Analyze Diet
Equine veterinary journal2020; 53(2); 379-384; doi: 10.1111/evj.13297

Oxidative state in equine neonates: Anti- and pro-oxidants.

Abstract: In newborns, exposure to the extrauterine environment with high oxygen tension and sudden pulmonary adaptation leads to an increase in reactive oxygen species (ROS). ROS have several physiological roles, which are essential for neonatal development, however, when unbalanced, these highly unstable molecules can cause cellular destabilisation, compromising vital processes. Objective: To characterise the oxidative status in healthy equine neonates, evaluating an indicator of lipid peroxidation and both enzymatic and nonenzymatic antioxidant systems, during the first week of life. Methods: Experimental cohort. Methods: Twenty-four foals were evaluated, with blood collections performed at 5 minutes, 12, 72 and 168 hours after birth. The degree of lipid peroxidation was quantified using Thiobarbituric Acid Reactive Substances (TBARS). Superoxide dismutase (SOD) and glutathione peroxidase (GPx) enzymatic activities, and total, conjugated and unconjugated serum bilirubin levels were also analysed. Comparisons were performed using ANOVA followed by a Tukey's test. Additionally, dependent variables were also evaluated with Pearson's correlation tests. Results: Higher GPx activity was observed at 12 and 72 hours when compared to 5 minutes. An increase in TBARS levels was found at 5 minutes after birth, followed by a decrease at 72 hours and stabilisation through subsequent moments until 168 hours after birth. No differences were observed in SOD activity when comparing the four time points. Bilirubin concentrations were lower at 5 minutes after birth and total and unconjugated bilirubin increased at 12 hours and decreased between 72 and 168 hours after birth. Conclusions: Lipid peroxidation at birth was high, suggesting an increase in ROS levels relating to physiological events in neonatal adaptation. Antioxidant systems, involving unconjugated bilirubin and GPx, were activated and these biomolecules act concomitantly to reduce ROS levels, thus maintaining oxidative homeostasis. Overall, our results suggest a pro-oxidant balance during the first 168 hours after birth in equine neonates.
Publication Date: 2020-07-09 PubMed ID: 32492758DOI: 10.1111/evj.13297Google 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 examines the role of reactive oxygen species (ROS) and various enzymatic and nonenzymatic antioxidant systems in the neonatal development of horses during their first week of life. The study found a high level of lipid peroxidation at birth, indicating a rise in ROS levels, while antioxidant systems were triggered to maintain oxidative balance.

Research Aim

  • The research aimed to characterise the oxidative status in healthy equine neonates in relation to reactive oxygen species (ROS) and both enzymatic and non-enzymatic antioxidant systems.

Methodology

  • The researchers conducted a cohort study with a sample of twenty-four foals.
  • They collected blood samples at 5 minutes, 12, 72 and 168 hours after birth.
  • They used the Thiobarbituric Acid Reactive Substance (TBARS) to measure the degree of lipid peroxidation.
  • They also analysed superoxide dismutase (SOD) and glutathione peroxidase (GPx) enzymatic activities, as well as total, conjugated and unconjugated serum bilirubin levels.
  • The findings were compared using ANOVA and Tukey’s test for statistical significance. Any dependent variables were further evaluated using Pearson’s correlation tests.

Results

  • The study reported an increase in GPx activity at 12 and 72 hours compared to 5 minutes after birth.
  • TBARS levels rose 5 minutes after birth, then decreased at 72 hours and stabilised thereafter until 168 hours after birth.
  • No significant differences were seen in SOD activity over the four time points.
  • Bilirubin concentrations were low at 5 minutes after birth, and total and unconjugated bilirubin levels rose at 12 hours, before decreasing between 72 and 168 hours after birth.

Conclusion

  • The research found that lipid peroxidation was high at birth, suggesting an increase in ROS levels related to physiological events in the adaptation of neonates.
  • The antioxidants, unconjugated bilirubin and GPx, were activated and functioned together to reduce ROS levels, which helped in maintaining oxidative balance.
  • The overall findings suggest that there is a pro-oxidant balance during the first 168 hours after birth in equine newborns.

Cite This Article

APA
França de Souza D, Alonso MA, Brito MM, Meirelles MG, Francischini MCP, Nichi M, Fernandes CB. (2020). Oxidative state in equine neonates: Anti- and pro-oxidants. Equine Vet J, 53(2), 379-384. https://doi.org/10.1111/evj.13297

Publication

ISSN: 2042-3306
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 53
Issue: 2
Pages: 379-384

Researcher Affiliations

França de Souza, Danilo
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, São Paulo, Brazil.
Alonso, Maria A
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, São Paulo, Brazil.
Brito, Maíra M
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, São Paulo, Brazil.
Meirelles, Marcela G
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, São Paulo, Brazil.
Francischini, Maria C P
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, São Paulo, Brazil.
Nichi, Marcilio
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, São Paulo, Brazil.
Fernandes, Claudia B
  • Department of Animal Reproduction, School of Veterinary Medicine and Animal Science, University of São Paulo, São Paulo, Brazil.

