Submit or Track your Manuscript LOG-IN

Effect of Organic Selenium Supplementation in Diet on Gastrointestinal Tract Performance and Meat Quality of Goat




Effect of Organic Selenium Supplementation in Diet on Gastrointestinal Tract Performance and Meat Quality of Goat

Saba Parveen Samo1, Moolchand Malhi1,*, Javed Gadahi2, Yan Lei3, Allah Bux Kaciwal1 and Saeed Ahmed Soomro1

1Department Veterinary Physiology and Biochemistry, Sindh Agricultural University, Tandojam 70060, Pakistan

2Department of Veterinary Parasitology, Sindh Agricultural University, Tandojam 70060, Pakistan

3Dairy Herd Improvement Center, Henan Animal Husbandry Bureau, Zhengzhou 450046, China


Ten cross-bred goats of about 4 months of age and 10.5 kg body weight were randomly selected for the study and divided into two groups (n=5/each). Basal diet given to the animals consist of roughage and concentrate at the ratio of 65:35. Group A was kept without any supplementation whereas group B was supplemented with selenium yeast (SY) at the dose rate of 0.3 mg/ for 8 weeks. The results showed that the weights (% of empty body weight) of rumen (4.18 ± 0.30 vs 3.49 ± 0.10); duodenum (0.32 ± 0.01 vs 0.27 ± 0.01); colon (1.14 ± 0.03 vs 1.06 ± 0.01), caecum (0.62 ± 0.03 vs 0.57 ± 0.01) and the whole large intestine (2.44 ± 0.04 vs 2.32 ± 0.03) significantly increased (P < 0.05) in B compared to A. The weights of liver, heart, kidney and spleen were not significantly different (P > 0.05) between the groups, however, the lung weight increased in B (1.15 ± 0.04 vs 0.99 ± 0.04, P < 0.05) compared to A. Digestibility trails revealed that utilization of dry matter (DM), crude protein (CP) and crude fiber (CF) increased (P < 0.05) by 13.71, 12.02 and 4.78% at week 3 and by 11.11, 11.8 and 3.46 % at week 6 in B compared to A. Among carcass characteristics the carcass dressing % (52.99 ± 0.77 vs 49.41 ± 0.6 ) and leg weight (kg) (1.28 ± 0.06 vs 1.05 ± 0.04) increased (P < 0.05) in B compared to A. The physico-chemical properties of meat were not significantly different between the groups except fat content (2.75 ± 0.25 vs 2.00 ± 0.05%, P < 0.096) which tended to increase in B compared to A. These data demonstrated that dietary SY supplementation increased gastrointestinal tract weight and nutrient digestibilities, and improved some carcass characteristics in goats.

Article Information

Received 13 December 2017

Revised 02 January 2018

Accepted 10 January 2018

Available online 19 April 2018

Authors’ Contribution

MM conceived and designed the study. SPS executed the study and wrote the manuscript. JG and ABK supervised the study and helped in data analysis. YL and SAS provided the technical assistance in writing the manuscript.

Key words

Selenium yeast, Gastrointestinal tract, Digestibility, Carcass, Goat.


* Corresponding author:

0030-9923/2018/0003-0995 $ 9.00/0

Copyright 2018 Zoological Society of Pakistan



Selenium (Se) is an important micro-nutrient which is necessarily required in smaller concentration in the animal feed for a wide range of physiological activities. In most of the areas of Pakistan, the soil Se level is too low, yielding Se-deficient plants, which ultimately leads to depletion of Se in animals (Khan et al., 2006; Ahmad et al., 2009). Depending upon the physiological status of animals, the Se deficiency is manifested by nutritional degenerative myopathy (white muscle disease) and early death in lambs and calves (Underwood, 2012), poor growth rate and delayed puberty in young animals and reproductive (dystocia, retained placenta, infertility) and productive (reduced milk and meat production) disorders in adults (Ramirez-Bribiesca et al., 2005; Enjalbert et al., 2006; Ahmad et al., 2009). Thus, Se supplementation in animal’s ration is extremely important to avoid Se-deficiency related problems. It is supplemented in either organic or inorganic forms to livestock, however, organic Se is extensively used as supplement in the diet of ruminants because of its increased bioavailability in the tissues and superior physiological role over inorganic Se (Arthur, 2000; Tapiero et al., 2003; Maiorino et al., 1999; McKenzie et al., 1998; Beck et al., 2005). Selenium yeast (SY) is an excellent source of synthetic organic Se frequently used as supplement in the ruminant’s diet (Kelly and Powers, 1995; Wang et al., 2009).

