Does Oxidative Stress Impact Bovine Reproductive Disorders?
DOI:
https://doi.org/10.48165/ijar.2021.42.2.1Keywords:
Oxidative stress, Bovine, Infertility, Pathogenesis, Reactive oxygen speciesAbstract
Oxidative stress indicates an imbalance between pro-oxidants and antioxidants mechanisms of the body. The elevated production of stress level affects physiological functions of female reproduction. Literatures pertaining to oxidative stress have become an active area of research investigation now a day in livestock species particularly in veterinary medicine in general and reproduction in particular. This is because of the increased incidence of infertility problems in livestock and perhaps will remain as emerging area of research in the coming decades. The oxidative stress is surmised to have role in pathophysiology of female infertility. From a clinical perspective, it is of utmost importance to have knowledge in respect to impact of oxidative stress in bovine infertility. This review focuses on the pathogenesis of various bovine reproductive disorders such as cystic condition, endometritis, retained fetal membrane, embryonic mortality and repeat breeding with respect to oxidative stress.
References
Agarwal, A., Aponte-Mellado, A., Premkumar, B.J., Shaman, A. and Gupta, S. (2012). The effects of oxidative stress on female reproduction: a review. Reprod. Biol. Endocrinol.,10: 1-31.
Agarwal, A., Gupta, S. and Sharma, R.K. (2005). Role of oxida tive stress in female reproduction: Review. Reprod. Biol. Endocrinol., 3: 1-21.
Ahmed, W.M., El-khadrawy, H.H., Hanafi, E.M., Ali, A.H. and Shalaby, S.A. (2010). Clinical Perspective of Repeat Breeding Syndrome in Buffaloes. J. Am. Sci., 6: 661- 666.
Allison, R.D. and Laven, R.A. (2000). Effect of vitamin E supple mentation on the health and fertility of dairy cows: a review. Vet. Rec., 147: 703-708.
Ansari-Lari, M., Mehdi, M. and Abbas, R. (2012). Causes of cull ing in dairy cows and its relation to age at culling and inter val from calving in Shiraz, Southern Iran. Vet. Res. Forum., 3: 233.
Aziz, E.S., Klesius, P.H. and Frandsen, J.C. (1984). Effect of sele nium on polymorphonuclear leukocyte function in goats. Am. J. Vet. Res., 45: 1715–1718.
Baruselli, P.S., Reis, E.L., Marques, M.O. Nasser, L.F. and Bó, G.A. (2004). The use of hormonal treatments to improve reproductive performance of anestrous beef cattle in tropi cal climates. Anim. Reprod. Sci., 82: 479-486.
Beg, M.A. and Ginther, O.J. (2006). Follicle selection in cattle and horses: role of intrafollicular factors. Reproduction, 132: 365-377.
Behrman, H.R. and Aten, R.F. (1991). Evidence that hydrogen peroxide blocks hormone-sensitive cholesterol transport into mitochondria of rat luteal cells. Endocrinology, 128: 2958-2966.
Birben, E., Sahiner, U.M., Sackesen, C., Erzurum, S. and Kalayci, O. (2012). Oxidative stress and antioxidant defense. World Allergy Organ. J., 5: 9-19.
Burton, G.J. and Jauniaux, E. (2011). Oxidative stress. Best Pract. Res. Clin. Obstet. Gynaecol., 25: 287-299.
Carlson, J.C., Sawada, M., Boone, D.L. and Stauffer, J.M. (1995). Stimulation of progesterone secretion in dispersed cells of rat corpora lutea by antioxidants. Steroids, 60: 272-276.
Ciani, F., Cocchia, N., d’Angelo, D. and Tafuri, S. (2015). Influence of ROS on ovarian functions. New Discov. Embryol., 3: 1-34.
Cooke, M.S., Evans, M.D., Dizdaroglu, M. and Lunec, J. (2003). Oxidative DNA damage: mechanisms, mutation, and dis ease. FASEB J., 17: 1195-1214.
Das, G.K. and Khan, F.A. 2010. Summer anoestrus in buffalo–a review. Reprod. Domest. Anim., 45: 483-494.
De Rensis, F. and Scaramuzzi, R.J. (2003). Heat stress and sea sonal effects on reproduction in the dairy cow—a review. Theriogenology, 60: 1139-1151.
Derar, D.R., Hasab-Enaby, H.S., Ali, H.H., Zain, A. and Shehata, S.H. (2011). Postpartum ovarian resumption in native dairy cows in upper Egypt and their relation to oxidant antioxi dant status. Endocrinol. Metab. Syndr., 4: 2-6.
Dunnam, R.C., Hill, M.J., Lawson, D.M. and Dunbar, J.C. (1999). Ovarian hormone secretory response to gonadotropins and nitric oxide following chronic nitric oxide deficiency in the rat. Biol. Reprod., 60: 959-963.
