Você está na página 1de 10

Vol 7 (2) Feb17

International Journal of Livestock Research eISSN : 2277-1964 NAAS Score -5.36

Review
Selenium for Calf Growth and Health - Mini Review
Vinu M. Nampoothiri1* and P. Gangadevi2

MRDF Total Mixed Ration Plant, Palakkad, Kerala, INDIA


1
Assistant Veterinary Officer,
2
Professor & Head, Division of Animal Nutrition, College of Veterinary and Animal Sciences, Mannuthy,
Kerala, INDIA

*Corresponding author: vinumnatl@gmail.com

Rec.Date: Jan 19, 2017 06:59


Accept Date: Feb 12, 2017 15:28
Published Online: February 16, 2017
DOI 10.5455/ijlr.20170212032834

Abstract
Dairy cattle form an integral part of Indian animal wealth, which accounts to 15 per cent of worlds total
cattle population. Production of healthy calves should be given due importance in dairy cattle
management. Dairy farmers are suffering from huge economic losses due to diseases of newly born calf.
Supplementation of selenium in inorganic/organic form to calves improves growth, immune response and
hence finally improve the health status of the animal. Selenium helps in the formation of thyroid
hormones, antioxidant enzyme glutathione peroxidase and also improves neutrophil activity.

Key words: Selenium, Calves, Immunity, Glutathione Peroxidase

How to cite: Nampoothiri, V., & GangaDevi, P. (2017). Selenium for calf growth and health: Mini
review. International Journal of Livestock Research, 7(2), 110. doi:10.5455/ijlr.20170212032834

Introduction

Selenium has attracted much attention recently in animal and human nutrition. Even though selenium in
excess is toxic, in trace amounts it exerts various beneficial effects in vivo. Selenium supplementation was
found to improve the growth and muscle development. Selenium influences the immune response by the
activation of phagocytosis, increased antibody production and enhanced lymphocyte proliferation.
Supplementation of selenium had increased the blood globulin level indicating the improved immunity
status in male buffalo calves of 8 to 9 months of age (Mudgal et al. 2008).

Selenium is an effective antioxidant in animal body being the key component in the antioxidant enzyme,
glutathione peroxidase (GSH-Px) which protects cells and unsaturated fatty acids in cell membranes from
damage by oxidizing materials. Selenium dependent enzymes deiodinases are responsible for the
1 Page

formation of biologically active thyroid hormone T 3 from T4, deficiency of which affects the production

Hosted@www.ijlr.org DOI 10.5455/ijlr.20170212032834


Vol 7 (2) Feb17
International Journal of Livestock Research eISSN : 2277-1964 NAAS Score -5.36

performance of the animal. Selenium has been approved as a feed additive for cattle ration since 1979,
first at an added level of 0.1 mg/kg of DM (FDA, 1979) and at 0.3 mg/kg of DM (FDA, 1987).

Growth
Selenium plays an important role in the formation of thyroid hormones. Enzyme 5 iodothyronine
deiodinase is a selenium dependent enzyme, which helps in the activation of T4 (tetra iodothyronine).
Selenium influences the growth performance through the formation and activation of thyroid hormones.
Selenium and Vitamin E functions are inter dependent. Selenium and Vitamin E, both are excellent anti
oxidants as they form part of the major antioxidant enzyme glutathione peroxidase. Selenium deficiency
can be partially compensated by Vitamin E supplementation. So the deficiency of Selenium and Vitamin
E results in thyroid malfunction which inturn results in retarded growth. Selenium requirement for calves
is 100 g/kg DM and Vitamin E about 40-60 IU (NRC, 2001).

Gleed et al. (1983) from his studies on the effects of selenium and copper supplementation on the growth
of beef steers reported that by supplementing 0.15 mg selenium/kg body weight increased growth rate by
0.041 and 0.060 kg/day respectively in two experiments. Phillips et al. (1989) reported increased weight
gain by selenium supplementation in suckling beef calves in the 90 to 120 days period of their test but
gains were not significantly different for the whole 120 days period. Tsai and Bukas (2003) also observed
14.1 per cent increase in the body weight gain of calves aged from two to three months when
supplemented with 0.2 mg sodium selenite/kg feed. Similarly, Reiss et al. (2008) also observed higher
weight gain in twelve month old Nellore calves when supplemented with 5.4 mg of selenium/ animal/
day.

