Research Article
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Year 2020, Volume: 4 Issue: 1, 1 - 8, 10.03.2020

Abstract

References

  • Abdelfatah-Hassan, A., Almería, S., Serrano, B., de Sousa, N.M., Beckers, J.F., López-Gatius, F., The inseminating bull and plasma pregnancy-associated glycoprotein (PAG) levels were related to peripheral leukocyte counts during the late pregnancy/early postpartum period in high-producing dairy cows. Theriogenology 2012; 77(7): 1390–7. Agarwal, A., Allamaneni, S.S.R., Role of free radicals in female reproductive diseases and assisted reproduction. Reprod Biomed Online 2004; 9: 338–347. Al-Gubory, KH., Fowler, P.A., Garrel, C., The roles of cellular reactive oxygen species, oxidative stress and antioxidants in pregnancy outcomes. Int J Biochem Cell Biol 2010; 42(10): 1634-1650.Anastasakis, E., Papantoniou, N., Daskalakis, G., Mesogitis, S., Antsaklis, A., Screening for pre-eclampsia by oxidative stress markers and uteroplacental blood flow. J. Obstet. Gynaecol., 2008. 28 (3), 285-289. Aurousseau, B., Durand, D., Gruffat, D., Contrôle des phéenoménes oxydatifs pendant la gestation chez les monogastriques et les ruminants. INRA Prod. Anim., 2004.17, 339–354. Ayad, A., Delahaut, P., Yahi, K., Iguer-Ouada, M., Benbarek, H., Validation of a new Elisa for measuring bovine pregnancy-associated glycoproteins in plasma and its application for early pregnancy diagnosis. Reprod. Dom. Anim., 2014.49, 55-56.Ayad, A., Sousa, N.M., Sulon, J., Hornick, J.L., Iguer-Ouada, M., Beckers, J.F., Correlation of five radioimmunoassay systems for measurement of bovine plasma pregnancy-associated glycoprotein concentrations at early pregnancy period. Res. Vet. Sci., 2009. 86(3), 377-382. Ayad, A., Sousa, N.M., Sulon, J., Hornick, J.L., Touati, K., Iguer-Ouada, M., Beckers, J.F., Endocrinologie de la gestation chez la vache: Signaux embryonnaires, hormones et protéines placentaires. Ann. Méd. Vét., 2006.150(4),212-226.Ayad, A., Sousa, N. M., Sulon, J., Iguer-Ouada, M., Beckers, J.F., 2007. Comparison of five radioimmunoassay systems for PAG measurement: ability to detect early pregnancy in cows. Reprod. Dom. Anim., 42, 433-440. Bomba-Opon, D., Samaha, R B.B., Kosinski, P., Kozlowski, S., Wegrzyn, P., Borowski, D., Bartoszewicz, Z., Bednarczuk, T., Wielgos, M., 2014. First trimester maternal serum vitamin d and markers of preeclampsia. J. Matern Fetal Neonatal. Med., 27(10), 1078-9. Breukelman, S.P., Perényi, Z., Taverne, M.A.M., Jonker, H., Van der Weijden, G.C., Vos, P.L.A.M., De Ruigh, L., Dieleman, S.J., Beckers, J.F., Szenci, O., 2012. Characterization of pregnancy losses after embryo transfer by measuring plasma progesterone and bovine pregnancy-associated glycoprotein-1 concentrations. Vet. J., 194, 71–76. Castillo, C., Hernandez, J., Bravo, A., Lopez Alonso, M., Pereira, V., Benedito, J.L., 2005. Oxidative status during late pregnancy and early lactation in dairy cows. Vet. J., 169, 286–292.Celi, P., Merlo, M., Barbato, O., Gabai, G., 2012. Relationship between oxidative stress and the success of artificial insemination in dairy cows in a pasture-based system. Vet. J., 193(2), 498–502.Chavatte-Palmer, P., Tarrade, A., 2016. Placentation in different mammalian species. Ann. Endocrinol., 77, 67–74.Codoñer-Franch, P., Valls-Bellés, V., Arilla-Codoñer, A., Alonso-Iglesias, E., 2011. Oxidant mechanisms in childhood obesity: the link between inflammation and oxidative stress. Transl. Res., 158(6), 369-84. Constant, F., Camous, S., Chavatte-Palmer, P., Heyman, Y., De Sousa, N., Richard, C., Beckers, J.F., Guillomot, M., 2011. Altered secretion of pregnancy-associated glycoproteins during gestation in bovine somatic clones. Theriogenology, 76, 1006–1021. Dosogne, H., Burvenich, C., Freeman, A.E., Kehrli, M.E.Jr., Detilleux, J.C., Sulon, J., Beckers, J.F., Hoeben, D., 1999. Pregnancy-associated glycoprotein and decreased polymorphonuclear leukocyte function in early post-partum dairy cows. Vet. Immunol. Immunopathol., 67(1), 47–54. Dosogne, H., Massart-Leen, A.M., Bervenich, C., 2000. Immunological aspects of pregnancy associated glycoproteins. Adv. Exp. Cell