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Equine veterinary journal2019; 52(2); 165-173; doi: 10.1111/evj.13206

Physiological development of the equine fetus during late gestation.

Abstract: In many species, the pattern of growth and physiological development in utero has an important role in determining not only neonatal viability but also adult phenotype and disease susceptibility. Changes in fetal development induced by a range of environmental factors including maternal nutrition, disease, placental insufficiency and social stresses have all been shown to induce adult cardiovascular and metabolic dysfunction that often lead to ill health in later life. Compared to other precocious animals, much less is known about the physiological development of the fetal horse or the longer-term impacts on its phenotype of altered development in early life because of its inaccessibility in utero, large size and long lifespan. This review summaries the available data on the normal metabolic, cardiovascular and endocrine development of the fetal horse during the second half of gestation. It also examines the responsiveness of these physiological systems to stresses such as hypoglycaemia and hypotension during late gestation. Particular emphasis is placed on the role of the equine placenta and fetal endocrine glands in mediating the changes in fetal development seen towards term and in response to nutritional and other environmental cues. The final part of the review presents the evidence that the early life environment of the horse can alter its subsequent metabolic, cardiovascular and endocrine phenotype as well as its postnatal growth and bone development. It also highlights the immediate neonatal environment as a key window of susceptibility for programming of equine phenotype. Although further studies are needed to identify the cellular and molecular mechanisms involved, developmental programming of physiological phenotype is likely to have important implications for the health and potential athletic performance of horses, particularly if born with abnormal bodyweight, premature or dysmature characteristics or produced by assisted reproductive technologies, indicative of an altered early life environment.
Publication Date: 2019-12-17 PubMed ID: 31721295DOI: 10.1111/evj.13206Google Scholar: Lookup
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  • Journal Article
  • Review

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The study explores physiological development of the equine fetus during the later stages of gestation, how various environmental factors can cause changes in fetal development leading to potential health problems later in life, and the role of the placenta and endocrine glands in these changes. It also discusses evolutionary programming as a mechanism, which can impact the horse’s postnatal growth, cardiovascular system, metabolism, and even athletic performance.

Understanding the Physiological Development

  • The research aims to develop an in-depth understanding of the physiological development of the fetal horse during the later half of pregnancy. This part of the research focuses on the metabolic, cardiovascular and endocrine development of the equine fetus.
  • It is acknowledged that difficulties in gaining access to the fetus in utero due to the horse’s size and long lifespan poses a challenge in researching this area. This makes this area less understood compared to other precocious animals.

Responsiveness to Stresses

  • The paper examines how these physiological systems respond to stresses like hypotension and hypoglycaemia during late gestation. The main focus here is to analyse how variances in development conditions can impact the fetus.
  • The paper recognizes a range of environmental factors, such as maternal nutrition, disease, social stresses, and placental insufficiency that can lead to altered fetal development and eventually result in cardiovascular and metabolic dysfunction in adult horses.

Role of the Placenta and Endocrine Glands

  • Particular emphasis is placed on the equine placenta and fetal endocrine glands. The study investigates how these play a role in mediating the changes in fetal development seen towards term and in response to various nutritional and other environmental cues.

Impact on Postnatal Development and Adult Phenotype

  • The research presents evidence that the early life environment could impact subsequent growth, cardiovascular and endocrine phenotype, and bone development in horses.
  • It also emphasizes on the immediate neonatal environment as a critical phase for evolutionary programming of the equine phenotype.

Implications for Health and Athletic Performance

  • The study suggests that the development programming of physiological phenotype could have important implications for the health and potential athletic performance of horses.
  • Particularly in cases where horses are born with abnormal bodyweight, premature or dysmature characteristics, or produced by assisted reproductive technologies, indicating an altered early life environment, could significantly affect their health and performance in adulthood.

Cite This Article

APA
Fowden AL, Giussani DA, Forhead AJ. (2019). Physiological development of the equine fetus during late gestation. Equine Vet J, 52(2), 165-173. https://doi.org/10.1111/evj.13206

Publication

ISSN: 2042-3306
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 52
Issue: 2
Pages: 165-173

Researcher Affiliations

Fowden, A L
  • Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.
Giussani, D A
  • Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.
Forhead, A J
  • Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK.

