Analyze Diet
The Journal of physiology2000; 528 Pt 1(Pt 1); 209-219; doi: 10.1111/j.1469-7793.2000.00209.x

Ontogenic and nutritionally induced changes in fetal metabolism in the horse.

Abstract: 1. Using the Fick principle and tracer methodology, the metabolic rates of chronically catheterized fetal foals (n = 24) were measured at different gestational ages during the second half of gestation and in response to maternal fasting for 36 h in late gestation (n = 4, term approximately 335 days). 2. Absolute rates of umbilical blood flow, fetal glucose utilization and umbilical uptake of oxygen (O2) and glucose increased from mid-gestation to 300 days and then plateauxed until term. The absolute rate of umbilical lactate uptake was significant after, but not before, 280 days of gestation. Weight specific rates of umbilical uptake and fetal utilization of glucose decreased progressively throughout the second half of gestation. 3. Weight specific rates of CO2 production from glucose carbon were also inversely correlated with gestational age. Umbilical lactate uptake per kilogram of fetus was lower after 320 days than between 281 and 300 days. In contrast, no gestational trends were observed in the weight specific rates of fetal O2 uptake and urea production. Glucose production by the fetal horse was negligible, even very close to term. 4. Maternal fasting for 36 h reduced the rate of umbilical uptake and utilization of glucose production but had no effect on the rates of endogenous glucose production and umbilical uptake of oxygen and lactate by the horse fetus. 5. The observations show that fetal metabolism is highly dependent on glucose in the horse compared to the sheep in mid- and late gestation. Different species therefore adopt different strategies in meeting the nutritional demands of the growing fetus during the second half of gestation.
Publication Date: 2000-10-06 PubMed ID: 11018119PubMed Central: PMC2270112DOI: 10.1111/j.1469-7793.2000.00209.xGoogle Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

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.

This research article investigates the metabolic rates and related changes in fetal foals throughout gestation and in response to maternal fasting. It found that maternal fasting reduces some aspects of glucose production, but not others, while highlighting differences between horse and sheep fetal metabolism.

Methodology

  • Researchers used the Fick principle, a model of physiological flow based on the concentration difference of substance metabolites, and tracer methodology to measure metabolic rates in fetal horses.
  • The experiments involved 24 chronically catheterized fetal foals at different gestational ages during the second half of gestation. An additional four foals were also tested during late gestation after their mothers were subject to 36 hours of fasting.

Foal Metabolism Changes Over Gestation

  • Metabolic changes were found in fetal foals throughout gestation. Notably, they observed an increased uptake of crucial nutrients (oxygen and glucose) from the umbilical cord as gestation progressed until around 300 days, after which a plateau was observed.
  • Weight-specific rates of umbilical glucose uptake and fetus utilization decreased progressively throughout the second half of gestation.
  • The study reveals that below 280 days of gestation, fetal uptake of lactate (a product of glucose metabolism) was negligible. However, after 280 days, lactate uptake became significant, suggesting a metabolic shift in the fetus as it grew larger.
  • Additionally, the researchers observed lower lactate uptake in the fetus after 320 days of gestation compared to the period from 281 to 300 days.

Effects of Maternal Fasting on Fetal Metabolism

  • The research provided insights into the impact of maternal fasting on fetal metabolism. Specifically, it showed that a 36-hour period of maternal fasting reduced the rate of umbilical uptake and utilization of glucose, but had no effect on the rates of endogenous glucose production and umbilical uptake of oxygen and lactate.

Comparative Analysis

  • By conducting a comparative analysis with another common domestic species (sheep), the researchers highlighted that fetal metabolism in horses is highly dependent on glucose in comparison to sheep, particularly during the mid- and late gestation periods.
  • They concluded that different species employ different strategies to meet the nutritional demands of the growing fetus during the second half of gestation.

