Analyze Diet
Veterinary clinical pathology2022; 52(2); 261-270; doi: 10.1111/vcp.13181

Transient increases in glutamate dehydrogenase (GLDH) activity occur in neonatal foals.

Abstract: Liver analyte measurement is important in the evaluation of sick animals. Liver injury in horses is recognized by increased glutamate dehydrogenase (GLDH), sorbitol dehydrogenase (SDH), and aspartate aminotransferase (AST) activities, whereas biliary pathology is identified by increased alkaline phosphatase and γ-glutamyl transferase (GGT) activities or bilirubin concentrations. We have observed high GLDH, but not SDH, activities in neonatal foals admitted for conditions other than liver disease. Only one previous study have evaluated GLDH activity over time in healthy neonatal foals; however, SDH activity was not measured. Objective: We aimed to evaluate changes in liver analytes in neonatal foals over time. Methods: We measured serum liver analytes (GLDH, SDH, GGT, AST, total, direct, and indirect bilirubin) and creatine kinase activity of 11 clinically healthy foals before and at various times after suckling until 46 days of age. Analytes were also measured in colostrum and mare serum. Results: Median GLDH activities increased after birth to peak at 3-4 days of age (106 U/L, reference interval, 0-8 U/L). Median SDH activities had a lower peak at 3-4 days (15 U/L, reference interval, 0-11 U/L) and were frequently discordant with GLDH. There was no association between foal and mare serum or colostral enzyme activities. AST activity plateaued at 5-6 days, whereas GGT activity and total and indirect bilirubin concentrations peaked at 14 and 3-4 days of age, respectively. Conclusions: Transient increases in GLDH, SDH, and GGT activities and total and indirect bilirubin concentrations occur in clinically healthy neonatal foals and do not necessarily indicate relevant liver disease.
Publication Date: 2022-11-28 PubMed ID: 36443639DOI: 10.1111/vcp.13181Google 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

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 research study found that temporary increases in levels of certain liver analytes, specifically glutamate dehydrogenase (GLDH), sorbitol dehydrogenase (SDH), and γ-glutamyl transferase (GGT), as well as total and indirect bilirubin concentrations, can occur in healthy newborn foals and do not always indicate significant liver disease.

Background of the Study

  • In the veterinary field, certain enzymes and chemical substances in the liver are often measured to assess the health of animals, especially when dealing with liver disease. Among these, increased activities of glutamate dehydrogenase (GLDH), sorbitol dehydrogenase (SDH), and aspartate aminotransferase (AST) suggest liver injury, while increased alkaline phosphatase and γ-glutamyl transferase (GGT) activities and heightened bilirubin concentrations imply biliary pathology.
  • The researchers had recorded an increased GLDH activity in newborn foals, although SDH activities were not elevated. There was only one prior study examining GLDH over time in healthy newborn foals, but it didn’t measure SDH activity.

Objective and Methodology

  • This research aimed to understand the changes in these liver enzymes and substances in healthy newborn foals over time. To accomplish this, serum liver analytes including GLDH, SDH, GGT, AST, total, direct, and indirect bilirubin were measured in 11 clinically healthy foals at various stages after birth up to 46 days. Levels of these analytes were also checked in colostrum and mare serum.

Research Findings

  • At 3-4 days of age, GLDH activities peaked (106 U/L), which is notably higher than the reference interval of 0-8 U/L. SDH also peaked at the same time, but at a lower level (15 U/L).
  • There was no correlation found between the foal and mare serum or colostral enzyme activities.
  • AST activity leveled off at 5-6 days, while GGT activity and total and indirect bilirubin concentrations peaked at 14 days and 3-4 days of age, respectively.

Conclusions

  • What was discovered in the study is that temporary increases in enzyme activities of GLDH, SDH, and GGT, and total and indirect bilirubin concentrations, do happen in healthy newborn foals. This suggests that these increases do not necessarily indicate significant liver disease. Therefore, these findings might have implications for diagnosing liver disease in foals. The detection of such increases should be evaluated further before making a diagnosis of liver disease.

Cite This Article

APA
Hoffman M, Cheong SH, Stokol T. (2022). Transient increases in glutamate dehydrogenase (GLDH) activity occur in neonatal foals. Vet Clin Pathol, 52(2), 261-270. https://doi.org/10.1111/vcp.13181

Publication

ISSN: 1939-165X
NlmUniqueID: 9880575
Country: United States
Language: English
Volume: 52
Issue: 2
Pages: 261-270

Researcher Affiliations

Hoffman, Martha
  • Department of Population Medicine and Diagnostic Sciences, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA.
Cheong, Soon Hon
  • Department of Clinical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA.
Stokol, Tracy
  • Department of Population Medicine and Diagnostic Sciences, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA.