MeSH Terms

  • Animals
  • Female
  • Fetal Development
  • Fetus
  • Horses
  • Phenotype
  • Placenta
  • Pregnancy

Grant Funding

  • RG/06/006/22028 / British Heart Foundation
  • RG/11/16/29260 / British Heart Foundation
  • University of Cambridge

References

This article includes 90 references
  1. Silver M. Some aspects of equine placental exchange and foetal physiology.. Equine Vet. J. 16, 227-233.
  2. Jellyman J.K., Valenzuela O.A., Fowden A.L.. Glucocorticoid programming of the hypothalamic-pituitary-adrenal axis and metabolic function: animal studies from mouse to horse.. J. Anim. Sci. 93, 3245-3260.
  3. Peugnet P., Robles M., Wimel L., Tarrade A., Chavatte-Palmer P.. Management of the pregnant mare and long-term consequences on the offspring.. Theriogeneology 86, 99-109.
  4. Platt H. Growth of the equine fetus.. Equine Vet. J. 16, 247-252.
  5. Fowden A.L., Comline R.S., Silver M. Insulin secretion and carbohydrate metabolism during pregnancy in the mare.. Equine Vet. J. 16, 239-246.
  6. George L.A., Stanier W.B., Cubitt T.A., Treiber K.H., Harris P.A., Geor R.J.. Evaluation of the effects of pregnancy on insulin sensitivity, insulin secretion, and glucose dynamics in Thoroughbred mares.. Am. J. Vet. Res. 72, 666-674.
  7. Beythien E., Aurich C., Wulf M., Aurich J.. Effects of season on placental, foetal and neonatal development in horses.. Theriogenology 97, 98-103.
  8. Fowden A.L., Forhead A.J., White K.L., Taylor P.M.. Equine uteroplacental metabolism at mid and late gestation.. Exp. Physiol. 85, 539-545.
  9. Fowden A.L., Taylor P.M., White K.L., Forhead A.J.. Ontogenic and nutritionally-induced changes in fetal metabolism in the horse.. J. Physiol. 528, 209-219.
  10. Hennecke D.R., Potter G.D., Kreider J.L.. Body condition during pregnancy and lactation and reproductive efficiency of mares.. Theriogenology 21, 897-909.
  11. Kubiak J.R., Evans J.W., Potter G.D., Harris P.G., Jenkins W.L.. Parturition in the multiparous mare fed to obesity.. J. Equine Vet. Sci. 8, 135-149.
  12. Ousey J.C., Fowden A.L., Wilsher S., Allen W.R.. The effects of maternal health and body condition on the endocrine responses of neonatal foals.. Equine Vet. J. 40, 673-679.
  13. Smith S., Marr C.M., Dunnett C., Menzies-Gow N.J.. The effect of mare obesity and endocrine function on foal birthweight in Thoroughbreds.. Equine Vet. J. 49, 461-466.
  14. Meznarich H.K., Hay W.W., Sparks J.W., Meschia G., Battaglia F.. Fructose disposal and oxidation rates in the ovine fetus.. Q. J. Exp. Physiol. 72, 617-625.
  15. Stammers J.P., Hull D., Silver M., Fowden A.L., Ousey J.C., Rossdale P.D.. Release of lipid from the equine placenta during in vitro incubation.. Placenta 15, 857-872.
  16. Fowden A.L.. Comparative aspects of fetal carbohydrate metabolism.. Equine Vet. J. 29, Suppl. 24, 19-25.
  17. Wooding F.B.P., Fowden A.L.. Nutrient transfer across the equine placenta: correlation of structure and function.. Equine Vet. J. 38, 175-183.
  18. Macdonald A.A., Chavatte P., Fowden A.L.. Scanning electron microscopy of the microcotyledonary placenta of the horse, Equus caballus.. Placenta 21, 565-574.
  19. Samuel C.A., Allen W.R., Steven D.H.. Studies on the equine placenta. II. Ultrastructure of the placental barrier.. J. Reprod. Fertil. 48, 257-264.
  20. Ehrhart R.A., Bell A.W.. Developmental increase in glucose transporter concentration in the sheep placenta.. Am. J. Physiol. 273, R1132-R1141.
  21. Wooding F.B.P., Morgan G., Fowden A.L., Allen W.W.. Separate sites and mechanisms for placental transport of calcium, iron and glucose in the equine placenta.. Placenta 21, 635-645.