Elsayed, D.H., Abdelrazek, H.M., El Nabtiti, A.A., Mahmoud, Y.K. and Abd El-Hameed, N.E. (2019). Associations between metabolic profiles, post-partum delayed resump tion of ovarian function and reproductive performance in Egyptian buffalo: Roles of IGF-1 and antioxidants. Anim. Reprod. Sci., 208: 106-134.
Forman, H.J. and Torres, M. (2002). Reactive oxygen species and cell signaling: respiratory burst in macrophage signaling. Am. J. Respir. Crit. Care Med.,166: 4–8.
Fucci, L., Oliver, C.N., Coon, M.J. and Stadtman, E.R. (1983). Inactivation of key metabolic enzymes by mixed-func tion oxidation reactions: possible implication in pro tein turnover and ageing. Proc. Natl. Acad. Sci. USA, 80: 1521–1525.
Gilbert, R.O., Shin, S.T., Guard, C.L., Erb, H.N. and Frajblat, M. (2005). Prevalence of endometritis and its effects on repro ductive performance of dairy cows. Theriogenology, 64: 1879–1888.
Givens, M.D. (2006). A clinical, evidence-based approach to infectious causes of infertility in beef cattle. Theriogenology, 66: 648-654.
Gupta, S., Gupta, H.K. and Soni, J. (2005). Effect of Vitamin E and selenium supplementation on concentrations of plasma cortisol and erythrocyte lipid peroxides and the incidence of retained fetal membranes in crossbred dairy cattle. Theriogenology, 64: 1273–1286.
Hajhashemi, V., Vaseghi, G., Pourfarzam, M. and Abdollahi, A. (2010). Are antioxidants helpful for disease prevention? Res. Pharm. Sci., 5: 1.
Heidarpour, M., Mohri, M., Fallah-Rad, A.H., Shahreza, F.D. and Mohammadi, M. (2012). Oxidative stress and trace elements before and after treatment in dairy cows with clinical and subclinical endometritis. Revue Méd. Vét., 163: 628-633.
Imai, K., Khandoker, M.A.M.Y., Yonai, M., Takahashi, T., Sato, T., Ito, A., Hasegawa, Y. and Hashizume, K. (2003). Matrix metalloproteinases-2 and-9 activities in bovine follicular fluid of different-sized follicles: relationship to intra-fol
licular inhibin and steroid concentrations. Domest. Anim. Endocrinol., 24: 171-183.
Jan, M.H., Das, G., Singh, J., Khan, S., Kumar, P., Singh, G., Sarkar, M. and Pathak, M. (2015). Oxidative stress during cystic ovarian disease in water buffalo. Indian J. Anim. Sci., 85: 356-360.
Jan, M.H., Khan, F.A., Pande, M., Kumar, B., Das, G.K. and Sarkar, M. (2011). Follicular attributes and intra- follicular nitric oxide and ascorbic acid concentrations in cyclic and acyclic buffaloes during summer season. Therio. Insight, 2: 83- 88.
Kankofer, M., Albera, E., Feldman, M., Gundling, N. and Hoedemaker, M. (2010). Comparison of antioxidative/oxi dative profiles in blood plasma of cows with and without retained fetal placental membranes. Theriogenology, 74: 1385-1395.
Khan, F.A. and Das, G.K. (2011). Follicular fluid nitric oxide and ascorbic acid concentrations in relation to follicle size, functional status and stage of estrous cycle in buffalo. Anim. Reprod. Sci.,125: 62- 68.
Khan, F.A. and Das, G.K. (2012). Follicular characterisctics and intrafollicular concentrations of nitric oxide and ascorbic acid during ovarian acyclicity in water buffalo (Bubalasbubalis). Trop. Anim. Health Prod., 44: 125- 131.
Khan, F.A., Das, G.K., Pande, M., Pathak, M.K. and Sarkar, M. (2011). Biochemical and hormonal composition of follic ular cysts in water buffalo (Bubalus bubalis). Anim.Reprod. Sci., 124: 61-64.
Kimura, K., Goff, J.P., Kehrli Jr, M.E. and Reinhardt, T.A. (2002). Decreased neutrophil function as a cause of retained pla centa in dairy cattle. J. Dairy Sci., 85: 544-550.
Krishnan, B.B., Kumar, H., Mehrotra, S., Singh, S.K., Goswami, T.K. and Narayanan, K. (2014). Subclinical endometritis increases oxidative stress and modulates polymorhonu clear leukocyte functions in crossbred cows. Indian J. Anim. Reprod., 84: 1192- 1195.