MeSH Terms

  • Animals
  • Glutathione Peroxidase / metabolism
  • Horses
  • Humans
  • Lipid Peroxidation
  • Oxidative Stress
  • Reactive Oxygen Species
  • Thiobarbituric Acid Reactive Substances

Grant Funding

  • 001 / Coordination for Improvement of People with Higher Level Education-Brazil (CAPES)
  • 2017/05425-0 / Su00e3o Paulo Research Foundation (FAPESP)

References

This article includes 37 references
  1. Castagnetti C, Pirrone A, Mariella J, Mari G. Venous blood lactate evaluation in equine neonatal intensive care.. Theriogenology 2010;73:343-57.
  2. Tennent-Brown B. Blood lactate measurement and interpretation in critically ill equine adults and neonates.. Vet Clin North Am Equine Pract 2014;30:399-413.
  3. Barsotti C, Ipata PL. Metabolic regulation of ATP breakdown and of adenosine production in rat brain extracts.. Int J Biochem Cell Biol 2004;36(11):2214-25.
  4. Ryu HM, Kim YJ, Oh EJ, Oh SH, Choi JY, Cho JH. Hypoxanthine induces cholesterol accumulation and incites atherosclerosis in apolipoprotein E-deficient mice and cells.. J Cell Mol Med 2016;20(11):2160-72.
  5. Sgorbini M, Bonelli F, Marmorine P, Biagi G, Corozza M, Pasquini A. Maternal and neonatal evaluation of derivated reactive oxygen metabolites (d-ROMs) and biological antioxidant potential in the horse.. Theriogenology 2015;83(1):48-51.
  6. Tsatmali M, Walcott EC, Crossin KL. Newborn neurons acquire high levels of reactive oxygen species and increased mitochondrial proteins upon differentiation from progenitors.. Brain Res 2005;1040(1-2):137-50.
  7. Augusto O. Radicais livres como maus à vida.. In: Radicais livres: bons, maus e naturais. 1st ed. São Paulo: Oficina de Textos; 2006. p. 120.
  8. Rey-Santano C, Mielgo VE, Gastiasoro E, Murgia X, Lafuente H, Ruiz-Del-Yerro E. Early cerebral hemodynamic, metabolic, and histological changes in hypoxic-Ischemic fetal lambs during postnatal life.. Front Neurosci 2011;5:111.
  9. Rao G, Kamath U, Raghothama C, Pradeep KS, Rao P. Maternal and fetal indicators of oxidative stress in various obstetric complications.. Indian J Clin Biochem 2003;18(2):80-6.
  10. Kamath U, Rao G, Kamath SU, Rai L. Maternal and fetal indicators of oxidative stress during intrauterine growth retardation (IUGR).. Indian J Clin Biochem 2006;21(1):111-5.
  11. Frank L, Sosenko IR. Prenatal development of lung antioxidant enzymes in four species.. J Pediatr 1987;110(1):106-10.
  12. Frank L, Groseclose EE. Preparation for birth into an O2-rich environment: the antioxidant enzymes in the developing rabbit lung.. Pediatr Res 1984;18(3):240-4.
  13. Shekeeb Shahab M, Kumar P, Sharma N, Narang A, Prasad R. Evaluation of oxidant and antioxidant status in term neonates: a plausible protective role of bilirubin.. Mol Cell Biochem 2008;317(1-2):51-9.
  14. Gurzanova-Durnev L, Zisovska E, Dosic-Markovska B. Cord blood superoxide dismutase and glutathione peroxidase activity in premature infants.. J Med Biochem 2014;33:208-15.
  15. Huertas JR, Palomino N, Carrasco R, Quiles J, Ramirez-Tortosa MC, Ochoa J. Lipid peroxidation and antioxidants in newborns.. Mol Aspects Med 1997;18(Suppl):229-32.
  16. Robles R, Palomino N, Robles A. Oxidative stress in the neonate.. Early Hum Dev 2001;65(Suppl):75-81.
  17. Abdul-Razzak KK, Nusier MK, Obediat AD, Salim AM. Antioxidant vitamins and hyperbilirubinemia in neonates.. Ger Med Sci 2007;5:Doc03.
  18. Wiedemann M, Kontush A, Finckh B, Hellwege H-H, Kohlschutter A. Neonatal blood plasma is less susceptible to oxidation than adult plasma owing to its higher content of bilirubin and lower content of oxidizable fatty acids.. Pediatr Res 2003;53:843-9.
  19. Sedlak TW, Snyder SH. Bilirubin benefits: cellular protection by a biliverdin reductase antioxidant cycle.. Pediatrics 2004;113(6):1776-82.
