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Dietary Supplementation with Oregano and Linseed in Garganica Suckling Kids: Effects on Growth Performances and Meat Quality




Dietary Supplementation with Oregano and Linseed in Garganica Suckling Kids: Effects on Growth Performances and Meat Quality

Pasqua Rotondi1, Maria Antonietta Colonna1, Giuseppe Marsico1, Francesco Giannico1, Marco Ragni1 and Anna Maria Facciolongo2,*

1Department of Agricultural and Environmental Science, University of Bari “Aldo Moro”, Bari, Italy

2Institute of Biosciences and Bioresources (IBBR), National Research Council (CNR), Bari, Italy


Meat from Garganica kids fed diets containing oregano and linseed was analysed for physical and sensory properties, chemical and fatty acid composition of intramuscular lipids. Twenty-one three-week-old kids were divided into three homogeneous groups (n = 7), according to age and body weight, and assigned to one of the following feeding treatments: C) control: commercial pelleted feed; L) pelleted feed containing 3% extruded linseed; LO) pelleted feed containing 3% extruded linseed and 0.6% dried oregano inflorescences. Kids were slaughtered at 60 days of age. Diet did not affect in vivo performances, dressing percentage, pH and meat colour, but it influenced meat tenderness, that was lower (P<0.01) in meat from kids receiving oregano, probably due to the lesser (P<0.05) fat content of their meat. The use of oregano also resulted in a lower muscle fat oxidation and in a better meat flavour. As for human health, the dietary supplementation with linseed improved the muscle fatty acid composition, resulting in higher levels of α-linolenic acid (P<0.05) and in a lower n-6/n-3 ratio.

Article Information

Received 08 June 2017

Revised 24 January 2018

Accepted 13 March 2018

Available online 20 June 2018

Authors’ Contribution

GM conceived and designed the study. PR performed experimental work and laboratory analysis. MAC carried out meat analysis. FG and MR helped in preparation of the manuscript. AMF analysed the data and wrote the article.

Key words

Garganica breed, Kids, Oregano, Linseed, Meat quality, Fatty acid composition.


* Corresponding author:

0030-9923/2018/0004-1421 $ 9.00/0

Copyright 2018 Zoological Society of Pakistan



The crisis affecting animal production may be overcome by rediscovering “biodiverse” animal breeds. The recovery of autochthonous breeds is an important factor in maintaining biodiversity. The Garganica breed is a native Apulian goat breed well adapted to the harsh environmental conditions of Southern Italy marginal areas. The exploitation of this goat breed passes through the improvement of meat production and quality, which has a relationship with human health.

In the last ten years, research on human nutrition has shown that a diet containing high levels of saturated fatty acids (SFA) increases the risk of cancer, atherosclerosis and cardiovascular diseases (Hooper et al., 2006; Erkkilä et al., 2008; Webb and O’Neill, 2008; Leon et al., 2009).

Consequently, consumers of the technologically advanced countries have begun paying attention to the link between health and nutrition, directing their food choices towards good quality, healthy and wholesome products. People prefer meats with a low fat and cholesterol content along with high levels of n-3 polyunsaturated fatty acids (n-3 PUFA).

Ruminant meat can be considered a good dietary source of several nutrients (Wahle et al., 2004), however, it has also been censured for its high level of intramuscular fat, which is particularly rich in SFA due to rumen biohydrogenation of dietary fats, especially PUFAs (Doreau and Ferlay, 1993; Glasser et al., 2008).

Therefore, the improvement of ruminant meat requires feeding strategies (Wood et al., 1999; Wachira et al., 2002; Demirel et al., 2004) able to optimize its chemical and nutritional composition and fatty acid profile, in order to obtain a product with a low SFA content, a high PUFA concentration (especially n-3; Cooper et al., 2004), and n-6/n-3 and PUFA/SFA (Chilliard et al., 2000; Vatansever et al., 2000; Caputi Jambrenghi et al., 2004) ratios close to the levels recommended by the Department of Health (1994).

Several studies have shown that the supplementation of the animal diet with linseed resulted in a higher content of α-linolenic acid in the muscle and increased the amount of long-chain n-3 PUFAs (Wachira et al., 2002; Demirel et al., 2004; Bas et al., 2007; Berthelot et al., 2010); moreover, changes in the feed level in the diet affect the ruminal ecosystem reducing PUFA biohydrogenation (Glasser et al., 2008).

Although dietary supplementation with PUFAs improves its nutritional characteristics, meat becomes more susceptible to lipid oxidation and peroxidation, resulting in consistent worsening of its colour (browning), flavour and shelf life (Wood et al., 2004).

Animal feeding supplementation with natural antioxidant essences such as oregano, sage, thyme and rosemary (Rice-Evans et al., 1997) has proved to delay or limit the oxidative process (Elmore et al., 1999) during meat storage and exposure at the meat counter, thus prolonging its shelf life.

Oregano (Origanum vulgare L.) is a common aromatic plant in the Mediterranean area (Kokkini et al., 2004). Its essential oil is known to have several properties: antimicrobial (Lambert et al., 2001; Marino et al., 2001; Friedman et al., 2002), antifungal (Paster et al., 1995; Adam et al., 1998) and antioxidant (Bendini et al., 2002; Botsoglou et al., 2002; Papageorgiou et al., 2003). Oregano’s antioxidant activity is attributed to carvacrol and thymol; these molecules make the bacterial cell membrane permeable (Lambert et al., 2001) and convert lipids and hydroxyl radicals into stable products (Yanishlieva-Maslarova, 2001).

Studies on animal feeding supplementation with oregano have given controversial growth performance results for pigs (Namkung et al., 2004) and broilers (Botsoglou et al., 2004a; Giannenas et al., 2005). However, oregano improves the oxidative stability of chicken (Botsoglou et al., 2003) and rabbit meat (Botsoglou et al., 2004b), protecting it from the negative effects that slaughtering stress may have on quality (Young et al., 2003). Studies on oregano used in lamb feeding have confirmed its effectiveness in giving greater oxidative stability and in improving the sensory qualities of meat (Bampidis et al., 2005; Simitzis et al., 2008), although little information is available regarding the effects of oregano supplementation to the kid ration.

This study aimed to evaluate the effect of dietary supplementation with oregano and extruded linseed on the chemical, physical and sensory characteristics, intramuscular fat oxidation and fatty acid profile of meat from suckling Garganica kids.


Materials and methods

Animal management and diet

The study involved twenty-one male Garganica kids, born as twins, carried out in the Research Unit for Extensive Animal Husbandry (Zootecnia Estensiva - ZOE) in Muro Lucano (PZ, Italy, latitude: 40°45’13”64 N, longitude: 15°29’17.1” E, 650 m a.s.l.) between March and May 2015 for a total of 40 days. Kids were reared according to the traditional farming system for the Garganica breed: they were exclusively milk-fed, suckling from the dams until they reached the age of about 21 days. Then they were assigned to one the following groups (n=7), homogeneous for body weight and age: C) control group, that received a commercial pelleted feed; L) group that received a pelleted feed containing 3% extruded linseed; LO) group fed a pelleted feed containing 3% extruded linseed and 0.6% dried oregano inflorescences. The three pelleted total mixed rations (PTMR) (Tables I, II) were formulated to be isocaloric and isonitrogenous, in order to meet the nutritional requirements of kids (INRA, 1988) and were provided ad libitum.