Biol., 480, 295−305. Fainaru, O., Almog, B., Pinchuk, I., Kupferminc, M.J., Lichtenberg, D., Many, A., 2002. Active labour is associated with increased oxidisibility of serum lipids ex vivo. B.J.O.G., 109 (9), 938-941.Friedrich, M., Holtz, W., 2010. Establishment of an ELISA for measuring bovine pregnancy associated glycoprotein in serum or milk and its application for early pregnancy detection. Reprod. Dom. Anim., 45, 142–146. Gajewski, Z., Petrajtis-Golobow, M., De Sousa, N.M., Beckers, J.F., Pawlinski, B., Wehrend, A., 2014. Comparison of accuracy of pregnancy-associated glycoprotein (PAG) concentration in blood and milk for early pregnancy diagnosis in cows. Schweiz. Arch. Tierh., 156, 585-590. García-Ispierto, I., Rosselló-Visa, M.A., Serrano-Pérez, B., Mur-Novales, R., De Sousa, N.M.,, Beckers, J.F., López-Gatius, F., 2015. Plasma concentrations of pregnancy-associated glycoproteins I and II and progesterone on day 28 post-AI as markers of twin pregnancy in dairy cattle. Livestock Sciences,192, 44–47. Garrel, C., Fowler, P.A., Al-Gubory, K.H., 2010. Developmental changes in antioxidant enzymatic defences against oxidative stress in sheep placentomes. J. Endocrinol., 205, 107–116. Gilbert, R.O., 2011.The effects of endometritis on the establishment of pregnancy in cattle. Reprod. Fertil. Dev., 24, 252–257. Green, J.A., Parks, T.E., Avalle, M.P., Telugu, B.P., McLain, A.L., Peterson, A.J., McMillan, W., Mathialagan, N., Hook, R.R., Xie, S., Roberts, R.M., 2005. The establishment of an ELISA for the detection of pregnancy-associated glycoproteins (PAGs) in the serum of pregnant cows and heifers. Theriogenology, 63, 1481–1503. Green, L.E., Huxley, J.N., Banks, C., Green, M.J., 2014. Temporal associations between low body condition, lameness and milk yield in a UK dairy herd. Prev. Vet.y Med., 113 (1), 63-71. Gupta, S., Agarwal, A., Banerjee, J., Alvarez, J.G., 2007. The role of oxidative stress in spontaneous abortion and recurrent pregnancy loss: A systematic review. Obstet. Gynecol. Sur., 62, 335-347. Hoeben, D., Monfardini, E., Opsomer, G., Burvenich, C., Dosogne, H., De Kruif, A., Beckers, J.F., 2000. Chemiluminescence of bovine polymorphonuclear leucocytes during the periparturient period and relation with metabolic markers and bovine pregnancy-associated glycoprotein. J. Dairy Res., 67, 249–59. Jauniaux, E., Gulbis, B., Burton, G.J., 2003. The human first trimester gestational sac limits rather than facilities oxygen transfer to the foetus: a review. Placenta, 24, S86–S93. Karen, A., Bajcsy, Á. C., Minoia, R., Kovács, R., De Sousa, N.M., Beckers, J.F., Tibold, J.,Mádl, I.,Szenci, O., 2014. Relationship of progesterone, bovine pregnancy-associated glycoprotein-1 and nitric oxide with late embryonic and early fetal mortalities in dairy cows. J. Reprod. Dev., 60 (2), 162-167. Kindahl, H., Kornmatitsuk, B., Gustafsson, H., 2004. The cow in endocrine focus before and after calving. Reprod. Dom. Anim., 39, 217–221. Ledezma-Torres, R.A., Beckers, J.F., Holtz, W., 2006. Assessment of plasma profile of pregnancy-associated glycoprotein (PAG) in sheep with a heterologous (anti-caPAG55+59) RIA and its potential for diagnosing pregnancy. Theriogenology, 66 (4), 906-912. Liu, A.X., Jin, F., Zhang, W.W., Zhou, T.H., Zhou, C.Y., Yao, W.M., Qian, Y.L., Huang, H.F., 2006. Proteomic analysis on the alteration of protein expression in the placental villous tissue of early pregnancy loss. Biol. Reprod., 75, 414–420. Lobago, F., Bekana, M., Gustafsson, H., Beckers, J.F., Yohannes, G., Aster, Y., Kindahl, H., 2009. Serum profiles of pregnancy‐associated glycoprotein, oestrone sulphate and progesterone during gestation and some factors influencing the profiles in Ethiopian Borana and crossbred cattle. Reprod. Dom. Anim., 44 (4), 685-692. Lopez-Gatius, F., Garbayo, J.M., Santolaria, P., Yaniz, J., Ayad, A., De Sousa, N.M., Beckers, J.F., 2007. Milk production correlates negatively with plasma levels of pregnancy-associated glycoprotein (PAG) to plasma pregnancy-associated glycoprotein (PAG) during the early fetal period in high producing dairy cows with live