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Somatotropin

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DOI: 10.1081/E-EAS2-120019802

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Somatotropin
Dale E. Baumana; Frank R. Dunsheab
a
Department of Animal Science, Cornell University, Ithaca, New York, U.S.A. b Department of
Primary Industries, Werribee, Victoria, Australia

Online publication date: 19 November 2010

To cite this Chapter Bauman, Dale E. and Dunshea, Frank R.(2010) 'Somatotropin', Encyclopedia of Animal Science,
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Somatotropin

Dale E. Bauman
Department of Animal Science, Cornell University, Ithaca, New York, U.S.A.
Frank R. Dunshea
Department of Primary Industries, Werribee, Victoria, Australia

Abstract
Somatotropin is a protein hormone secreted from the anterior pituitary gland under the action of growth
hormone-releasing factor (stimulatory) and somatostatin (inhibitory) released from the hypothalamus. So-
matotropin can vary slightly in size, generally about 191 amino acids, and the amino acid sequence also var-
ies among species. Whereas bST and pST share a high degree of sequence similarity (ca. 90%), both have
Downloaded By: [Bauman, Dale E.][Cornell University Library] At: 14:34 20 January 2011

a much lower homology with human ST (ca. 65%) and hence are inactive in humans. Since ST is a protein,
it is digested if consumed orally, and exogenous ST has to be administered via injection or implant.

Introduction of amino acids to maximize response. Also, reductions in


In the 1920s, it was discovered that a crude pituitary extract fat deposition and feed intake appear less in young rumi-
stimulated growth in rats, and this extract was referred to nants compared to pigs.
as somatotropin or growth hormone, after the Greek deri- There is little effect of pST on digestibility, so effects
vation meaning tissue growth.[1] Results were extended to are due to an increase in the efficiency of use of dietary pro-
farm animals when somatotropin (ST) was shown to en- tein and/or an increase in the requirement of dietary protein
hance growth rates in pigs[2] and stimulate milk produc- to support the increased protein deposition. In grower pigs
tion in lactating goats[3] and cows.[4] However, the supply (30–60 kg), pST has little or no effect on dietary protein re-
of ST was extremely limited until the advent of recombi- quirements, but there is an improvement in the efficiency of
nant technology. In 1982, the first study with recombinant amino acid use. In finisher pigs (60–120 kg), pST has little
ST in domestic animals was reported, in this case bovine effect on the efficiency of dietary protein use, but there is
ST (bST) in lactating dairy cows.[5] Commercial use of an increase in protein requirement commensurate with the
bST and porcine ST (pST) began in 1994 and 1996 in the increase in protein deposition.[6] As a consequence of the
United States and Australia, respectively. increased protein mass and protein synthesis, there is also an
increase in maintenance requirement. That increase, when
combined with the reduced intake, means that dietary en-
ergy may often limit the response to pST. Protein deposition
Efficacy of Exogenous Somatotropin
in growing ruminants is virtually always limited by dietary
energy consumption, and this may explain why ruminants
Growth
treated with ST do not decrease feed intake, since energy
spared from the reduction in lipid synthesis is partitioned
Somatotropin alters nutrient partitioning to improve growth
toward protein deposition (or milk secretion in lactation, as
performance and body composition, and pST has been ap-
discussed subsequently). Therefore, if the full benefits of
proved commercially in 14 countries.[6,7] Exogenous pST
exogenous ST are to be achieved, feed intake needs to be
results in dose-dependent increases in lean deposition and
maximized regardless of species or physiological state.[9]
reductions in fat (Fig. 1). It is effective in increasing pro- Slaughter –
tein deposition and decreasing fat deposition in all sexes Lactation Turkeys
and genotypes. Although the greatest responses occur in
finisher pigs (60–120 kg), exogenous pST also improves Exogenous ST has been shown to enhance lactational per-
growth in younger pigs (30–60 kg). As a result of the formance in mammals ranging from laboratory animals to
reduction in fat deposition, there is a corresponding reduc- humans. The most extensive work is with lactating cows,
tion in feed intake.[8] Since pST stimulates protein deposi- and bST has been approved for commercial use in 19
tion in all tissues, there are increases in visceral and skin countries.[10,11] Commercial use over the last decade has
mass, and reductions in dressing percent. In general, lean clearly demonstrated a consistent milk response, generally
tissue responses in growing ruminants have been less than about 5 kg/day, and a marked improvement in productive
in pigs, although much of these differences may relate to efficiency while maintaining normal cow health and herd
the difficulty of ensuring an adequate balance and quantity life.[11] There is generally little response to bST in early
Encyclopedia of Animal Science, Second Edition DOI: 10.1081/E-EAS2-120019802
Copyright © 2011 by Taylor & Francis. All rights reserved. 995