  22. Wooding F.B.P., Bell A.W., Ehrhardt R.A., Limesand S.W., Hay W.W.. Localisation of glucose transport in the ruminant placenta: implications for sequential use of transporter isoforms.. Placenta 26, 626-640.
  23. Gibson C., de Ruijter-Villani M., Reitveld J., Stout T.A.E.. Expression of glucose transporters in the endometrium and early conceptus membranes of the horse.. Placenta 68, 23-32.
  24. Stammers J., Hull D., Silver M., Fowden A.L.. Fetal and maternal plasma lipids in chronically catheterized mares in late gestation: effects of different nutritional states.. Reprod. Fertil. Dev. 7, 1275-1284.
  25. Wilsher S., Allen W.R.. Effects of Streptococcus equi infection-mediated nutritional insulin during mid-gestation in primiparous Thoroughbred fillies. Part 1: placental and fetal development.. Equine Vet. J. 38, 549-557.
  26. Robles M, Noveau E, Gautier C, Mendoza L, Dubois M, Dahirel L, Lagofun B, Aubriere M.C., Lejeune J.P., Caudron I., Gueron I., Viguie C., Wimel L., Bouraima-Lelong H., Serteyn D., Couturier-Tarrade A., Chavatte-Palmer P.. Maternal obesity increases insulin resistance, low-grade inflammation and osteochondrosis in foals and yearlings until 18 months of age.. PLoS One 13, e01900309.
  27. Robles M., Couturier-Tarrade A., Derisoud E., Geeverding A., Dubois C., Dahirel M., Aioun J., Prezelin A., Calvez J., Richard C., Wimel L., Chavatte-Palmer P.. Effects of dietary arginine supplementation in pregnant mares on maternal metabolism, placental structure and function and foal growth.. Sci. Rep. 9, 6461.
  28. Allen W.R., Wilsher S., Turnbull C., Stewart F., Ousey J., Rossdale P.D., Fowden A.L.. The influence of maternal size on placental, fetal and postnatal growth in the horse: I Development in utero.. Reproduction 123, 454-465.
  29. Robles M, Peugnet P.M., Valentino S.A., Dubois C., Dahirel M., Aubriere M-C, Reigner F, Serteyn D, Wimel L, Couturier-Tarrade A, Chavatte-Palmer P. Placental alterations in structure and function in intra-uterine growth-related horses.. Equine. Vet J. 50, 405-414.
  30. Stammers J.P., Silver M., Fowden A.L.. Effects of nutrition on uterine and umbilical venous plasma lipids in chronically catheterized mares in late gestation.. Equine Vet J. 20, Suppl. 5, 37-40.
  31. Fowden A.L., Ralph M., Silver M.. Nutritional regulation of uteroplacental prostaglandin production and metabolism in pregnant ewes and mares during late gestation.. Exp. Clin. Endocrinol. 102, 212-221.
  32. Fowden A.L., Mundy L., Ousey J.C., McGladdery A., Silver M.. Tissue glycogen and glucose-6-phosphatase activity in the fetal and newborn foals.. J. Reprod. Fertil. Suppl. 44, 537-542.
  33. Fowden A.L., Mundy L., Silver M.. Developmental regulation of glucogenesis in the sheep fetus during late gestation.. J. Physiol. 508, 937-947.
  34. Jeffcott L.B., Whitwell K.E.. Twinning as a cause of foetal and neonatal loss in the Thoroughbred mare.. J. Comp. Pathol. 83, 91-106.
  35. Forhead A.J., Broughton-Pipkin F., Taylor P.M., Baker K., Balouzet V., Giussani D.A., Fowden A.L.. Developmental changes in blood pressure and the renin-angiotensin system in the fetal foal during the second half of gestation.. J. Reprod. Fertil. Suppl. 56, 693-703.
  36. Giussani D.A., Forhead A.J., Fowden A.L.. Development of cardiovascular function in the horse fetus.. J. Physiol. 565, 1019-1030.
  37. Baska-Vincze B., Baska F., Szenci O.. Fetal heart rate and fetal heart rate variability in Lipizzaner broodmares.. Acta Vet. Hung. 63, 89-99.
  38. Nagel C., Erber R., Ille N., Wulf M., Aurich J., Möstl E., Aurich C.. Heart rate and salivary cortisol concentrations at birth.. Vet. J. 203, 250-252.