fetuses. Dom. Anim. Endocrinol., 32 (1), 29-42. Mocatta, T.J., Winterbourn, C.C., Inder, T.E., Darlow, B.A., 2004. The effect of gestational age and labour on markers of lipid and protein oxidation in cord plasma. Free Radical Res., 38, 185–191. Mohanty, S., Sahu, P.K., Mandal, M.K., Mohapatra, P.C., Panda, A., 2006. Evaluation of oxidative stress in pregnancy induced hypertension. Indian J. Clin. Biochem., 21 (1), 101-105. Nathan, C., Cunningham-Bussel, A., 2013. Beyond oxidative stress: an immunologist's guide to reactive oxygen species. Nat. Rev. Immunol., 13(5), 349. Nemmar, A., Raza, H., Yuvaraju, P., Beegam, S., John, A., Yasin, J., Hameed, R.S., Adeghate, E., Ali, B.H., 2013. Nose-only water-pipe smoking effects on airway resistance, inflammation, and oxidative stress in mice. J. Appl. Physiol., 115(9), 1316-1323. Ness, R.B., 2004. The consequences for human reproduction of a robust inflammatory response. Q. Rev. Biol., 79(4), 383–393. Piechotta, M., Bollwein, J., Friedrich, M., Heilkenbrinker, T., Passavant, C., Branen, J., Bollwein, H., 2011. Comparison of commercial ELISA blood tests for early pregnancy detection in dairy cows. J. Reprod. Dev., 57(1), 72-75. Poston, L., Igosheva, N., Mistry, H.D., Seed, P.T., Shennan, A.H., Rana, S., Karumanchi, S.A., Chappell, L.C., 2011. Role of oxidative stress and antioxidant supplementation in pregnancy disorders. Am. J. Clin. Nutr., 94, 1980S-5S. Qanungo, S., Mukherjea, M., 2000. Ontogenic profile of some antioxidants and lipid peroxidation in human placental and fetal tissues. Mol. Cell. Biochem., 215, 11–19. Smith, S.K., Charnock-Jones, D.S., Sharkey, A.M., 1998. The role of leukemia inhibitory factor and interleukin-6 in human reproduction. Hum. Reprod., 13(3), 237–43. Soehnlein, O., Weber, C., Lindbom, L., 2009. Neutrophil granule proteins tune monocytic cell function. Trends Immunol., 30, 538–46. Sordillo, L.M., Aitken, S.L., 2009. Impact of oxidative stress on thehealthandimmune function of dairy cattle. Vet. Immunol. Immunopathol., 128(1-3), 104-9. Sorg, O., 2004. Oxidative stress: a theoretical model or a biological reality?. C. R. Biol., 327, 649–662. Sousa, N.M., Ayad, A., Beckers, J.F., Gajewski, Z., 2006. Pregnancy-associated glycoproteins (PAG) as pregnancy markers in the ruminants. J. Physiol. Pharmacol., 57(8), 153-71.Talukder, S., Kerrisk, K.L., Ingenhoff, L., Gabai, G., Garcia, S.C., Celi, P., 2014. Changes in plasma oxidative stress biomarkers in dairy cows after oestrussynchronisation with controlled internal drug release (CIDR) and prostaglandin F2α (PGF2α). Anim. Product. Sci., 54(9), 1490–6.Trevisan, M., Browne, R., Ram, M., Muti, P., Freudenheim, J., Carosella, A.N., Armstrong, D., 2001. Correlates of markers of oxi- dative status in the general population. Am. J. Epidemiol., 154, 348–356. Tuuli, M.G., Longtine, M.S., Nelson, D.M., 2011. Review: oxygen and trophoblast biology—a source of controversy. Placenta, 32 (2), S109–18. Wall, P.D., Pressman, E.K., Woods, J.R.Jr., 2002. Preterm premature rupture of the membranes and antioxidants: the free radical connection. J. Perinat. Med., 30, 447–457. Wallace, D.C., 2005. A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine. Ann. Rev. Gen., 39, 359–407. Wilde, D., 2006. Influence of macro and micro minerals in the peri- parturient period on fertility in dairy cattle. Anim. Reprod. Sci., 96, 240–249. Witko-Sarsat, V., Friedlander, M., Capeillère-Blandin, C., Nguyen-Khoa, T., Nguyen, A. T., Zingraff, J., Jungers, P., Descamps-Latscha, B., 1996. Advanced oxidation protein products as a novel marker of oxidative stress in uraemia. Kidney Int., 49, 1304–1313. Wooding, F.B., Roberts, R.M., Green, J.A., 2005. Light and electron microscope immunocytochemical studies of the distribution of pregnancy-associated glycoproteins (PAGs) throughout pregnancy in the cow: possible functional implications. Placenta, 26, 807–827. Younis, A., Clower, C., Nelsen, D., Butler, W., Carvalho, A., Hok, E., Garelnebi, M., 2012. The relationship between pregnancy and oxidative stress markers on patients undergoing ovarian stimulations. J. Assist. Reprod. Gen., 29(10), 1083–9.

