Effect of clinical endometritis on physiological, hematological, biochemical and endocrinological profiles in crossbred cows under tropical island ecosystem
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Keywords:
Andaman and Nicobar islands, Antioxidants, Blood, Crossbred cows, Endometritis, Hormone, Island ecosystem, Physiological profilesAbstract
The present study was carried out to assess the effect of endometritis on hematological, physiological, antioxidant, oxidative and endocrinological profiles in crossbred cows under tropical island ecosystem of Andaman and Nicobar Islands. Each 12 number of cows affected with clinical endometritis was selected as group 2 and without endometritis as group 1. These cows were in same parity in same locality with similar type management. Physiological profiles, hematological profiles, antioxidant profiles and hormone profiles were estimated. The result revealed that the crossbred cows with endometritis were suffering severe anaemia. The endometritis affected animals were shown significantly low level of antioxidant profiles and higher MDA level than the unaffected animal groups. Similarly endocrinological profiles revealed that the endometritis affected animals have significantly higher level of CORT and lower level of E2, P4, FSH, LH and T4 than the unaffected crossbred cows. It was concluded that the endometritis was due to anaemia, lack of antioxidants, over production of free radicals and disturbances of endocrinological profiles in crossbred cows of Andaman and Nicobar Islands.Downloads
References
Ahmed W M, Shalaby S I A and Zaabal M M. 2010. Some biochemical constituents of preovulatory and cystic ovarian follicular fluids in buffalo-cows with emphasis on protein polymorphism. International Journal of Animal Science 13: 53–57.
Azawi O I. 2008. Review: Postpartum uterine infection in cattle. Animal Reproduction Science 105: 187–208. DOI: https://doi.org/10.1016/j.anireprosci.2008.01.010
Behiman H I, Kodman P H, Preston S L and Gao S. 2001. Oxidative stress and the ovary. Journal of Society for Gynaecological Investigations 8: 540–42. DOI: https://doi.org/10.1177/1071557601008001S13
Binsila B K. 2011. ‘Effect of immunomodulators on the recovery of subclinical endometritis in crossbred cows’. MVSc. Thesis, submitted to IVRI, Izatnagar, Bareilly.
Chenault J R, Mc Allister J F, Chester S T, Dame K J, Kausche F M and Robb E J. 2004. Efficacy of ceftiofur hydrochloride sterile suspension administered parenterally for the treatment of acute postpartum metritis in dairy cows. Journal of the American Veterinary Medical Association 224: 1634–39. DOI: https://doi.org/10.2460/javma.2004.224.1634
Cheong S H, Sa Filho O G, Absalon-Medina V A, Pelton S H, Butler W R and Gilbert R O. 2016. Metabolic and endocrine differences between dairy cows that do or do not ovulate first postpartum dominant follicles. Biology of Reproduction 94(18): 1–11. DOI: https://doi.org/10.1095/biolreprod.114.127076
Gautam G, Nakao T, Yusuf M and Koike K. 2009. Prevalence of endometritis during the postpartum period and its impact on subsequent reproductive performance in two Japanese dairy herds. Animal Reproduction Science 116(3): 175–87. DOI: https://doi.org/10.1016/j.anireprosci.2009.02.001
Hazeldine J, Arlt W and Lord J M. 2010. Dehydroepiandrosterone as a regulator of immune cell function. Journal of Steroid Biochemistry 120: 127–36. DOI: https://doi.org/10.1016/j.jsbmb.2009.12.016
Herath S, Lilly S T, Fischer D P, Williams E J, Dobson H, Bryant C E and Sheldon I M. 2009. Bacterial lipopolysacharide induces an endocrine switch from prostaglandin F2 alpha to prostaglandin E2 in bovine endometrium. Endocrinology 150: 1912–20. DOI: https://doi.org/10.1210/en.2008-1379
Islam R. 2012. ‘Studies on immune-endocrine profile of peripartum cows in relation to post-partum reproductive health’. PhD Thesis, submitted to IVRI, Izatnagar, Bareilly, UP, India.
Karsch F J, Battaglia D F, Breen K M, Debus N and Harris T G. 2002. Mechanisms for ovarian cycle disruption by immune/ inflammatory stress. Stress 5: 101–12. DOI: https://doi.org/10.1080/10253890290027868
Kim I H, Na K J and Yang M P. 2005. Immune responses during the peripartum period in dairy cows with postpartum endometritis. Journal of Reproduction and Development 51(6): 757–64. DOI: https://doi.org/10.1262/jrd.17036
Lee E K and Kehrli M. 1998. Expression of adhesion molecules on neutrophils of Periparturient cows and neonatal calves. American Journal of Veterinary Research 59: 37–43.
Macfarlane M S, Breen K M, Sakurai H, Adams B M and Adams T E. 2000. Effect of duration of infusion of stress-like concentrations of cortisol on follicular development and the preovulatory surge of LH in sheep. Animal Reproduction Science 63(3–4): 167–75. DOI: https://doi.org/10.1016/S0378-4320(00)00179-2
Madebo T, Lindtjorn B, Aukrust P and Berge R K. 2003. Circulating antioxidants and lipid peroxidation products in untreated tuberculosis patients in Ethiopia. American Journal of Clinical Nutrition 78: 117–22. DOI: https://doi.org/10.1093/ajcn/78.1.117
Noakes D E, Parkinson T J and England G C W. 2001. Arthur´s Veterinary Reproduction and Obstetrics. 8th ed. W.B. Saunders, London.
Peter A T, Bosu W T K and DeDecker R J. 1989. Suppression of preovulatory luteinizing hormone surges in heifers after intrauterine infusions of Escherichia coli endotoxin. American Journal of Veterinary Research 50: 368–73.
Senosy W S, Izaike Y and Osawa T. 2011. Influences of metabolic traits on sub-clinical endometritis at different intervals postpartum in high milking cows. Reproduction in Domestic Animals 47(4): 666–74. DOI: https://doi.org/10.1111/j.1439-0531.2011.01941.x
Sharma A, Singh M, Kumar P, Sharma A, Neelam Aaqib, Majid Jan and Sharma P. 2017. Postpartum uterine infections in cows and factors affecting it. International Journal of Current Microbiology and Applied Science 6(9): 1020–28. DOI: https://doi.org/10.20546/ijcmas.2017.609.123
Sheldon I M, Noakes D E, Rycroft A N, Pfeiffer D U and Dobson H. 2002. Influence of uterine bacterial contamination after parturition on ovarian dominant follicle selection and follicle growth and function in cattle. Reproduction 123: 837–45. DOI: https://doi.org/10.1530/rep.0.1230837
Sordillo L M. 2016. Nutritional strategies to optimize dairy cattle immunity. Journal of Dairy Science 99(6): 4967–82. DOI: https://doi.org/10.3168/jds.2015-10354
Williams C Y, Harris T G, Battaglia D F, Viguie C and Karsch F J. 2001. Endotoxin inhibits pituitary responsiveness to gonadotropin-releasing hormone. Endocrinology 142: 1915– 22. DOI: https://doi.org/10.1210/endo.142.5.8120
Williams E J, Fischer D P, Noakes D E, England G C, Rycroft A, Dobson H and Sheldon I M. 2007. The relationship between uterine pathogen growth density and ovarian function in the postpartum dairy cow. Theriogenology 68: 549–59 DOI: https://doi.org/10.1016/j.theriogenology.2007.04.056
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