Kumar, A., Mehrotra, S., Singh, G., Narayanan, K., Das, G.K., Soni, Y.K., Singh, M., Mahla, A.S., Srivastava, N. and Verma, M.R. (2015). Sustained delivery of exogenous melatonin influences biomarkers of oxidative stress and total antioxidant capacity in summer-stressed anestrous water buffalo (Bubalus bubalis). Theriogenology., 83: 1402-1407.
Kumawat, B.L. (2014). Studies on oxidative stress, ovarian func tion and estrus response in delayed pubertal heifers treated
with Aegle marmelos and Murrayakoenigii. M.V.Sc Thesis. Indian Veterinary Research Institute, Izatnagar, India. Lenaz, G. (2001). The mitochondrial production of reactive oxygen species: mechanisms and implications in human pathology. IUBMB Life., 52: 159-164.
Li, Y., Ding, H.Y., Wang, X.C., Feng, S.B., Li, X.B., Wang, Z., Liu, G.W. and Li, X.W. (2016). An association between the level of oxidative stress and the concentrations of NEFA and BHBA in the plasma of ketotic dairy cows. J. Anim. Physiol. Anim. Nutr.,100: 844-851.
Liou, G.Y. and Storz, P. (2010). Reactive oxygen species in cancer. Free Radic. Res.,44: 479-496.
Maji, A.K. and Samanta, A. (2013). Analysis of incidence of infertility in cattle of Howrah district in West Bengal, India. Explor. Anim. Med. Res., 3: 154-158.
Murdoch, W.J. and Gottsch, M.L. (2003). Proteolytic mech anisms in the ovulatory folliculo-luteal transformation. Connect. Tissue Res., 44: 50-57.
Pande, M., Das, G.K., Khan, F.A., Sarkar, M., Pathak, M.C., Prasad, J.K. and Kumar, H. (2013). Endometritis impairs luteal development, function, and nitric oxide and ascor bic acid concentrations in buffalo (Bubalus bubalis). Trop. Anim. Health Prod., 45: 805- 810.
Pedernera, M., Celi, P., García, S.C., Salvin, H.E., Barchia, I. and Fulkerson, W.J. (2010). Effect of diet, energy balance and milk production on oxidative stress in early-lactating dairy cows grazing pasture. Vet. J., 186: 352-357.
Plaizier, J.C.B., King, G.J., Dekkers, J.C.M. and Lissemore, K. (1998). Modelling the relationship between reproductive performance and net-revenue in dairy herds. Agric. Sys., 56: 305–322.
Prabaharan, V., Selvaraju, M., Napolean, R.E., Duraisamy, K.A. and Natarajan, A. (2014). Role of oxidative stress biomark ers on embryonic mortality in bovines. Inter. J. Vet. Sci., 4: 6-9.
Rautela, R., Das, G.K., Khan, F.A., Prasad, S., Kumar, A., Prasad, J.K., Ghosh, S.K., Dhanze, H., Katiyar, R. and Srivastava, S.K. (2018). Antibacterial, anti-inflammatory and antioxi dant effects of Aegle marmelos and Murrayakoenigii in dairy cows with endometritis. Livestock Sci., 214: 142-148.
Rizzo, A., Minoia, G., Trisolini, C., Mutinati, M., Spedicato, M., Jirillo, F. and Sciorsci, R.L. (2009). Reactive oxygen species (ROS): involvement in bovine follicular cysts etiopathogen esis. Immunopharmacol. Immunotoxicol., 31: 631-635.
Sharma, R.K. and Agarwal, A. (2004). Role of reactive oxygen spe cies in gynecologic diseases. Reprod. Med. Biol., 3: 177-199. Ster, C., Loiselle, M.C. and Lacasse, P. (2012). Effect of postcalving serum nonesterified fatty acids concentration on the func tionality of bovine immune cells. J. Dairy Sci., 95: 708-717.
Tripathi, A., Shrivastav, T.G. and Chaube, S.K. (2013). An increase of granulosa cell apoptosis mediates aqueous neem (Azadirachtaindica) leaf extract-induced oocyte apoptosis in rat. Int. J. Appl. Basic Med. Res., 3: 27–36.
Veerkamp, R.F., Beerda, B. and Van der Lende, T. (2003). Effects of genetic selection for milk yield on energy balance, levels of hormones, and metabolites in lactating cattle, and possible links to reduced fertility. Livestock Prod. Sci., 83: 257-275.
Vega, M., Carrasco, I., Castillo, T., Troncoso, J.L., Videla, L.A. and Devoto, L. (1995). Functional luteolysis in response to hydrogen peroxide in human luteal cells. J. Endocrinol., 147: 177-182.
Walsh, S.W., Williams, E.J. and Evans, A.C.O. (2011). A review of the causes of poor fertility in high milk producing dairy cows. Anim. Reprod. Sci., 123: 127-138.
Downloads
Published
Issue
Section
How to Cite