Cite This Article

APA
Fowden AL, Taylor PM, White KL, Forhead AJ. (2000). Ontogenic and nutritionally induced changes in fetal metabolism in the horse. J Physiol, 528 Pt 1(Pt 1), 209-219. https://doi.org/10.1111/j.1469-7793.2000.00209.x

Publication

ISSN: 0022-3751
NlmUniqueID: 0266262
Country: England
Language: English
Volume: 528 Pt 1
Issue: Pt 1
Pages: 209-219

Researcher Affiliations

Fowden, A L
  • Departments of Physiology and Clinical Veterinary Medicine, University of Cambridge, Cambridge CB2 3EG, UK. alf1000@cam.ac.uk
Taylor, P M
    White, K L
      Forhead, A J

        MeSH Terms

        • Animal Nutritional Physiological Phenomena
        • Animals
        • Aorta / embryology
        • Aorta / physiology
        • Blood Flow Velocity / physiology
        • Blood Gas Analysis
        • Blood Glucose
        • Female
        • Fetal Weight / physiology
        • Food Deprivation / physiology
        • Gestational Age
        • Glucose / metabolism
        • Horses / embryology
        • Horses / metabolism
        • Hydrocortisone / blood
        • Insulin / blood
        • Lactic Acid / blood
        • Oxygen Consumption / physiology
        • Pregnancy
        • Umbilical Veins / physiology
        • Urea / blood
        • Vena Cava, Inferior / embryology
        • Vena Cava, Inferior / physiology