Selenium supplementation can be done through different routes. Studies were also done regarding
supplementation of selenium through intra ruminal and parenteral routes. Results will be quicker while
supplying through parenteral route compared with that of oral route. Wichtel et al. (1996) got higher
mean daily body weight gain for Friesian calves on supplementation with selenium as intra ruminal
pellets than that of the non supplemented group.

Increased growth response on parenteral supplementation of selenium was reported by different authors.
Spears et al. (1986) noticed increased weaning weight in calves when injected with 5.5mg selenium and
75 IU Vitamin E /100 kg body weight at 60 days intervals from first to fifth or seventh month of age
when compared with un supplemented calves. Reffett et al. (1986) found that selenium injection at 15
2

mg/head increased calf weight gains in first fourteen days after weaning. Yuhua et al. (1996) also got
Page

similar result in goats. Castellan et al. (1999) obtained higher average daily gain than the control group on

Hosted@www.ijlr.org DOI 10.5455/ijlr.20170212032834


Vol 7 (2) Feb17
International Journal of Livestock Research eISSN : 2277-1964 NAAS Score -5.36

parenteral administration of selenium to suckling beef calves at the rate of 0.05 mg/kg within two days of
birth and on days 70, 114 and 149.

Selenium is available in inorganic and organic form. Common inorganic forms include Sodium selenite
and selenate. Organic form exists as Seleno methionine. The organic source of selenium yeast is more
digestible than commonly used inorganic selenium (sodium selenite) (Pagan et al., 1999). Guyot et al.
(2007) observed higher growth in calves fed diets with organic selenium (Y-Se) when given at the rate of
0.5 ppm compared to those fed diets containing inorganic selenium as sodium selenite. Lambs fed diet
with 0.15 ppm selenium as sodium selenite or organic selenium (Jevsel-101) recorded improved growth
rate, humoral immune response and antioxidant status compared to non supplemental control (Kumar et
al., 2009) and the effect being higher for organic selenium group than those fed inorganic selenium
supplemented diet.

Several works showed no effects of selenium supplementation on growth. Mehdi and Dufrasne (2016)
explained that the selenium dependent selenoprotein, 5 iodo thyronine deiodinase is one of the last protein
to be affected due to selenium deficiency, which may be the reason for this non effect of Selenium on
growth performance. Dietary supplementation of selenium at 0, 0.1 and 1 ppm in Holstein calves of 120
days of age for a period of 28 days by Kincaid et al. (1977) could not observe any significant difference
in calf weight gains. Growth studies conducted in sheep and crossbred steers by Ullrey et al. (1977) also
could not obtain any significant improvement in average daily gain by dietary supplementation of
selenium at 100 and 200 ppb as sodium selenite for six weeks. Ammerman et al. (1980) supplemented
selenium at 0.1 or 0.2 ppm as sodium selenite to beef cows and suckling calves along with soybean meal,
corn and linseed meal and observed that selenium supplementation did not significantly influence live
weight of the cows or birth weight of calves, but had an increasing trend in weaning weight of the calves.
Siddons and Mills (1981) tested three basal diets containing 0.05, 0.025, and 0.024 ppm of selenium as
sodium selenite on four week old Friesian bull calves and noticed no significant difference in average
daily gain during the feeding trial of 36 weeks. When calves were fed skim milk powder based milk
replacer containing either 0.2, 1, 3, 5 or 10 ppm selenium added as sodium selenite from 3 to 45 days of
age to estimate the lowest amount of dietary selenium that would reduce calf performance and feed
utilization by Jenkins and Hidiroglou (1986), only the highest selenium (10 ppm) fed calves showed
reduced average daily gain. They also opined that preruminant calves were very tolerant of high inorganic
selenium concentration in skim milk powder based milk replacer.
3 Page

