, the inclusion of oregano in the diet did not provide noticeable effects on meat quality traits [12].
The supplementation of ruminant diets with lipid sources rich in polyunsaturated fatty acids (PUFA) is moderately effective in improving the nutritional value of meat fat due to the biohydrogenation of unsaturated fatty acids, which occurs in the rumen [13]. There is general agreement that during the pre-ruminant stage of life, the fatty acid composition of the muscular and adipose tissues reflects that of the milk consumed, as investigated in lambs [14,15] and kids [16]. Since the nutritional properties of ruminant milk are largely affected by the diet [17,18] and by the season [19], the improvement in meat quality in suckling animals is closely related to the enhancement of the dam’s milk quality [20,21].
The aim of the study was to investigate the effects of dietary supplementation with extruded linseed and oregano on goat milk quality and whether the characteristics of goat milk affect the physical and chemical features, fatty acid profile, meat lipid oxidation, and sensory properties of meat from suckling kids of the autochthonous population named “Facciuta Lucana”.
2. Materials and Methods
2.1. Animal Management and Diet
All procedures involving animals were ethically and responsibly conducted, according to the Italian government guidelines (Directive 2003/50/EC, received in Italy by D.L. 193/2005) [22].
The study was carried out during February–April 2020 on a dairy farm located in Gorgoglione (in the province of Matera, Basilicata region, Italy; Latitude: 40.3785846, Longitude: 16.1454083, 700 m a.s.l.).
Two weeks before parturition, in order to allow adaptation to the experimental diets, fifty-one female pluriparous goats of the autochthonous “Facciuta Lucana” breed, homogeneous for weight (52 ± 3 kg) and parity (3–4), were randomly divided into three homogeneous groups (n = 17) and fed the following diets: control feed (“C”); a diet containing 3% extruded linseed (Linum usitatissimum L., “L”), or 3% linseed plus 0.6% dried oregano inflorescences (Origanum vulgare L., “L + O”). The three pelleted feeds were formulated to be isocaloric and isonitrogenous, and to meet or exceed the nutritional requirements of goats [23] (Table 1). The goats received hay ad libitum and 600 g of the pelleted feeds per head/day. Animals had free access to water all the time.
Table 1.
Ingredients (%) | Diet 1 | Hay | ||
---|---|---|---|---|
C | L | L + O | ||
Corn | 31.00 | 31.00 | 30.40 | |
Faba bean | 10.00 | 8.50 | 8.50 | |
Wheat bran | 10.00 | 10.00 | 10.00 | |
Barley | 9.00 | 9.00 | 9.00 | |
Wheat flour shorts | 9.00 | 9.00 | 9.00 | |
Sunflower meal | 8.00 | 7.50 | 7.50 | |
Dehulled soybean | 6.00 | 6.00 | 6.00 | |
Sugar beet pulp | 6.00 | 6.00 | 6.00 | |
Soybean hulls | 4.00 | 4.00 | 4.00 | |
Extruded linseed | - | 3.00 | 3.00 | |
Molasses | 3.00 | 3.00 | 3.00 | |
Vitamin-mineral premix | 3.00 | 3.00 | 3.00 | |
Soybean oil | 1.00 | - | - | |
Oregano | - | - | 0.60 | |
Chemical composition (% on DM basis) |
||||
Crude protein | 15.51 | 15.60 | 15.61 | 10.72 |
Ether extract | 3.66 | 3.70 | 3.71 | 1.37 |
Ash | 3.41 | 3.49 | 3.56 | 9.58 |
Crude fiber | 7.91 | 7.92 | 8.32 | 33.94 |
NDF 2 | 21.19 | 21.24 | 21.15 | 60.38 |
ADF 3 | 9.58 | 9.56 | 9.53 | 37.43 |
ADL 4 | 1.79 | 1.86 | 1.85 | 9.31 |
ME (MJ) | 10.16 | 10.18 | 10.05 | 11.25 |
Fatty acids (% FA methyl esters) |
||||
C16:0 (palmitic) | 9.23 | 7.47 | 7.39 | 13.45 |
C18:0 (stearic) | 1.18 | 3.55 | 4.08 | 3.03 |
C18:1 n-9, cis 9 (oleic) | 17.78 | 18.76 | 17.99 | 12.13 |
C18:2 n-6 (linoleic) | 15.16 | 22.15 | 20.42 | 31.00 |
C18:3 n-3 (α-linolenic) | 4.65 | 31.00 | 30.68 | 2.57 |
C22:5 n-3 (DPA) | 0.46 | 0.17 | 0.27 | 0.00 |
C22:6 n-3 (DHA) | 0.29 | 0.28 | 0.28 | 0.01 |
1 C, control feed; L, feed containing 3% extruded linseed; L + O, feed containing 3% extruded linseed + 0.6% oregano. 2 NDF, neutral detergent fiber; 3 ADF, acid detergent fiber; 4 ADL, acid detergent lignin.
At delivery, three groups of ten male kids born as singletons and homogeneous for live weight (3.50 ± 0.30 kg) were made out from the corresponding goat groups; the kids were reared according to the traditional farming system, suckling only maternal milk ad libitum until weaning, which occurred when kids were about 45 days old. After weaning, kids received ad libitum the same feed administered to their mothers until they were 60 days old.
Beginning on 9 March 2020, the COVID–19 pandemic state was declared in Italy; therefore, it was not possible to assess growth performances during the trial as well as to collect data at slaughtering and carcass sectioning.
The kids were slaughtered altogether, after fasting for 12 h, according to the official veterinary rules. After 24 h of refrigeration (0–4 °C), the carcasses were split into two halves by the mid-line, and the right side was divided into different cuts (neck, shoulder, leg, steaks, and brisket). Loins were transported from the slaughterhouse to the laboratory under refrigerated conditions for analysis of the Longissimus lumborum muscle.
2.2. Chemical Composition of Feed
Representative samples of the pelleted feeds were taken every 20 days and mixed to obtain a single final pool for each diet, which was analyzed to determine the chemical composition and fatty acid profile (Table 1). Samples were ground in a hammer mill with a 1-mm screen and analyzed using the following Association of Official Agricultural Chemistry AOAC [24] procedures: dry matter (method 934.01), ether extract (method 920.39), ash (method 942.05), crude protein (method 954.01), crude fiber (method 945.18), ADF and ADL (method 973.18), and amylase-treated neutral detergent fiber (NDF) (method 2002.04). Metabolizable energy was calculated using the INRA system [23].
2.3. Chemical Composition and Fatty Acid Profile of Milk
On days 10 and 30 after delivery, milk samples were collected from each goat twice a day (at 7:00 am and 6:00 pm) and pooled together within each group. Milk was stored at 4 °C and immediately transported to the laboratory for the analysis of fat, protein, lactose, and total solids using an infrared milk analyzer (Milkoscan 133-B, Foss Electric, Hillerød, Denmark) previously standardized for goat’s milk. Ash content was detected after burning a sample in a muffle furnace at 550 °C for 5 h.
Total lipids were extracted according to the chloroform/methanol method described by Folch et al. [25]. FAs were methylated using a BF3-methanol solution (12% v/v) [26]. The FA profile was assessed by using a Chrompack CP 9000 gas chromatograph, with a silicate glass capillary column (70% cyanopropyl polysilphenylene-siloxane BPX 70 of SGE Analytical Science, length 50 m, internal diameter 0.22 mm, film thickness 0.25 μm). The temperature program was 135 °C for 7 min, followed by increases of 4 °C per minute up to 210 °C. Fatty acid peaks were identified using a comparative analysis with standard reference mixtures. The fatty acid content was expressed as the percentage of total fatty acid methyl esters (FAME).