  39. O’Connor S.J., Fowden A.L., Holdstock N., Giussani D.A., Forhead A.J.. Developmental changes in pulmonary and renal angiotensin converting enzyme concentration in fetal and neonatal horses.. Reprod. Fertil. Dev. 14, 413-417.
  40. O’Connor S.J., Gardner D.S., Ousey J.C., Holdstock N.B., Rossdale P.D., Edwards C.M.B., Fowden A.L., Giussani D.A.. Development of the baroreflex and endocrine response to hypotensive stress in the newborn foal and lamb.. Pflugers Arch. 450, 298-306.
  41. O’Connor S.J., Ousey J.C., Gardner D.S., Fowden A.L., Giussani D.A.. Development of baroreflex function and peripheral vascular reactivity in the horse fetus.. J. Physiol. 572, 155-164.
  42. Macdonald A.A., Fowden A.L., Ousey J., Silver M., Rossdale P.D.. The foramen ovale of the fetal and neonatal foal.. Equine Vet. J. 20, 255-260.
  43. Fowden A.L., Forhead A.J.. Hormones as epigenetic signals in developmental programming.. Exp. Physiol. 94, 607-625.
  44. Fowden A.L., Forhead A.J., Ousey J.C.. Endocrine adaptations in the foal during the perinatal period.. Equine Vet. J. 44, Suppl. 41, 130-139.
  45. Fowden A.L., Barnes R.J., Comine R.S., Silver M.. Pancreatic β cell function in the fetal foal and mare.. J. Endocrinol. 87, 293-301.
  46. Fowden A.L., Gardner D.S., Ousey J.C., Giussani D.A., Forhead A.J.. Maturation of pancreatic beta cell function in the fetal horse during late gestation.. J. Endocrinol. 186, 467-473.
  47. Fowden A.L., Forhead A.J., Bloomfield M., Taylor P.M., Silver M.. Pancreatic α cell function in the fetal foal during late gestation.. Exp. Physiol. 84, 697-705.
  48. Holdstock N.B., Allen V.L., Fowden A.L.. Pancreatic endocrine function in newborn pony foals after induced or spontaneous delivery at term.. Equine Vet J. 44, Suppl. 41, 30-37.
  49. Silver M., Fowden A.L.. Sympathoadrenal and other endocrine and metabolic responses to hypoglycaemia in the fetal foal during late gestation.. Exp. Physiol. 80, 651-662.
  50. Silver M., Fowden A.L.. Prepartum adrenocortical maturation in the fetal foal: responses to ACTH(1-24).. J. Endocrinol. 142, 417-425.
  51. Sferruzzi-Perri A.N., Vaughan O.R., Forhead A.J., Fowden A.L.. Hormonal and nutritional drivers of intrauterine growth.. Curr. Opin. Clin. Nutr. Metab. Care 16, 298-309.
  52. Comline R.S., Silver M.. Catecholamine secretion by the adrenal medulla of the foetal and new-born foal.. J. Physiol. 216, 659-682.
  53. Fowden A.L., Li J., Forhead A.J.. Glucocorticoids and the preparation for life after birth: are there long-term consequences of the life insurance?. Proc. Nutr. Soc. 57, 113-122.
  54. Rossdale P.D., Silver M., Comline R.S., Hall L.W., Nathanielsz P.W.. Plasma cortisol in the foal during the late fetal and early neonatal period.. Res. Vet. Sci. 15, 395-397.
  55. Fowden A.L., Silver M.. Comparative development of the pituitary-adrenal axis in the fetal foal and lamb.. Reprod. Domest. Anim. 30, 170-177.
  56. Han X., Rossdale P., Ousey J., Holdstock N., Allen W., Silver M., Fowden A., McGladdery A., Challis J.. Localisation of 15-hydroxy-prostaglandin dehydrogenase (PGDH) and steroidogenic enzymes in the equine placenta.. Equine Vet. J. 25, 334-339.
  57. Cudd T.A., LeBlanc M., Silver M., Norman W., Madison J., Keller-Wood M., Wood C.E.. Ontogeny and ultradian rhythms of adrenocorticotrophin and cortisol in the late gestation fetal horse.. J. Endocrinol. 144, 271-283.
  58. Silver M., Fowden A.L., Knox J., Ousey J.C., Cash R., Rossdale P.D.. Relationship between circulating tri-iodothyronine and cortisol in the perinatal period of the foal.. J. Reprod. Fertil. Suppl. 44, 619-626.
  59. Rossdale P.D., Silver M.. The concept of readiness for birth.. J. Reprod. Fertil. Suppl. 32, 507-510.
  60. Rossdale P.D.. Clinical view of disturbances in equine foetal maturation.. Equine Vet. J. 25, Suppl. 14, 3-7.