Hosted@www.ijlr.org DOI 10.5455/ijlr.20170212032834


Vol 7 (2) Feb17
International Journal of Livestock Research eISSN : 2277-1964 NAAS Score -5.36

McClure and Mahan (1988) had not observed any effect on the growth rate of growing and finishing
lambs received diet with 0.25, 1or 2 ppm of selenium as selenium yeast. When calves were supplemented
with sodium selenite, selenium enriched yeast and live yeast culture, Nicholson et al. (1991a) obtained no
difference in weight gain due to treatment. Nursing cows when supplemented with 113 g/day of free
choice mineral mixture containing 26 ppm selenium as sodium selenite or selenium yeast (selplex),
Gunter et al. (2003) noticed no significant improvement in average daily gain of nursing calves. Lawler et
al. (2004) also reported that dietary selenium supplementation (2.84ppm) had no effect on the average
daily gain of crossbred steer heifers. Slavik et al. (2008) observed no significant increase in weight gain
in the calves that were supplemented with both organic and inorganic forms of selenium at the rate of
1mg per head per day. Juniper et al. (2008) noticed no treatment effect on body weight by giving
selenium at varying levels (0.15 to 6.63 ppm) as selenium enriched yeast to cattle, calves and lambs.
Feeding calves on torula yeast based diet with or without sodium selenite (0.1 to 0.45 ppm selenium) did
not influence growth rate and feed intake (Lum et al., 2009). Richards et al. (2011) had given 0.34 ppm of
supplemental selenium from selenium yeast for a 130 day finishing period to beef cattle and obtained no
improvement in body weight gain.

In calves received 0, 1 or 2 injections of selenium and vitamin E at a dose rate of 0.078 mg and 5.4 IU/
100 kg respectively during a period of 14 to 56 days of age, Weiss et al. (1983) had not observed any
improvement in weight gain in treatment groups. Afzal et al. (1988) had not obtained any significant
difference in weight gain when newborn jersey calves and buffalo calves were supplemented with 500mg
of vitamin E and 200 g selenium daily from birth to 30 days of age. Effect of preweaning parenteral
supplementation of vitamin E and selenium at the rate of 300 U and 6mg/45 kg body weight to new born
calves at 24 to 48 hours and 14 days after birth up to three months of age was studied by Mohri et al.
(2005) and observed no significant differences for weight gain from birth to three months compared to un
supplemented control. Non significant effect of dietary supplementation of selenium enriched yeast and
vitamin E at varying levels on body weight gain was also reported by Skrivanova et al. (2007) in calves.
Supplementation of selenium at 0.3 ppm alone or vitamin E at 300 IU/ day plus selenium at 0.3 ppm as
sodium selenite had not improved the growth performance and nutrient utilization in male buffalo calves
of 10 to 12 months of age (Shinde et al., 2008). Swecker et al. (2008) found no effect on weight gain in
weaned beef calves when fed with 0.1 mg of selenium and 0.22 IU vitamin E/kg of body weight.

Immune Response and Health


4

Relationship between selenium and udder health due to its antioxidant properties are well known.
Page

Selenium supplementation can improve humoral and cellular immune responses. Selenium

Hosted@www.ijlr.org DOI 10.5455/ijlr.20170212032834


Vol 7 (2) Feb17
International Journal of Livestock Research eISSN : 2277-1964 NAAS Score -5.36

supplementation cause improved expression of natural killer (NK) cells. Phagocytic activity of
neutrophils also increases by selenium supplementation.