An animal’s growth and production performance requires efficient digestion and absorption of nutrients throughout the GIT and the efficient peripheral flow of absorbed nutrient for suitable utilization. Growth of digestive organs is an important indicator of body growth because it represents the amount of nutrient utilization and therefore makes it available to the periphery (Johnson et al., 1990).

Supplementation of trace minerals including Se in diet influences the growth and nutrient digestibility rates in GIT. Inorganic Se supplemented in diet at the dose rate 0.2 – 0.6 mg/kg.DM either in selenate or selenite forms increased total tract digestibility in sheep fed high concentrate diet (Del Razo-Rodriguez et al., 2013) whereas no effect was observed in sheep fed low concentrate diet (Del Razo-Rodriguez et al., 2013; Alimohamady et al., 2013; Serra et al., 1994). Total tract digestibility of nutrients was higher in multiparous dairy cattle fed organic selenium at 0.15 and 0.3 g/kg DM compared to control but no difference in the digestibility was found at 0.45 g/kg DM (Wang et al., 2009).

Oxidation reactions adversely affects the nutritive value and flavors of meat products and can be prevented by the antioxidant ability of glutathione peroxidase (GSH-Px) (DeVore et al., 1983; Morrissey et al., 1998; Gatellier et al., 2004). Reduction in the oxidation maintain the meat quality, which requires the availability of an antioxidant in the meat (Faustman and Cassens, 1989; Sanchez-Escalante et al., 2001).

There is scarcity of information concerning the effects of Se on nutrient utilization and GIT growth of ruminants thus the recent study aimed to evaluate the effects of SY on nutrient digestibility, GIT growth and meat quality of goat.


Materials And Methods

Selection and management of animals

Ten cross-bred goats of around 4 months of age, weighing 10.5 kg body weight were used in this study. After four weeks of acclimatization to the environment, the animals were housed in distinct pens of 2.5 × 4 ft area per pen and randomly divided into two groups; i.e. A and B (n=5/group). Animals in group A received basal diet consisting of roughage and concentrate (65:35) and that in group B along with basal diet supplemented with organic selenium (selenium yeast, SY) at the dose of 0.3 mg/kg diet. Feed and water were provided ad libitum. On the basis of percent dry matter, the basal diet contained 20.89% crude protein, 3.64% crude fat, 6.67% crude fiber and 7.73% ash. The metabolizable energy (ME) in basal diet was 10.85 MJ/kg DM and the Se concentration was 0.03 mg/kg diet. The experiment lasted for eight weeks.

Sample collection, slaughter and measurements

Throughout experimental period feed samples were collected once in a week and composited for chemical analysis. Fecal samples were collected on 3rd and 6th week of trial. The wet fecal samples were instantly dried in forced air oven at 65°C for 48 h, grinded and then stored at -20°C for chemical analysis. Feed and fecal samples were analyzed for dry matter (DM), crude protein (CP), ether extract (EE) and ash according to the methods of AOAC (2000) and Viram et al. (2017). Immediately after slaughter, the abdominal cavity of the animal was opened and the entire gastrointestinal tract as well as other visceral organs were removed and collected in a clean tub. Whole stomach and its various parts (Rumen, reticulum, omasum and abomasum) were isolated from the rest of the viscera, emptied and washed with cold phosphate buffer solution (PBS) and then weighed. The parts of small intestine such as duodenum, jejunum, and ileum, and the parts of large intestine such as caecum, rectum and colon were identified and isolated as described by Neville et al. (2008). After identification and careful separation, each part was emptied, washed in PBS and weighed. Visceral organs (heart, liver, lungs, kidneys and spleen) were collected and weighed.

