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Shearing during late pregnancy increases size at birth but does not alter placental endocrine responses in sheep

Published online by Cambridge University Press:  06 November 2019

C. A. Rosales Nieto
Affiliation:
Department of Animal Science, College of Agriculture and Natural Resources, Michigan State University, East Lansing, Michigan 48824, USA
A. Mantey
Affiliation:
Department of Animal Science, College of Agriculture and Natural Resources, Michigan State University, East Lansing, Michigan 48824, USA
B. Makela
Affiliation:
Department of Animal Science, College of Agriculture and Natural Resources, Michigan State University, East Lansing, Michigan 48824, USA
T. Byrem
Affiliation:
Antel Biosystems, East Lansing, Michigan 48910, USA
R. Ehrhardt
Affiliation:
Department of Animal Science, College of Agriculture and Natural Resources, Michigan State University, East Lansing, Michigan 48824, USA Department of Large Animal Clinical Sciences, College of Veterinary Medicine, Michigan State University, East Lansing, Michigan 48824, USA
A. Veiga-Lopez*
Affiliation:
Department of Animal Science, College of Agriculture and Natural Resources, Michigan State University, East Lansing, Michigan 48824, USA
*
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Abstract

Shearing during the latter half of pregnancy is a common practice to improve flock health and productivity. Previous studies have demonstrated that shearing pregnant ewes at mid or late pregnancy is associated with an increase in lamb birth weight. In the present study, we used singleton Polypay × Dorset pregnant sheep, to investigate the potential roles of placental function and changes in maternal metabolism in underlying this increased birth weight response. Two groups were randomly established and blocked at enrollment by animal BW, body condition score and subcutaneous adipose tissue depth. The groups were shorn (SH; n = 18) or not (C; n = 20) at gestational day (GD) 107 ± 1 (mean ± SEM). Weekly maternal plasma samples were collected between shearing and birth, but only six samples were assayed for progesterone, pregnancy-associated glycoproteins (PAG1), glucose and non-esterified fatty acids (NEFAs). At birth, sex, birth weight, and newborn body mass index (BMI) were recorded. Maternal BW during mid- to late-pregnancy was similar between groups. Shearing resulted in increased lamb birth weight and BMI (P < 0.05) regardless of fetal sex but did not affect the maternal concentration of PAG1 or progesterone from GDs 100 to 142. After shearing (GD100) and up to lambing, shorn females had higher circulating glucose concentrations (P < 0.05), but not NEFA, compared to the control group. Maternal circulating PAG1, progesterone, glucose or NEFA concentration across pregnancy did not differ according to lamb sex. Across pregnancy, birth weight was positively associated with PAG1 (P < 0.001), but not with progesterone concentrations. In conclusion, weight and BMI at birth were higher in both sexes upon shearing in singleton pregnancies. Despite PAG1 being associated with birth weight, late-pregnancy shearing did not alter the placental endocrine response. Whether other placental factors are altered upon shearing and may influence the increase in birth weight and BMI remain to be investigated.

Type
Research Article
Copyright
© The Animal Consortium 2019 

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Footnotes

a

Present address: Facultad de Agronomía y Veterinaria, Universidad Autónoma de San Luis Potosí, San Luis Potosí 78321, México