  61. Fowden A.L., Forhead A.J., Ousey J.C.. The endocrinology of equine parturition.. Exp. Clin. Endocrinol. Diabetes 116, 393-403.
  62. Ousey J.C., Forhead A.J., Rossdale P.D., Grainger L., Houghton E., Fowden A.L.. The ontogeny of uteroplacental progestagen production in pregnant mares during the second half of gestation.. Biol. Reprod. 69, 540-548.
  63. Ousey J.C.. Peripartal endocrinology in the mare and foetus.. Reprod. Domest. Anim. 39, 222-231.
  64. Hay M.F., Allen W.R.. An ultrasound and histochemical study of the interstitial cells in the gonads of the fetal horse.. J. Reprod. Fertil. Suppl. 23, 557-561.
  65. Pashen R.L., Allen W.R.. The role of fetal gonads and placenta in steroid production, maintenance of pregnancy and parturition in the mare.. J. Reprod. Fertil. Suppl. 27, 499-509.
  66. Pashen R.L., Allen W.R.. Endocrine changes after foetal gonadectomy and during normal and induced parturition in the mare.. Anim. Reprod. Sci. 2, 271-288.
  67. Coverdale J.A., Hammer C.J., Walter K.W.. Nutritional programming and the impact on mare and foal performance.. J. Anim. Sci. 93, 3261-3267.
  68. Chavatte-Palmer P., Velazquez M.A., Jammes H., Durathon V.. Review: Epigenetics, develppmental programming anf nutrition in herbivores.. Animal 12, Suppl. 2, 363-371.
  69. Fowden A.L., Giussani D.A., Forhead A.J.. Intrauterine programming of physiological systems: causes and consequences.. Physiology 21, 29-37.
  70. Rossdale P.D., Ousey J.C., Cottrill C.M., Chavatte P., Allen W.R., McGladdery A.J.. Effects of placental pathology on maternal plasma progestogen and mammary secretion calcium concentrations and on neonatal adrenocortical function in the horse.. J. Reprod. Fertil. Suppl. 44, 579-590.
  71. George L.A., Stanier W.B., Treiber K.H., Harris P.A., Geor R.J.. Insulin sensitivity and glucose dynamics during pre-weaning foal development and in response to maternal diet composition.. Domest. Anim. Endocrinol. 37, 23-29.
  72. Peugnet P., Robles M., Mendoza L., Wimel L., Dubois C., Dahriel M., Guillaume D., Camous S., Berthelot V., Toquet M.P., Richard E., Sandersen C., Chaffaux S., Lejeune J.P., Tarrade A., Sertyn D., Chavatte-Palmer P.. Effects of moderate amounts of barley in late pregnancy on growth, glucose metabolism and osteoarticular status of pre-weaning horses.. PLoS One 10, e0122596.
  73. Robles M., Gautier C., Mendoza L., Peugnet P., Dubois M., Lejeune J.P., Caudron I., Gueron I., Camous S., Tarrade A., Wimel L., Serteyn D., Bouraima-Lelong H., Chavatte-Palmer P.. Maternal nutrition during pregnancy affects testicular and bone development, glucose metabolism and response to overnutrition in weaned horses up to two years.. PLoS One 12, e0169295.
  74. Ousey J.C., Rossdale P.D., Fowden A.L., Palmer L., Turnbull C., Allen W.R.. The effects of manipulating intra-uterine growth on postnatal adrenocortical development and other parameters of maturity in neonatal foals.. Equine Vet. J. 36, 616-621.
  75. Peugnet P., Wimel L., Duchamp G., Sandersen C., Camous S., Guillaume D., Dahirel L., Dubois D., Jouneau L., Reigner F., Berthelot V., Chaffaux S., Tarrade A., Sertyn D., Chavatte-Palmer P.. Enhanced or reduced fetal growth induced by embryo transfer into smaller or larger breeds alters post-natal growth and metabolism in pre-weaning horses.. PLoS One 9, e102044.
  76. Giussani D.A., Forhead A.J., Gardner D.S., Fletcher A.J.W., Allen W.R., Fowden A.L.. Postnatal cardiovascular function after manipulation of fetal growth by embryo transfer in the horse.. J. Physiol. 547, 67-76.
  77. Forhead A.J., Ousey J.C., Allen W.R., Fowden A.L.. Postnatal insulin secretion and sensitivity after manipulation of fetal growth by embryo transfer in the horse.. J. Endocrinol. 181, 459-467.