2.4. Physical Parameters of Muscles
The Longissimus lumborum (Ll) muscle was excised from the right half carcass of each kid in order to assess meat color and tenderness. The whole Ll was split into two halves: the proximal one was used for color readings and tenderness assessment, while the second half was used for lipid oxidation, chemical, and fatty acid analysis.
The color features (L* = Lightness, a* = red index, b* = yellow index) were determined using a Hunter Lab MiniscanTM XE Spectrophotometer (Model 4500/L, 45/0 LAV, 3.20 cm diameter aperture, 10° standard observer, focusing at 25 mm, illuminant D65/10; Hunter Associates Laboratory Inc., Reston, VA, USA). Three readings were taken for each sample by placing the instrument on different meat areas. The instrument was normalized to a standard white tile before performing the analysis (Y = 92.8, x = 0.3162, and y = 0.3322). The reflectance measurements were performed after the samples were allowed to oxygenate in the air for at least 30 min, to take stable measurements [27]. Three samples (1.25 cm in diameter and thickness) of each muscle were tested for tenderness by the Warner-Bratzler Shear (WBS) force system using an Instron 5544 testing machine; samples were assessed in triplicate and perpendicularly sheared in the muscle fiber direction (load cell 50 kg, shearing speed 200 mm/min). Peak force was expressed as kg/cm2 [28].
2.5. Chemical Composition and Fatty Acid Profile of Kid Meat
In order to analyze the chemical composition of meat, representative sub-samples of the Longissimus lumborum muscle from each kid were homogenized [24].
Fat was extracted using a 2:1 chloroform/methanol (v/v) solution to determine the fatty acid profile [25]. The fatty acids were methylated using a KOH/methanol 2N solution [26] and analyzed by gas chromatography (Shimadzu GC-17A, Shimadzu Corp., Kyoto, Japan) using a silicone-glass capillary column (70% Cyanopropyl Polysilphenylene–siloxane BPX 70, length = 60 m, internal diameter = 0.25 mm, film thickness = 0.25 µm by Thermo Scientific, Waltham, MA USA). The starting temperature was 135 °C for 7 min, and then it was increased by 4 °C/min up to 210 °C. Fatty acids were expressed as a percentage (wt/wt) of total methylated fatty acids.
The Conjugated Linoleic Acid (CLA) content in goat milk and kid meat was assessed as previously described [29].
The food risk factors of meat were determined by calculating the Atherogenic (AI) and Thrombogenic (TI) Indices [30]:
AI = [(C12:0 + 4 × C14:0 + C16:0)] ÷ [ΣMUFA + Σn−6 + Σn−3];
TI = [(C14:0 + C16:0 + C18:0)] ÷ [(0.5 × ΣMUFA + 0.5 × Σn−6 + 3 × Σn−3 + Σn−3)/Σn−6];
where MUFA are monounsaturated fatty acids.
Lipid oxidation was evaluated in Longissimus lumborum muscle samples stored at 4 °C for 48 h after slaughtering by measuring the concentration of 2-thiobarbituric acid reactive substances (T-BARS) [31] and expressed as mg malondialdehyde (MDA)/kg meat.
2.6. Sensorial Analysis
The sensory attributes of kid meat were assessed according to the procedures described by Pimentel et al. [32]. The Longissimus lumborum muscle from the left half carcass of each animal was roasted in a pre-heated oven (170 °C) until the meat temperature was 71 °C at the geometric center of the cut, as recorded by a thermocouple (Hanna Instruments, Villafranca Padovana, PD, Italy). Afterward, fragments of the Ll meat were cut into cubes (2 cm3) weighing about 8–10 g and grouped by treatment.
The consumer test was carried out using forty-one untrained persons, that are habitual consumers of meat (21 men and 20 women, aged 18–72 years). During the sensory evaluation, each taster was provided one meat sample per group without condiments on plastic plates with coded lids containing random three-digit numbers; each taster also received water and crackers for ingestion between tastings to remove residual flavor. Consumer tasters evaluated the following parameters, indicating the intensity of sensation on a 9-point scale: flavor, aroma, softness, juiciness, and overall acceptance. The intensities of the goat meat flavor and aroma characteristics were also evaluated [33].
The analysis was based on five sensory descriptors (Table 2); each descriptor was evaluated using a 9-point semi-structured hedonic scale and continuously anchored at extremities with terms that express intensity.
Table 2.
Descriptor | Definition |
---|---|
“Kid” flavor a | Mixed experience of olfactory, gustatory, and tactile sensations perceived during the tasting. Flavor intensity of kid meat. |
Succulence b | First perception of the quantity of liquid liberated by the sample of meat in the mouth. |
Tenderness c | The force required to compress a piece of meat between the molar teeth, evaluated at the first bite. |
Juiciness d | Perception of the amount of liquid released from the meat sample in the mouth after the fifth bite. |
Overall acceptance e | Sum of quality attributes that will contribute to determine the degree of product acceptance by panelists. |
a 0 = Not detected, 9 = very intense; b 0 = extremely dry, 9 = extremely succulent; c 0 = very tough, 9 = very tender; d 0 = very dry, 9 = very juicy; e 0 = very bad, 9 = very good.
2.7. Statistical Analysis
Data were analyzed using a GLM procedure of SAS software [34] with treatment (diet) as the fixed effect: Yij = M + Ai + Ej; where Yij = analyzed trait of meat; M = overall mean; Ai = fixed effect of diet; Ej = residual error.
When the diet effect was significant (p < 0.05), means were separated and compared using Tukey’s HSD. Significance was declared at p < 0.05; results are reported as least squares mean and standard error of the mean (SEM).
3. Results
3.1. Chemical and Fatty Acid Composition of Goat Milk
The two diets containing linseed resulted in a significantly (p < 0.01) lower content of dry matter in the milk (Table 3). Diet did not significantly affect either the protein or the fat concentration of goat milk, although the linseed + oregano diet determined a lower content of fat.
Table 3.