References

Banchero, G, Vázquez, A, Montossi, F, de Barbieri, I and Quintans, G 2010. Pre-partum shearing of ewes under pastoral conditions improves the early vigour of both single and twin lambs. Animal Production Science 50, 309314.CrossRefGoogle Scholar
Bell, AW and Ehrhardt, RA 2002. Regulation of placental nutrient transport and implications for fetal growth. Nutrition Research Reviews 15, 211230.CrossRefGoogle ScholarPubMed
Corner, RA, Kenyon, PR, Stafford, JK, West, DM and Oliver, MH 2006. The effect of mid-pregnancy shearing or yarding stress on ewe post-natal behaviour and the birth weight and post-natal behaviour of their lambs. Livestock Science 102, 121129.CrossRefGoogle Scholar
Corner, RA, Kenyon, PR, Stafford, KJ, West, DM and Oliver, MH 2007. The effect of mid-pregnancy shearing and litter size on lamb birth weight and postnatal plasma cortisol response. Small Ruminant Research 73, 115121.CrossRefGoogle Scholar
De Barbieri, I, Montossi, F, Viñoles, C and Kenyon, PR 2018. Time of shearing the ewe not only affects lamb live weight and survival at birth and weaning, but also ewe wool production and quality. New Zealand Journal of Agricultural Research 61, 5766.CrossRefGoogle Scholar
deNicolo, G, Kenyon, PR, Morris, ST, Morel, PCH and Wall, AJ 2008. Mid-pregnancy shearing of autumn-lambing ewes in New Zealand. Australian Journal of Experimental Agriculture 48, 957960.CrossRefGoogle Scholar
Gardner, DS, Buttery, PJ, Daniel, Z and Symonds, ME 2007. Factors affecting birth weight in sheep: maternal environment. Reproduction 133, 297307.CrossRefGoogle ScholarPubMed
Gingrich, J, Pu, Y, Roberts, J, Karthikraj, R, Kannan, K, Ehrhardt, R and Veiga-Lopez, A 2018. Gestational bisphenol S impairs placental endocrine function and the fusogenic trophoblast signaling pathway. Archives of Toxicology 92, 18611876.CrossRefGoogle ScholarPubMed
Green, JA, Xie, S, Quan, X, Bao, B, Gan, X, Mathialagan, N, Beckers, J-Fo and Roberts, RM 2000. Pregnancy-associated bovine and ovine glycoproteins exhibit spatially and temporally distinct expression patterns during pregnancy. Biology of Reproduction 62, 16241631CrossRefGoogle ScholarPubMed
Jenkinson, CMC, Kenyon, PR, Blair, HT, Breier, BH and Gluckman, PD 2009. Birth weight effect in twin-born lambs from mid-pregnancy shearing is associated with changes in maternal IGF-I concentration. New Zealand Journal of Agricultural Research 52, 261268.CrossRefGoogle Scholar
Karkalas, J 1985. An improved enzymic method for the determination of native and modified starch. Journal of the Science of Food and Agriculture 36, 10191027.CrossRefGoogle Scholar
Kenyon, PR, Morris, ST, Revell, DK and McCutcheon, SN 2002. Maternal constraint and the birthweight response to mid-pregnancy shearing. Australian Journal of Agricultural Research 53, 511517.CrossRefGoogle Scholar
Kenyon, PR, Sherlock, RG, Morris, ST and Morel, PCH 2006. The effect of mid- and late-pregnancy shearing of hoggets on lamb birthweight, weaning weight, survival rate, and wool follicle and fibre characteristics. Australian Journal of Agricultural Research 57, 877882.CrossRefGoogle Scholar
Kleemann, DO, Walker, SK and Seamark, RF 1994. Enhanced fetal growth in sheep administered progesterone during the first three days of pregnancy. Journal of Reproduction and Fertility 102, 411417.CrossRefGoogle ScholarPubMed
Matsubara, C, Nishikawa, Y, Yoshida, Y and Takamura, K 1983. A spectrophotometric method for the determination of free fatty acid in serum using acyl-coenzyme A synthetase and acyl-coenzyme A oxidase. Analytical Biochemistry 130, 128133.CrossRefGoogle ScholarPubMed
Morris, ST, McCutcheon, SN and Revell, DK 2000. Birth weight responses to shearing ewes in early to mid gestation. Animal Science 70, 363369.CrossRefGoogle Scholar