Feed was offered daily at 08:00 h at a rate of 110% of ad libitum intake calculated by weighing-back refusal weekly. Feed samples were taken weekly and stored at -20°C until analysis. In addition, kids had access to maternal milk throughout the trial period. Suckling occurred twice daily, in the morning at about 07:00, before taking the dams out to pasture, and in the evening at about 19:00, when the dams came back from pasture. The amount of milk suckled by the kids was calculated by weighing them before and after suckling.


Table I.- Composition of experimental diets.






Ingredient % (as-fed basis)

Dehulled soybeans



Wheat flour shorts

Faba bean


Sugar beet pulp dehydrated

Extruded linseed

Soybean oil

Sunflower meal


Soybean hulls

Oregano (dried inflorescences)

Vitamin mineral premix















































1Diets: C, control feed; L, control feed + 3% extruded linseed; LO, control feed + 3% extruded linseed + 0.6% Oregano.


The dams grazed during the day, receiving hay ad libitum and commercial feed (500 g/head/day) at housing, in the evening.

Samples of maternal milk were taken every two weeks for analysis of chemical and fatty acid composition (Table II).

The kids were housed in individual pens (0.8 m2/head) with free access to water, and the temperature in the pens ranged from 7 °C to 15 °C.

Feed refusals were recorded weekly to calculate average daily gain (ADG), average daily feed intake (ADFI) and feed conversion ratio (FCR).


Table II.- Chemical and fatty acid composition of the diets and maternal milk.



Maternal milk




Chemical composition % (dry matter basis)





Crude protein





Ether extract















Crude fiber






























Fatty acid composition (% fatty acid methyl esters)















C12:0 (lauric)





C14:0 (myristic)





C16:0 (palmitic)










C18:0 (stearic)





C18:1 n-9, cis 9 (oleic)





C18:2 n-6 (linoleic)





C18:3 n-3 (α-linolenic)





C20:4 n-6 (arachidonic)





C22:5 n-3 (DPA)





C22:6 n-3 (DHA)





1Diets: C, control feed; L, control feed + 3% extruded linseed; LO, control feed + 3% extruded linseed + 0.6% Oregano. 2NDF, neutral detergent fiber; ADF, acid detergent fiber; ADL, acid detergent lignin; AIA, acid insoluble ash.


The kids were slaughtered at 60 days of age, by exsanguination, according to the veterinary police rules (D.P.R. 320/54) after fasting for 12 h, with free water access, and recording of body weights. The hot carcass, skin, fleece, pluck, and full and empty gastro-intestinal tract (GIT) were weighed. Carcasses were hung by the Achilles tendon, chilled at 4 °C (80-82% relative humidity) for 24 h and then reweighed. The weight of the digestive content (full-empty GIT) was used to calculate the net dressing percentage after dressing and chilling (hot carcass weight/empty body weight; cold carcass weight/empty body weight).

Chemical composition of feed

Representative samples of the pelleted feeds were taken at fifteen-day intervals, and mixed to obtain a single final pool for each diet, which was then analysed to determine its chemical composition and fatty acid profile. Samples of each PTMR were ground in a hammer mill with a 1 mm screen and analysed using the following AOAC (2004) procedures: DM (Method 934.01), EE (Method 920.39), ash (Method 942.05), CP (Method 954.01), CF (Method 945.18), ADF and ADL (Method 973.18), and amylase-treated NDF (Method 2002.04).

The chemical composition of the dams’ milk was analysed as follows: total protein (N×6.38), fat and lactose content, using an infrared spectrophotometer (Milko Scan 133B; Foss Electric, DK-3400, Denmark).

Physical and chemical parameters of meat

The pH values were measured on the Longissimus lumborum (Ll) muscle at the time of slaughter (pH0) and after that the carcasses were refrigerated at 4 °C for 24 h (pH24), using a portable instrument (Model HI 9025; Hanna Instruments, Woonsocket, RI) with an electrode (FC 230C; Hanna Instruments) and performing a two-point calibration (pH 7.01 and 4.01). The refrigerated carcasses were divided into left and right halves, and samples of the Ll muscle were taken from the right side in order to measure meat colour and tenderness.

Meat colour (L* = lightness, a* = redness, b* = yellowness) 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, Virginia, 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 analysis (Y = 92.8, x = 0.3162, and y = 0.3322). The reflectance measurements were performed after the samples were allowed to oxygenate in air for at least 30 min, in order to take stable measurements (Šicklep and Čandek-Potokar, 2007).

Three Ll samples (1.25 cm diameter and thick) were tested for tenderness by the Warner-Bratzler Shear Force (WBSF) system using an Instron 5544 testing machine. Shear forces were determined perpendicular to fiber direction.

Chemical composition and fatty acid analyses

In order to analyse the chemical composition of meat (moisture, ether extract, raw protein, ash) (AOAC, 1995), representative sub-samples of Ll were homogenised and fat was extracted according to the method suggested by Folch et al. (1957), using a 2:1 chloroform/methanol (v/v) solution in order to determine the fatty acid profile. The fatty acids were then methylated using a KOH/methanol 2N solution (Christie, 1982) and analysed by gas chromatography (Shimadzu GC-17A) using a silicone-glass capillary column (70% Cyanopropyl Polysilphenylene-siloxane BPX 70 by Thermo Scientific, length = 60 m, internal diameter = 0.25 mm, film thickness = 0.25 µm). The starting temperature was 135 °C for 7 min, then increased by 4 °C/min up to 210 °C.

The analysis of milk fatty acids was performed by applying the same extraction procedure described for meat. The methylated fatty acids were prepared following AOAC (2000) procedure and analysed by gas chromatography, the only differences being that the starting temperature was 140 °C, and increased by 5 °C/min up to 230 °C. The single fatty acids were expressed as a percentage of the total methylated fatty acids.

Samples of each concentrate mixture were used for fatty acid analysis according to the method described above for the meat fatty acid profile.

Morover, Δ9 desaturase and elongase enzymatic activities were determined as described by Malau-Aduli et al. (1997), using mathematical indices. The calculations were performed as follows: Δ9 desaturase 16 index = 100 [(C16:1cis9)/(C16:1cis9 + C16:0)]; Δ9 desaturase 18 index = 100 [(C18:1cis9)/(C18:1cis9 + C18:0)]; elongase index = 100 [(C18:0 + C18:1cis9)/(C16:0 + C16:1cis9 + C18:0 + C18:1cis9)].

The food risk factor of meat was evaluated by calculating the n-6/n-3 and PUFA/SFA ratios and the nutritive value of the fat (Bonanome and Grundy, 1988); the latter was calculated as follows: (C18:0 + C18:1cis9)/C16:0.

Lipid oxidation

Lipid oxidation on meat samples from Ll muscle was evaluated by measuring 2-thiobarbituric acid reactive substances (TBARS), according to the method of Salih et al. (1987), and was expressed as mg MDA/kg meat.