Glutathione Peroxidase Activity


Siddons and Mills (1981) observed that in calves, the plasma and whole blood activity of GSH-Px was
reduced to a minimum level of approximately 15 units/g haemoglobin at 16 weeks in low selenium group
where as in the selenium supplemented group, activity increased continuously during the first 22 weeks to
a maximum level of approximately 300 units/g haemoglobin. Stabel et al. (1989) from his studies on
effect of selenium on GSH-Px and the immune response of stressed calves challenged with Pasteurella
hemolytica, noticed a higher GSH-Px activity for selenium supplemented group. The GSH-Px of whole
blood was numerically higher in cows fed with selenium fertilized silage than that with inorganic
selenium though the differences were not significant (Nicholson et al., 1991b). Gerloff (1992) observed
that when selenium was given at 0.3 and 6mg per day, the whole blood GSH-Px increased from 15 mU to
25 mU/mg of haemoglobin. Walsh et al. (1993) noted that erythrocyte GSH-PX activity in calves fed on
diets supplemented with selenium increased steadily reaching a plateau of between 250 and 320 IU/g
haemoglobin compared to that of erythrocyte GPX activity (55 IU/g Hb) in calves fed on diets low in
selenium. Rowntree et al. (2004) also found that dairy cows drenched with 20 mg selenium as sodium
selenite weekly once for two months showed significant increase in GSH-Px, the values being 14.91 vs
24.61 EU/g of haemoglobin. Lum et al. (2009) observed that GSH-Px activity was greater for calves fed
selenium adequate diet than for selenium deficient calves by 84 days of age. Edward et al. (1985)
observed that selenium treated calves showed higher blood GSH-Px concentrations (143 units/g
haemoglobin) when compared to non supplemented control. Activities of superoxide dismutase and GSH-
Px were significantly increased by selenium supplementation at 0 or 1 ppm level in Liaoning cashmere
goats (Qin et al., 2011).

Influence of organic and inorganic selenium supplements on GSH-Px activity was also studied by several
authors and organic selenium was found to have higher GSH-Px activity. Significant increase in GSH-Px
activities were noticed by Gunter et al. (2003) in calves born to cows supplemented with selenium yeast
compared to those fed selenium as sodium selenite. In Belgium blue cows and calves Guyot et al. (2007)
obtained higher GSH-Px activity in erythrocytes for 0.5 ppm selenium yeast diet against 0.1 ppm sodium
selenite. Beef cattle fed diets supplemented with 6.47 ppm of selenium as selenium yeast showed
significant GSH-Px activity of 1283 compared to 844 units per gram haemoglobin in control which
received 0.2 ppm selenium diet (Juniper et al., 2008). Kumar et al. (2009) by giving 0.15 ppm of
5 Page

Hosted@www.ijlr.org DOI 10.5455/ijlr.20170212032834


Vol 7 (2) Feb17
International Journal of Livestock Research eISSN : 2277-1964 NAAS Score -5.36

selenium through sodium selenite and organic selenium (Jevsel 101) found increased RBC GSH- Px
activity in lambs when fed diets supplemented with 0.15 ppm of selenium as sodium selenite.

But in contradiction to these results Ortman and Pehrson (1997) reported that calves fed diets
supplemented with sodium selenite (3mg) and selenium in yeast (0.75 and 3mg) showed similar GSH-Px
activity in erythrocytes. Slavik et al. (2008) also reported significantly higher GSH-Px activity in late
pregnant beef cows and calves fed diet supplemented with organic and inorganic selenium.

Combinations of selenium and Vitamin E also showed similar results as they work in an interdependent
manner. When selenium (5.5 mg) and vitamin E (75 IU) injections were given in calves, Spears et al.
(1986) also noticed improved whole blood GSH-Px activity than that of control group. Kennedy et al.
(1987) studied the experimental myopathy in vitamin E and selenium depleted calves with and without
added dietary polyunsaturated fatty acids as a model for nutritional degenerative myopathy in ruminant
cattle and reported high GSH-Px activity in vitamin E-selenium supplemented group with no clinical
abnormalities or evidence of myo degeneration.