Item | Diet 1 | SEM 2 | p-Value | ||
---|---|---|---|---|---|
C | L | L + O | |||
Dry matter | 11.67 A | 11.00 B | 10.09 B | 0.336 | 0.005 |
Protein | 3.57 | 3.50 | 3.57 | 0.116 | 0.376 |
Fat | 2.66 | 2.55 | 1.95 | 0.325 | 0.143 |
Ash | 0.77 | 0.78 | 0.78 | 0.0.12 | 0.829 |
Lactose | 4.67 | 4.17 | 3.78 | 0.350 | 0.057 |
C4:0 | 0.78 B | 1.15 A | 1.11 A | 0.082 | 0.007 |
C6:0 | 1.12 b | 1.58 a | 1.40 a | 1.114 | 0.014 |
C8:0 | 1.80 | 2.25 | 2.02 | 0.166 | 0.354 |
SCFA 3 | 3.70 | 4.98 | 4.53 | 0.076 | 0.214 |
C10:0 (capric) | 8.20 | 8.35 | 8.51 | 0.882 | 0.526 |
C11:0 | 0.06 | 0.08 | 0.06 | 0.014 | 0.192 |
C12:0 (lauric) | 3.59 | 3.55 | 3.32 | 0.286 | 0.503 |
C13:0 | 0.08 | 0.09 | 0.08 | 0.011 | 0.294 |
C14:0 (myristic) | 9.38 | 8.87 | 9.13 | 0.431 | 0.429 |
C15:0 | 1.07 | 0.88 | 0.96 | 0.139 | 0.370 |
C16:0 (palmitic) | 25.19 | 24.93 | 24.28 | 0.716 | 0.136 |
C17:0 | 0.64 | 0.60 | 0.66 | 0.049 | 0.370 |
MCFA 4 | 48.21 | 48.35 | 46.00 | 0.074 | 0.163 |
C18:0 (stearic) | 12.31 a | 11.10 b | 11.87 b | 0.793 | 0.0296 |
C20:0 | 0.46 b | 0.69 a | 0.78 a, b | 0.057 | 0.016 |
C21:0 | 0.18 a, b | 0.19 a | 0.14 b | 0.013 | 0.023 |
LCFA 5 | 12.95 | 10.98 | 13.79 | 0.742 | 0.087 |
∑ SFA 6 | 64.86 | 64.37 | 64.40 | 1.837 | 0.812 |
C14:1 | 0.35 a, b | 0.23 b | 0.42 a | 0.057 | 0.035 |
C15:1 | 0.29 a | 0.22 b | 0.28 a | 0.019 | 0.040 |
C16:1 trans (palmitoleic) | 0.27 | 0.26 | 0.24 | 0.022 | 0.347 |
C16:1 cis | 0.40 | 0.41 | 0.32 | 0.056 | 0.333 |
C17:1 | 0.16 | 0.16 | 0.20 | 0.022 | 0.282 |
C18:1 n9 (oleic) | 23.55 | 23.51 | 23.63 | 1.392 | 0.747 |
C20:1 n9 | 0.15 a | 0.12 a, b | 0.06 b | 0.03 | 0.046 |
∑ MUFA 7 | 25.17 | 24.91 | 25.16 | 1.433 | 0.902 |
C18:2 n6 (linoleic) | 3.78 | 3.96 | 3.23 | 0.326 | 0.177 |
C18:2 trans10,cis12 | 0.05 | 0.08 | 0.09 | 0.007 | 0.060 |
C18:2 cis9,trans11 | 0.10 | 0.12 | 0.13 | 0.012 | 0.664 |
Total Conjugated Linoleic Acid (CLA) | 0.15 b | 0.20 a | 0.22 a | 0.060 | 0.050 |
C18:3 n6 (γ-linolenic) | 0.51 | 0.72 | 0.66 | 0.090 | 0.147 |
C18:3 n3 (α-linolenic) | 0.04 B | 0.10 A | 0.10 A | 0.008 | 0.001 |
C20:2 n6 | 0.07 | 0.07 | 0.18 | 0.069 | 0.247 |
C20:3 n6 | 0.04 | 0.04 | 0.04 | 0.002 | 0.055 |
∑ PUFA 8 | 4.44 | 4.59 | 4.22 | 0.356 | 0.493 |
∑ UFA 9 | 29.61 | 29.48 | 29.46 | 1.683 | 0.945 |
* Results are reported as least square means; 1 C, control feed; L, feed containing 3% extruded linseed; L + O, feed containing 3% extruded linseed + 0,6% oregano; 2 SEM: Standard error of means; 3 SCFA: Short Chain Fatty Acids; 4 MCFA: Medium Chain Fatty Acids; 5 LCFA: Long Chain Fatty Acids; 6 SFA: Saturated Fatty Acids (sum of C4:0 + C6:0 + C8:0 + C10:0 + C12:0 + C13:0 + C14:0 + C15:0 + C16:0 + C17:0 + C18:0 + C20:0 + C21:0); 7 MUFA: Mono Unsaturated Fatty Acids (sum of C14:1 + C15:1 + C16:1 c + C16:1 t + C17:1 + C18:1 n9 + C20:1 n9); 8 PUFA: Poly Unsaturated Fatty Acids (sum of C18:2 n6 + C18:2 c12;t10 + C18:2 c9;t11 + C18:3 n6 + C18:3 n3 + C20:2 n6 + C20:3 n6); 9 UFA: Unsaturated Fatty Acids (sum of MUFA + PUFA). Means with different letters within each row significantly differ: a, b: p < 0.05; A, B: p < 0.01.
The fatty acid composition of the goat milk was significantly influenced by the diet. Dietary supplementation with linseed, with or without oregano, significantly increased the concentration of butyric (C4:0; p < 0.01) and caproic (C6:0; p < 0.05) fatty acids, while it led to a decrease in the concentration of stearic acid (C18:0; p < 0.05).
The linseed diet without oregano supplementation lowered (p < 0.05) the concentration of several milk fatty acids, such as C20:0, C14:1, and C15:1. The concentration of C20:1 was the lowest in the L + O group (p < 0.05). The concentration of total Conjugated Linoleic Acid (CLA) was significantly higher in both of the groups fed linseed as compared to the control (p < 0.05). Likewise, the two linseed diets significantly increased (p < 0.01) the concentration of C18:3 n3 (α-linolenic) acid.
3.2. Kid Meat Physical, Chemical, and Fatty Acid Composition
The loin dissection data are shown in Table 4. The diet did not affect either the loin weight or the percentages of lean, fat, and bone.
Table 4.
Item | Diet 1 | SEM 2 | p-Value | ||
---|---|---|---|---|---|
C | L | L + O | |||
Loin weight (g) | 219.50 | 209.73 | 220.34 | 9.588 | 0.449 |
Lean (%) | 48.46 | 48.37 | 49.65 | 5.207 | 0.301 |
Dissectible fat (%) | 11.71 | 9.94 | 10.30 | 0.503 | 0.204 |
Bone (%) | 39.83 | 41.69 | 10.05 | 0.509 | 0.112 |
* Results are reported as least squares mean; 1 C, control feed; L, feed containing 3% extruded linseed; L + O, feed containing 3% extruded linseed + 0.6% oregano. 2 SEM: Standard error of means.
Table 5 shows the results concerning meat features from the Longissimus lumborum muscle. No significant differences between groups were observed for the pH values of meat, either at slaughtering or after 24 h of refrigeration. None of the meat color parameters were affected by the diet. Meat hardness, assessed by the WBS system, was similar between groups.
Table 5.
Item | Diet 1 | SEM 2 | p-Value | ||
---|---|---|---|---|---|
C | L | L + O | |||
pH1 (pH at 1 h post-mortem) | 6.53 | 6.63 | 6.64 | 0.136 | 0.054 |
pH24 (pH at 24 h post-mortem) | 5.81 | 5.83 | 5.74 | 0.134 | 0.059 |
L * (Lightness) | 47.75 | 50.04 | 47.39 | 1.019 | 0.112 |
a * (Red index) | 4.26 | 4.08 | 4.45 | 0.753 | 0.753 |
b * (Yellow index) | 11.20 | 11.68 | 11.14 | 0.176 | 0.101 |
WBS 3 (kg/cm2) | 4.90 | 4.80 | 5.09 | 0.540 | 0.537 |
MDA 4 (mg/kg meat), Day 1 | 0.06 | 0.06 | 0.05 | 0.006 | 0.107 |
MDA 4 (mg/kg meat), Day 10 | 0.36 A | 0.30 A | 0.13 B | 0.014 | 0.001 |
* Results are reported as least squares mean; 1 C, control feed; L, control feed + 3% extruded linseed; L + O, control feed + 3% extruded linseed + 0.6% oregano; 2 SEM: Standard error of means; 3 WBS, Warner–Bratzler shear force; 4 MDA, malondialdehyde. Means with different letters within each row significantly differ: A, B: p < 0.01.
While the concentration of malondialdehyde (MDA) was similar between the dietary treatment groups on Day 1 of assessment, after 10 days of storage, meat from the group fed L + O showed the lowest MDA concentration (p < 0.01) compared to the other groups, proving that oregano is effective in preserving meat from oxidative processes.
The chemical composition of the meat is shown in Table 6. The fat content of the kid meat was significantly lowest (p < 0.05), following feeding with linseed + oregano, as compared to the diet containing only linseed and to the control. Furthermore, the two diets containing linseed led to a significantly higher (p < 0.05) concentration of N-free extracts in the kid meat with respect to the control group.
Table 6.