Sensory properties of meat

Consumer tests were carried out in a single session to record consumer responses to the sensory properties of meat: tenderness, juiciness, flavour and overall acceptability (Meilgaard et al., 1991). Each consumer was asked to score each attribute on an intensity scale ranging from 1 (very bad) to 9 (excellent).

The lumbar region from the kids’ half carcasses was refrigerated at 4 °C for 24 h and cut into ribs. The meat was grilled at 180 °C until it reached an internal temperature of 75 °C, monitored using an internal thermocouple. It was then served to the members of the consumer panel, consisting of 41 adult men and women aged between 18 and 60. The educational level was medium-high and panel members belonged to three job categories of approximately equal numbers: (1) students, (2) office workers and (3) technicians. Most were non-smokers and habitual meat eaters (eating meat more than once a week).

Statistical analysis

Statistical analysis was performed using the GLM procedure of the SAS application package (SAS, 2000). The statistical model included the effect of diet treatment and experimental error. When the diet effect was significant (P<0.05), means were compared by the Student’s t-test.


Table III.- Effect of diet on in vivo performances and slaughtering data of kids.




P value




Initial BW (Kg)






Final BW (Kg)






Average daily feed intake (Kg/d)






Average daily milk intake (Kg/d)






Average daily gain (Kg/d)






Feed conversion ratio (F+M)3 (Kg/Kg)






Net hot dressing percentage4






Net cold dressing percentage4






1Diets: C, control feed; L, control feed + 3% extruded linseed; LO, control feed + 3% extruded linseed + 0.6% Oregano. 2Standard error of means. 3Feed + milk. 4% of empty body weight.


Results and discussion

Growth performances in vivo and slaughtering data

Performances in vivo and slaughtering data were not affected by the diet (Table III). Feed intake was very low for all the groups (107-118 g head/day), therefore growth performances were more affected by milk consumption (840-910 g head /day) than by the experimental diets.

Other studies in lambs showed that dietary supplementation with linseed oil or seeds did not influence slaughtering weight or daily weight gain (Bas et al., 2007; Radunz et al., 2009; Berthelot et al., 2010, 2012). In agreement with previous observations involving lambs (Simitzis et al., 2008), broilers (Botsoglou et al., 2004a) and rabbits (Botsoglou et al., 2004b), the oregano inclusion in the diet did not influence growth performances, although the components of oregano could have affected these by limiting the growth and colonisation of many pathogenic and non-pathogenic bacteria species in the gut (Bampidis et al., 2005).

The dressing percentage is similar to that reported by Todaro et al. (2006) in Girgentana kids slaughtered at the same age, but higher in comparison with other studies (Santos et al., 2007, 2008; Peña et al., 2011). The discrepancies can probably be attributed to differences in slaughtering weights (Marichal et al., 2003) and genotype (Peña et al., 2011).


Table IV.- Effect of diet on physical characteristics and lipid oxidation of meat from the Longissimus lumborum muscle.




P value
















MDA (mg/Kg meat)






1 d L*


















WBS (kg/cm2)






5 d L*


















WBS (kg/cm2)






a, b, P<0.05; A, B, P<0.01. 1Diets: C, control feed; L, control feed + 3% extruded linseed; LO, control feed + 3% extruded linseed + 0.6% Oregano.


Physical and chemical parameters of meat

The data regarding pH, colour and tenderness of the Longissimus lumborum muscle are reported in Table IV.

The pH values were not significantly affected by the diet. The final pH that we recorded was between 5.45 and 5.60, with values similar to those reported by Stanisz et al. (2009) and lower than those of other genotypes (Dhanda et al., 2003; Santos et al., 2007; Bonvillani et al., 2010). In agreement with observations recorded in Manchego lambs (de la Fuente-Vázquez et al., 2014), the final pH values were not influenced neither by linseed nor by oregano supplementation, while Simitzis et al. (2008) reported significant increases in final pH values only for female Chios lambs, but not for males, when diet was supplemented with oregano essential oil.

Considering the effects on shelf life, colour and quality of meat, the final pH values are essential for refrigerated meat; levels above 5.8 generally indicate poor quality caused by pre-slaughtering stress (Lawrie, 1998; Dhanda et al., 2003). However, the levels we found are within the acceptable range (5.5-5.8) considered as optimal for high quality goat meat (Herold et al., 2007; Solaiman et al., 2011).

The colorimetric characteristics (L*, a*, b*) measured at 1 and 5 days after slaughter were not influenced by the diet. de la Fuente-Vázquez et al. (2014) found that dietary linseed had no effect on the colorimetric features of lamb meat. Dietary supplementation with oregano, instead, determined slightly higher levels of the parameters studied, in partial agreement with observations on lambs (Simitzis et al., 2008) fed with a diet containing oregano essential oil, that showed slightly increased meat lightness and significantly increased a* and b* values.

The lightness values (L*) were intermediate results compared to those observed by Peña et al. (2009) in Criollo Cordobes (L* = 42.54) and Anglonubian (L* = 48.82) kids slaughtered at the same weight of the kids of our study. The same suthors, moreover, registered a significant effect due to genotype and reported, like Santos et al. (2007), higher a* and b* values, in contrast with our observations.

Meat tenderness recorded the day after slaughtering was significantly affected by the diet; WBS values (kg/cm2) were higher in group LO compared with group C (P<0.05) and especially with group L (P<0.01). However, these differences disappeared at the 5th day (Table IV). Linseed used alone, however, lowered tenderness in comparison with group C (Table IV), although not significantly.

This result is consistent with previous studies on kids (Abuelfatah et al., 2016), lambs (Nute et al, 2007; Díaz et al., 2011) and beef cattle (Juárez et al., 2012) fed using different PUFA sources.

The higher WBS values in kids receiving oregano can probably be ascribed to the lower fat content of their meat (Table V); Kemp et al. (1981) found that fatter lambs actually had more tender meat.


Table V.- Effect of diet on chemical composition of the meat from Longissimus lumborum muscle.



SEM P value
Moisture (%) 76.65



0.595 0.043
Crude protein (%) 19.97 20.27 19.51 0.503 0.055
Ether extract (%)




0.232 0.018
Ash (%) 1.33 1.46 1.52 0.199


a, b, P<0.05. 1Diets: C, control feed; L, control feed + 3% extruded linseed; LO, control feed + 3% Extruded linseed + 0.6% Oregano.


The WBS values are also similar to those reported by other researchers (Dhanda et al., 2003; Todaro et al., 2004; Bonvillani et al., 2010) and lower than those recorded by Santos et al. (2007), who observed significant differences due to genotype, sex and to the different muscle samples. The shear force values reported for kid meat vary widely in relation to factors such as pre-slaughter treatment, post mortem carcass treatment, the type of muscle and the sample preparation method (Webb et al., 2005).