Determination of carcass and meat characteristics

The carcass characteristics including carcass weight, dressing percentage and leg length were measured as described by Lawler et al. (2004). The meat samples were isolated from longissimus dorsi (LD) muscle to evaluate the physico-chemical characteristics. The LD muscle was exercised from the carcasses from left side, between the 8th and 11th thoracic vertebrae, according to descriptions by Honikel (1998) and all visible fat was trimmed from the muscles before any physical and chemical analyses were carried out. A piece of meat (10 g) was homogenized in distilled water (90 ml) and the pH was determined by pH meter (Ockreman, 1985). The water holding capacity (WHC) was analyzed by following the protocol given by Wardlaw et al. (1973). Meat sample (8 g) was mixed in 12 ml of 0.6 M NaCl solution in the test tube and then centrifuged at (4°C) at 10,000 rpm for 15 min. The supernatant was poured and WHC was measured and expressed in percentage. Cooking loss was measured according to the method as given by Kondaiah et al. (1985). Meat sample (20g) was placed in a polyethylene bag and heated for 1 h in a water bath at core temperature of 72°C. Cooked out was drained, cooled and then weighed to determine the cooking loss. According to the method described by Sen et al. (2004) drip loss was measured. Meat sample (50g) was placed in polyethylene bag with sealad cover and refrigerated (4°C) for 24 h, then wiped and dried with filter paper and weighed. The difference among definite weight of sample and after refrigeration was expected as drip loss. Chemical characteristics of meat were determined by the method of Association of Official Analytical Chemists (AOAC, 2000). Lipids were extracted and purified from the homogenized sample with a chloroform: methanol mixture (1:1 v/v) according to the method of Hanson and Olley (1963). The total lipids were gravimetrically determined.


Table I.- Effects of dietary selenium yeast supplementation fed for 8 weeks on weights of gastrointestinal tract and other visceral organs of goat.

Weights (% EBW)

Basal diet (n=5)

Basal diet ± Se yeast (n=5)



3.49 ± 0.10

4.18 ± 0.30



0.58 ± 0.05

0.53 ± 0.04



0.66 ± 0.05

0.64 ± 0.04


Whole stomach

4.73 ± 0.07

5.34 ± 0.33



0.27 ± 0.01

0.32 ± 0.01



0.59 ± 0.01

0.63 ± 0.02



1.46 ± 0.01

1.49 ± 0.03


Small intestine

2.31 ± 0.01

2.34 ± 0.02



1.06 ± 0.01

1.14 ± 0.03



0.57 ± 0.01

0.62 ± 0.03



0.69 ± 0.03

0.68 ± 0.05


Large intestine

2.32 ± 0.03

2.44 ± 0.04



0.40 ± 0.02

0.43 ± 0.02



0.99 ± 0.04

1.15 ± 0.04



2.07 ± 0.11

2.03 ± 0.12



0.51 ± 0.02

0.57 ± 0.04



0.31 ± 0.02

0.27 ± 0.06


EBW, empty body weight. Values (mean ± SE) differ significantly at P < 0.05.




Table I shows the effects of dietary SY supplementation on weights (percent empty body weight, % EBW) of visceral organ of goats. The weight of rumen increased in B (4.18 ± 0.30 vs 3.49 ± 0.10, P < 0.05) compared to A, however, the weights of whole stomach, omasum and abomasum were not significantly different (P > 0.05) between the groups. The weights of small intestine as a whole, and ileum and jejunum were not different (P > 0.05) between the groups however duodenal weight increased in B (0.32 ± 0.01 vs 0.27 ± 0.01, P < 0.05) compared to A. The weight of rectum was not significantly different between the groups, however, the weights of colon (1.14 ± 0.03 vs 1.06 ± 0.01) and caecum (0.62 ± 0.03 vs 0.57 ± 0.01) increased (P < 0.05) in A compared to B, which resulted in the increase of whole large intestine weight (2.44 ± 0.04 vs 2.32 ± 0.03, P < 0.05) in B compared to A. No significant difference (P > 0.05) was observed between the two dietary groups on the weights of liver, heart, kidney and spleen, however, the lung weight increased in B (1.15 ± 0.04 vs 0.99 ± 0.04, P < 0.05) compared to A.


Table II.- Effects of dietary selenium yeast supplementation for 8 weeks on nutrient digestibility in goats.


Basal diet (n=5)

Basal diet ± Se yeast (n=5)


Week 3
Dry matter

66.43 ± 1.33

75.54 ± 0.95


Crude protein

65.82 ± 0.86

73.73 ± 1.34


Ether extract

71.32 ± 2.41

72.46 ± 1.05


Crude fiber

79.04 ± 1.15

82.89 ± 0.53


Week 6
Dry matter

70.61 ± 1.82

78.46 ± 0.55


Crude protein

68.47 ± 2.48

76.55 ± 0.34


Ether extract

73.94 ± 2.33

76.5 ± 1.06


Crude fiber

80.55 ± 0.55

83.75 ± 0.57


Values (mean ± SE) differ significantly at P < 0.05.


Table III.- Effects of dietary selenium yeast supplementation for 8 weeks on carcass characteristics of goats.


