Veterinary World

     Open access and peer reviewed journal  

ISSN (Online): 2231-0916

 

Home l Editorial board l Instructions for authors l Reviewer guideline l Open access policy l Archives l FAQ


Open Access


Research (Published online: 08-10-2016)

4. Determination of ceruloplasmin, some other acute phase proteins, and biochemical parameters in cows with endometritis - S. Kaya, O. Merhan, C. Kacar, A. Colak and K. Bozukluhan

Veterinary World, 9(10): 1056-1062

 

 

   doi: 10.14202/vetworld.2016.1056-1062

 

 

S. Kaya: Department of Obstetrics and Gynecology, Faculty of Veterinary Medicine, University of Kafkas, Kars, Turkey; semra-kafkas@hotmail.com

O. Merhan: Department of Biochemistry, Faculty of Veterinary Medicine, University of Kafkas, Kars, Turkey; oguzmerhan@hotmail.com

C. Kacar: Department of Obstetrics and Gynecology, Faculty of Veterinary Medicine, University of Kafkas, Kars, Turkey; cihan3000@hotmail.com

A. Colak: Department of Obstetrics and Gynecology, Faculty of Veterinary Medicine, University of Ataturk, Erzurum, Turkey; fgacolak@hotmail.com

K. Bozukluhan: Department of Veterinary Health, Kars School of Higher Vocational Education, University of Kafkas, Kars, Turkey; kbozukluhan@hotmail.com

 

Received: 26-05-2016, Accepted: 22-08-2016, Published online: 08-10-2016

 

Corresponding author: S. Kaya, e-mail: semra-kafkas@hotmail.com


Citation: Kaya S, Merhan O, Kacar C, Colak A, Bozukluhan K (2016) Determination of ceruloplasmin, some other acute phase proteins, and biochemical parameters in cows with endometritis, Veterinary World, 9(10): 1056-1062.



Aim: The aim of this study is to determine serum ceruloplasmin levels in cows with endometritis of varying degrees of severity and to establish whether or not there is a correlation between acute phase protein (APP) levels and biochemical parameters.

Material and Methods: The study was conducted with 100 Brown Swiss cows (3-8 years of age) on days 28-32 postpartum. Cows were divided into endometritis (mild, moderate, and severe endometriosis) and healthy groups based on ultrasonography, vaginoscopy, and cytological examination. Blood samples were collected from all cows. Levels of haptoglobin (Hp), serum amyloid A (SAA), ceruloplasmin, albumin, and some biochemical parameters were analyzed.

Results: Hp, SAA, and ceruloplasmin levels were higher in cows with endometritis than in healthy cows (p=0.001), and the levels of these APPs increased as endometritis became more severe (p=0.001). Some significant correlations were found between APPs and the biochemical parameters that were analyzed. In conclusion, it was determined that ceruloplasmin levels increase significantly in the presence of endometritis and proportionate to the severity of endometritis. A significant correlation was found between ceruloplasmin levels and Hp and SAA levels.

Conclusion: It was concluded that ceruloplasmin levels can be used in the diagnosis of endometritis as an alternative to Hp and SAA levels.

Keywords: albumin, ceruloplasmin, cow, endometritis, haptoglobin, serum amyloid A.



1. Cray, C., Zaias, J. and Altman, N.H. (2009) Acute phase response in animals: A review. Comp. Med., 59: 517-526.
PMid:20034426 PMCid:PMC2798837
 
2. Biswal, S.S., Das, S., Balasubramanian, S., Mohanty, D.N., Sethy, K. and Dasgupta, M. (2014) Serum amyloid A and haptoglobin levels in crossbred cows with endometritis following different therapy. Vet. World, 7: 1066-1070.
http://dx.doi.org/10.14202/vetworld.2014.1066-1070
 
3. Tothova, C., Nagy, O. and Kovac, G. (2011) Acute phase proteins and their use in the diagnosis of diseases in ruminants: A review. Vet. Med. Czech., 59: 163-180.
 