Item | Diet 1 | SEM 2 | p-Value | ||
---|---|---|---|---|---|
C | L | L + O | |||
Moisture | 72.70 | 72.71 | 74.53 | 1.808 | 0.497 |
Protein | 20.01 | 20.45 | 19.38 | 1.094 | 0.502 |
Lipid | 5.07 a | 3.82 b | 3.37 c | 0.674 | 0.049 |
Ash | 2.01 | 2.58 | 2.30 | 0.267 | 0.170 |
N free-extract | 0.21 b | 0.44 a | 0.42 a | 0.185 | 0.035 |
* Results are reported as least squares mean; 1 C, control feed; L, feed containing 3% extruded linseed; L + O, feed containing 3% extruded linseed + 0.6% oregano. 2 SEM: Standard error of means. Means with different letters within each row significantly differ: a, b, c: p < 0.05.
The fatty acid profile of the kid meat is reported in Table 7. The total concentration of Saturated Fatty Acids (SFAs) was significantly higher (p < 0.05) in the control group compared to the L and L + O groups. Among SFAs, greater amounts of myristic (C14:0) and palmitic (C16:0) acids were found in the kid meat from the control group while, in contrast, feeding linseed, with or without oregano, led to a markedly (p < 0.05) higher amount of C23:0.
Table 7.
Item | Diet 1 | SEM 2 | p-Value | ||
---|---|---|---|---|---|
C | L | L + O | |||
C10:0 (capric) | 0.20 | 0.17 | 0.15 | 0.029 | 0.214 |
C12:0 (lauric) | 0.73 | 0.55 | 0.57 | 0.085 | 0.151 |
C14:0 (myristic) | 8.14 a | 6.27 b | 7.03 b | 0.448 | 0.012 |
C15:0 | 0.66 | 0.53 | 0.61 | 0.043 | 0.063 |
C16:0 (palmitic) | 26.73 a | 23.62 b | 24.49 b | 0.820 | 0.020 |
C17:0 | 1.00 | 0.91 | 0.98 | 0.062 | 0.319 |
C18:0 (stearic) | 14.44 | 14.64 | 14.80 | 0.622 | 0.691 |
C20:0 | 0.07 | 0.09 | 0.12 | 0.017 | 0.077 |
C21:0 | 0.04 | 0.05 | 0.03 | 0.004 | 0.056 |
C22:0 | 0.16 | 0.22 | 0.18 | 0.021 | 0.079 |
C23:0 | 0.28 b | 0.48 a | 0.35 a | 0.051 | 0.011 |
∑ SFA | 52.45 a | 47.53 b | 49.31 b | 1.157 | 0.011 |
C14:1 | 0.14 | 0.12 | 0.19 | 0.024 | 0.069 |
C15:1 | 0.25 | 0.22 | 0.24 | 0.023 | 0.401 |
C16:1 trans (palmitoleic) | 0.41 | 0.35 | 0.38 | 0.023 | 0.102 |
C16:1 cis | 1.52 | 1.36 | 1.68 | 0.146 | 0.153 |
C17:1 | 0.28 b | 0.47 a | 0.48 a | 0.052 | 0.018 |
C18:1 n-9 trans (elaidic) | 0.17 | 0.15 | 0.17 | 0.011 | 0.092 |
C18:1 n-9 cis (oleic) | 31.05 | 31.08 | 32.68 | 0.667 | 0.109 |
C20:1 n-9 | 0.12 | 0.12 | 0.25 | 0.064 | 0.165 |
C22:1 n-9 | 1.63 b | 2.95 a | 2.00 a | 0.360 | 0.024 |
∑ MUFA | 35.57 b | 36.82 a | 38.07 a | 0.584 | 0.013 |
C18:2 n-6 trans | 0.16 | 0.48 | 0.17 | 0.128 | 0.102 |
C18:2 n-6 cis (linoleic) | 5.00 b | 6.75 a | 5.87 b | 0.504 | 0.022 |
C18:2 trans10,cis12 | 0.02 b | 0.05 a | 0.06 a | 0.001 | 0.048 |
C18:2 cis9,trans11 | 0.05 b | 0.08 a | 0.10 a | 0.003 | 0.047 |
Total Conjugated Linoleic Acid (CLA) | 0.07 b | 0.13 a | 0.16 a | 0.020 | 0.049 |
C18:3 n-6 (γ-linolenic) | 0.40 B | 0.70 Aa | 0.55 b | 0.048 | 0.001 |
C18:3 n-3 (α-linolenic) | 0.13 | 0.13 | 0.12 | 0.007 | 0.110 |
C20:2 n-6 | 0.33 | 0.50 | 0.36 | 0.057 | 0.069 |
C20:4 n-6 (ARA) | 0.06 | 0.09 | 0.06 | 0.011 | 0.088 |
C20:5 n-3 (EPA) | 0.15 a, b | 0.21 a | 0.13 b | 0.020 | 0.029 |
C22:5 n-3 (DPA) | 0.67 B | 1.13 Aa | 0.81 b | 0.102 | 0.008 |
C22:6 n-3 (DHA) | 0.19 B | 0.39 A | 0.25 B | 0.032 | 0.001 |
∑ PUFA | 7.16 b | 10.51 a | 8.48 b | 0.792 | 0.018 |
∑ UFA | 42.73 b | 47.33 a | 46.55 a | 1.600 | 0.015 |
Other acids | 4.82 | 5.14 | 4.15 | 1.446 | 0.417 |
n-3 | 1.14 B | 1.86 A | 1.31 B | 0.270 | 0.002 |
n-6 | 5.95 b | 8.52 a | 7.01 b | 2.379 | 0.020 |
n-6/n-3 | 5.22 a | 4.58 b | 5.35 a | 1.624 | 0.047 |
A.I. | 1.54 A | 1.15 B | 1.38 B | 0.074 | 0.003 |
T.I. | 2.23 A | 1.86 B | 2.00 B | 0.107 | 0.003 |
* Results are reported as least squares mean; 1 C, control feed; L, feed containing 3% extruded linseed; L + O, feed containing 3% extruded linseed + 0.6% oregano. 2 SEM: Standard error of means. SFA—saturated fatty acids (sum of C10:0 + C12:0 + C14:0 + C15:0 + C16:0 + C17:0 + C18:0 + C21:0 + C22:0 +C24:0); MUFA—monounsaturated fatty acids (sum of C14:1 + C15:1 + C16:1 c + C16:1 t + C17:1 + C18:1 n-9 t + C18:1 n-9 c + C20:1 n-9 + C22:1 n-9); Total n-6 (sum of C18:2 n-6 t + C18:2 n-6 c + C18:2 c12;t10 + C18:2 c9;t11 + CLA + C18:3 n-6 + C20:2 n-6 + C20:4 n-6); Total n-3 (sum of C18:3 n-3 + C20:5 n-3 + C22:5 n-3 + C22:6 n-3); PUFA—polyunsaturated fatty acids (sum of n-6 + n-3); means with different letters within each row significantly differ: a, b: p < 0.05; A, B: p < 0.01.
On the other hand, dietary linseed determined a significantly greater (p < 0.05) concentration of total Mono Unsaturated Fatty Acids (MUFAs) with respect to the control, especially for C17:1 and C22:1 n-9.
The concentration of total Poly Unsaturated Fatty Acids (PUFAs) was significantly greater (p < 0.05) following the diet containing linseed, due to a higher concentration of the individual fatty acids C18:2 n-6, C18:3 n-6, C20:5 n-3, C22:5 n-3, and C22:6 n-3.
The two diets containing linseed, regardless of the presence of oregano, demonstrated a significantly higher (p < 0.05) concentration of conjugated linoleic acid (CLA) isomers C18:2trans10,cis12 and C18:2cis9,trans11, along with the total CLA content, compared with the control diet.