Basal diet (n=5)

Basal diet ± Se yeast (n=5)


Carcass weight (kg)

6.45 ± 0.59

7.58 ± 0.66


Carcass length (cm)

52.25 ± 3.22

55.75 ± 3.71


Dressing (%)

49.41 ± 0.6

52.99 ± 0.77


Leg length (cm)

29.50 ± 1.26

31.0 ± 1.22


Leg weight (kg)

1.05 ± 0.04

1.28 ± 0.06


Rib cage weight (kg)

1.28 ± 0.06

1.5 ± 0.15


Values (mean ± SE) differ significantly at P < 0.05.


The effects of dietary SY supplementation on digestibility in goats at weeks 3 and 6 are shown in Table II. At week 3, the digestibilities of dry matter (DM) (75.54 ± 0.95 vs 66.43 ± 1.33), crude protein (CP) (73.73 ± 1.34 vs 65.82 ± 0.86) and crude fiber (CF) (82.89 ± 0.53 vs 79.04 ± 1.15) increased (P < 0.05) in B compared to A, however, the digestibility of ether extract (EE) was not different (P > 0.05) between two A and B. Similarly, at week 6, the digestibilities of DM (78.46 ± 0.55 vs 70.61 ± 1.82), CP (76.55 ± 0.34 vs 68.47 ± 2.48), CF (83.75 ± 0.57 vs 80.55 ± 0.55) and EE (76.5 ± 1.06 vs 73.94 ± 2.33) significantly increased (P < 0.05) in B compared to A.

Table III shows the effects of dietary SY supplementation on carcass characteristics of goats. The result showed that the carcass dressing % and leg weight (kg) increased (P < 0.05) in B (52.99 ± 0.77 and 1.28 ± 0.06) compared to A (49.41 ± 0.6 and 1.05 ± 0.04). However, the other carcass traits such as rig cage weight, carcass length, leg length, rib cage girth, lion weight, and back weight were not different (P > 0.05) between the groups.

The physic-chemical properties of goat meat are depicted in Table IV. The physical properties of meat including pH, WHC, cooking loss and drip loss were not different between A and B. However, the pH was reduced by 0.15 units, and the cooking and drip losses were reduced by approximately 11 and 13.5 % in B compared to A. Amongst the chemical properties of meat the moisture, protein and ash contents were not different (P > 0.05) between the groups, however, the fat content (2.75 ± 0.25 vs 2.00 ± 0.05%, P < 0.096) tended to increase in B compared to A.


Table IV.- Effects of dietary selenium yeast supplementation for 8 weeks on physico-chemical properties of meat of goats.


Basal diet (n=5)

Basal diet ± Se yeast (n=5)



5.59 ± 0.15

5.44 ± 0.20


WHC (%)

76 ± 4.10

79.5 ± 2.87


Cooking loss (%)

40.41 ± 1.51

36.34 ± 1.91


Drip loss (%)

2.51 ± 0.25

2.21 ± 0.11


Moisture (%)

56.88 ± 3.59

51.75 ± 1.01


CP (%)

22.91 ± 0.67

21.77 ± 0.37


Fat (%)

2.0 ± 0.5

2.75 ± 0.25


Ash (%)

0.85 ± 0.12

0.83 ± 0.12


Values (mean ± SE) differ significantly at P < 0.05.




The GIT of ruminants is characterized by the presence of complex stomachs (especially rumen) followed by the small and large intestines. The rumen and large intestine (particularly colon and caecum) produce as well as absorb short chain fatty acids (SCFA) and fulfills ~ 90% energy requirement of the ruminant’s body needed for maintenance, growth and production (Malhi et al., 2013). In the current study, the dietary selenium yeast (SY) supplementation resulted in the increase of weights of rumen, colon, caecum and the intact large intestine of goats. Previous studies have shown that addition of organic selenium in the diet improved fermentation by elevating the concentrations of propionate and total SCFA and by increasing microbial counts in rumen, caecum and colon of animals (Kim et al., 1997; Liu et al., 2007; Wang et al., 2009; Faixová et al., 2016). The SCFA have trophic effect on GIT epithelium which may stimulate epithelial growth and thereby increase the organ weight (Malhi et al, 2013; Moolchand et al., 2013). Thus, in the present study, the increase in ruminal and large intestine weights in goats fed SY diet might be due to its positive effects on fermentation. In addition to rumen and large intestine, the present study showed an increase in the weight of duodenum and jejunum of SY-fed goats. In agreement with our results, earlier studies have shown an increase in duodenal and jejunal weight of goats and steers fed organic Se compared to their control (Soto-Navarro et al., 2004; Ahmed et al., 2016). The improved growth in these segments of intestine is due to proliferative action of Se (Neville et al., 2008).