4. Thomas, F.C., Waterston, M., Hastie, P., Parkin, T., Haining, H. and Eckersall, P.D. (2015) The major acute phase proteins of bovine milk in a commercial dairy herd. BMC Vet. Res., 11: 207.
http://dx.doi.org/10.1186/s12917-015-0533-3
PMid:26276568 PMCid:PMC4536752
 
5. Brodzki, P., Kostro, K., Brodzki, A., Wawron, W., Marczuk, J. and Kurek, Ł. (2015) Inflammatory cytokines and acute-phase proteins concentrations in the peripheral blood and uterus of cows that developed endometritis during early postpartum. Theriogenology, 84: 11-18.
http://dx.doi.org/10.1016/j.theriogenology.2015.02.006
PMid:25765299
 
6. Chan, J.P.W., Chu, C.C., Fung, H.P., Chuang, S.T., Lin, Y.C., Chu, R.M. and Lee, S.L. (2004) Serum haptoglobin concentration in cattle. J. Vet. Med. Sci., 66: 43-46.
http://dx.doi.org/10.1292/jvms.66.43
PMid:14960809
 
7. Green, M.P., Ledgard, A.M., Berg, M.C., Peterson, A.J. and Back, P.J. (2009) Prevalence and identification of systemic markers of sub-clinical endometritis in postpartum dairy cows. Proc. N. Z. Soc. Anim., 69: 37-42.
 
8. Humblet, M.F., Guyot, H., Boudry, B., Mbayahi, F., Hanzen, C., Rollin, F. and Godeau, J.M. (2006) Relationship between haptoglobin, serum amyloid A, and clinical status in a survey of dairy herds during a 6-month period. Vet. Clin. Pathol., 35: 188-193.
http://dx.doi.org/10.1111/j.1939-165X.2006.tb00112.x
PMid:16783711
 
9. Floris, G., Medda, R., Padiglia, A. and Musci, G. (2000) The physiopathological significance of ceruloplasmin. Biochem. Pharmacol., 60: 1735-1741.
http://dx.doi.org/10.1016/S0006-2952(00)00399-3
 
10. Lóvstad, R.A. (2006) A kinetic study on the phenothiazine dependent oxidation of NADH by bovine ceruloplasmin. BioMetals, 19: 1-5.
http://dx.doi.org/10.1007/s10534-005-2627-z
PMid:16502325
 
11. Cerone, S.I., Sansinanea, A.S., Streitenberger, S.A., Garcia, M.C. and Auza, N.J. (2000) Cytochrome c oxidase, Cu, Zn-superoxide dismutase, and ceruloplasmin activities in Copper-deficient bovines. Biol. Trace. Elem. Res., 73: 269-278.
http://dx.doi.org/10.1385/BTER:73:3:269
 
12. Banuvalli, N., Bhaskaran, R., Krishnamurthy, U., Gruraj, P.M., Kumar, K.P.H. and Rames, H.S. (2014) Effect of body condition score at parturition on post-partum productive and reproductive performance in crossbred dairy cows. Int. J. Livest. Res., 4: 5-13.
 
13. Weber, C., Hametner, C., Tucscherer, A., Losand, B., Kanitz, E., Otten, W., Singh, S.P., Bruckmaier, R.M., Becker, F., Kanitz, W. and Hammon, H.M. (2013) Variation in fat mobilization during early lactation differently affects feed intake, body condition, and lipid and glucose methabolism in high-yielding dairy cows. J. Dairy Sci., 96: 165-180.
http://dx.doi.org/10.3168/jds.2012-5574
PMid:23127904
 
14. Gong, J.G., Lee, W.J., Garnworthy, P.C. and Webb, R. (2002) Effect of dietary-induced increases in circulating insulin concentrations during the early postpartum period on reproductive function in dairy cows. Reproduction, 123: 419-427.
http://dx.doi.org/10.1530/rep.0.1230419
PMid:11882019
 
15. Liu, P., He, B.X., Yang, X.L., Hou, X.L., Zhao, H.Y., Han, Y.H., Nie, P., Deng, H.F. and Cheng, L. (2012) Activities of aspartate aminotransferase, alanine aminotransferase, gamma-glutamyl transferase, alkaline phosphatase in plasma of postpartum Holstein cows. J. Anim. Vet. Adv., 11: 1270-1274.
http://dx.doi.org/10.3923/javaa.2012.1270.1274
 