  20. Knottenbelt D, Holdstock N, Madigan JE. Intensive care, therapeutics and nursing.. In: Equine neonatology medicine and surgery. 1st ed. Edinburgh: Saunders; 2004. p. 405-65.
  21. Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction.. Anal Biochem 1979;95(2):351-8.
  22. Nichi M, Goovaerts IG, Cortada CN, Barnabe BH, De Clercq JB, Bols PE. Roles of lipid peroxidation and cytoplasmic droplets on in vitro fertilization capacity of sperm collected from bovine epididymides stored at 4 and 34 degrees C.. Theriogenology 2007;67(2):334-40.
  23. Flohé L, Ötting F. Formation or removal of oxygen radicals.. Meth Enzimol 1984;105:92-104.
  24. Salomone F, Li Volti G, Rosso C, Grosso G, Bugianese E. Unconjugated bilirubin, a potent endogenous antioxidant, is decreased in patients with non-alcoholic steatohepatitis and advanced fibrosis.. J Gastroenterol Hepatol 2013;28(7):1202-8.
  25. Jansen T, Hortmann M, Oelze M, Opitz B, Steven S, Schell R. Conversion of biliverdin to bilirubin by biliverdin reductase contributes to endothelial cell protection by heme oxygenase-1-evidence for direct and indirect antioxidant actions of bilirubin.. J Mol Cell Cardiol 2010;49(2):186-95.
  26. Axon JE, Palmer JE. Clinical pathology of the foal.. Vet Clin North Am Equine Pract 2008;24(2):357-85.
  27. Stocker R, Glazer AN, Ames BN. Antioxidant activity of albumin-bound bilirubin.. Proc Natl Acad Sci USA 1987;84(16):5918-22.
  28. Sedlak TW, Saleh M, Higginson DS, Paul DB, Juluri KR, Sneyder SH. Bilirubin and glutathione have complementary antioxidant and cytoprotective roles.. Proc Natl Acad Sci USA 2009;106(13):5171-6.
  29. Ferencz A, Orvos H, Hermesz E. Major differences in the levels of redox status and antioxidant defence markers in the erythrocytes of pre- and full-term neonates with intrauterine growth restriction.. Reprod Toxicol 2015;53:10-4.
  30. Ishida N, Sato F, Asai Y, Masumizo T, Mukoyama H. Chronological changes in the superoxide-scavenging ability of the plasma of mares and foals at delivery.. J Equine Sci 1997;8(4):109-11.
  31. Perry JJP, Shin DS, Getzoff ED, Tainer JA. The structural biochemistry of the superoxide dismutases.. Biochim Biophys Acta 2010;1804(2):245-62.
  32. Kwak JY, Takeshige K, Cheung BS, Minakami S. Bilirubin inhibits the activation of superoxide-producing NADPH oxidase in a neutrophil cell-free system.. Biochim Biophys Acta 1991;1076(3):369-73.
  33. Yin J, Ren W, Liu G, Duan J, Yang G, Wu L. Birth oxidative stress and the development of an antioxidant system in newborn piglets.. Free Radic Res 2013;47(12):1027-35.
  34. Gaal T, Ribiczeyne-Szabo P, Stadler K, Jakus J, Reiczigel J, Kover P. Free radicals, lipid peroxidation and the antioxidant system in the blood of cows and newborn calves around calving.. Comp Biochem Physiol B Biochem Mol Biol 2006;143(4):391-6.
  35. Ng CF, Schafer FQ, Buettner GR, Rodgers VGJ. The rate of cellular hydrogen peroxide removal shows dependency on GSH: mathematical insight into in vivo H2O2 and GPx concentrations.. Free Radic Res 2007;41(11):1201-11.
  36. Ayala A, Munoz MF, Arguelles S. Lipid peroxidation: production, metabolism, and signaling mechanisms of malondialdehyde and 4-hydroxy-2-nonenal.. Oxid Med Cell Longev 2014;2014:1-31.
  37. Lazar R, Orvos H, Szollosi R, Varga IS. The quality of the antioxidant defence system in term and preterm twin neonates.. Redox Rep 2015;20(3):103-8.

Citations

This article has been cited 1 times.
  1. Sgorbini M, Bonelli F, Percacini G, Pasquini A, Rota A. Maternal and Neonatal Evaluation of Derived Reactive Oxygen Metabolites and Biological Antioxidant Potential in Donkey Mares and Foals.. Animals (Basel) 2021 Oct 3;11(10).
    doi: 10.3390/ani11102885pubmed: 34679906google scholar: lookup