        References

        This article includes 43 references
        1. Armitage P. Statistical Methods in Medical Research. Oxford, UK: Blackwells; 1971.
        2. Baur R. Morphometry of the placental exchange area. Advances in Anatomy, Embryology and Cell Biology 1977;53:1–63.
          pubmed: 878950
        3. Bell AW, Kennaugh JM, Battaglia FC, Makowski EL, Meschia G. Metabolic and circulatory studies of the fetal lamb at mid gestation. American Journal of Physiology 1986;250:E538–544.
          pubmed: 3706520
        4. Bell AW, Kennaugh JJ, Battaglia FC, Meschia G. Uptake of amino acids and ammonia at mid gestation by the fetal lamb. Quarterly Journal of Experimental Physiology 1989;74:635–643.
          pubmed: 2594925
        5. Chavatte P, Holtan D, Ousey JC, Rossdale PD. Biosynthesis and possible biological roles of progestagens during equine pregnancy and in the newborn foal. Equine Veterinary Journal 1997;(suppl. 24):89–95.
          pubmed: 9355808
        6. Ehrhardt RA, Bell AW. Developmental increase in glucose transporter concentration in the sheep placenta. American Journal of Physiology 1997;273:R1132–1142.
          pubmed: 9321896
        7. Fowden AL. Comparative aspects of fetal carbohydrate metabolism. Equine Veterinary Journal 1997;(suppl. 24):19–25.
          pubmed: 9355798
        8. Fowden AL, Comline RS. The effects of pancreatectomy on the sheep fetus in utero. Quarterly Journal of Experimental Physiology 1984;69:319–330.
          pubmed: 6374729
        9. Fowden AL, Forhead AJ. The distribution of uterine glucose uptake between the fetal and uteroplacental tissues in the pregnant mare during the second half of gestation. The Journal of Physiology 1999;517.P:9–10P.
        10. Fowden AL, Forhead AJ. The ontogeny of glucose metabolism in the fetal horse during the second half of gestation. The Journal of Physiology 2000;523.P:177–178P.
        11. Fowden AL, Hay WW. The effects of pancreatectomy on the rates of glucose utilization, oxidation and production in the sheep fetus. Quarterly Journal of Experimental Physiology 1988;73:973–984.
          pubmed: 3070626
        12. Fowden AL, Mijovic J, Silver M. The effects of cortisol on hepatic and renal gluconeogenic enzyme activities in the sheep fetus during late gestation. Journal of Endocrinology 1993;137:213–222.
          pubmed: 8326249
        13. Fowden AL, Mundy L, Ousey JC, McGladdery A, Silver M. Tissue glycogen and glucose-6-phosphate activity in the fetal and newborn foal. Journal of Reproduction and Fertility 1991;(suppl. 44):537–542.
          pubmed: 1665518
        14. Fowden AL, Mundy L, Silver M. Developmental regulation of glucogenesis in the sheep fetus during late gestation. The Journal of Physiology 1998;508:937–947.
          pmc: PMC2230917pubmed: 9518744
        15. Fowden AL, Ralph MM, Silver M. Nutritional regulation of uteroplacental prostaglandin production and metabolism in pregnant ewes and mares during late gestation. Experimental and Clinical Endocrinology 1994;102:212–221.
          pubmed: 7995343
        16. Fowden AL, Silver M. Glucose and oxygen metabolism in the fetal foal during late gestation. American Journal of Physiology 1995;268:R1455–1461.
          pubmed: 8594949
        17. Hay WW. Regulation of placental metabolism by glucose supply. Reproduction, Fertility and Development 1997;7:365–375.
          pubmed: 8606945
        18. Hay WW, Molina RA, D'Giacomo JE, Meschia G. Model of placental glucose consumption and glucose transfer. American Journal of Physiology 1990;258:R569–577.
          pubmed: 2316706
        19. Hay WW, Myers SA, Sparks JW, Wilkening RB, Meschia G, Battaglia FC. Glucose and lactate oxidation rates in the fetal lamb. Proceedings of the Society for Experimental Biology and Medicine 1983;173:553–563.
          pubmed: 6412239
        20. Hay WW, Sparks JW, Quissell BJ, Battaglia FC, Meschia G. Simultaneous measurements of umbilical uptake, fetal utilization rate and fetal turnover rate of glucose. American Journal of Physiology 1981;240:E662–668.
          pubmed: 7246734
        21. Leiser R, Kaufmann P. Placental structure: in a comparative aspect. Experimental and Clinical Endocrinology 1995;102:122–134.
          pubmed: 7995333
        22. Macdonald AA, Chavatte P, Fowden AL. Scanning electron microscopy of the microcotyledonary placenta of the horse. Equus cabellus. Placenta 2000;21 (in the Press).
          pubmed: 10940207
        23. Meschia G, Cotter JR, Breathnach EJ, Barron DH. Simultaneous measurements of uterine and umbilical blood flow and oxygen uptakes. Quarterly Journal of Experimental Physiology 1967;52:1–18.
        24. Meyer H, Ahleswede L. The intrauterine growth and body composition of foals and the nutrient requirements of pregnant mares. Animal Research and Development 1978;8:86–112.
        25. Meznarich HK, Hay WW, Sparks JW, Meschia G, Battaglia FC. Fructose disposal and oxidation rates in the ovine fetus. Quarterly Journal of Experimental Physiology 1987;72:617–625.
          pubmed: 3122263
        26. Molina RD, Carver TD, Hay WW. Ontogeny of insulin effect in fetal sheep. Paediatric Research 1993;34:654–660.
          pubmed: 8284105
        27. Molina RD, Meschia G, Battaglia FC, Hay WW. Gestational maturation of placental glucose transfer capacity in sheep. American Journal of Physiology 1991;261:R697–704.
          pubmed: 1887958
        28. Platt H. Growth of the equine fetus. Equine Veterinary Journal 1984;16:247–252.
          pubmed: 6383808
        29. Silver M. An assessment of the chronically catheterised fetal preparation in sheep and other species. Placenta 1981;(suppl. 2):89–108.
        30. Silver M, Barnes RJB, Comline RS, Fowden AL, Clover L, Michell MD. Prostaglandins in maternal and fetal plasma and in allantonic fluid during the second half of gestation in the mare. Journal of Reproduction and Fertility 1979;27:531–539.
          pubmed: 289833
        31. Silver M, Comline RS. Transfer of gases and metabolite in the equine placenta: a comparison with other species. Journal of Reproduction and Fertility 1975;(suppl. 23):589–594.
          pubmed: 1529
        32. Silver M, Fowden AL. Uterine prostaglandin of metabolite production in relation to glucose availability in late gestation – The possible influence of diet on the time of delivery in the mare. Journal of Reproduction and Fertility 1982;(suppl. 32):511–519.
          pubmed: 6962892
        33. Silver M, Fowden AL, Taylor PM, Knox J, Hill CM. Blood amino acids in the pregnant mare and fetus: the effects of maternal fasting and intrafetal insulin. Experimental Physiology 1994;79:423–433.
          pubmed: 8074855
        34. Silver M, Steven DH, Comline RS. Placental exchange and morphology in ruminants and mare. In: Comline RS, Cross KW, Dawes GS, Nathanielsz PW, editors. Proceedings Fetal and Neonatal Physiology. Cambridge: CUP; 1973. pp. 245–271.
        35. Simmons MA, Meschia G, Makowski EL, Battaglia FC. Fetal metabolic response to maternal starvation. Pediatric Research 1974;8:830–836.
          pubmed: 4471599
        36. Sparks JW, Hay WW, Bonds D, Meschia G, Battaglia FC. Simultaneous measurements of lactate turnover rate and umbilical lactate uptake in the fetal lamb. Journal of Clinical Investigation 1982;70:179–192.
          pmc: PMC370240pubmed: 7085882
        37. Stammers JP, Hill D, Silver M, Fowden AL. Fetal and maternal plasma lipids in chronically catheterised mares in late gestation: effects of different nutritional states. Reproduction, Fertility and Development 1995;7:1275–1284.
          pubmed: 8848600
        38. Stammers JP, Hill D, Silver M, Fowden AL, Ousey JC, Rossdale PD. Release of lipid from the equine placenta during in utero incubation. Placenta 1994;15:857–872.
          pubmed: 7886026
        39. Stegeman JH. Placental development in the sheep and its relation to fetal development. Bijdragentot de Dierkunde 1974;44:3–73.
        40. Steven DH. Placentation in the mare. Journal of Reproduction and Fertility 1982;(suppl. 31):41–55.
          pubmed: 6762433
        41. Taylor PM. Anaesthesia of pregnant animals. Equine Veterinary Journal 1997;(suppl. 24):1–6.
          pubmed: 9355795
        42. Taylor PM, Silver M, Fowden AL. Intravenous catheterisation of fetus and mare in late pregnancy: management and respiratory, circulatory and metabolic effects. Equine Veterinary Journal 1992;24:391–396.
          pubmed: 1396515
        43. Wooding FBP, Morgan G, Fowden AL, Allen WW. Separate sites and mechanisms for placental transport of calcium, iron, and glucose in the equine placenta. Placenta 2000;21 (in the Press).
          pubmed: 10985966