The diet containing only linseed demonstrated a significantly greater concentration of the total fatty acids of the n-3 (p < 0.01) and n-6 (p < 0.05) series, along with a lower n-6/n-3 ratio (p < 0.05).
The presence of linseed in the diet, with or without oregano, significantly lowered (p < 0.01) the indices of atherogenicity and thrombogenicity of the kid meat compared to the control group.
3.3. Sensory Analysis of the Kids’ Longissimus lumborum Muscle
The results of the sensory analysis of the kid meat from the Ll muscle are shown in Table 8. In this study, feeding with L + O influenced kid meat organoleptic features. Meat from the L + O group was perceived as being more succulent (p < 0.05), tender (p < 0.01), and juicy (p < 0.01) compared to meat from the other two groups. Similarly, the overall acceptability (p < 0.05), which expresses the sum of descriptors contributing to the acceptance of the kid meat, was highest following the L + O diet.
Table 8.
Item | Dietary Treatment 1 | SEM 2 | p-Value | ||
---|---|---|---|---|---|
C | L | L + O | |||
Tasters (n.) | 41 | 41 | 41 | ||
Flavor | 6.07 | 5.61 | 5.78 | 2.473 | 0.068 |
Succulence | 6.46 b | 6.50 b | 7.22 a | 1.248 | 0.044 |
Tenderness | 6.63 B | 6.68 B | 7.54 A | 1.388 | 0.007 |
Juiciness | 4.23 B | 4.39 B | 5.60 A | 1.426 | 0.006 |
Overall acceptance | 8.41 b | 8.10 b | 8.71 a | 1.317 | 0.038 |
* Results are reported as least squares mean; 1 C, control feed; L, feed containing 3% extruded linseed; L + O, feed containing 3% extruded linseed + 0.6% oregano. 2 SEM: Standard error of means. Means with different letters within each row significantly differ: a, b: p < 0.05; A, B: p < 0.01.
4. Discussion
This is a preliminary study aimed at enhancing the native Facciuta Lucana goat population reared according to the traditional farming system through dietary supplementation with local and economically sustainable feeds. In order to limit the genetic erosion of native genotypes, it would be desirable to promote interventions that encourage farmers to preserve these populations, which produce milk and meat endowed with interesting nutritional and sensory qualities, that are related to the characteristics of the environment.
Dietary linseed has been used in sheep [35,36], cows [37], and goats [38] to improve the fatty acid profile of milk; in this study, the diet did not substantially affect the chemical composition of the goat milk, in accordance with previous findings [39,40]. Supplementation with linseed, with or without oregano, significantly increased the concentration of the short-chain saturated fatty acids (SCFA) butyric (C4:0) and caproic (C6:0), as also found by other authors [40,41]. The concentration of palmitic and stearic acids in goat milk decreased following linseed supplementation [36]. In our study, the concentration of total SFAs was lower than that observed in other native goat breeds, showing the effect of the genotype on the fatty acid profile of milk [42].
Interestingly, in our study, the milk content of Conjugated Linoleic Acid (CLA) increased following the linseed diets, in accordance with the findings reported by other authors [38,43]. Total CLA are intermediates of the biohydrogenation of C18:2cis9,cis12, which is present in high concentrations in linseed. Many authors have indicated that feeding linseed in different forms leads to an increased proportion of CLA in milk fat following Δ9 desaturase activity in the mammary gland [44]. The concentration of CLA in goat milk in this trial was lower compared to previous research carried out on Ionica goats [45]; CLA content in milk and meat depends on many factors, such as the animal genotype, age, and diet [46,47].
Ruminants are born with underdeveloped rumen and are considered functionally monogastric animals before weaning; during the pre-ruminant stage of life, the animal status is influenced by the mother’s diet [14,16], the feeding methods [19], and the microbial colonization. All these factors may affect meat quality, with particular concern given to the intramuscular fatty acid profile [48].
With regards to the chemical composition of kid meat, the fat content was significantly the lowest following feeding with linseed + oregano, compared to the diet containing only linseed and to the control. This result is in accordance with Rotondi et al. [9] in Garganica suckling kids.
In this trial, the analysis of the fatty acid profile of kid meat highlighted a higher total concentration of Saturated Fatty Acids (SFAs) in the control group compared to those containing linseed, with or without oregano. Among SFAs, lower amounts of myristic (C14:0) and palmitic (C16:0) acids were found in kid meat from the linseed diets; this is a desirable result from a nutritional point of view, since these fatty acids are held responsible for elevating blood cholesterol [49].
Dietary linseed determined a significantly greater concentration of total MUFAs and PUFAs, and it led to a greater concentration of the total fatty acids of the n-3 and n-6 series, along with a lower n-6/n-3 ratio. In our study, the n-6/n-3 ratio fell within the range 4.58–5.35, which may be considered suitable [50]. In sucking lambs and kids, the n-6/n-3 ratio has been proven to be strongly affected by the breed, the traditional production system, and the environment [51].
Although CLA accounts for a relatively small amount of the total fatty acid composition of foods, it is very important for human health [52,53]. Its main isomer, C18:2 cis-9, trans-11, is effective against cancer and atherogenic diseases and also has positive effects on diabetes and the immune system [54,55]. In our study, the linseed diets determined a significant increase in the CLA content in kid meat, which reflects the difference also found in goat’s milk, in agreement with previous investigations [11,45].
Linseed diets lowered the indices of the atherogenicity and thrombogenicity of kid meat compared to the control, in agreement with the results obtained in meat from Jonica kids [11]. These indices provide useful information on the quality of fat, and values below 2.0 are considered appropriate for a healthy diet.
Feeding strategies aiming to increase the concentration of PUFAs in meat may increase tissue susceptibility to oxidation and perioxidation [9]. In order to limit these processes, several authors have studied the association of plants and herbs having antioxidant properties due to the presence of bioactive compounds (i.e., terpenoids and phenylpropanoids), which are effective in lowering or delaying the occurrence of lipid oxidation [56,57]. Among these, oregano contains carvacrol, thymol, and terpinene, and is considered an alternative to antibiotics due to its antioxidant and antimicrobial properties [58,59].
While the concentration of malondialdehyde (MDA) was similar between the dietary treatment groups on Day 1 of the assessment, after 10 days of storage, meat from the group fed linseed + oregano showed the lowest MDA concentration compared to the other groups, proving that oregano may have been effective in preserving meat from oxidative processes. This may be attributed to oregano’s antioxidant compounds, which are incorporated into muscle cell membranes, thus protecting them against oxidation and increasing meat lipid stability and shelf-life [60].
Several studies have reported that the sensorial properties of goat meat are influenced by the animal’s diet, age at slaughtering, and the farming system [61]. In general, meat from animals fed with concentrate demonstrates higher flavor intensity than those grazed on grass. In this study, feeding with linseed and oregano positively influenced kid meat organoleptic features. Tasters expressed better overall acceptability and appreciated meat for its tenderness, succulence, and juiciness, according to the results obtained from lambs fed extruded linseed in association with oregano [12].
5. Conclusions
This paper contributes to a better understanding of meat quality in a local goat population from Basilicata. Due to the small number of individuals of this genotype, further studies are needed to confirm our findings and to strengthen our knowledge of this goat population.
As expected, the fatty acid profile of the goat milk was affected by the diet, and this also influenced the fatty acid composition of suckling kid meat, which was improved following linseed diets. Furthermore, the addition of oregano to linseed improved overall acceptance by consumers, who appreciated its succulence, tenderness, and juiciness.
Following these preliminary results, the Basilicata Region decided to include the Facciuta Lucana goat population among the local autochthonous goat breeds to be protected by genetic erosion, thus representing an opportunity for the valorization and promotion of this genotype and its products.
