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Evaluation of oxidant/antioxidant status, metabolic profile and milk production in cows with metritis

. 2020 ; 73 () : 8. [epub] 20200527

Status PubMed-not-MEDLINE Language English Country Ireland Media electronic-ecollection

Document type Journal Article

BACKGROUND: The aim of the study was to evaluate oxidant/antioxidant status in 21 Holstein dairy cows with metritis compared to 8 healthy controls. Blood samples were taken during the first 21 days postpartum. Malondialdehyde (MDA), a marker of oxidative stress, total antioxidant status (TAS) and antioxidant parameters such as glutathione peroxidase (GPx), selenium (Se), vitamins A and E and beta-carotene were determined from all cows. The differences in beta-hydroxybutyrate (BHB), non-esterified fatty acids (NEFA), calcium, bilirubin concentrations and aspartate aminotransferase (AST) activity were also monitored, as were milk production and milk composition. Metritis was defined by an unpleasant discharge of varying color (milky-grey/brown/sanguineous) and consistency (muco-purulent/purulent/watery) and by the presence of increased temperature (> 38.5 °C) in cows within 21 days postpartum. Rectal examination revealed increased uterine size, thickened uterine wall and increased uterine tone. The affected cows had significantly reduced daily milk production. Additionally, hematological parameters and haptoglobin concentration were also measured in metritic cows. RESULTS: Higher MDA concentration (P < 0.001) was recorded in cows with metritis, while vitamin A and vitamin E concentrations were lower (P < 0.01) compared to healthy cows. Higher BHB (P < 0.05), NEFA (P < 0.05), AST (P < 0.05) and bilirubin (P < 0.001) concentrations was recorded in cows with metritis as compared to the control group. Significant differences in beta-carotene concentration, GPx activity, and Se, TAS and Ca concentrations in cows with metritis compared to control group were not observed in the present study (P > 0.05). Milk production was decreased in the cows with metritis (P < 0.001) and alterations in milk composition were also observed in metritic cows as compared to healthy cows. CONCLUSIONS: The results of the study showed that cows with metritis in early postpartum are exposed to a higher degree of oxidative stress and that the incidence of metritis can negatively affect milk production in dairy cows.

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Goff JP, Horst RL. Physiological changes at parturition and their relationship to metabolic diseases. J Dairy Sci. 1997;80:1260–1268. PubMed

LeBlanc SJ. Managing transition period health for reproductive performance in dairy cows. Cattle Pract. 2013;21:209–215.

Wathes DC, Swangchan-Uthai T, Oguejiofor CF, Cheng Z. Energy balance, immune function and fertility in the postpartum dairy cows. Cattle Pract. 2013;21:129–137.

LeBlanc SJ, Herdt TH, Seymour WM, Duffield TF, Leslie KE. Peripartum serum vitamin E, retinol and beta-carotene in dairy cattle and their association with disease. J Dairy Sci. 2004;87:609–619. PubMed

Sheldon IM, Dobson H. Postpartum uterine health in cattle. Anim Reprod Sci. 2004;82–83:295–306. PubMed

Zerbe H, Schuberth HJ, Engelke F, Frank J, Klug W, Leibold W. Development and comparison of in vivo and in vitro models for endometritis in cows and mares. Theriogenology. 2003;60:209–223. PubMed

Gier HT, Marion GB. Uterus of the cow after parturition: involutional changes. Am J Vet Res. 1968;29:83–96. PubMed

Janeway CA, Jr, Travers P, Walport M, Shlomchik MJ. Immunobiology: the immune system in health and disease. New York: Garland Publishing; 2001. Infectious agents and how they cause disease; pp. 382–388.

Lewis GS. Uterine health and disorders. J Dairy Sci. 1997;80:984–994. PubMed

Lewis GS. Steroidal regulation of uterine immune defenses. Anim Rep Sci. 2004;82–83:281–294. PubMed

Sheldon IM, Lewis GS, LeBlanc S, Gilbert RO. Defining postpartum uterine disease in cattle. Theriogenology. 2006;65:1516–1530. PubMed

Kennedy PC, Miller RB. The female genital system. In: Jubb KVF, Kennedy PC, Palmer N, editors. Pathology of domestic animals. 4. San Diego: Academic Press; 1993. pp. 378–387.