16. Đoković, R., Šamanc, H., Petrović, M.D., Ilić, Z. and Kurćibić, Z. (2012) Relationship among blood metabolites and lipid content in the liver in transitional dairy cows. Biotechnol. Anim. Husb., 28: 705-714.
http://dx.doi.org/10.2298/BAH1204705D
 
17. Burke, C.R., Meier, S., Mcdougall, S., Compton, C., Mitchell, M. and Roche, J.R. (2010) Relationships between endometritis and metabolic state during the transition period in pasture-grazed dairy cows. J. Dairy Sci., 93: 5363-5373.
http://dx.doi.org/10.3168/jds.2010-3356
PMid:20965352
 
18. Williams, E.J., Fischer, D.P., Pfeiffer, D.U., England, G.C.W., Noakes, D.E., Dobson, H. and Sheldon, I.M. (2005) Clinical evaluation of postpartum vaginal mucus reflects uterine bacterial infection and the immune response in cattle. Theriogenology, 63: 102-117.
http://dx.doi.org/10.1016/j.theriogenology.2004.03.017
PMid:15589277
 
19. Kasimanickam, R., Duffield, T.F., Foster, R.A., Gartley, C.J., Leslie, K.E., Walton, J.S. and Johnson, W.H. (2004) Endometrial cytology and ultrasonography for the detection of subclinical endometritis in postpartum dairy cows. Theriogenology, 62: 9-23.
http://dx.doi.org/10.1016/j.theriogenology.2003.03.001
PMid:15159097
 
20. Mari, G., Iacono, E., Toni, F., Predieri, P.G. and Merlo, B. (2012) Evaluation of the effectiveness of intrauterine treatment with formosulphathiazole of clinical endometritis in postpartum dairy cows. Theriogenology, 78: 189-200.
http://dx.doi.org/10.1016/j.theriogenology.2012.01.036
PMid:22464185
 
21. Edmonson, A.J., Lean, I.J., Weaver, L.D., Farver, T. and Webster, G. (1989) A body condition score chart for Holstein dairy cows. J. Dairy Sci., 72: 68-78.
http://dx.doi.org/10.3168/jds.S0022-0302(89)79081-0
 
22. Skinner, J.G., Brown, R.A. and Roberts, L. (1991) Bovine haptoglobin response in clinically defined field conditions. Vet. Rec., 128: 147-149.
http://dx.doi.org/10.1136/vr.128.7.147
PMid:1903006
 
23. Colombo, J.P. and Richterich, R. (1964) On the determination of ceruloplasmin in plasma. Schweiz. Med. Wochenschr., 94: 715-720.
PMid:14242015
 
24. Gardner, I.A. and Greiner, M. (2006) Receiver-operating characteristic curves and likelihood ratios: Improvements over traditional methods for evaluation and application of veterinary clinical pathology tests. Vet. Clin. Pathol., 35: 8-17.
http://dx.doi.org/10.1111/j.1939-165x.2006.tb00082.x
 
25. Biswal, S.S.H., Das, S. and Mohanty, D.N. (2013) Immunomodulatory effect of oyster glycogen on endometritic crossbred cows. Indian J. Anim. Reprod., 34: 21-24.
 
26. Chan, J.P.W., Chang, C.C., Hsu, W.L., Liu, W.B. and Chen, T.H. (2010) Association of increased serum acute-phase protein concentrations with reproductive performance in dairy cows with postpartum metritis. Vet. Clin. Pathol., 39: 72-78.
http://dx.doi.org/10.1111/j.1939-165X.2009.00182.x
PMid:19747184
 
27. Dubuc, J., Duffield, T.F., Leslie, K.E., Walton, J.S. and Leblanc, S.J. (2010) Risk factors for postpartum uterine diseases in dairy cows. J. Dairy Sci., 93: 5764-5771.
http://dx.doi.org/10.3168/jds.2010-3429
PMid:21094748
 
28. Alberghina, D., Piccione, G., Casella, S., Panzera, M., Morgante, M. and Gianesella, M. (2013) The effect of the season on some blood metabolites and haptoglobin in dairy cows during postpartum period. Arch. Tierzucht., 56: 354-359.
 
29. Khoshvaghti, A., Nazifi, S., Vafafar, A. and Gheisari, H.R. (2009) Evaluation of serum and milk haptoglobin in some inflammatory diseases of cattle. Int. J. Vet. Res., 3: 31-36.
 