TBARS values (mg malondialdehyde MDA/kg-1 meat) were similar for groups C and L, and were significantly (P<0.01) reduced by using oregano. The higher level of meat oxidation due to the linseed diet agrees with observations reported in Manchego lambs (de la Fuente-Vázquez et al., 2014); the antioxidant activity of oregano is confirmed in trials on lambs (Simitzis et al., 2008), calves (Zinoviadou et al., 2009), pigs (Simitzis et al., 2010) and rabbits (Cardinali et al., 2015). Oregano is thought to delay oxidation because lipids and hydroxyl radicals are rendered more stable by reaction with its phenolic components (Jadhav et al., 1996; Yanishlieva-Maslarova, 2001).

In agreement with Simitzis et al. (2008), it is therefore possible to state, although indirectly, that after oregano was ingested with feed, its phenolic compounds acted at tissue level after being absorbed.

Chemical composition of meat

The chemical composition data of the Longissimus dorsi are shown in Table V. The moisture content was higher (P<0.05) in group LO than in group L. However, the fat proportion was lower (P<0.05) in group LO than in the other two groups, while the protein and ash proportion was not influenced by diet. No information is available about the influence of oregano on the chemical composition of kid meat, while a study on rabbit meat did not report any significant differences in chemical composition that could be ascribed to oregano included in the diet (Cardinali et al., 2015).


Table VI.- Effect of diet on fatty acid profile (% of total fatty acid methyl esters) and indices related to human health of meat from the Longissimus lumborum muscle.

Fatty acids



P value




C12:0 (lauric)






C14:0 (myristic)






C16:0 (palmitic)












C18:0 (stearic)






Total SFA2






C16:1 n-7 (palmitoleic)






C18:1 n-9 t9






C18:1 n-9 c9 (oleic)






Total MUFA3






C18:2 n-6, c9, c12 (linoleic)






C18:3 n-3 (α-linolenic)






Total n-64






Total n-35






Total PUFA6






Nutritive value7


















Δ9 desaturase 16 index8






Δ9 desaturase 18 index9






Elongase index10






a, b, P<0.05. 1Diets: C, control feed; L, control feed + 3% extruded linseed; LO, control feed + 3% extruded linseed + 0.6% Oregano. SFA, saturated fatty acids; MUFA, monounsaturated fatty acids; PUFA, polyunsaturated fatty acids. 2Sum of C12:0 + C14:0 + C15:0 + C16:0 + C17:0 + C18:0 + C22:0 + C24:0. 3Sum of C16:1n-7 + C18:1trans-9 + C18:1cis-9. 4Sum of C18:2cis-9,cis-12 + C18:2cis-9,trans-11+ C18:3 + C20:4. 5Sum of C18:3 + C20:3 + C20:5 + C22:6. 6Sum of n-6 + n-3. 7Nutritive value: (C18:0 + C18:1cis9)/C16:0. 8Δ9 desaturase 16 index = index of desaturase enzyme activity in C16 fatty acids = 100 [(C16:1cis9) / (C16:1cis9 + C16:0)]. 9Δ9 desaturase 18 index = index of desaturase enzyme activity in C18 fatty acids = 100 [(C18:1cis9) / (C18:1cis9 + C18:0)]. 10elongase index = 100 [(C18:0 + C18:1cis9) / (C16:0 + C16:1cis9 + C18:0 + C18:1cis9)].


Fatty acid profile

The fatty acid profile of the Longissimus lumborum intramuscular fat is shown in Table VI.

Dietary treatment did not significantly influence the percentage of total saturated fatty acids (SFA), monounsaturated fatty acids (MUFA) and polyunsaturated fatty acids (PUFA). The most represented (23-25 %) fatty acids were oleic (C18:1 n-9 cis9) and palmitic acids (C16:0), followed (12-15%) by stearic (C18:0) and linoleic acids (C18:2 n-6 cis9 cis12). This trend, except for linoleic acid, is in agreement with that observed in other studies (Banskalieva et al., 2000; Todaro et al., 2006; Ebrahimi et al., 2014), which reported oleic, palmitic and stearic acids (in decreasing order) as the fatty acids found in the largest amounts; however, the percentage of stearic and oleic acids was lower than that found in the literature for lambs and kids, while the levels of linoleic acid were higher (Bas et al., 2005; Werdi Pratiwi et al., 2006; Bonvillani et al., 2010). In agreement with Kim et al. (2007), the lower levels of stearic acid we found in the muscle could have been caused by a greater amount of linoleic acid escaping ruminal biohydrogenation, and given that stearic acid acts as a Δ9 desaturase substrate (Cook, 1996) in the synthesis of oleic acid, lower levels of C18:0 in muscle tissue can also determine lower concentrations of C18:1 n-9 cis 9.

In cattle, however, feeding high levels of concentrates (Latham et al., 1972) has shown to determine a reduction of the bacteria responsible for the rumen biohydrogenation, probably due to higher acidity (Harfoort and Hazelwood, 1997). The different proportions of acids we found might also be due to the heterogeneity of the trial conditions reported in literature, dissimilar for breeds (de Smet et al., 2004), diets (Bas et al., 2005; Lee et al., 2008) or slaughtering weights (Sañudo et al., 1998); it has been observed, in fact, that the fatty acid profile can be significantly affected by diet changes after weaning and by weight increases at slaughtering (Dhanda et al., 2003; Beserra et al., 2004).

The use of linseed in the diet did not affect the proportion of oleic acid in meat intramuscular fat, as also observed in calves (Aharoni et al., 2004; Bartoň et al., 2007).

In agreement with previous studies in lambs (de la Fuente-Vázquez et al., 2014), linoleic acid levels (11.89-14.21%) were not influenced by linseed supplementation. In Black Goat kids fed with sesame, sunflower or linseed oil, and slaughtered at a higher age than that of our kids, the linoleic acid content in the muscle was approximately a third (3.48-3.89%) of the level we found (Saqhir et al., 2012). It is likely that diet, genotype and the age difference were conditioning factors also in this case. Beserra et al. (2004) showed, indeed, that the linoleic acid content is influenced significantly by genotype and by slaughtering age of kids.

However, in a study involving Girgentana kids fed with maternal milk, or with maternal milk and feed, and slaughtered at the same age as our kids, the meat linoleic acid level was lower than the level we found (Todaro et al., 2006).

Regarding PUFAs, the C18:3 n-3 proportion was significantly lower (P<0.05) in the kids of group C than in those fed with linseed and linseed + oregano, in agreement with a previous study carried out in lambs fed with extruded linseed and linseed oil that showed an intramuscular content increase of the α-linolenic acid as related to the diet (Colonna et al., 2011).

The total PUFA n-6 and the total PUFA n-3 percentages were not influenced by dietary treatment, whereas the n-6/n-3 ratio was significantly higher (P<0.05) in group C than in the other two groups. This ratio reduction due to linseed supplementation agrees with the findings reported in Boer kids (Abuelfatah et al., 2016) and Manchego lambs (de la Fuente-Vázquez et al., 2014) also fed with linseed.

However, regardless of the diet, the ratio value was higher than that reported in other studies carried out in different genotypes (Todaro et al., 2006; Peña et al., 2009), and resulted unsatisfactory in terms of meat healthful properties. In relation to human health, this ratio should not exceed 4. The differences with the findings of other Authors may be due to the genotype (Peña et al., 2009), or to the amount and composition of the maternal milk received by the kids in our study, which suckled mostly milk, as showed by the feed intake values (Table III). The fatty acid composition of suckling kid meat, in fact, is mainly related to maternal milk composition (Zygoyiannis et al., 1992; Dhanda et al., 1999).