        Citations

        This article has been cited 4 times.
        1. Filippi L, Pascarella F, Pini A, Cammalleri M, Bagnoli P, Morganti R, Innocenti F, Castagnini N, Melosi A, Scaramuzzo RT. Fetal Oxygenation from the 23rd to the 36th Week of Gestation Evaluated through the Umbilical Cord Blood Gas Analysis. Int J Mol Sci 2023 Aug 6;24(15).
          doi: 10.3390/ijms241512487pubmed: 37569862google scholar: lookup
        2. Filippi L, Scaramuzzo RT, Pascarella F, Pini A, Morganti R, Cammalleri M, Bagnoli P, Ciantelli M. Fetal oxygenation in the last weeks of pregnancy evaluated through the umbilical cord blood gas analysis. Front Pediatr 2023;11:1140021.
          doi: 10.3389/fped.2023.1140021pubmed: 37152310google scholar: lookup
        3. O'Connor SJ, Ousey JC, Gardner DS, Fowden AL, Giussani DA. Development of baroreflex function and hind limb vascular reactivity in the horse fetus. J Physiol 2006 Apr 1;572(Pt 1):155-64.
          doi: 10.1113/jphysiol.2006.105635pubmed: 16469779google scholar: lookup
        4. Giussani DA, Forhead AJ, Fowden AL. Development of cardiovascular function in the horse fetus. J Physiol 2005 Jun 15;565(Pt 3):1019-30.
          doi: 10.1113/jphysiol.2004.078469pubmed: 15790668google scholar: lookup