Acknowledgments
The authors would like to thank Massimo Lacitignola, Nicolò De Vito, and Domenico Gerardi for their technical support.
Supplementary Materials
The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ani13193050/s1, Table S1: Description of the “Facciuta Lucana” authocthonous goat population. Refs in Supplementary Materials [62,63,64].
Author Contributions
Conceptualization, M.A.C., S.T., F.G. and P.F.; validation, M.A.C., S.T., C.C. (Carlo Cosentino) and V.T.; formal analysis, M.A.C., S.T., F.G., M.S. and C.L.; investigation, M.A.C., S.T., D.K., C.C. (Claudia Carbonara) and C.L.; resources, M.R.; data curation, M.A.C., S.T. and M.S.; writing—original draft preparation, M.A.C. and S.T.; writing—review and editing, M.A.C., S.T. and V.T.; visualization, M.A.C., S.T. and V.T.; supervision, M.A.C., S.T. and M.R.; project administration, F.G. and S.T.; funding acquisition, M.R. All authors have read and agreed to the published version of the manuscript.
Institutional Review Board Statement
Ethical review and approval were waived for this study due to animals were cared for and handled in compliance with the EU legislation on animal welfare regulations (Directive 2010/63/EU, which updates and replaces the 1986 Directive 86/609/EEC on the protection of animals used for scientific purposes) and following the University research polices.
Informed Consent Statement
Not applicable.
Data Availability Statement
All data generated or analyzed during this study are included in this article.
Conflicts of Interest
The authors declare no conflict of interest.
Funding Statement
The present research was part of the project founded and supported by the Basilicata Region, Italy “VAL.BI.OVI.CAP.—PSR Basilicata 2014–2020—Misura 10—Sottomisura 10.2—Sostegno per la conservazione, l’uso e lo sviluppo sostenibili delle risorse genetiche in agricoltura”.
Footnotes
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.
References
- 1.Colonna M.A., Rotondi P., Selvaggi M., Jambrenghi A.C., Ragni M., Tarricone S. Sustainable Rearing for Kid Meat Production in Southern Italy Marginal Areas: A Comparison among Three Genotypes. Sustainability. 2020;12:6922. doi: 10.3390/su12176922. [DOI] [Google Scholar]
- 2.Pophiwa P., Webb E.C., Frylinck L. A review of factors affecting goat meat quality and mitigating strategies. Small Rum. Res. 2020;183:106035. doi: 10.1016/j.smallrumres.2019.106035. [DOI] [Google Scholar]
- 3.Almeida O.C., Ferraz M.V., Jr., Susin I., Gentil R.S., Polizel D.M., Ferreira E.M., Barroso J.P.R., Pires A.V. Plasma and milk fatty acid profiles in goats fed diets supplemented with oils from soybean, linseed or fish. Small Rum. Res. 2019;170:125–130. doi: 10.1016/j.smallrumres.2018.11.002. [DOI] [Google Scholar]
- 4.Manso T., Gallardo B., Salvá A., Guerra-Rivas C., Mantecón A.R., Lavín P., De la Fuente M. Influence of dietary grape pomace combined with linseed oil on fatty acid profile and milk composition. J. Dairy. Sci. 2016;99:1111–1120. doi: 10.3168/jds.2015-9981. [DOI] [PubMed] [Google Scholar]
- 5.Tarricone S., Colonna M.A., Giannico F., Facciolongo A.M., Caputi Jambrenghi A., Ragni M. Effects of dietary extruded linseed (Linum usitatissumum L.) on performance and meat quality in Podolian young bulls. S. Afr. J. Anim. Sci. 2019;49:781–789. doi: 10.4314/sajas.v49i4.20. [DOI] [Google Scholar]
- 6.Tarricone S., Colonna M.A., Giannico F., Lestingi A., Facciolongo A.M. Effect of an extruded linseed diet on meat quality traits in Nero Lucano pigs. S. Afr. J. Anim. Sci. 2019;49:1093–1103. doi: 10.4314/sajas.v49i6.13. [DOI] [Google Scholar]
- 7.Wood J.D., Richardson R.I., Nute G.R., Fisher A.V., Campo M.M., Kasapidou E., Sheard P.R., Enser M. Effects of fatty acids on meat quality: A review. Meat Sci. 2004;66:21–32. doi: 10.1016/S0309-1740(03)00022-6. [DOI] [PubMed] [Google Scholar]
- 8.Pérez-Rosés R., Risco E., Vila R., Peñalver P., Cañigueral S. Biological and non biological antioxidant activity of some essential oils. J. Agric. Food Chem. 2016;64:4716–4724. doi: 10.1021/acs.jafc.6b00986. [DOI] [PubMed] [Google Scholar]
- 9.Rotondi P., Colonna M.A., Marsico G., Giannico F., Ragni M., Facciolongo A.M. Dietary Supplementation with Oregano and Linseed in Garganica Suckling Kids: Effects on Growth Performances and Meat Quality. Pak. J. Zool. 2018;50:1421. doi: 10.17582/journal.pjz/2018.50.4.1421.1433. [DOI] [Google Scholar]
- 10.Tarricone S., Giannico F., Ragni M., Colonna M.A., Rotondi P., Cosentino C., Tufarelli V., Laudadio V. Effects of dietary extruded linseed (Linum usitatissimum L.) and oregano (Origanum vulgare) on growth traits, carcass composition and meat quality of Grigia di Potenza suckling kids. Intern. J. Agric. Biol. 2021;25:1147–1152. doi: 10.17957/IJAB/15.1775. [DOI] [Google Scholar]
- 11.Vizzielli F., Tarricone S., Claps S., De Mastro G., Ragni M. Extruded Linseed and Oregano Dietary Supplementation: Effects on Growth Performance, Carcass Composition, and Meat Quality of Jonica Kids. Ruminants. 2021;1:127–136. doi: 10.3390/ruminants1020010. [DOI] [Google Scholar]
- 12.Scarpa G., Tarricone S., Ragni M. Carcass Composition, Meat Quality and Sensory Quality of Gentile di Puglia Light Lambs: Effects of Dietary Supplementation with Oregano and Linseed. Animals. 2021;11:607. doi: 10.3390/ani11030607. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Ungerfeld E.M., Cancino-Padilla N., Vera-Aguilera N. Fermentation in the rumen. In: Hurst C.J., editor. Microbial Fermentations in Nature and as Designed Processes. Wiley; Hoboken, NJ, USA: 2023. p. 133. [Google Scholar]
- 14.Bas P., Morand-Fehr P. Effect of nutritional factors on fatty acid composition of lamb fat deposits. Livest. Prod. Sci. 2000;64:61–79. doi: 10.1016/S0301-6226(00)00176-7. [DOI] [Google Scholar]
- 15.Vicenti A., Colonna M.A., Ragni M., Toteda F. Effect of type of suckling and polyunsaturated fatty acid use on lamb production. Chemical and fatty acid composition of raw and cooked meat. Ital. J. Anim. Sci. 2004;3:81–91. [Google Scholar]
- 16.Zygoyiannis D., Kufidis D., Katsaounis N.N., Phillips P. Fatty acid composition of carcass fat of indigenous (Capra prisca) suckled Greek kids and milk of their does. Small Rumin. Res. 1992;8:83–95. doi: 10.1016/0921-4488(92)90010-2. [DOI] [Google Scholar]
- 17.Chilliard Y., Ferlay A., Loor J. Trans and conjugated fatty acids in milk from cows and goats consuming pasture or receiving vegetable oils or seeds. Ital. J. Anim. Sci. 2002;1:243–254. doi: 10.4081/ijas.2002.243. [DOI] [Google Scholar]
- 18.Antongiovanni M., Buccioni A., Petacchi F. Upgrading the lipid fraction of foods of animal origin by dietary means: Rumen activity and presence of trans fatty acids and CLA in milk and meat. Ital. J. Anim. Sci. 2003;2:3–28. doi: 10.4081/ijas.2003.3. [DOI] [Google Scholar]
- 19.Ostrowska E., Walker G.P., Doyle P.T. Milk conjugated linoleic and transvaccenic acids are highest in Spring in grazing cows. Asia Pac. J. Clin. Nutr. 2004;13:53. [Google Scholar]
- 20.Tedone L., Giannico F., Tufarelli V., Laudadio V., Selvaggi M., De Mastro G., Colonna M.A. Camelina sativa (L. Crantz) Fresh Forage Productive Performance and Quality at Different Vegetative Stages: Effects of Dietary Supplementation in Ionica Goats on Milk Quality. Agriculture. 2022;12:91. doi: 10.3390/agriculture12010091. [DOI] [Google Scholar]
- 21.Giorgino A., Raspa F., Valle E., Bergero D., Cavallini D., Gariglio M., Bongiorno V., Bussone G., Bergagna S., Cimino F., et al. Effect of Dietary Organic Acids and Botanicals on Metabolic Status and Milk Parameters in Mid–Late Lactating Goats. Animals. 2023;13:797. doi: 10.3390/ani13050797. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Decreto Legislativo 193/2005. [(accessed on 20 March 2020)]. Available online: https://www.gazzettaufficiale.it/eli/id/2005/10/15/05A09902/sg.