In the existing study, weights of liver, heart and spleen did not differ significantly between the groups; however, lung weight increased in SY-fed goats compared to control. Previous studies reported no differences in weights of liver, spleen and kidney in steers and finishing cattle fed organic selenium at the dose rate of approximately 0.3 g/kg of dry matter (Lawler et al., 2004; Sretenović et al., 2012). However, in relation with our results, Reed et al. (2007) reported an increase in lung weight of ewes fed SY supplemented diet. Apart from kidney, significant amount of organic Se is expelled in the form of its metabolite, dimethyl selenide (Se (CH3)2) through lungs (Behne and Kyriakopoulos, 2001). Explaining the reason of higher lung weight, Reed et al. (2007) suggested that the removal of excess Se caused increased respiration and thus lung capacity which was reflected in its weight.

In the current study, digestibility of dry matter (DM), crude protein (CP) and crude fiber (CF) increased by 13.71, 12.02 and 4.78% at week 3 and by 11.11, 11.8 and 3.46% at week 6, in goats fed diet supplemented with SY compared to control. Consistent with our findings, previous studies have reported an increase in nutrients digestibility in pigs and cattle (Wang et al., 2009; Adkins and Evans, 1984). Moreover, the increase in digestibility at week 3 and 6 were of equal magnitude, which suggests that numerical increase in digestibility of nutrients is independent of treatment period. Consistently, Adkins and Evans (1984) did not observe temporal effects of SY on nutrient digestibility analyzed at week 2 and 4 in young pigs. However, SY supplementation produced dose-dependent effects on nutrient utilization. Animals fed diet supplemented with SY at various doses between 0.1 to 0.3 mg/kg. DM of diet showed linear increase in nutrient digestibility in dose-dependent manner while the SY supplementation at the dose rate of 0.45 mg/kg DM of diet reduced nutrient digestibility (Wang et al., 2009; Adkins and Evan, 1984). These data show that SY at higher doses (≥ 0.45 mg/kg of dietary DM) may cause adverse effects on nutrient digestibility.

In the present study, the dressing percentage, carcass weight and leg weight increased by 7.2%, 17.5% and 21.9% respectively, in goats fed SY supplemented diet compared with control. Consistent with the present results, Hernandez-Calva et al. (2013) reported that Se increased leg weight and dressing percentage in lambs and they suggested that the increase in carcass weight and dressing percentage may be due to increase in leg weight. The increase in the meat cuts weight suggests improved muscle growth which might be due to antioxidant and hypertrophic effects of Se in muscles. Dietary Se has been shown to elevate glutathione peroxidase (GSH-Px) activity in muscle (Chung et al., 2007) and induce hypertrophy in type-I skeletal muscle fibers (Rannem et al., 1995). In the present study, the physical properties of meat including pH, WHC; cooking loss and drip loss were not different between the two groups. In accordance with our results previous studies have shown no significant effect of SY supplementation on pH, WHC, cooking loss and drip loss in meat of lambs and calves (Marounek et al., 2006; Esterhuyse, 2012; Hernandez-Calva et al., 2013). Amongst the chemical properties, the moisture, protein and ash contents (%) of meat showed no any difference between the groups, however, the fat content of meat increased by 37.5 % in B compared to A. Consistent with our results, Marounek et al. (2006) observed no significant effects of Se supplemented diet on moisture, protein and ash contents, however, they observed non-significant increase in fat content of meat by 11.76 % in calves fed Se supplemented diet compared to those fed diet without Se supplementation. The elevated fat synthesis in muscles of SY fed goats may be attributed to insulin-like effects of Se because insulin has been shown to haveS anabolic effects on fat (McNeill et al., 1991; Berg et al., 1995).




The results of present study showed that dietary SY supplementation increased weight of some parts of gastrointestinal tract, enhanced nutrient digestibility and improved some carcass characteristics in goats.


Statement of conflict of interest

Authors have declared no conflict of interest.




Adkins, R.S. and Ewan, R.C., 1984. Effect of supplemental selenium on pancreatic function and nutrient digestibility in the pig. J.Anim Sci., 58: 351-355.

Ahmad, K., Khan, Z.I., Ashraf, M., Shah, Z.A., Ejaz, A. and Valeem, E.E., 2009. Time-course changes in selenium status of soil and forage in a pasture in Sargodha, Punjab, Pakistan. Pak. J. Bot., 41: 2397-2401.