With regards to the nutritional value, in terms of the fatty acid ratio (C18:0 + C18:1)/C16:0) of meat, Banskalieva et al. (2000) suggested that its assessment could be a useful way to describe the potential effects on human health of the different fatty acids ingested with food. It has been highlighted that palmitic acid (C16:0) increases blood cholesterol, while stearic acid (C18:0) has no effect and oleic acid (C18:1) reduces it. In the present study, the ratio ranged from 1.59-1.73 and did not present any differences related to diet. However, the ratio was lower than that recorded in other genotypes (Todaro et al., 2002; Santos et al., 2007; Peña et al., 2009; Bonvillani et al., 2010), and consequently less satisfactory for human health.

The PUFA/SFA ratio was unaffected by the diet, and the values ranging between 0.28 and 0.33 are comparable to those obtained in finishing lambs receiving forage (Enser et al., 1998a), linseed supplementation (de la Fuente-Vázquez et al., 2014), fish, rapeseed or soybean meal (Ponnampalam et al., 2001), or fish oil (Wachira et al., 2002; Cooper et al., 2004). However, the ratio values we obtained were below the level of 0.45, recommended for human health (Enser et al., 1998b).

Sensory characteristics of meat

The sensory characteristics of meat are shown in Table VII. Overall acceptability, tenderness and juiciness were not significantly influenced by the feeding treatment, although the tasters gave a higher flavour score to the meat of kids fed with oregano than to group L subjects and especially to group C (P<0.01). The lack of the diet influence on meat tenderness and juiciness is in agreement with other research carried out in lambs whose ration was supplemented with different lipid sources including linseed oil (Nute et al., 2007; Diaz et al., 2011) and with the findings reported in Kivircik lambs (Demirel et al., 2013) receiving oregano supplementation. About the flavor, instead, the best values were recorded following the administration of oregano in contrast with the observations of Demirel et al. (2013), which did not show the influence of oregano oil supplementation on meat flavor in lambs.


Table VII.- Effect of diet on sensory characteristics of meat.




P value




Tasters (n.)






Overall acceptability
























1Diets: C, control feed; L, control feed + 3% extruded linseed; LO, control feed + 3% extruded linseed + 0.6% Oregano.




The results lead us to conclude that, under our experimental conditions, the ration supplementation with extruded linseed does not affect the productive performance, the chemical and physical characteristics of meat and fatty acid profile of muscle lipids. The fatty acid composition, however, shows higher linolenic acid content and a better n-6/n-3 ratio. This poor response may be probably attributed to the low kid feed intake and, therefore, to the greater influence of maternal milk on kid growth and body composition.

Oregano supplementation enhances meat lipids oxidative stability and its flavor, confirming results that have been already observed in other species.




Research supported by the Basilicata Region within the project “Valorization of meat from Basilicata native sheep and goats for the conservation of biodiversity”, Basilicata 2007-2013 PSR - Miss. 214 Action 5, Agrobiodiversity: Integrated Action Projects DGR No. 1096 of 08/08/2012.


Statement of conflict of interest

Authors have declared no conflict of interest.




Abuelfatah, K., Zuki, A.B.Z., Goh, Y.M. and Sazili, A.Q., 2016. Effects of enriching goat meat with n-3 polyunsaturated fatty acids on meat quality and stability. Small Rum. Res., 136: 36-42.

Adam, K., Sivropoulou, A., Kokkini, S., Lanaras, T. and Arsenakis, M., 1998. Antifungal activities of Origanum vulgare subsp. hirtum, Mentha spicata, Lavandula angustifolia, and Salvia fruticosa essential oils against human pathogenic fungi. J. Agric. Fd. Chem., 46: 1739-1745.

Aharoni, Y., Orlov, A. and Brosh, A., 2004. Effects of high-forage content and oilseed supplementation of fattening diets on conjugated linoleic acid (CLA) and trans fatty acids profiles of beef lipid fractions. Anim. Feed Sci. Technol., 117: 43-60.

AOAC, 1995. Official methods of analysis of association of official analytical chemists, 16th edn. Association of Official Analytical Chemists, Arlington, VA, USA.

AOAC, 2000. Official methods of analysis of association of official analytical chemists, 17th edn. Association of Official Analytical Chemists, Arlington, VA, USA.

AOAC, 2004. Official methods of analysis of association of official analytical chemists, 18th edn. Association of Official Analytical Chemists, Arlington, VA, USA.

Bampidis, V.A., Christodoulou, V., Florou-Paneri, P., Christaki E., Spais, A.B. and Chatzopoulou, P.S., 2005. Effect of dietary dried oregano leaves supplementation on performance and carcass characteristics of growing lambs. Anim. Feed Sci. Tech., 121: 285-295.

Banskalieva, V., Sahlu, T. and Goest, A.L., 2000. Fatty acid composition of goat muscles and fat depot: a review. Small Rum. Res., 37: 255-268.

Bartoň, L., Marounek, M., Kudrna, V., Bureš, D. and Zahradkova, R., 2007. Growth performance and fatty acid profiles of intramuscular and subcutaneous fat from Limousin and Charolais heifers fed extruded linseed. Meat Sci., 76: 517-523.

Bas, P., Berthelot, V., Pottier, E. and Normand, J., 2007. Effect of linseed on fatty acid composition of muscles and adipose tissues of lambs with emphasis on trans fatty acids. Meat Sci., 77: 678-688.

Bas, P., Dahbi, E., El Aich, A., Morand-Fehr, P. and Araba, A., 2005. Effect of feeding on fatty acid composition of muscles and adipose tissues in young goat raised on the Argan tree forest of Moroco. Meat Sci., 71: 317-326.

Bendini, A., Gallina Toschi, T. and Lercker, G., 2002. Antioxidant activity of oregano (Origanum vulgare L.) leaves. Ital. J. Fd. Sci., 14: 17-24.

Berthelot, V., Bas, P., Pottier, E. and Normand, J., 2012. The effect of maternal linseed supplementation and/or lamb linseed supplementation on muscle and subcutaneous adipose tissue fatty acid composition of indoor lambs. Meat Sci., 90: 548-557.

Berthelot, V., Bas, P. and Schmidely, P., 2010. Utilization of extruded linseed to modify fatty composition of intensively-reared lamb meat: Effect of associated cereals (wheat vs. corn) and linoleic acid content of the diet. Meat Sci., 84: 114-124.

Beserra, F.J., Madruga, M.S., Leite, A.M., Silva, E.M.C. and Maia, E.L., 2004. Effect of age at slaughter on chemical composition of meat from Moxotó goats and their crosses. Small Rum. Res., 55: 177-181.

Bonanome, A. and Grundy, S.M., 1988. Effect of dietary stearic acids on plasma cholesterol and lipoprotein levels. New Engl. J. Med., 318: 1244-1248.