30. Hassanpour, A., Gholipour, M. and Rezaie, A. (2011) The effect of using monensin on haptoglobin serum level in dairy cattle. J. Anim. Vet. Adv., 10: 1364-1367.
http://dx.doi.org/10.3923/javaa.2011.1364.1367
 
31. Jeremejeva, J., Orro, T. and Kask, K. (2015) Relationship between acute phase proteins and subsequent fertility of dairy cows after postpartum uterine inflammation and healthy cows. Vet. Med. Zoot., 70: 37-41.
 
32. Musal, B., Seyrek, K. and Ulutaş, P.A. (2004) Serum sialic acid, total protein and albumin levels in cows with metritis treated with intrauterine oxytetracycline. Uludağ Univ. J. Fac. Vet. Med., 23: 71-75.
 
33. Tóthová, C.S., Nagy, O., Seidel, H., Konvićná, J., Farkašová, Z. and Kovác, G. (2008) Acute phase proteins and variables of protein metabolism in dairy cows during the pre - and postpartal period. Acta Vet. Brno., 77: 51-57.
http://dx.doi.org/10.2754/avb200877010051
 
34. Chassagne, M., Barnouin, J. and Chacornac, J.P. (1998) Biological predictors for early clinical mastitis occurrence in Holstein cows under field conditions in France. Prev. Vet. Med., 35: 29-38.
http://dx.doi.org/10.1016/S0167-5877(97)00092-5
 
35. Szczubiał, M., Dąbrowski, R., Kankofer, M., Bonchniarz, M. and Komar, M. (2012) Concentration of serum amyloid A and ceruloplasmin activity in milk from cows with subclinical mastitis caused by different pathogens. Pol. J. Vet. Sci., 15: 291-296.
http://dx.doi.org/10.2478/v10181-011-0149-x
PMid:22844707
 
36. Hussein, H.A. and Staufenbiel, R. (2012) Variations in copper concentration and ceruloplasmin activity of dairy cows in relation to lactation stages with regard to ceruloplasmin to copper ratios. Biol. Trace Elem. Res., 146: 47-52.
http://dx.doi.org/10.1007/s12011-011-9226-3
PMid:22006222
 
37. Kankofer, M., Albera, E., Feldman, M., Gundling, N. and Hoedemaker, M. (2010) Comparison of antioxidative/oxidative profiles in blood plasma of cows with and without retained fetal placental membranes. Theriogenology, 74: 1385-1395.
http://dx.doi.org/10.1016/j.theriogenology.2010.06.009
PMid:20663543
 
38. Lamand, M. and Levieux, D. (1981) Effects of infection on plasma levels of copper and zinc in ewes. Ann. Rech. Vét., 12: 133-136.
PMid:7200753
 
39. Talukder, S., Kerrisk, K.L., Gabai, G., Fukutomi, A. and Celi, P. (2015) Changes in milk oxidative stress biomarkers in lactating dairy cows with ovulatory and an-ovulatory oestrous cycles. Anim. Reprod. Sci., 158: 86-95.
http://dx.doi.org/10.1016/j.anireprosci.2015.05.004
PMid:26006094
 
40. Ahmad, I., Lodhi, L.A., Qureshi, Z.I. and Younis, M. (2004) Studies on blood glucose, total proteins, urea and cholesterol levels in cyclic, non-cyclic and endometritic crossbred cows. Pak. Vet. J., 24: 92-94.
 
41. Kaufmann, T.B., Drillich, M., Tenhagen, B.A. and Heuwieser, W. (2010) Correlations between periparturient serum concentrations of non-esterified fatty acids, betahydroxybutyric acid, bilirubin, and urea and the occurrence of clinical and subclinical postpartum bovine endometritis. BMC. Vet. Res., 6: 1-6.
http://dx.doi.org/10.1186/1746-6148-6-47
PMid:20979598 PMCid:PMC2988005
 
42. Heidarpour, M., Mohri, M., Fallah-Rad, A.H., Shahreza, F.D. and Mohammadi, M. (2012) Acute phase protein concentration and metabolic status affect the outcome of treatment in cows with clinical and subclinical endometritis. Vet. Rec., 171: 219.
http://dx.doi.org/10.1136/vr.100947
PMid:22865113