Immune Response
Highest density of selenium is found in kidney, while it is found in highest amount on muscles. So the
first organs to be affected due to selenium deficiency are heart, skeletal muscle and liver (Meschy, 2010).
Nutritional muscular dystrophy is a common occurrence due to selenium deficiency. Hidiroglou et al.
(1985) found that administration of intraruminal pellets to cows during last three months of pregnancy
had reduced the case of nutritional muscular dystrophy in calves. Along with kidney, liver, testis and
lungs also store large amount of selenium. Reffett et al. (1988) noticed the effect of dietary selenium on
the primary and secondary immune response in calves challenged with infectious bovine rhinotracheitis
virus found that whole blood and plasma GSH-Px activity increased in selenium supplemented group (0.2
mg/kg diet) but not in selenium deficient calves. Gill and Walker (2008) reported that mice fed with high
selenium diet (121 g/100g feed) for 49 days showed proliferation of spleen lymphocytes compared to
that fed selenium sufficient control (18 g/100g feed) indicating improved immune response of selenium
fed animals. Vinu et al., (2012) observed lower incidence of disease in crossbred calves when
supplemented with selenium yeast at the rate of 0.3 ppm.

Spears et al. (1986) found that selenium- vitamin E injections reduced calf death losses. Oxidative stress
is associated with the production of free radicals and the inability of body to counteract or detoxify these
6

harmful substances. Antioxidant activity of selenium prevents the production of free radicals due to
Page

peroxidation reactions. Reffett et al. (1986) concluded that selenium or zinc supplementation may

Hosted@www.ijlr.org DOI 10.5455/ijlr.20170212032834


Vol 7 (2) Feb17
International Journal of Livestock Research eISSN : 2277-1964 NAAS Score -5.36

individually improve an animals response to stress. Selenium improves neutrophil activity. Arthur et al.
(2003) reported significantly higher candidacidal activity of neutrophils when selenium deficient mice
were given intra peritoneal injection of sodium selenite at > 10 g per kilogram body weight in 0.9 per
cent sodium chloride solution.

But certain studies showed non-significant effect of selenium supplementation on immunity. Weiss et al.
(1983) studied the role of selenium/vitamin E in disease prevention and weight gain of neonatal calves by
injecting 0.078 mg selenium and 5.4 IU vitamin E/kg body weight and reported no reduction in the
incidence of respiratory diseases. Effect of vitamin E (500 mg) and selenium (200g) supplementation on
immunity was studied in newborn jersey and buffalo calves from birth to 30 days by Afzal et al. (1988)
could not found any significance in total leucocyte count, differential leucocyte count, antibody titre and
susceptibility to disease on supplementing vitamin E (500mg) and selenium (200g) to new born jersey
and buffalo calves. Hoshino et al. (1989) from their studies on serum tocopherol, selenium levels and
blood GSH-Px activities in calves with white muscle disease observed that white muscle disease in calves
was attributable to nutritional muscular dystrophy caused by deficiencies in tocopherol and selenium in
feed stuffs supplied to their dams.

Conclusion
Selenium was first given importance because of its toxicity, later it was identified that selenium is
essential for animals for various life activities and also for developing proper immune mechanism against
the invaders. There is only a narrow gap between toxic dose and dietary essential dose in case of
selenium. Deficiency of selenium leads to white muscle disease in calves and toxicity leads to alkali
disease. So it is better to follow FDA guidelines during supplementation of selenium (0.3 ppm) in the
diet. As of now research works had proved the efficiency of organic form of selenium over inorganic
selenium. Proper supplementation of selenium keeps the animal in good growth and health condition.

Conflicts of Interests
The author have not declared any conflict of interests

Reference

1. Afzal, M., Hussain, M., Khan, K.N. and Munir, R. 1988. Effect of vitamin E and selenium on
immunity in newborn jersey and buffalo calves. AJ. AS. 1: 13-19
2. Ammerman, C.B., Chapman, H.L., Bouwman, G.W., Fontenot, J.P., Bagley, C.P. and Moxon, A.L.
1980. Effect of supplemental selenium for beef cows on the performance and tissue selenium
7

concentrations of cows and suckling calves. J. Anim. Sci. 51: 1381-1386


Page

Hosted@www.ijlr.org DOI 10.5455/ijlr.20170212032834


Vol 7 (2) Feb17
International Journal of Livestock Research eISSN : 2277-1964 NAAS Score -5.36