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996 Somatotropin

for the reduction in feed intake observed in response to


pST treatment.[14]
Treatment with somatotropin also causes an increase
in lipolytic response to adrenergic stimulation in pigs and
cattle.[10,15] In animals that are in a positive energy bal-
ance, where fat synthesis in adipose tissue is high and fat
mobilization is low, effects of ST are predominantly a re-
duction in lipogenesis with little effect on lipolysis. On the
other hand, if animals are in negative energy balance or
need to draw on energy reserves, ST-treated animals have
an enhanced ability to mobilize fat. Thus, the overall effect
is that less nutrients are partitioned to body fat and more
Fig. 1  Relationship between porcine somatotropin (pST) dose nutrients are available for productive functions.
and parameters of growth performance.
Source: From National Research Council.[9] Protein
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lactation before peak yield, so commercial use is during Although it is well established that ST increases protein
the declining phase of lactation (Fig. 2). deposition and milk protein synthesis in growing and lac-
The composition of milk is unaltered by bST treatment. tating animals, respectively, the precise mechanisms and
Therefore, the use of bST has no impact on nutrient re- extent to which effects on protein metabolism are direct
quirements per unit of milk or the nutritional and manu- or indirect via IGF-I remains an active area of investiga-
facturing properties of milk.[9,10] Responses to bST have tion. Most studies suggest that in growing animals, the in-
been observed for all dairy breeds, regardless of parity and crease in protein deposition is due primarily to an increase
genetic potential. Cows receiving bST increase intake in in protein synthesis, with little effect on protein degrada-
an amount that matches nutrient needs for the extra milk tion. The increase in protein synthesis is also associated
and allows for the normal replenishment of body reserves with a reduction in amino acid oxidation, so that a greater
over the lactation cycle. Thus, offering a balanced diet in proportion of absorbed amino acids is used for protein ac-
adequate amounts is important; if nutrition and manage- cretion.[6,15]
ment are inadequate or poor, the lactational response to
bST will be attenuated or even abolished.[9,10,13] Mammary Gland

Treatment of lactating cows with ST results in an increased


Mechanisms synthesis of all milk constituents consistent with the in-
crease in milk yield. The mechanism involves both an
Fat and Carbohydrate increase in the synthetic capacity and an improved mainte-
nance of mammary epithelial cells. Coordinated increases
The multitude of effects that have been ascribed to ST in the
regulation of growth and lactation are outlined in Table 1.
Depending on physiological state, ST coordinates me-
tabolism to partition nutrients toward lean tissue and bone
during growth or toward milk synthesis during lactation.
Many effects of ST are direct and mediated through chang-
ing responses to homeostatic hormones such as insulin or
catecholamines. Other effects are indirect and thought to be
mediated by the insulin-like growth factor (IGF) system.
Slaughter –

Basal lipogenesis in adipose tissue from growing pigs


Turkeys

treated with pST is decreased by up to 85%.[14] In addition,


the ability of insulin to stimulate lipogenesis and glucose
transport is similarly reduced in adipose tissue obtained
from ST-treated animals, and this is mainly due to a de-
creased sensitivity to insulin. Also, ST treatment reduces
rates of glucose clearance in response to an insulin or glu- Fig. 2  Effect of bovine somatotropin (bST) on milk yield in
cose challenge, and there is an augmented plasma insulin lactating dairy cows. Commencing at week 0 (84 ± 10 days
response to a glucose load. It has been suggested that the postpartum) cows received a daily injection of excipient (dotted
insulin resistance and resultant reduced adipose tissue li- line) or bST (27 mg/day; solid line) for 26 weeks.
pogenesis and glucose oxidation are largely responsible Source: Adapted from Bauman et al.[12]

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Somatotropin 997

Table 1  Biological and production effects of somatotropin in farm animals during growth and lactation.
Tissue Physiological process affected
Skeletal muscle (growth) � Protein gain
� Protein synthesis
� Amino acid and glucose uptake
� Partial efficiency of amino acid utilization
Bone (growth) � Mineral gain (paralleling tissue growth)
Mammary tissue (lactation) � Milk with normal composition
� Uptake of nutrients used for milk synthesis
� Maintenance and activity of secretory cells
� Blood flow consistent with milk yield
Adipose tissue ¯ Lipid gain
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¯ Lipid synthesis
� Lipid mobilization (especially if in negative energy
balance)
� Catecholamine-stimulated lipolysis
¯ Insulin-stimulated lipid synthesis and glucose metabolism
Liver ¯ Ability of glucose to inhibit gluconeogenesis
� Glucose output (in lactation) to meet glucose needs
¯ Glucose output (in growth of pigs) to meet glucose needs
Systemic effects ¯ Glucose clearance and oxidation
¯ Insulin sensitivity
¯ Amino acid oxidation and catabolism
� Plasma glucose, insulin, IGF-I, and IGFBP-3
¯ Plasma urea and IGFBP-2
� = increase; ¯ = decrease; IGF-I = insulin-like growth factor I; IGFBP = insulin-like growth factor binding protein.
Source: Adapted from Bauman and Vernon,[10] and Etherton and Bauman.[15]