NRC 2007. Nutrient requirements of small ruminants, sheep, goats, cervids, and new world camelids, 1st edition. National Academy Press, Washington, DC.Google Scholar
Parker, WJ, Morris, ST and McCutcheon, SN 1991. Wool production and feed intake in unmated and mated Border Leicester × Romney crossbred ewes shorn in July or November. New Zealand Journal of Agricultural Research 34, 427437.CrossRefGoogle Scholar
Petterson, JA, Slepetis, R, Ehrhardt, RA, Dunshea, FR and Bell, AW 1994. Pregnancy but not moderate undernutrition attenuates insulin suppression of fat mobilization in sheep. The Journal of Nutrition 124, 24312436.CrossRefGoogle ScholarPubMed
Ranilla, MJ, Sulon, J, Carro, MD, Mantecón, AR and Beckers, JF 1994. Plasmatic profiles of pregnancy-associated glycoprotein and progesterone levels during gestation in Churra and Merino sheep. Theriogenology 42, 537545.CrossRefGoogle ScholarPubMed
Revell, DK, Main, SF, Breier, BH, Cottam, YH, Hennies, M and McCutcheon, SN 2000. Metabolic responses to mid-pregnancy shearing that are associated with a selective increase in the birth weight of twin lambs. Domestic Animal Endocrinology 18, 409422.CrossRefGoogle ScholarPubMed
Revell, DK, Morris, ST, Cottam, YH, Hanna, JE, Thomas, DG, Brown, S and McCutcheon, SN 2002. Shearing ewes at mid-pregnancy is associated with changes in fetal growth and development. Australian Journal of Agricultural Research 53, 697705.CrossRefGoogle Scholar
Roberts, JN, May, KJ and Veiga-Lopez, A 2017. Time-dependent changes in pregnancy-associated glycoproteins and progesterone in commercial crossbred sheep. Theriogenology 89, 271279.CrossRefGoogle ScholarPubMed
Rosales Nieto, CA, Ferguson, MB, Macleay, CA, Briegel, JR, Wood, DA, Martin, GB, Bencini, R and Thompson, AN 2018. Milk production and composition, and progeny performance in young ewes with high merit for rapid growth and muscle and fat accumulation. Animal 12, 22922299.CrossRefGoogle ScholarPubMed
SAS Institute 2010. SAS/Stat user’s guide, version 9.3. SAS Institute Inc., Cary, NC, USA.Google Scholar
Sousa, NM, Ayad, A, Beckers, JF and Gajewski, Z 2006. Pregnancy-associated glycoproteins (PAG) as pregnancy markers in the ruminants. Journal of Physiology Pharmacology 57, 153171.Google ScholarPubMed
Sphor, L, Banchero, G, Correa, G, Osório, MTM and Quintans, G 2011. Early prepartum shearing increases milk production of wool sheep and the weight of the lambs at birth and weaning. Small Ruminant Research 99, 4447.CrossRefGoogle Scholar
Symonds, ME, Bryant, MJ and Lomax, MA 1986. The effect of shearing on the energy metabolism of the pregnant ewe. British Journal of Nutrition 56, 635643.CrossRefGoogle ScholarPubMed
Symonds, ME, Bryant, MJ and Lomax, MA 1988. Metabolic adaptation during pregnancy in winter-shorn sheep. The Journal of Agricultural Science 111, 137145.CrossRefGoogle Scholar
Tanaka, T, Akaboshi, N, Inoue, Y, Kamomae, H and Kaneda, Y 2002. Fasting-induced suppression of pulsatile luteinizing hormone secretion is related to body energy status in ovariectomized goats. Animal Reproduction Science 72, 185196.CrossRefGoogle ScholarPubMed
Vandaele, L, Verberckmoes, S, El Amiri, B, Sulon, J, Duchateau, L, Van Soom, A, Beckers, J-F and de Kruif, A 2005. Use of a homologous radioimmunoassay (RIA) to evaluate the effect of maternal and foetal parameters on pregnancy-associated glycoprotein (PAG) concentrations in sheep. Theriogenology 63, 19141924.CrossRefGoogle Scholar
Vipond, JE, King, ME, Inglis, DM and Hunter, EA 1987. The effect of winter shearing of housed pregnant ewes on food intake and animal performance. Animal Science 45, 211221.CrossRefGoogle Scholar