3. Arthur, J.R., Mckenzie, R.C. and Beckett, G.J. 2003. Selenium in the immune system. J. Nutr. 133:
1457-1459
4. Castellan, D.M., Maas, J.P., Gardner, I.A., Oltjen, J.W. and Sween, M.L. 1999. Growth of suckling
beef calves in response to parenteral administration of selenium and the effect of dietary protein
provided to their dams. J. Am. Vet. Med. Ass. 15; 214(6): 816-821
5. Edward, C., Segerson and Spears, J.W. 1985. Selenium status and phytohemaglutinin-stimulated T
lymphocytes from beef calves. Biol. Trace Ele. Res. 70: 173-180
6. Food and Drug Administration. 1979. Food additives permitted in feed and drinking water of
animals:selenium. Fed. Reg. 44: 5392p
7. Food and Drug Administration. 1987. Food additives permitted in feed and drinking water of
animals:selenium. Fed. Reg. 52: 10668p
8. Gerloff, B.J. 1992. Effect of selenium supplementation on dairy cattle. J. Anim. Sci. 70: 3934-3940
9. Gill, H. and Walker, G. 2008. Selenium, immune function and resistance to viral infections. Nutr.
Dietetics 65: 41-47
10. Gleed, P.T., Allen, W.M., Mallinson, C.B., Rowlands, G.J., Sansom, B.F., Vagg, M.J. and Caswell,
R.D. 1983. Effects of selenium and copper supplementation on the growth of beef steers. Vet. Rec.
113: 388-392
11. Gunter, S.A., Beck, P.A. and Phillips, J.M. 2003. Effects of supplementary selenium source on the
performance and blood measurements in beef cows and their calves. J. Anim. Sci. 81: 856-864
12. Guyot, H., Spring, P., Andrieu, S. and Rollin, F. 2007. Comparative responses to sodium selenite and
organic selenium supplements in Belgium blue cows and calves. Livestock Sci. 111: 259-263
13. Hidiroglou, M., Proulx, J. and Jolette, J. 1985. Intraruminal selenium pellet for control of nutritional
muscular dystrophy in cattle. J. Dairy Sci. 68: 57-66
14. Hoshino, Y., Ichijo, S., Osame, S. and Takahashi, E. 1989. Studies on serum tocopherol, selenium
levels and blood glutathione peroxidase activities in calves with white muscle disease. Nihon Juigaku
Zasshi. 51(4): 741-748
15. Jenkins, K.J. and Hidiroglou, M. 1986. Tolerence of the preruminant calf for selenium in milk
replacer. J. Dairy Sci. 69: 1865-1870
16. Juniper, D.T., Phipps, R.H., Givens, D.I., Jones, A.K., Green, C. and Bertin, G. 2008. Tolerence of
ruminant animals to high dose in feed administration of a selenium enriched yeast. J. Anim. Sci. 86:
197-204
17. Kennedy, S., Rice, D.A. and Davidson, W.B. 1987. Experimental myopathy in vitamin E and
selenium depleted calves with and without added dietary polyunsaturated fatty acids as a model for
nutritional degenerative myopathy in ruminant cattle. Res. Vet. Sci. 43(3): 384-394
18. Kincaid, R.L., Miller, W.J., Neathery, M.W., Gentry, R.P. and Hampton, D.L. 1977. Effect of added
dietary selenium on metabolism and tissue distribution of radioactive and stable selenium in calves.
J. Anim. Sci. 44:147-151
19. Kumar, N., Garg, A.K, Dass, R.S, Chaturvedi, V.K., Mudgal, V., Varshney, V.P. 2009. Selenium
supplementation influences growth performance, antioxidant status and immune response in lambs.
Anim. Feed Sci. Technol. 153: 77-87
20. 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
21. Lum, G.E., Rowntree, J.E., Bondioli, K.R., Southern, L.L. and Williams, C.C. 2009. The influence
of dietary selenium on common indicators of selenium status and liver glutathione peroxidase-1
messenger ribonucleic acid. J. Anim. Sci. 87: 1739-1746
22. McClure, K.E. and Mahan, D.C. 1988. Effect of dietary selenium source on retention, digestibility
and wool accumulation of selenium in growing lambs. Nutr. Rep. Int. 37, 839-846
8

