Professional Documents
Culture Documents
net/publication/279752264
Somatotropin
CITATIONS READS
0 809
2 authors, including:
SEE PROFILE
Some of the authors of this publication are also working on these related projects:
Understand and reduce impacts of in utero heat stress in pigs View project
Implementation of machine learning and artificial intelligence to assess beer foamability and quality View project
All content following this page was uploaded by Frank Rowland Dunshea on 06 July 2015.
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
To cite this Chapter Bauman, Dale E. and Dunshea, Frank R.(2010) 'Somatotropin', Encyclopedia of Animal Science,
Second Edition, 1: 1, 995 — 998
This article may be used for research, teaching and private study purposes. Any substantial or
systematic reproduction, re-distribution, re-selling, loan or sub-licensing, systematic supply or
distribution in any form to anyone is expressly forbidden.
The publisher does not give any warranty express or implied or make any representation that the contents
will be complete or accurate or up to date. The accuracy of any instructions, formulae and drug doses
should be independently verified with primary sources. The publisher shall not be liable for any loss,
actions, claims, proceedings, demand or costs or damages whatsoever or howsoever caused arising directly
or indirectly in connection with or arising out of the use of this material.
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.
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
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
Downloaded By: [Bauman, Dale E.][Cornell University Library] At: 14:34 20 January 2011
¯ 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.
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-
Downloaded By: [Bauman, Dale E.][Cornell University Library] At: 14:34 20 January 2011
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.
Slaughter –
Turkeys