BonDurant RH. Inflammation in the bovine reproductive tract. J Dairy Sci. 1999;82:101–110. PubMed

Huszenica G, Fodor M, Gacs M, Kulcsar M, Dohmen MJW, Vamos M, Porkolab L, Kegl T, Miller JK. Brzezinska–Slebodzinska E, Madsen FC. Oxidative stress, antioxidants, and animal function. J Diary Sci. 1993;76:2812–2823. PubMed

Sicsic R, Goshen T, Dutta R, Kedem-Vaanunu N, Kaplan-Shabtai V, Pasternak Z, Gottlieb Y, Shpigel NY, Raz T. Microbial communities and infammatory response in the endometrium difer between normal and metritic dairy cows at 5–10 days post-partum. Vet Res. 2018;49:77. PubMed PMC

Sheldon IM, Cronin J, Goetze L, Donofrio G, Schuberth HJ. Defining postpartum uterine disease and the mechanisms of infection and immunity in the female reproductive tract in cattle. Biol Reprod. 2009;81:1025–1032. PubMed PMC

Miller JK, Brzezinska-Slebodzinska E, Madsen FC. Oxidative stress, antioxidants, and animal function. J Dairy Sci. 1993;76:2812–2823. PubMed

Kankofer M. Placental release/retention in cows and its relation to peroxidative damage of macromolecules. Reprod Domest Anim. 2002;37:27–30. PubMed

Bernabucci U, Ronchi B, Lacetera N, Nardone A. Influence of body condition score on relationship between metabolic status and oxidative stress in periparturient dairy cows. J Dairy Sci. 2005;88:2017–2026. PubMed

Castillo C, Hernandez J, Bravo A, Lopez-Alonso M, Pereira V, Benedito JL. Oxidative status during late pregnancy and early lactation in dairy cows. Vet J. 2005;169:286–292. PubMed

Wilde D. Influence of macro and micro minerals in the periparturient period on fertility in dairy cattle. Anim Rep Sci. 2006;69:240–249. PubMed

Sordillo LM. Factors affecting mammary gland immunity and mastitis susceptibility. Livestock Prod Sci. 2005;98:89–99.

Brzezinska-Slebodzinska E, Miller JK, Quigley JD, III, Moore JR, Madsen FC. Antioxidant status of dairy cows supplemented prepartum with vitamin E and selenium. J Diary Sci. 1994;77:3087–3095. PubMed

Kizil O, Akar Y, Yuksel M, Saat N. Oxidative stress in cows with acute puerperal metritis. Revue Med Vet. 2010;161:353–357.

Matějčková J, Samec M, Jaček M, Tůma P. HPLC monitoring of malondialdehyde in patients with endometrial and ovarial cancer. Chem List. 2011;105:375–380.

Paglia DE, Valentine WN. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med. 1967;70:158–169. PubMed

Jones ML, Allison RW. Evaluation of the ruminant complete blood cell count. Vet Clin Food Anim. 2007;23:377–402. PubMed

Kramer JW. Normal hematology of cattle, sheep, and goats. In: Feldman BF, Zinkl JG, Jain NC, editors. Schalm’s veterinary hematology. 5. Philadelphia: Lippincott Williams & Wilkins; 2000. pp. 1075–1084.

Kraft W, Dürr UM. Klinische Labordiagnostik in der Tiermedizin [clinical laboratory diagnostics in veterinary medicine], 6th Schattauer, Stuttgart, Germany. In German. 2005. p. 552.