MeSH Terms

  • Animals
  • Horses
  • Female
  • Glutamate Dehydrogenase
  • Liver Diseases / veterinary
  • Bilirubin
  • Aspartate Aminotransferases
  • Horse Diseases

References

This article includes 39 references
  1. Gerber H. Serum enzyme determination in equine medicine.. Eq Vet J 1969;1:129-139.
  2. Armengou L, Jose-Cunilleras E, Ríos J, Cesarini C, Viu J, Monreal L. Metabolic and endocrine profiles in sick neonatal foals are related to survival.. J Vet Intern Med 2013;27:567-575.
  3. Haggett EF, Magdesian KG, Kass PH. Clinical implications of high liver enzyme activities in hospitalized neonatal foals.. J Am Vet Med Assoc 2011;239:661-667.
  4. Hoffman WE, Solter PF, Kaneko JJ, Harvey HJ, Bruss M. Diagnostic enzymology of domestic animals.. In: Kaneko JJ, Harvey JW, Bruss M, eds. Clinical Biochemistry of Domestic Animals. 6th ed.; San Diego, CA: Elsevier; 2008:351-378.
  5. Tomlinson JE, Jager M, Struzyna A. Tropism, pathology, and transmission of equine parvovirus-hepatitis.. Emerg Microbes Infect 2020;9:651-663.
  6. West HJ. Evaluation of total plasma bile acid concentrations for the diagnosis of hepatobiliary disease in horses.. Res Vet Sci 1989;46:264-270.
  7. Marrs J, Small J, Milne EM, John HA. Liver and biliary system pathology in equine dysautonomia (grass sickness).. J Vet Med A Physiol Pathol Clin Med 2001;48:243-255.
  8. Satué K, Miguel-Pastor L, Chicharro D, Gardón JC. Hepatic enzyme profile in horses.. Animals (Basel) 2022;12(7):861.
  9. Gronwall R, Engelking LR, Noonan N. Direct measurement of biliary bilirubin excretion in ponies during fasting.. Am J Vet Res 1980;41:125-126.
  10. Waelchli RO, Lutz H, Hermann M, Eggenberger E. Clinico-chemical blood parameters in foals in the first two months of life.. Schweiz Arch Tierheilkd 1992;134:471-482.
  11. Barton MH, LeRoy BE. Serum bile acids concentrations in healthy and clinically ill neonatal foals.. J Vet Intern Med 2007;21:508-513.
  12. Patterson WH, Brown CM. Increase in serum gamma-glutamyl transferase in neonatal Standardbred foals.. Am J Vet Res 1986;47:2461-2463.
  13. Bauer JE, Asquith RL, Kivipelto J. Serum biochemical indicators of liver function in neonatal foals.. Am J Vet Res 1989;50:203-2041.
  14. Gossett KA, French DD. Effect of age on liver enzyme activities in serum of healthy quarter horses.. Am J Vet Res 1984;45:354-356.
  15. Aoki T, Ishii M. Hematological and biochemical profiles in peripartum mares and neonatal foals (heavy draft horse).. J Eq Vet Sci 2012;32:170-176.
  16. Boyd JW. Serum enzyme changes in newborn calves fed colostrum.. Vet Clin Pathol 1989;18:47-51.
  17. Perino LJ, Sutherland RL, Woollen NE. Serum gamma-glutamyltransferase activity and protein concentration at birth and after suckling in calves with adequate and inadequate passive transfer of immunoglobulin G.. Am J Vet Res 1993;54:56-59.
  18. Tessman RK, Tyler JW, Parish SM, Johnson DL, Gant RG, Grasseschi HA. Use of age and serum gamma-glutamyltransferase activity to assess passive transfer status in lambs.. J Am Vet Med Assoc 1997;211:1163-1164.
  19. Maden M, Altunok V, Birdane FM, Aslan V, Nizamlioglu M. Blood and colostrum/milk serum gamma-glutamyltransferase activity as a predictor of passive transfer status in lambs.. J Vet Med B Infect Dis Vet Public Health 2003;50:128-131.
  20. Harr KE, Flatland B, Nabity M, Freeman KP, ASVCP. ASVCP guidelines: allowable total error guidelines for biochemistry.. Vet Clin Pathol 2013;42:424-436.
  21. Friedrichs KR, Harr KE, Freeman KP. ASVCP reference interval guidelines: determination of de novo reference intervals in veterinary species and other related topics.. Vet Clin Pathol 2012;41:441-453.