Ahmed, Z., Malhi, M., Soomro, S.A., Gandahi, J.A., Arijo A., Bhutto, B. and Qureshi, T.A., 2016. Dietary selenium yeast supplementation improved some villi morphological characteristics in duodenum and jejunum of young goats. J. Anim. Pl. Sci., 26: 382-387.

Alimohamady, R., Aliarabi, H., Bahari, A. and Dezfoulian, A.H., 2013. Influence of different amounts and sources of selenium supplementation on performance, some blood parameters, and nutrient digestibility in lambs. Biol. Trace Element Res., 154: 45-54.

AOAC, 2000. Official methods of analysis, 16th edn. Association of Official Analytical Chemists, Arlington V.A.

Arthur, J.R., 2000. The glutathioneperoxidases. Cell Mol. Life Sci., 57: 1825-1835.

Beck, P.A, Wistuba, T.J, Davis, M.E. and Gunter, S.A., 2005. Effect of feeding supplemental organic or inorganic selenium to cow-calf pairs on Selenium status and immune responses of weaned beef calves. Profess. Anim. Sci., 21: 114-120.

Behne, D. and Kyriakopoulos, A., 2001. Mammalian selenium-containing proteins. Annu. Rev. Nutr., 21: 453-473.

Berg, E.A., Wu, J.Y., Campbell, L., Kagey, M. and Stapleton, S.R., 1995. Insulin-like effects of vanadate and selenate on the expression of glucose-6-phosphate dehydrogenase and fatty acid synthase in diabetic rats. Biochimie., 12: 919–924.

Chung, J.Y., Kim, J.H., Ko, Y.H. and Jang, I.S., 2007. Effects of dietary supplemented inorganic and organic selenium on antioxidant defense systems in the intestine, serum, liver and muscle of Korean native goats. Asian-Aust. J. Anim. Sci., 20: 52-59.

Del Razo-Rodriguez, O.E., Ramirez-Bribiesca, J.E., Lopez-Arellano, R., Revilla-Vazquez, A.L., Gonzalez-Munoz, S.S., Cobos-Peralta, M.A., Hernandez-Calva, L.M. and McDowell, L.R., 2013. Effects of dietary level of selenium and grain on digestive metabolism in lambs. J. Anim. Sci., 58: 253-261.

DeVore, V.R., Colnago, G.L., Jensen, L.S. and Greene, B.E., 1983. Thiobarbituric acid values and Glutathione peroxidase activity in meat from chickens fed a selenium supplemented diet. J. Food. Sci., 48: 300-301.

Enjalbert, F., Lebretonand, P. and Salat, O., 2006. Effects of copper, zinc and selenium status on performance and health in commercial dairy and beef herds: Retrospective study. J. Anim. Physiol. Anim. Nutr., 90: 459-466.

Esterhuyse, J.J. 2012. The effects of different selenium sources on the meat quality and bioavailability of selenium in lamb. MS thesis, Stellenbosch University.

Faixová, Z., Faix, Š., Leng, Váczi, P., Maková, Z. and Szabóová. R., 2007. Haematological, blood and Rumen chemistry changes in lambs following supplementation with se-yeast. Acta Vet Brno., 76: 3-8.

Faustman, C. and Cassens. R.G., 1989. Strategies for improving fresh meat colour. Proc. 35th Int. Cong. Meat Sci. Technol., 11: 446-452.

Gatellier, P., Mercier, Y., Juin, H. and Renerre, M., 2004. Effect of finishing mode (pasture- or mixed –diet) on lipid composition, colour stability and lipid oxidation in meat from Charolais cattle. Meat Sci., 69: 175-186.

Hanson, S.W.F. and Olley, J., 1963. Application of the Bligh and Dyer method of lipid extraction to tissue homogenates. Biochem. J., 89: 101-102.

Hernandez-Calva L.M., Ramirez-Bribiesca, J.E., Guerrero-Legarreta, I., Hernandez-Cruz, L., Avendaño-Reyes, L., Dominguez-Vara, I. and McDowell., L.R. 2013. Influence of dietary magnesium and selenium level on growth performance and carcass-meat quality in finishing diets for feedlot Pelibuey lambs. Archiv Tierzucht. 30: 1-16.

Honikel, KO. 1998. Reference methods for the assessment of physical characteristics of meat. Meat Sci., 4: 447-457.