Relationship between oxidative stress status and glycoprotein-associated pregnancy concentrations during the early pregnancy period in dairy cows

Year 2020, Volume: 4 Issue: 1, 1 - 8, 10.03.2020

Abstract

Objective:This study was planned to
assess the possible relationships with PAG concentrations by the determination
of the biomarkers of oxidative stress in the plasma of
dairy cattle during the early period of
gestation. 

Materials and Methods:Blood samples were
collected in pregnant females (n = 54) and
non-pregnant females (n
= 45). Measurement of
biomarkers of oxidative stress (LPO, GSH and SOD) was carried out in females using
spectrophotometric method. 

Results:The levels of SOD were
significantly lower (
P< 0.05) in pregnant
females from day 25 to 35 (7.08 ±0.31 U.ml
-1) and day 36 to 50 after
AI (6.6 ± 0.29 U.ml
-1) compared with non-pregnant ones (7.59 ± 0.35
U.ml
-1). Concerning the levels of LPO and GSH, the values obtained
were also significant lower (
P <
0.05) in pregnant females in the period 25-35 days post AI (122.7 ±10.27 μM and
6.46 ±1.24 μmol/min.ml
-1, respectively) and 36-50 days post AI
(108.05±6.17 μM and 6.2±0.77 μmol/min.ml
-1, respectively) than in
the non-pregnant ones (124.8 ± 12.16 μM and 6.96 ± 0.92 μmol/min.ml
-1,
respectively). 