  22. Mariella J, Castagnetti C, Prosperi A, Scagliarini A, Peli A. Cytokine levels in colostrum and in foals' serum pre- and post-suckling.. Vet Immunol Immunopathol 2017;185:34-37.
  23. Secor EJ, Matychak MB, Felippe MJB. Transfer of tumour necrosis factor-α via colostrum to foals.. Vet Rec 2012;170:51.
  24. Paltrinieri S, Giordano A, Villani M, Manfrin M, Panzani S, Veronesi MC. Influence of age and foaling on plasma protein electrophoresis and serum amyloid A and their possible role as markers of equine neonatal septicaemia.. Vet J 2008;176:393-396.
  25. Stoneham SJ, Palmer L, Cash R, Rossdale PD. Measurement of serum amyloid A in the neonatal foal using a latex agglutination immunoturbidimetric assay: determination of the normal range, variation with age and response to disease.. Equine Vet J 2001;33:599-603.
  26. Keller P. Enzyme activities in the dog: tissue analyses, plasma values, and intracellular distribution.. Am J Vet Res 1981;42:575-582.
  27. Braakman I, Keij J, Hardonk MJ, Meijer DK, Groothuis GM. Separation of periportal and perivenous rat hepatocytes by fluorescence-activated cell sorting: confirmation with colloidal gold as an exogenous marker.. Hepatology 1991;13:73-82.
  28. Boyd JW. The mechanisms relating to increases in plasma enzymes and isoenzymes in diseases of animals.. Vet Clin Pathol 1983;12:9-24.
  29. Schmidt ES, Schmidt FW. Glutamate dehydrogenase: biochemical and clinical aspects of an interesting enzyme.. Clin Chim Acta 1988;173:43-55.
  30. Wimmer M, Pette D. Microphotometric studies on intraacinar enzyme distribution in rat liver.. Histochemistry 1979;64:23-33.
  31. Craig AM, Pearson EG, Meyer C, Schmitz JA. Clinicopathologic studies of tansy ragwort toxicosis in ponies: sequential serum and histopathological changes.. J Eq Vet Sci 1991;11:261-271.
  32. Noonan NE. Variations of plasma enzymes in the pony and the dog after carbon tetrachloride administration.. Am J Vet Res 1981;42:674-678.
  33. Bernard WV, Divers TJ. Variations in serum sorbitol dehydrogenase, aspartate transaminase, and isoenzyme 5 of lactate dehydrogenase activities in horses given carbon tetrachloride.. Am J Vet Res 1989;50:622-623.
  34. Collis KA, Symonds HW, Sansom BF. The half-life of glutamate dehydrogenase in plasma of dry and lactating dairy cows.. Res Vet Sci 1979;27:267-268.
  35. Jaeschke H, McGill MR. Serum glutamate dehydrogenase-biomarker for liver cell death or mitochondrial dysfunction?. Toxicol Sci 2013;134:221-222.
  36. Rollins D, Larsson A, Steen B. Glutathione and gamma-glutamyl cycle enzymes in human fetal liver.. J Pharmacol Exp Ther 1981;217:697-700.
  37. Rico AG, Braun JP, Benard P, El Hassan AA, Cazieux A. Tissue distribution and blood levels of gamma-glutamyl transferase in the horse.. Equine Vet J 1977;9:100-101.
  38. Fujiwara R, Maruo Y, Chen S, Tukey RH. Role of extrahepatic UDP-glucuronosyltransferase 1A1: advances in understanding breast milk-induced neonatal hyperbilirubinemia.. Toxicol Appl Pharmacol 2015;289:124-132.
  39. Horney BS, Honor DJ, MacKenzie A, Burton S. Stability of sorbitol dehydrogenase activity in bovine and equine sera.. Vet Clin Pathol 1993;22:5-9.

Citations

This article has been cited 1 times.
  1. Wilkins PA, Wong D, Slovis NM, Collins N, Barr BS, MacKenzie C, De Solis CN, Castagnetti C, Mariella J, Burns T, Perkins G, Delvescovo B, Sanchez LC, Kemper AM, Magdesian KG, Bedenice D, Taylor SD, Gold J, Dunkel B, Pranzo G, Constable PD. The Systemic Inflammatory Response Syndrome and Predictors of Infection and Mortality in 1068 Critically Ill Newborn Foals. J Vet Intern Med 2025 Mar-Apr;39(2):e70004.
    doi: 10.1111/jvim.70004pubmed: 40091577google scholar: lookup