- 23.National Research Council . Nutrient Requirements of Small Ruminants: Sheep, Goats, Cervids and New World Camelids. The National Academy Press; Washington, DC, USA: 2007. [Google Scholar]
- 24.Association of Official Agricultural Chemistry . Official Methods of Analysis of the AOAC. 17th ed. Association of Official Analytical Chemists; Arlington, VA, USA: 2000. [Google Scholar]
- 25.Folch J., Lees M., Sloan-Stanley G.H. A simple method for the isolation and purification of total lipids from animal tissues. J. Biol. Chem. 1957;226:497–509. doi: 10.1016/S0021-9258(18)64849-5. [DOI] [PubMed] [Google Scholar]
- 26.Christie W.W. Lipid Analysis-Isolation, Separation, Identification and Structural Analysis of Lipids. Pergamon; Oxford, UK: 1982. p. 270. [Google Scholar]
- 27.Sicklep M., Candek-Patokar M. Pork color measurements as affected by bloom time and measurement location. J. Muscle Fds. 2007;18:78–87. [Google Scholar]
- 28.ASPA (Scientific Association of Animal Production) Metodiche per la Determinazione Delle Caratteristiche Qualitative Della Carne (Methods for Meat Quality Assessment) University of Perugia; Perugia, Italy: 1996. [Google Scholar]
- 29.Colonna M.A., Giannico F., Tufarelli V., Laudadio V., Selvaggi M., De Mastro G., Tedone L. Dietary Supplementation with Camelina sativa (L. Crantz) Forage in Autochthonous Ionica Goats: Effects on Milk and Caciotta Cheese Chemical, Fatty Acid Composition and Sensory Properties. Animals. 2021;11:1589. doi: 10.3390/ani11061589. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Ulbricht T.L., Southgate D.A.T. Coronary heart disease: Seven dietary factors. Lancet. 1991;338:985–992. doi: 10.1016/0140-6736(91)91846-M. [DOI] [PubMed] [Google Scholar]
- 31.Salih A.M., Smith D.M., Price J.F., Dawson L.E. Modified extraction 2-tiobarbituricacid method for measuring lipid oxidation in poultry. Poult. Sci. 1987;66:1483–1488. doi: 10.3382/ps.0661483. [DOI] [PubMed] [Google Scholar]
- 32.Pimentel P.R.S., Pellegrini C.B., Lanna D.P.D., Brant L.M.S., Ribeiro C.V.D.M., Silva T.M., Barbosa A.M., da Silva Júnior J.M., Bezerra L.R., Oliveira R.L. Effects of Acacia mearnsii extract as a condensed-tannin source on animal performance, carcass yield and meat quality in goats. Anim. Feed Sci. Technol. 2021;271:114733. doi: 10.1016/j.anifeedsci.2020.114733. [DOI] [Google Scholar]
- 33.Madruga M.S., Elmore J.S., Oruna-Concha M.J., Balagiannis D., Mottram D.S. Determination of some water-soluble aroma precursors in goat meat and their enrolment on flavour profile of goat meat. Food Chem. 2010;123:513–520. doi: 10.1016/j.foodchem.2010.04.004. [DOI] [Google Scholar]
- 34.SAS . SAS/STAT 9.13 User’s Guide. Statistical Analysis System Inst; Cary, NC, USA: 2004. [Google Scholar]
- 35.Mughetti L., Sinesio F., Acuti G., Antonini C., Moneta E., Peparaio M., Trabalza-Marinucci M. Integration of extruded linseed into dairy sheep diets: Effects on milk composition and quality and sensorial properties of Pecorino cheese. Anim. Feed Sci. Technol. 2012;178:27–39. doi: 10.1016/j.anifeedsci.2012.09.005. [DOI] [Google Scholar]
- 36.Buccioni A., Serra A., Minieri S., Mannelli F., Cappucci A., Benvenuti D., Rapaccini S., Conte G., Mele M. Milk production, composition, and milk fatty acid profile from grazing sheep fed diets supplemented with chestnut tannin extract and extruded linseed. Small Rum. Res. 2015;130:200–207. doi: 10.1016/j.smallrumres.2015.07.021. [DOI] [Google Scholar]
- 37.Martin C., Rouel J., Jouany J.P., Doreau M., Chilliard Y. Methane output and diet digestibility in response to feeding dairy cows crude linseed, extruded linseed, or linseed oil. J. Anim. Sci. 2008;86:2642–2650. doi: 10.2527/jas.2007-0774. [DOI] [PubMed] [Google Scholar]
- 38.Nudda A., Battacone G., Usai M.G., Fancellu S., Pulina G. Supplementation with extruded linseed cake affects concentrations of conjugated linoleic acid and vaccenic acid in goat milk. J. Dairy Sci. 2006;89:277–282. doi: 10.3168/jds.S0022-0302(06)72092-6. [DOI] [PubMed] [Google Scholar]
- 39.Nudda A., Cannas A., Correddu F., Atzori A.S., Lunesu M.F., Battacone G., Pulina G. Sheep and goats respond differently to feeding strategies directed to improve the fatty acid profile of milk fat. Animals. 2020;10:1290. doi: 10.3390/ani10081290. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Cosentino C., Colonna M., Musto M., Dimotta A., Freschi P., Tarricone S., Ragni M., Paolino R. Effects of dietary supplementation with extruded linseed and oregano in autochthonous goat breeds on the fatty acid profile of milk and quality of Padraccio cheese. J. Dairy Sci. 2021;104:1445–1453. doi: 10.3168/jds.2020-18805. [DOI] [PubMed] [Google Scholar]
- 41.Bennato F., Ianni A., Innosa D., Grotta L., D’Onofrio A., Martino G. Chemical-nutritional characteristics and aromatic profile of milk and related dairy products obtained from goats fed with extruded linseed. Asian-Austr. J. Anim. Sci. 2020;33:148. doi: 10.5713/ajas.18.0868. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Florio M., Cimini C., Ianni A., Bennato F., Grotta L., Valbonetti L., Martino G. New Insight into the Quality Traits of Milk and Cheese from Teramana Goats, a Native Italian Breed. Animals. 2023;13:1344. doi: 10.3390/ani13081344. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Kholif S.M., Morsy T.A., Matloup O.H., Ebeid H.M., Kholif A.M. Effects of crushed linseed or linseed oil supplementation on performance of dairy goats and fatty acid profile in milk. Life Sci. J. 2015;12:94–99. doi: 10.12816/0016602. [DOI] [Google Scholar]
- 44.Bernard L., Mouriot J., Rouel J., Glasser F., Capitan P., Pujos-Guillot E., Chardigny J.M., Chilliard Y. Effects of fish oil and starch added to a diet containing sunflower-seed oil on dairy goat performance, milk fatty acid composition and in vivo Δ9-desaturation of [13C] vaccenic acid. Brit. J. Nutr. 2010;104:346–354. doi: 10.1017/S0007114510000486. [DOI] [PubMed] [Google Scholar]