in mammary blood flow and mammary uptake of nutrients ordinated changes in the physiological processes, and many
also occur. The increased milk synthesis is supported by a of these adaptations involve changes in tissue response to
series of orchestrated changes in other body tissues to en- homeostatic signals. Overall, these orchestrated adaptations
sure that the mammary gland is supplied with the quantity allow for a greater partitioning of nutrients for lean tissue
and pattern of nutrients to support milk synthesis.[10,11,13] accretion (during growth) or milk synthesis (during lacta-
These coordinated adaptations involve most tissues in the tion), thereby allowing for increases in performance and
Slaughter –
Turkeys
body, a portion of which is illustrated in Table 1. productive efficiency while preserving animal well-being.

Conclusions References

Exogenous ST treatment of domestic animals markedly 1. Evans, H.M.; Simpson, M.E. Hormones of the anterior hy-
improves production efficiency by increasing the amount pophysis. Am. J. Physiol. 1931, 98, 511–546.
of lean meat or milk produced per unit of feed intake. As 2. Giles, D.D. An experiment to determine the effect of the
a result, ST is used commercially in the dairy and swine growth hormone of the anterior lobe of the pituitary gland
industries in many countries. The mechanisms involve co- on swine. Am. J. Vet. Res. 1942, 3, 77–85.

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998 Somatotropin

3. Asdell, S.A. The effect of the injection of hypophyseal extract 9. National Research Council, Metabolic Modifiers: Effects on
in advanced lactation. Am. J. Physiol. 1932, 20, 137–140. the Nutrient Requirements of Food-Producing Animals;
4. Asimov, G.J.; Krouze, N.K. The lactogenic preparations National Academy Press: Washington, DC, 1994.
from the anterior pituitary and the increase in milk yield 10. Bauman, D.E.; Vernon, R.G. Effects of exogenous bovine
from cows. J. Dairy Sci. 1937, 20, 289–306. somatotropin on lactation. Annu. Rev. Nutr. 1993, 13, 437–
5. Bauman, D.E.; DeGeeter, M.J.; Peel, C.J.; Lanza, G.M.; 461.
Gorewit, R.C.; Hammond, R.W. Effect of recombinantly 11. Bauman, D.E. Bovine somatotropin and lactation: From
derived bovine growth hormone (bGH) on lactational per- basic science to commercial application. Domest. Anim.
formance of high yielding dairy cows. J. Dairy Sci. 1982, Endocrinol. 1999, 17, 101–116.
65 (Suppl. 1), 121. 12. Bauman, D.E.; Eppard, P.J.; DeGeeter, M.J.; Lanza, G.M.
6. Dunshea, F.R. Nutrient requirements of pigs treated with met- Responses of high-producing dairy cows to long-term treat-
abolic modifiers. Proc. Nutr. Soc. Austr. 1994, 18, 102–114. ment with pituitary somatotropin and recombinant somato-
7. Campbell, R.G.; Johnson, R.J.; Taverner, M.R.; King, R.H. tropin. J. Dairy Sci. 1985, 68, 1352–1362.
Interrelationships between exogenous porcine somatotropin 13. Burton, J.L.; McBride, B.W.; Block, E.; Glimm, D.R.;
(PST) administration and dietary protein and energy intake Kennelly, J.J. A review of bovine growth hormone. Can. J.
on protein deposition capacity and energy metabolism of Anim. Sci. 1994, 74, 167–201.
pigs. J. Anim. Sci. 1991, 69, 1522–1531. 14. Dunshea, F.R. Effect of metabolism modifiers on lipid me-
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8. Boyd, R.D.; Bauman, D.E.; Fox, D.G.; Scanes, C.G. Impact tabolism in the pig. J. Anim. Sci. 1993, 71, 1966–1977.
of metabolism modifiers on protein accretion and protein 15. Etherton, T.D.; Bauman, D.E. Biology of somatotropin in
and energy requirements of livestock. J. Anim. Sci. 1991, growth and lactation of domestic animals. Physiol. Rev.
69 (Suppl. 2), 56–75. 1998, 78, 745–761.
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