Barragan AA, Pineiro JM, Schuenemann GM, Rajala-Schultz PJ, Sanders DE, Lakritz J. Assesment of daily activity patterns and biomarkers of pain, inflammation, and stress in lactating dairy cows diagnosed with clinical metritis. J Dairy Sci. 2018;101:8248–8258. PubMed

Gruys E, van Ederen AM, Alsemgeest SPM, Kalsbeek HC, Wensing T. Acute phase protein values in blood of cattle as indicator of animals with pathological processes. Arch Lebensmittelhygiene. 1993;44:107–112.

Trevisi E, Amadori M, Cogrossi S, Razzuoli E, Bertoni G. Metabolic stress and inflammatory response in high-yielding, periparturient dairy cows. Res Vet Sci. 2012;93:695–704. PubMed

Hirvonen J, Huszenicza G, Kulcsar M, Pyörälä S. Acute-phase response in dairy cows with acute postpartum metritis. Theriogenology. 1999;51:1071–1083. PubMed

Huzzey JM, Veira DM, Weary DM, von Keyserlingk MAG. Prepartum behavior and dry matter intake identify cows at risk for metritis. J Dairy Sci. 2007;90:3220–3233. PubMed

Sheldon IM, Noakes DE, Rycroft AN, Dobson H. Acute phase protein responses to uterine bacterial contamination in cattle after calving. Vet Rec. 2001;148:172–175. PubMed

Chan JPW, Chang CC, Hsu WL, Liu WB, Chen TH. Association of increased serum acute-phase protein concentrations with reproductive performance in dairy cows with postpartum metritis. Vet Clin Pathol. 2010;39:72–78. PubMed

Pohl A, Burfeind O, Heuwieser W. The associations between postpartum serum haptoglobin concentration and metabolic status, calving difficulties, retained fetal membranes, and metritis. J Dairy Sci. 2015;98:4544–4551. PubMed

Dervishi E, Zhang G, Hailemariam D, Goldansaz SA, Deng Q, Dunn SM, Ametaj BN. Alterations in innate immunity reactants and carbohydrate and lipid metabolism precede occurrence of metritis in transition dairy cows. Res Vet Sci. 2016;104:30–39. PubMed

Niki E. Biomarkers of lipid peroxidation in clinical material. Biochim Biophys Acta. 1840;2014:809–817. PubMed

Niki E. Lipid peroxidation: physiological concentrations and dual biological effects. Free Radic Biol Med. 2009;47:469–484. PubMed

Gong J, Xiao M. Selenium and antioxidant status in dairy cows at different stages of lactation. Biol Trace Elem Res. 2016;171:89–93. PubMed

Goff JP, Kimura K, Horst RL. Effect of mastectomy on milk fever, energy, and vitamins a, E, and β-carotene at parturition. J Dairy Sci. 2002;85:1427–1436. PubMed

Rizzo A, Pantaleo M, Mutinati M, Minoia G, Trisolini C, Ceci E, Sciorsci RL. Blood and milk oxidative status after administration of different antioxidants during early postpartum in dairy cows. Res Vet Sci. 2013;95:1171–1174. PubMed

Sordillo LM. Nutritional strategies to optimize dairy cattle immunity. J Dairy Sci. 2016;99:4967–4982. PubMed

Pontes GCS, Monteiro PLJ, Jr, Prata AB, Guardieiro MM, Pinto DAM, Fernandes GO, Wiltbank MC, Santos JEP, Sartori R. Effect of injectable vitamin E on incidence of retained fetal membranes and reproductive performance of dairy cows. J Dairy Sci. 2015;98:2437–2449. PubMed

Michal JJ, Heirman LR, Wong TS, Chew BP, Frigg M, Volker L. Modulatory effects of dietary β-carotene on blood mammary leukocyte function in periparturient dairy cows. J Dairy Sci. 1994;77:1408–1421. PubMed

Spears JW, Weiss WP. Role of antioxidant and trace elements in health and immunity of dairy cows. Vet J. 2008;176:70–76. PubMed

Kendall NR, Bone P. Fertility and trace elements - an understand problem. Cattle Pract. 2006;14:17–22.