Bonvillani, A., Peña, F., Domenech, V., Polvillo, O., García, P.T. and Casal, J.J., 2010. Meat quality of Criollo Cordobes goat kids produced under extensive feeding conditions. Effects of sex and age/weight at slaughter. Span. J. agric. Res., 8: 116-125.

Botsoglou, N.A., Christaki, E., Fletouris, D.J., Florou-Paneri, P. and Spais, A.B., 2002. The effect of dietary oregano essential oil on lipid oxidation in raw and cooked chicken during refrigerated storage. Meat Sci., 62: 259-265.

Botsoglou, N.A., Christaki, E., Florou-Paneri, P., Giannenas, I., Papageorgiou, G. and Spais, A.B., 2004a. The effect of a mixture of herbal essential oils or a-tocopheryl acetate on performance parameters and oxidation of body lipid in broilers. S. Afri. J. Anim. Sci., 34: 52-61.

Botsoglou, N.A., Florou-Paneri, P., Christaki, E., Giannenas, I. and Spais, A.B., 2004b. Performance of rabbits and oxidative stability of muscle tissues as affected by dietary supplementation with oregano essential oil. Arch. Anim. Nutr., 58: 209-218.

Botsoglou, N.A., Govaris, A., Botsoglou, E.N., Grigoropoulou, S.H. and Papageorgiou, G., 2003. Antioxidant activity of dietary oregano essential oil and alpha-tocopheryl acetate supplementation in long term frozen stored turkey meat. J. Agric. Fd. Chem., 51: 2930-2936.

Caputi Jambrenghi, A., Giannico F., Sanapo, S., Bozzo, F., Colonna, M.A., Vicenti, A. and Vonghia, G., 2004. Effect of dietary linseed oil on fatty acid composition of lamb meat. Proc. 50th Int. Congr. Meat Sci. Tech., 8-14 August, Helsinki, Finland.

Cardinali, R., Cullere, M., Dal Bosco, A., Mugnai, C., Ruggeri, S., Mattioli, S., Castellini, C., Trabalza Marinucci, M. and Dalle Zotte, A., 2015. Oregano, rosemary and vitamin E dietary supplementation in growing rabbits: Effect on growth performance, carcass traits, bone development and meat chemical composition. Livest. Sci., 175: 83-89.

Chilliard, Y., Ferlay, A., Mansbridge, R. and Doreau, M., 2000. Ruminant milk fat plasticity: nutritional control of saturated, polyunsaturated, trans and conjugated fatty acids. Annls. Zootech., 49: 181-205.

Christie, W.W., 1982. Lipid analysis-isolation, separation, identification and structural analysis of lipids. Pergamon Press, Oxford, pp. 270.

Colonna, M.A., Giannico, F., Coluccia, A., Di Bello, G., Vonghia, G. and Caputi Jambrenghi, A., 2011. Dietary supplementation with extruded linseed and linseed oil in lamb feeding: Productive performances and meat quality traits. Progr. Nutr., 13: 111-124.

Cook, H.W., 1996. Fatty acid desaturation and chain elongation in eukaryotes. In: Biochemistry of lipids, lipoproteins and membranes (eds. D.E. Vance and J.E. Vance). Elsevier, Amsterdam, the Netherlands, pp. 129.

Cooper, S.L., Sinclair, L.A., Wilkinson, R.G., Hallett, K.G., Enser, M. and Wood, J.D., 2004. Manipulation of the n-3 polyunsaturated fatty acid content of muscle and adipose tissue in lambs. J. Anim. Sci., 82: 1461-1470.

de la Fuente-Vázquez, J., Díaz-Díaz-Chirón, M.T., Pérez-Marcos, C., Cañeque-Martínez, V., Sánchez-González, C.I., Álvarez-Acero, I., Fernández-Bermejo, C., Rivas-Cañedo, A. and Lauzurica-Gómez, S., 2014. Linseed, microalgae or fish oil dietary supplementation affects performance and quality characteristics of light lambs. Span. J. agric. Res., 12: 436-447.

de Smet, S., Raes, K. and Demeyer, D., 2004. Meat fatty acid composition as affected by fatness and genetic factors: A review. Anim. Res., 53: 81-98.

Demirel, G., Ekiz, B., Unal, A., Yalcintan, A., Kocabagli, N. and Yilmaz, A., 2013. Effects of dietary oregano essential oil on carcass and meat quality of Kivircik Lambs. J. Anim. Vet. Adv., 12: 991-995.

Demirel, G., Wachira, A.M., Sinclair, L.A., Wilkinson, R.G., Wood, J.D. and Enser, M., 2004. Effects of dietary n-3 polyunsaturated fatty acids, breed and dietary vitamin E on the fatty acids of lamb muscle, liver and adipose tissue. Br. J. Nutr., 91: 551-565.

Department of Health, 1994. Nutritional aspects of cardiovascular disease. Report on Health and Social Subjects, No. 46 HMSO, London, UK.

Dhanda, J.S., Taylor, D.G. and Murray, P.J., 2003. Carcass composition and fatty acid profiles of adipose tissue of male goats: effects of genotype and live weight at slaughter. Small Rum. Res., 50: 67-74.

Dhanda, J.S., Taylor, D.G., Murray, P.J. and McCosker, J.E., 1999. The influence of goat genotype on the production of Capretto and Chevon carcasses. 4. Chemical composition of muscle and fatty acid profiles of adipose tissue. Meat Sci., 52: 375-379.

Díaz, M.T., Cañeque, V., Sánchez, C.I., Lauzurica, S., Pérez, C., Fernández, C., Álvarez, I. and de la Fuente, J., 2011. Nutritional and sensory aspects of light lamb meat enriched in n-3 fatty acids during refrigerated storage. Fd. Chem., 124: 147-155.

Doreau, M. and Ferlay, A., 1993. Digestion and utilisation of fatty acids by ruminants. Anim. Feed Sci. Tech., 45: 379-396.

Ebrahimi, M., Rajion, M.A. and Goh, Y.M., 2014. Effects of oils rich in linoleic and α-linolenic acids on fatty acid profile and gene expression in goat meat. Nutrients, 6: 3913-3928.

Elmore, J.S., Mottram, D.S., Enser, M. and Wood, J.D., 1999. Effect of the polyunsaturated fatty acid composition of beef muscle on the profile of aroma volatiles. J. Agric. Fd. Chem., 47: 1619-1625.

Enser, M., Hallett, K.G., Hewitt, B., Fursey, G.A.J. and Wood, J.D., 1998a. The polyunsaturated fatty acid composition of beef and lamb. Meat Sci., 49: 321-327.

Enser, M., Hallet, K.G., Hewit, B., Fursey, G.A.J., Wood, J.D. and Harrington, G., 1998b. Fatty acid content and composition of UK beef and lamb muscle in relation to production system and implication for human nutrition. Meat Sci., 49: 329-341.

Erkkilä, A., De Mello, V.D.F., Risérus, U. and Laaksonen, D.E., 2008. Dietary fatty acids and cardiovascular disease: An epidemiological approach. Progr. Lipid Res., 47: 172-187.

Folch, A.J., Lees, M. and Stanley, G.H., 1957. A simple method for the isolation and purification of total lipids from animal tissues. J. biol. Chem., 226: 497-509.