23. Mehdi, Y. and Dufrasne, I. 2016. Selenium in cattle: A review. Molecules. 21: 545-559
Page

Hosted@www.ijlr.org DOI 10.5455/ijlr.20170212032834


Vol 7 (2) Feb17
International Journal of Livestock Research eISSN : 2277-1964 NAAS Score -5.36

24. Mohri, M., Seifi, H.A. and Khodadadi, J. 2005. Effects of preweaning parenteral supplementation of
vitamin E and selenium on hematology, serum proteins, and weight gain in dairy calves. Comp. Clin.
Puchol. 14: 149-154
25. Mudgal, V., Garg, A.K., Dass, R.S. and Varshney, V.P. 2008. Effect of selenium and copper
supplementation on blood metabolic profile in male buffalo ( Bubalus bubalis ) calves. Biol.
Trace Ele. Res. 121: 31-38
26. National Research Council (NRC). 2001. Nutrient Requirements of Dairy Cattle. Seventh Revised
Edition; National Acedemy Press: Washington, DC, USA.
27. Nicholson, J.W.G., St-Laurent, A.M., McQueen, R.E. and Charmley, E. 1991a. The effect of feeding
organically bound selenium and alpha tocopherol to dairy cows on susceptibility of milk to
oxidation. Can. J. Anim. Sci. 71: 135-143
28. Nicholson, J.W.G., McQueen, R.E. and Bush, R.S. 1991b. Response of growing cattle to
supplementation with organically bound or inorganic sources of selenium or yeast cultures. Can. J.
Anim. Sci. 71: 803-811
29. Ortman, K. and Pehrson, B. 1997. Selenite and selenium yeast as feed supplements for dairy cows. J.
Vet. Med. 44: 373-380
30. Pagan, J.D., P. Karnezos, M.A.P. Kennedy, T. Currier and K.E. Hoekstra. 1999. Effect of selenium
source on selenium digestibility and retention in exercised Thoroughbreds. Proc. Equine Nutrition &
Physiology Soc., Raleigh, N.C.
31. Phillips, J.M., Brown, A.H. and Parham, R.W. 1989. Growth of the beef calf with selenium
supplementation. Nutr. Rep. Int. 39(3): 537-545
32. Qin, F., Zhu, X., Zhang, W., Zhou, J., Zhang, S. and Jia, Z. 2011. Effects of dietary iodine and
selenium on nutrient digestibility, serum thyroid hormones and antioxidant status of Liaoning
cashmere goats. Biol. Trace Ele. Res. 143: 1480-1488
33. Reffett. J.K., Spears, J.W., Hatch, P.A. and Brown, T.T. 1986. Influence of selenium and zinc on
performance, blood constituents and immune response in stressed calves. Biol. Trace Ele. Res. 9:
139-149
34. Reffett, J.K., Spears, J.W. and Brown, T.T. Jr. 1988.Effect of dietary selenium on the primary and
secondary immune response in calves challenged with infectious bovine rhinotracheitis virus. J.
Nutr. 118: 229-235
35. Reis, L.S., Chiacchio, S.B., Pardo, P.E., Oba, E., Giuffrida, R. and Frazatti-Gallina, N.M. 2008.
Selenium supplementation enhances weight gain in cattle. Arch. Zootec. 57 ( 218 ): 271-274
36. Richards, C.J., Blalock, H.M., Jacques, K.A. and Loveday, H.D. 2011. Efficiency of feeding
selenium enriched yeast to finishing beef cattle. Proff. Anim. Scient. 27: 1-8
37. Rowntree, J.E., Hill, G.M., Hawkins, D.R., Link, J.E., Rincker, M.J., Bednar, G.W. and Kreft, R.A.
2004. Effect of selenium on selenoprotein activity and thyroid hormone metabolism in beef and dairy
cows and calves. J. Anim. Sci. 82: 2995-3005
38. Shinde, P.L., Dass, R.S., Garg, A.K. and Bhadane, K.P. 2008. Effect of vitamin E and selenium
supplementation on growth, nutrient utilization and their balance in male buffalo calves. Anim. Nutr.
Feed Technol. 8: 157-165
39. Siddons, R.C. and Mills, C.F. 1981. Glutathione peroxidase activity and erythrocyte stability in
calves differing in selenium and vitamin E status. Br. J. Nutr. 46: 345-355
40. Skrivanova, E., Marounek, M., De Smet, S. and Raes, K. 2007. Influence of dietary selenium and
vitamin E on quality of veal. Meat Sci. 76: 495-500
41. Slavik, P., Illek, J., Rajmon, R., Zeleny, T. and Jilek, F. 2008. Selenium dynamics in the blood of
beef cows and calves fed diets supplemented with organic and inorganic selenium sources and the
effect on reproduction. Acta Vet. Brno. 77: 11-15
42. Spears, J.W., Harvey, R.W. and Segerson, E.C. 1986. Effects of marginal selenium deficiency and
9