Pilarczyk B, Jankowiak D, Tomza-Marciniak A, Pilarczyk R, Sablik P, Drozd R, Tylkowska A, Skolmowska M. Selenium concentration and glutathione peroxidase (GSH-Px) activity in serum of cows at different stages of lactation. Biol Trace Elem Res. 2012;147:91–96. PubMed

Pavlata L, Pechová A, Illek J. Direct and indirect assessment of selenium status in cattle –a comparison. Acta Vet. 2000;69:281–287.

O’Boyle N, Corl CM, Gandy JC, Sordillo LM. Relationship of body condition score and oxidant stress to tumor necrosis factor expression in dairy cattle. Vet Immunol Immunopathol. 2006;113:297–304. PubMed

Ghiselli A, Serafini M, Natella F, Scaccini C. Total antioxidant capacity as a tool to assess redox status: critical view and experimental data. Free Radic Biol Med. 2000;29:1106–1114. PubMed

Bionaz E, Trevisi E, Calamari L, Librandi F, Ferrari A, Bertoni G. Plasma paraoxonase, health, inflammatory conditions and liver function in transition dairy cows. J Dairy Sci. 2007;90:1740–1750. PubMed

Omur A, Kirbas A, Aksu E, Kandemir F, Dorman E, Kaynar O, Ucar O. Effects of antioxidant vitamins (a, D, E) and trace elements (cu, Mn, se, Zn) on some metabolic and reproductive profiles in dairy cows during transition period. Pol J Vet Sci. 2016;19:697–706. PubMed

LeBlanc SJ. Monitoring programs for transition dairy cows. In: Proceedings of the 26th World Buiatrics Congress, Nice. 2006. pp. 460–472.

Huzzey JM, Duffeild TF, LeBlanc SJ, Veira DM, Weary DM, von Keyserlingk MAG. Short communication: Haptoglobin as an early indicator of metritis. J Dairy Sci. 2009;92:621–625. PubMed

Herdt TH. Ruminant adaptation to negative energy balance. Influences on the etiology of ketosis and fatty liver. Vet Clin North Am Food Anim Pract. 2000;16:215–230. PubMed

Hammon DS, Evjen IM, Dhiman TR, Goff JP, Walters JL. Neutrophil function and energy status in Holstein dairy cows with uterine health disorders. Vet Immunol Immunopathol. 2006;113:21–26. PubMed

Ingvartsen KL, Moyes K. Nutrition, immune function and health of dairy cattle. Animal. 2013;7:112–122. PubMed

Martinez N, Sinedino LDP, Bisinotto RS, Ribeiro ES, Gomes GC, Lima FS, Greco LF, Risco CA, Galväo KN, Taylor-Rodriguez D, Driver JP, Thatcher WW, Santos JEP. Effect of induced subclinical hypocalcemia on physiological responses and neutrophil function in dairy cows. J Dairy Sci. 2014;97:874–887. PubMed

Park AF, Shirley JE, Titgemeyer EC, Meyer MJ, VanBaale MJ, VandeHaar MJ. Effect of protein concentration in prepartum diets on metabolism and performance of dairy cows. J Dairy Sci. 2002;85:1815–1828. PubMed

Moretti P, Probo M, Morandi N, Trevisi E, Ferrari A, Minuti A, Venturini M, Paltrinieri S, Giordano A. Early post-partum hematological changes in Holstein dairy cows with retained placenta. Anim Reprod Sci. 2015;152:17–25. PubMed

Wittrock JM, Proudfoot KL, Weary DM, von Keyserlingk MAG. Short communication: metritis affects milk production and cull rate of Holstein multiparous and primiparous dairy cows differently. J Dairy Sci. 2011;94:2408–2412. PubMed

Mordak R, Anthony SP. Periparturient stress and immune suppression as a potential cause of retained placenta in highly productive dairy cows: examples of prevention. Acta Vet Scand. 2015;57:84. PubMed PMC

Vries MJ, Veerkamp RF. Energy balance of dairy cattle in relation to milk production variables and fertility. J Dairy Sci. 2000;83:62–69. PubMed

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