Friedman, M., Henika, P.R. and Mandrell, R.E., 2002. Bactericidal activities of plant essential oils and some of their isolated constituents against Campylobacter jejuni, Escherichia coli, Listeria monocytogenes, and Salmonella enterica. J. Fd. Protec., 65: 1545-1560.

Giannenas, I.A., Florou-Paneri, P., Botsoglou, N.A., Christaki, E. and Spais, A.B., 2005. Effect of supplementing feed with oregano and/or a-tocopheryl acetate on growth of broiler chickens and oxidative stability of meat. J. Anim. Feed Sci., 14: 521-535.

Glasser, F., Schmidely, P., Sauvant, D. and Doreau, M., 2008. Digestion of fatty acids in ruminants: A meta-analysis of flows and variation factor 2. C18 fatty acids. Animal, 2: 691-704.

Harfoot, C.G. and Hazelwood, G.P., 1997. Lipid metabolism in the rumen. In: The rumen microbial ecosystem (eds. P.N. Hobson and C.S. Stewart). Blackie Academic & Professional, London, UK, pp. 382-426.

Herold, P., Snell, H. and Tawfik, E.S., 2007. Growth carcass and meat quality parameters of pure bred and crossbred goat kids in extensive pasture. Arch. Tierzucht., 50: 186-196.

Hooper, L., Thompson, R.L., Harrison, R.A., Summerbell, C.D., Ness, A.R., Moore, H.J., Worthington, H.V., Durrington, P.N., Higgins, J.P., Capps, N.E., Riemersma, R.A., Ebrahim, S.B. and Davey Smith, G., 2006. Risks and benefits of omega 3 fats for mortality, cardiovascular disease, and cancer: Systematic review. Br. med. J., 332: 752-755.

INRA, 1988. Alimentation des Bovines, Ovins et Caprins. INRA, Paris.

Jadhav, S.J., Nimbalkar, S.S., Kulkarni, A.D. and Madhavi, D.L., 1996. Role of antioxidants in inhibiting lipid peroxidation. In: Food antioxidants, technological, toxicological and health perspectives (eds. D.L. Madhavi, S.S. Deshpande and D.K. Salunkhe). M. Dekker Inc., NY, USA, pp. 41-53.

Juárez, M., Dugan, M.E.R., Aldai, N., Basarab, J.A., Baron,V.S., McAllister, T.A. and Aalhus, J.L., 2012. Beef quality attributes as affected by increasing the intramuscular levels of vitamin E and omega-3 fatty acids. Meat Sci., 90: 764-769.

Kemp, J.D., Mahyuddin, M., Ely, D.G., Fox, J.D. and Moody, W.G., 1981. Effect of feeding systems, slaughter weight and sex on organic properties, and fatty acid composition of lamb. J. Anim. Sci., 51: 321-330.

Kim, S.C., Adesogan, A.T., Badinga, L. and Staples, C.R., 2007. Effects of dietary n-6:n-3 fatty acid ratio on feed intake, digestibility, and fatty acid profiles of the ruminal contents, liver, and muscle of growing lambs. J. Anim. Sci., 85: 706-716.

Kokkini, S., Karousou, R., Hanlidou, E. and Lanaras, T., 2004. Essential oil composition of Greek (Origanum vulgare ssp hirtum) and Turkish (O-onites) oregano: A tool for their distinction. J. Essen. Oil Res., 16: 334-338.

Lambert, R.J.W., Skandamis, P.N., Coote, P.J. and Nychas, G.J., 2001. A study of the minimum inhibitory concentration and mode of action of oregano essential oil, thymol and carvacrol. J. appl. Microbiol., 91: 453-462.

Latham, M.J., Storry, J.E. and Sharpe, M.E., 1972. Effects of low roughage diets on the microflora and lipid metabolism in the rumen. Appl. Microbiol., 24: 871-877.

Lawrie, R.A., 1998. Lawrie’s meat science, 6th edn. Woodhead Publishing Ltd., Cambridge, England.

Lee, J.H., Kouakou, B. and Kannan, G., 2008. Chemical composition and quality characteristics of chevron from goats fed three different post-weaning diets. Small Rum. Res., 75: 177-184.

Leon, H., Shibata, M.C., Sivakumaran, S., Dorgan, M., Chatterley, T. and Tsuyuki, R.T.T., 2009. Effect of fish oil on arrhythmias and mortality: Systematic review. Br. med. J., 338: 2931-2939.

Malau-Aduli, A.E.O., Siebert, B.D., Bottema, C.D.K. and Pitchford, W.S., 1997. A comparison of the fatty acid composition of triacylglycerols in adipose tissue from Limousin and Jersey cattle. Aust. J. agric. Res., 48: 715-722.

Marichal, A., Castro, N., Capote, J., Zamorano, M.J. and Argüello, A., 2003. Effects of live weight at slaughter (6, 10, 25 kg) on kid carcass and meat quality. Livest. Prod. Sci., 83: 247-256.

Marino, M., Bersani, C. and Comi, G., 2001. Impedance measurements to study the antimicrobial activity of essential oils from Lamiaceae and Compositae. Int. J. Fd. Microbiol., 67: 187-195.

Meilgaard, M., Civille, G.V. and Carr, B.T., 1991. Sensory evaluation techniques, 2nd edn. CRC Press Inc., Boca Raton, Florida, USA, pp. 135-235.

Namkung, H., Li, M., Gong, J., Yu, H., Cottrill, M. and de Lange, C.F.M., 2004. Impact of feeding blends of organic acids and herbal extracts on growth performance, gut microbiota and digestive function in newly weaned pigs. Can. J. Anim. Sci., 84: 697-704.

Nute, G.R., Richardson, R.I., Wood, J.D., Hughes, S.I., Wilkinson, R.G., Cooper, S.L. and Sinclair, L.A., 2007. Effect of dietary oil source on the flavour and the colour and lipid stability of lamb meat. Meat Sci., 77: 547-555.

Papageorgiou, G., Botsoglou, N., Govaris, A., Giannenas, I., Iliadis, S. and Botsoglou, E., 2003. Effect of dietary oregano oil and α-tocopheryl acetate supplementation on iron-induced lipid oxidation of turkey breast, thigh, liver and heart tissue. J. Anim. Physiol. Anim. Nutr., 87: 324-335.

Paster, N., Menasherov, M., Ravid, U. and Juven, B., 1995. Antifungal activity of oregano and thyme essential oils applied as fumigants against fungi attacking stored grain. J. Fd. Protec., 58: 81-85.

Peña, F., Bonvillani, A., Freireb, B., Juárezc, M., Perea, J. and Gómez, G., 2009. Effects of genotype and slaughter weight on the meat quality of Criollo Cordobes and Anglo Nubian kids produced under extensive feeding conditions. Meat Sci., 83: 417-422.

Peña, F., Bonvillani, A., Morandini, M., Freire, V., Domenech, V. and García, A., 2011. Carcass quality of Criollo Cordobes and Anglo Nubian suckling kids: Effects of age at slaughter. Arch. Zootec., 60: 225-235.