winter protein supplementation on growth, reproduction and selenium status of beef cattle. J. Anim.
Page

Sci. 63: 586-594

Hosted@www.ijlr.org DOI 10.5455/ijlr.20170212032834


Vol 7 (2) Feb17
International Journal of Livestock Research eISSN : 2277-1964 NAAS Score -5.36

43. Stabel, R.S., Spears, J.W., Brown, T.T. and Brake, J. 1989. Selenium effects on glutathione
peroxidase and the immune response of stressed calves challenged with Pasteurella hemolytica. J.
Anim. Sci. 67: 557-564
44. Swecker, W.S., Eversole, D.E., Thatcher, C.D., Blodgett, D.J., Schurig, G.G. and Meldrum, J.B.
2008. Influence of supplemental selenium on humoral immune responses in weaned beef calves. J.
Vet. Int. Med. 22: 443-449
45. Tsai, V.P. and Bukas, V.V. 2003. Selenium supplementation of mixed feeds for growing cattle.
Zootec. Sci. Belarus Collection of Scientific Papers 38: 300-305 Available : agris. fao. org/ agris-
search/ display. do i.f.
46. Ullrey, D.E., Brady, P.S., Whetter, P.A., Ku, P.K. and Magee, W.T. 1977. Selenium supplementation
of diets for sheep and beef cattle. J. Anim. Sci. 45: 559-565
47. Vinu, M. N., Gangadevi, P., Mercy, A. D., Anil, K. S. and Shyama, K. 2012.Effect of dietary
supplementation of organic selenium on growth performance and nutrient utilization in crossbred
calves. J. Vet. Anim. Sci. 43: 36-40
48. Walsh, D.M., Kennedy, D.G., Goodwall, E.A. and Kennedy, S. 1993. Antioxidant enzyme activity in
the muscles of calves depleted of vitamin E or selenium or both. Br. J. Nutr. 70: 621-630
49. Weiss, W.P., Colenbrander, V.F., Cunningham, M.D. and Callahan, C.J. 1983. Selenium/vitamin E :
Role in disease prevention and weight gain of neonatal calves. J. Dairy Sci. 66: 1101-1107
50. Wichtel, J.J., Craig, A.L., Freeman, D.A., Alvarez, V. and Williamson, N.B. 1996. Effect of
selenium and Iodine supplementation on growth rate and on thyroid and somatotrophic function in
dairy calves at pasture. J. Dairy Sci. 79: 1865-1872
51. Yuhua, L., Xingsuo, W. and Xiutian, D. 1996. Effects of selenium supplementation in diet on the
ruminal digestion and metabolism of goats. Acta Agric. Univ. Henanensis. 1: 1-7

10 Page

Hosted@www.ijlr.org DOI 10.5455/ijlr.20170212032834

Você também pode gostar