Johnson, D.E., Lee, P.L., Lu, J. and Williams, L.T., 1990. Diverse forms of a receptor for acidic and basic fibroblast growth factors. Mol. Cell. Biol., 10: 4728-4736.

Kelly, M.P. and Power, R.F., 1995. Fractionation and identification of the major selenium containing compounds in selenized yeast. J. Dairy Sci., 78: 237-248.

Kim, J., Van Soest, P.J. and Combs, G.F.J., 1997. Studies on the effects of selenium on rumen microbial fermentation in vitro. Biol. Trace Elem. Res., 56: 203-213.

Khan, Z., Hussain, A., Ashraf, M. and McDowell, L. 2006. Mineral status of soils and forages in Southwestern Punjab-Pakistan: Micro-minerals. Asian-Aust. J. Anim. Sci., 19: 1139-1147.

Koenig, K.M., Rode, L.M., Cohen, R.D.H. and Buckley, W.T., 1997. Effects of diet and chemical form of selenium on selenium metabolism in sheep. J. Anim. Sci., 75: 817-827.

Kondaiah, N., Anjaneyulu, A.S.R., Rao, K.V., Sharma, N. and Joshi, H.B., 1985. Effect of salt and phosphate on the quality of Buffalo and Goat meats. Meat Sci., 15: 183-192.

Koong, L.J. and Nienaber, J.A., 1985. Changes of fasting heat production and organ size of pigs during prolonged weight maintenance. Eur. Assoc. Anim. Prod. Publ., 32: 46-48.

Lawler, T.L., Taylor, J.B., Finley, J.W. and Caton, J.S., 2004. Effect of supranutritional and organically bound selenium on performance,carcass characteristics, and selenium distribution in finishing beef steers. J. Anim. Sci., 82: 1488-1493.

Liu, Q., Wang, C., Huang, Y.X., Miao, C.H. and Gao, D.H., 2007. Effects of Sel-Plex on rumen fermentation and purine derivatives in Simmental steers. J. Anim. Feed Sci., 16: 133–138.

Maiorino, M., Flohé, L., Roveri, A., Steinert, P., Wissing, J.B. and Ursini, F., 1999. Selenium and reproduction. BioFactor, 10: 251-256.

Malhi, M., Gui, H., Yao, L., Aschenbach, J.R., Gäbel, G. and Shen, Z., 2013. Increased papillae growth and enhanced short-chain fatty acid absorption in the rumen of goats are associated with transient increases in cyclin D1 expression after ruminal butyrate infusion. J. Dairy Sci., 96: 7603-7616.

Marounek. M., Skřivanová, E. and Skřivanová, V. 2006. Selenium content and antioxidant status in tissues of veal calves fed a diet supplemented with selenium yeast. Slovak J. Anim. Sci., 39: 51-54.

McKenzie., R.C., Rafferty., T.S. and Beckett, G.J., 1998. Selenium: An essential element for immune function. Trends, 19: 342-345.

McNeill, J.H., Delgatty, H.L.M. and Battell, M.L. 1991. Insulin-like effects of sodium selenate in streptozotocin-induced diabetic rats. Diabetes, 40: 1675–1679.

Moolchand, M., Wang, J., Gui, H. and Shen, Z., 2013. Ruminal butyrate infusion increased papillae size and digesta weight but did not change liquid flow rate in the rumen of goats. J. Anim. Pl. Sci., 23: 1516-1521.

Morrissey, P.A., Sheehy, P.J.A., Galvin, K., Kerry, J.P. and Buckley, D.J.1998. Lipid stability in meat and meat products. Meat Sci., 49: 73-86.

Naziroglu, M., Aksakal, M., Cay, M. and Celik, S., 1997. Effects of vitamin E and Se on some rumen parameters in lambs. Acta Vet. Hung., 45: 447-456.

Neville, T.L., Ward, M.A., Reed, J.J., Soto-Navarro, S.A., Julius, S.L., Borowicz, P.P., Taylor, J.B., Redmer, D.A., Reynolds, L.P. and Caton, J.S., 2008. Effects of level and source of dietary selenium on maternal and fetal body weight, visceral organ mass, cellularity estimates, and jejunal vascularity in pregnant ewe lambs. J. Anim. Sci., 86: 890-901.

National Research Council, 1983. Selenium in nutrition, 2nd Edition. National Academy Press, Washington, USA.

Ockerman, H.W., 1985. Quality control of post-mortem muscles tissue. 13th ed. The Ohio State University, Colombus, OH.