Ponnampalam, E.N., Sinclair, A.J., Egan, A.R., Blakeley, S.J. and Leury, B.J., 2001. Effect of diets containing n−3 fatty acids on muscle long-chain n−3 fatty acid content in lamb fed low- and medium-quality roughage diets. J. Anim. Sci., 79: 698-706.

Radunz, A.E., Wickersham, L.A., Loerch, S.C., Fluharty, F.L., Reynolds, C.K. and Zerby, H.N., 2009. Effects of dietary polyunsaturated fatty acid supplementation on fatty acid composition in muscle and subcutaneous adipose tissue of lambs. J. Anim. Sci., 87: 4082-4091.

Rice-Evans, C., Miller, N.J. and Paganga, G., 1997. Antioxidant properties of phenolic compounds. Trends Pl. Sci., 2: 152-159.

Salih, A.M., Smith, D.M., Price, J.F. and Dawson, L.E., 1987. Modified extraction 2-tiobarbituricacid method for measuring lipid oxidation in poultry. Poult. Sci., 66: 1483-1488.

Santos, V.A.C., Silva, A.O., Cardoso, J.V.F., Silvestre, A.J.D., Silva, S.R., Martins, C. and Azevedo, J.M.T., 2007. Genotype and sex effects on carcass and meat quality of suckling kid protected by the PGI ‘‘Cabrito de Barroso”. Meat Sci., 75: 725-736.

Santos, V.A.C., Silva, S.R. and Azevedo, J.M.T., 2008. Carcass composition and meat quality of equally mature kids and lambs. J. Anim. Sci., 86: 1943-1950.

Sañudo, C., Sierra, I., Olleta, J.L., Martín, L., Campo, M.M., Santolaria J.D., Wood, J.D. and Nute, G.R., 1998. Influence of weaning on carcass quality, fatty acid composition and meat quality in intensive lamb production systems. Anim. Sci., 66: 175-187.

Saqhir, S., Abo Omar, J., Naser, O., Ghanam, I. and Abdalla, J., 2012. Muscle fatty acids profile of finishing Black goat kids fed oil supplemented diets. Asian-Pac. J. Trop. Biomed., 1: 1-5.

SAS, 2000. SAS/STAT user’s guide: Statistics. SAS Institute Inc., Cary, NC, USA.

Šicklep, M. and Candek-Potokar, M., 2007. Pork color measurements as affected by bloom time and measurement location. J. Muscle Fds., 18: 78-87.

Simitzis, P.E., Deligeorgis, S.G., Bizelis, J.A., Dardamani, A., Theodosiou, I. and Fegeros, K., 2008. Effect of dietary oregano oil supplementation on lamb meat characteristics. Meat Sci., 79: 217-223.

Simitzis, P.E., Symeon, G.K., Charismiadou, M.A., Bizelis, J.A. and Deligeorgis, S.G., 2010. The effects of dietary oregano oil supplementation on pig meat characteristics. Meat Sci., 84: 670-676.

Solaiman, S., Kerth, C., Willian, K., Min, B.R., Shoemaker, C., Jones, W. and Bransby, D., 2011. Growth performance, carcass characteristics and meat quality of Boer-cross weather and buck goats grazing Marshall rye grass. Asian-Aust. J. Anim. Sci., 24: 351-357.

Stanisz, M., Ślósarz, P. and Gut, A., 2009. Slaughter value and meat quality of goat kids with various share of Boer blood. Anim. Sci. Pap. Rep., 27: 189-197.

Todaro, M., Corrao, A., Alicara, M.L., Schinelli, R., Giaccone, P. and Priolo, A., 2004. Effects of litter size and sex on meat quality traits of kid meat. Small Rum. Res., 54: 191-196.

Todaro, M., Corrao, A., Barone, C.M.A., Alicata, M.L., Schinelli, R. and Giaccone, P., 2006. Use of weaning concentrate in the feeding of suckling kids: effects on meat quality. Small Rum. Res., 66: 44-50.

Todaro, M., Corrao, A., Barone, C.M.A., Schinelli, R., Occidente, M. and Giaccone, P., 2002. The influence of age at slaughter and litter size on some quality traits of kid meat. Small Rum. Res., 44: 75-80.

Vatansever, L., Kurt, E., Enser, M., Nute, G.R., Scollan, N.D., Wood, J.D. and Richardson, R.I., 2000. Shelf life and eating quality of beef from cattle of different breeds given diets differing in n-3 polyunsaturated fatty acid composition. Anim. Sci., 71: 471-482.

Wachira, A.M., Sinclair L.A., Wilkinson, R.G., Enser, M., Wood, J.D. and Fisher, A.V., 2002. Effects of dietary fat source and breed on the carcass composition, n-3 polyunsaturated fatty acid and conjugated linoleic acid content of sheep meat and adipose tissue. Br. J. Nutr., 88: 697-709.

Wahle, K.W.J., Heys, S.D. and Rotondo, D., 2004. Conjugated linoleic acids: Are they beneficial or detrimental to health? Progr. Lipid Res., 43: 553-587.

Webb, E.C., Casey, N.H. and Simela, L., 2005. Goat meat quality. Small Rumin. Res., 60: 153-166.

Webb, E.C. and O’Neill, H.A., 2008. The animal fat paradox and meat quality. Meat Sci., 80: 28-36.

Werdi Pratiwi, N.M., Murray, P.J., Taylor, D.G. and Zhang, D., 2006. Comparison of breed, slaughter weight and castration on fatty acid profiles in the longissimus thoracic muscle from male Boer and Australian feral goats. Small Rum. Res., 64: 94-100.

Wood, J.D., Enser, M., Fisher, A.V., Nute, G.R., Richardson, R.I. and Sheard, P.R., 1999. Manipulating meat quality and composition. Proc. Nutr. Soc., 58: 363-370.

Wood, J.D., Richardson, R.I., Nute, G.R., Fisher, A.V., Campo, M.M., Kasapidou, M., Sheard, P.R. and Enser, M., 2004. Effects of fatty acids on meat quality: A review. Meat Sci., 66: 21-32.

Yanishlieva-Maslarova, N.V., 2001. Inhibiting oxidation. In: Antioxidants in food: Practical applications (eds. J. Pokorny, N. Yanishlieva and M. Gordon). Woodhead Publishing Limited, CRC Press, Cambridge, England, pp. 22-70.

Young, J.F., Stagsted, J., Jensen, S.K., Karlsson, A.H. and Henckel, P., 2003. Ascorbic acid, α-tocopherol and oregano supplements reduce stress-induced deterioration of chicken meat quality. Poult. Sci., 82: 1343-1351.

Zinoviadou, K.G., Koutsoumanis, K.P. and Biliaderis, C.G., 2009. Physico-chemical properties of whey protein isolate films containing oregano oil and their antimicrobial action against spoilage flora of fresh beef. Meat Sci., 82: 338-345.

Zygoyiannis, D., Kufidis, D., Katasaounis, N. and Phillips, P., 1992. Fatty acid composition of carcass of indigenous (Capra prisca) suckled Greek kids and milk of their does. Small Rum. Res., 8: 83-95.

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