  78. Robles M., Dubois C., Gautier C., Dahirel L., Gueron I., Bouraima-Lelong H., Viguie C., Wimel L., Couturier-Tarrade A., Chavatte-Palmer P.. Maternal parity affects placental development, growth and metabolism of foals until 1 year and a half.. Theriogenology 108, 321-330.
  79. Valenzuela O.A., Jellyman J.K., Allen V.L., Holdstock N.B., Fowden A.L.. Effects of maternal dexamethasone treatment on pancreatic β cell function in the pregnant mare and postnatal foal.. Equine Vet. J. 49, 99-106.
  80. Jellyman J.K., Allen V.L., Holdstock N.B., Fowden A.L.. Glucocorticoid over-exposure in neonatal life alters pancreatic β cell function in newborn foals.. J. Anim. Sci. 91, 104-110.
  81. Valenzuela O.A., Jellyman K.L., Allen V.L., Holdstock N.B., Forhead A.J., Fowden A.L.. Effects of birth weight, sex and neonatal glucocorticoid overexposure on glucose-insulin dynamics in young adult horses.. J. Dev. Orig. Health Dis. 8, 206-215.
  82. Jellyman J.K., Allen V.L., Forhead A.J., Holdstock N.B., Fowden A.L.. Hypothalamic-pituitary-adrenal axis function in pony foals after neonatal glucocorticoid overexposure.. Equine Vet J. 44, Suppl. 41, 38-42.
  83. Jellyman J.K., Valenzuela O.A., Allen V.L., Forhead A.J., Holdstock N.B., Fowden A.L.. Neonatal glucocorticoid overexposure programmes pituitary-adrenal function in ponies.. Domest. Anim. Endocrinol. 50, 45-49.
  84. Walton A., Hammond J.. The maternal effects on growth and conformation in Shire horse-Shetland pony crosses.. Proc. R. Soc. Lond. B Biol. Sci. 125, 311-335.
  85. Allen W.R., Wilsher S., Tiplady C., Butterfield R.M.. The influence of maternal size on pre- and post-natal growth in the horse: III Postnatal growth.. Reproduction 127, 67-77.
  86. Wilsher S., Allen W.R.. Uterine influences on embryogenesis and early placentation in the horse revealed by transfer of day 10 embryos to day 3 recipient mares.. Reproduction 137, 583-593.
  87. Stout T.A.E.. Clinical insights: assisted reproductive technologies.. Equine Vet. J. 51, 427-428.
  88. Jellyman J.K., Valenzuela O.A., Allen V.L., Forhead A.J., Holdstock N.B., Fowden A.L.. Sex-associated differences in pancreatic β cell function in healthy pre-weaning foals.. Equine Vet. J. 46, 722-728.
  89. Silver M., Cash R.S.G., Dudan F., Fowden A.L., Knox J., Ousey J.C., Rossdale P.D.. Postnatal adrenocortical activity in relation to plasma ACTH and catecholamine levels in term and premature foals.. Equine Vet. J. 16, 278-286.
  90. Rossdale P.D., Ousey J.C.. Fetal programming for athletic performance in the horse: potential effects of IUGR.. Equine Vet. Educ. 14, 98-112.

Citations

This article has been cited 3 times.
  1. Neto da Silva AC, Costa AL, Teixeira A, Alpoim-Moreira J, Fernandes C, Fradinho MJ, Rebordão MR, Silva E, Ferreira da Silva J, Bliebernicht M, Alexandre-Pires G, Ferreira-Dias G. Collagen and Microvascularization in Placentas From Young and Older Mares. Front Vet Sci 2021;8:772658.
    doi: 10.3389/fvets.2021.772658pubmed: 35059454google scholar: lookup
  2. Domino M, Borowska M, Kozłowska N, Zdrojkowski Ł, Jasiński T, Smyth G, Maśko M. Advances in Thermal Image Analysis for the Detection of Pregnancy in Horses Using Infrared Thermography. Sensors (Basel) 2021 Dec 28;22(1).
    doi: 10.3390/s22010191pubmed: 35009733google scholar: lookup
  3. Maśko M, Witkowska-Piłaszewicz O, Jasiński T, Domino M. Thermal features, ambient temperature and hair coat lengths: Limitations of infrared imaging in pregnant primitive breed mares within a year. Reprod Domest Anim 2021 Oct;56(10):1315-1328.
    doi: 10.1111/rda.13994pubmed: 34310786google scholar: lookup