- 45.Jambrenghi A.C., Colonna M.A., Giannico F., Coluccia A., Crocco D., Vonghia G. Meat quality in suckling kids reared by different production systems. Progr. Nutr. 2009;11:36–46. [Google Scholar]
- 46.Jahreis G., Fritsche J., Möckel P., Schöne F., Möller U., Steinhart H. The potential anticarcinogenic conjugated linoleic acid, cis-9, trans-11 C18:2, in milk of different species: Cow, goat, ewe, sow, mare, woman. Nutr. Res. 1999;19:1541–1549. doi: 10.1016/S0271-5317(99)00110-4. [DOI] [Google Scholar]
- 47.Dhiman T.R., Nam S.H., Ure A.L. Factors affecting conjugated linoleic acid content in milk and meat. Crit. Rev. Food Sci. Nutr. 2005;45:463–482. doi: 10.1080/10408390591034463. [DOI] [PubMed] [Google Scholar]
- 48.Cal-Pereyra L., González-Montaña J.R., Neimaur Fernández K., Abreu-Palermo M.C., Martín Alonso M.J., Velázquez-Ordoñez V., Acosta-Dibarrat J. Effects of Ewe’s Diet Supplementation with Polyunsaturated Fatty Acids on Meat Lipid Profile of Suckling Lambs. Agriculture. 2023;13:710. doi: 10.3390/agriculture13030710. [DOI] [Google Scholar]
- 49.Kris-Etherton P.M., Yu S. Individual fatty acid effects on plasma lipids and lipoproteins: Human studies. Am. J. Clin. Nutr. 1997;65:1628–1644. doi: 10.1093/ajcn/65.5.1628S. [DOI] [PubMed] [Google Scholar]
- 50.WHO (World Health Organization) Diet, Nutrition and the Prevention of Chronic Diseases. Report of the WHO/FAO Joint Expert Consultation. WHO; Geneva, Switzerland: 2003. [Google Scholar]
- 51.Sinanoglou V.J., Batrinou A., Mantis F., Bizelis I., Miniadis-Meimaroglou S. Lipid quality indices: Differentiation of suckling lamb and kid breeds reared by traditional sheep farming. Small Rum. Res. 2013;113:1–10. doi: 10.1016/j.smallrumres.2013.01.008. [DOI] [Google Scholar]
- 52.McGuire M.A., McGuire M.K. Conjugated linoleic acid (CLA): A ruminant fatty acid with beneficial effects on human health. Proc. Am. Soc. Anim. Sci. USA. 1999;77:1–8. doi: 10.2527/jas2000.00218812007700ES0033x. [DOI] [Google Scholar]
- 53.Rainer L., Heiss C.J. Conjugated linoleic acid: Health implications and effects on body composition. J. Am. Diet. Assoc. 2004;104:963–968. doi: 10.1016/j.jada.2004.03.016. [DOI] [PubMed] [Google Scholar]
- 54.Cook M.E., Pariza M. The role of conjugated linoleic acid on health. Int. Dairy J. 1998;8:459–462. doi: 10.1016/S0958-6946(98)00069-7. [DOI] [Google Scholar]
- 55.Pariza M.W., Park Y., Cook M.E. The biologically active isomers of conjugated linoleic acid. Prog. Lipid. Res. 2001;40:283–298. doi: 10.1016/S0163-7827(01)00008-X. [DOI] [PubMed] [Google Scholar]
- 56.Muñoz-Cuautle A., Ortega-Cerrilla M.E., Herrera-Haro J.G., Nava-Cuellar C., Gutiérrez-Olvera C., Ramírez-Bribiesca J.E., Zetina-Córdoba P. Effect of Oregano (Lippia graveolens) Essential Oil as a Phytogenic Feed Additive on Productive Performance, Ruminal Fermentation, and Antioxidant Activity in Lamb Meat. Agriculture. 2022;12:973. doi: 10.3390/agriculture12070973. [DOI] [Google Scholar]
- 57.Petcu C.D., Mihai O.D., Tăpăloagă D., Gheorghe-Irimia R.A., Pogurschi E.N., Militaru M., Borda C., Ghimpețeanu O.M. Effects of Plant-Based Antioxidants in Animal Diets and Meat Products: A Review. Foods. 2023;12:1334. doi: 10.3390/foods12061334. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58.Memar M.Y., Raei P., Alizadeh N., Aghdam M.A., Kafil H.S. Carvacrol and thymol: Strong antimicrobial agents against resistant isolates. Rev. Med. Microbiol. 2017;28:63–68. doi: 10.1097/MRM.0000000000000100. [DOI] [Google Scholar]
- 59.Valdivieso-Ugarte M., Gomez-Llorente C., Plaza-Díaz J., Gil Á. Antimicrobial, antioxidant, and immunomodulatory properties of essential oils: A systematic review. Nutrients. 2019;11:2786. doi: 10.3390/nu11112786. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 60.Moyo B., Masika P.J., Muchenje V. Effect of feeding Moringa (Moringa oleifera) leaf meal on the physico-chemical characteristics and sensory properties of goat meat. S. Afr. J. Anim. Sci. 2014;44:64–70. doi: 10.4314/sajas.v44i1.9. [DOI] [Google Scholar]
- 61.De Medeiros G.C.B.S., Mesquita G.X.B., Lima S.C.V.C., Silva D.F.D.O., de Azevedo K.P.M., Pimenta I.D.S.F., de Oliveira A.K.D.S.G., de Oliveira Lyra C., Martínez D.G., Piuvezam G. Associations of the consumption of unprocessed red meat and processed meat with the incidence of cardiovascular disease and mortality, and the dose-response relationship: A systematic review and meta-analysis of cohort studies. Crit. Rev. Food. Sci. Nutr. 2022:1–14. doi: 10.1080/10408398.2022.2058461. [DOI] [PubMed] [Google Scholar]
- 62.Landi V., Tarricone S., Ragni M., Giannico F., Marsico G., Sarti F.M., Lasagna E., Ceccobelli S., Crepaldi P., Pilla F., et al. Selection signatures in Italian goat breeds sharing the “facciuto” phenotype; Proceedings of the International Conference on “Management of Animal and Plant Genetic Resources”; Tirana, Albania. 19 November 2021. [Google Scholar]
- 63.Tarricone S., Landi V., Ragni M., Giannico F., Rillo L., Matassino D., Crepaldi P., Marsico G., Ciani E. The “Murciunara” goat population from Southern Italy: Insights into its possible genetic origin; Proceedings of the International Conference on “Management of Animal and Plant Genetic Resources”; Tirana, Albania. 19 November 2021. [Google Scholar]
- 64.Landi V., Tarricone S., Ragni M., Giannico F., Marsico G., Sarti F.M., Lasagna E., Ceccobelli S., Crepaldi P., Pilla F., et al. Segnali di Selezione per il fenotipo facciuto in alcune razze caprine italiane; Proceedings of the Biodiversità 2021: Agricoltura, Ambiente e Salute: XIII Convegno Nazionale sulla Biodiversità; Foggia, Italy. 7–9 September 2021; ISBN 9788874271016. [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
All data generated or analyzed during this study are included in this article.