Ramirez-Bribiesca, J., Tortora, J., Huerta, M., Hernandez, L., López, R. and Crosby, M., 2005. Effect of selenium-vitamin E injection in selenium-deficient dairy goats and kids on the Mexican plateau. Arqu. Bras. Med. Vet. Zootec., 57: 77-84.

Rannem, T., Ladefoged, K., Hylander, E., Christiansen, J., Laursen, H., Kristensen, J.H., Linstow M., Beyer, N., Liguori, R., Dige-Petersen, H., Jensen, B.H. and Jarnum, S., 1995. The effect of selenium supplementation on skeletal and cardiac muscle in selenium-depleted patients. J. Parent Enter. Nutr., 19: 351-355.

Reed, J.J., Ward, M.A., Vonnahme, K.A., Neville, T.L., Julius, S.L., Borowicz, P.P., Taylor, J.B., Redmer, D.A., Grazul-Bilska, A.T., Reynolds, L.P. and Caton, J.S., 2007. Effects of selenium supply and dietary restriction on maternal and fetal body weight, visceral organ mass, cellularity estimates, and jejeunal vascularity in pregnant ewe lambs. J. Anim. Sci., 85: 2721-2733.

Sainz, R.D. and Bentley, B.E., 1997. Visceral organ mass and cellularity in growth-restricted and refed beef steers. J. Anim. Sci., 75: 1229-1236.

Sánchez-Escalante, A., Djenane, D., Torrescano, G., Beltrán, J.A., Roncalés, P., 2001. The effects of ascorbic acid, taurine, carnosine and rosemary powder on colour and lipid stability of beef patties packaged in modified atmosphere. Meat Sci., 58: 421-429.

Sen, A.R., Santra, A. and Karim, S.A., 2004. Carcass yield, composition and meat quality attributes of sheep and goat under semiarid conditions. Meat Sci., 66: 757-763.

Serra, A.B., Nakamura, K., Matsui, T., Harumoto, T. and Fujihar, T., 1994. Inorganic selenium for sheep II. Its influence on rumen bacterial yield, volatile fatty acid production and total tract digestion of timothy hay. Asian J. Anim. Sci., 7: 91-96.

Soto-Navarro, S., Lawler, T., Taylor, J., Reynolds, L., Reed, J., Finley, J. and Caton, J., 2004. Effect of high-selenium wheat on visceral organ mass, and intestinal cellularity and vascularity in finishing beef steers. J. Anim Sci., 82: 1788-1793.

Sretenović, L.J., Novaković, Ž., Petrović, M.M., Todorović, M., Pantelić, V., Aleksić, S. and Petrićević, M., 2012. Producing of beef meat enriched with organically bound selenium. Biotech. Anim. Husb., 28: 219-229.

Tapiero, H., Townsend, D.M. and Tew, K.D., 2003. The antioxidant role of selenium and seleno-compounds. Biomed. Pharmacother., 57: 134-44.

Tian, J.Z., Yun, M.S., Kong, C.S., Piao, L.G.,. Long, H.F., Kim, J.H., Lee, J.H., Lim, J.S., Kim, C.H., Kimand, Y.Y. and Han, I.K., 2006. Effects of different products and levels of selenium on growth, nutrient digestibility and selenium retention of growing-finishing pigs. Asian-Aust. J. Anim. Sci., 19: 6-66.

Underwood, E., 2012. Trace elements in human and animal nutrition. Elsevier.

Viram, K., Malhi, M., Soomro, S.A., Qureshi, T.A., Sanjrani, M.N. and Malhi, K. D., 2017. Gender differences in some haematological and blood biochemical parameters in Wild Indian Peafowl (Pavo cristatus) of Thar Desert, Pakistan. Pakistan J. Zool., 49: 1477-1481.

Wang, C., Liu, Q., Yang, W., Dong, Q., Yang, X., He, D., Zhang, P., Dong, K. and Huang, Y., 2009. Effects of selenium yeast on rumen fermentation, lactation performance and feed digestibilities in lactating dairy cows. Livest. Sci., 126: 239-244.

Wardlaw, F.B., McCaskill, L.H. and Acton, J.C., 1973. Effect of postmortem muscle changes on poultry meat loaf properties. J. Food Sci., 38: 421-423.

To share on other social networks, click on P-share. What are these?


Pakistan Journal of Zoology


Vol. 50, Iss. 3, Pages 799-1198


Click here for more

Subscribe Today

Receive free updates on new articles, opportunities and benefits

Subscribe Unsubscribe