Conclusion:We have demonstrated that
the markers of oxidative stress were higher in non-pregnant females compared
with pregnant females during the early period of gestation in dairy cattle. 



References

  • Abdelfatah-Hassan, A., Almería, S., Serrano, B., de Sousa, N.M., Beckers, J.F., López-Gatius, F., The inseminating bull and plasma pregnancy-associated glycoprotein (PAG) levels were related to peripheral leukocyte counts during the late pregnancy/early postpartum period in high-producing dairy cows. Theriogenology 2012; 77(7): 1390–7. Agarwal, A., Allamaneni, S.S.R., Role of free radicals in female reproductive diseases and assisted reproduction. Reprod Biomed Online 2004; 9: 338–347. Al-Gubory, KH., Fowler, P.A., Garrel, C., The roles of cellular reactive oxygen species, oxidative stress and antioxidants in pregnancy outcomes. Int J Biochem Cell Biol 2010; 42(10): 1634-1650.Anastasakis, E., Papantoniou, N., Daskalakis, G., Mesogitis, S., Antsaklis, A., Screening for pre-eclampsia by oxidative stress markers and uteroplacental blood flow. J. Obstet. Gynaecol., 2008. 28 (3), 285-289. Aurousseau, B., Durand, D., Gruffat, D., Contrôle des phéenoménes oxydatifs pendant la gestation chez les monogastriques et les ruminants. INRA Prod. Anim., 2004.17, 339–354. Ayad, A., Delahaut, P., Yahi, K., Iguer-Ouada, M., Benbarek, H., Validation of a new Elisa for measuring bovine pregnancy-associated glycoproteins in plasma and its application for early pregnancy diagnosis. Reprod. Dom. Anim., 2014.49, 55-56.Ayad, A., Sousa, N.M., Sulon, J., Hornick, J.L., Iguer-Ouada, M., Beckers, J.F., Correlation of five radioimmunoassay systems for measurement of bovine plasma pregnancy-associated glycoprotein concentrations at early pregnancy period. Res. Vet. Sci., 2009. 86(3), 377-382. Ayad, A., Sousa, N.M., Sulon, J., Hornick, J.L., Touati, K., Iguer-Ouada, M., Beckers, J.F., Endocrinologie de la gestation chez la vache: Signaux embryonnaires, hormones et protéines placentaires. Ann. Méd. Vét., 2006.150(4),212-226.Ayad, A., Sousa, N. M., Sulon, J., Iguer-Ouada, M., Beckers, J.F., 2007. Comparison of five radioimmunoassay systems for PAG measurement: ability to detect early pregnancy in cows. Reprod. Dom. Anim., 42, 433-440. Bomba-Opon, D., Samaha, R B.B., Kosinski, P., Kozlowski, S., Wegrzyn, P., Borowski, D., Bartoszewicz, Z., Bednarczuk, T., Wielgos, M., 2014. First trimester maternal serum vitamin d and markers of preeclampsia. J. Matern Fetal Neonatal. Med., 27(10), 1078-9. Breukelman, S.P., Perényi, Z., Taverne, M.A.M., Jonker, H., Van der Weijden, G.C., Vos, P.L.A.M., De Ruigh, L., Dieleman, S.J., Beckers, J.F., Szenci, O., 2012. Characterization of pregnancy losses after embryo transfer by measuring plasma progesterone and bovine pregnancy-associated glycoprotein-1 concentrations. Vet. J., 194, 71–76. Castillo, C., Hernandez, J., Bravo, A., Lopez Alonso, M., Pereira, V., Benedito, J.L., 2005. Oxidative status during late pregnancy and early lactation in dairy cows. Vet. J., 169, 286–292.Celi, P., Merlo, M., Barbato, O., Gabai, G., 2012. Relationship between oxidative stress and the success of artificial insemination in dairy cows in a pasture-based system. Vet. J., 193(2), 498–502.Chavatte-Palmer, P., Tarrade, A., 2016. Placentation in different mammalian species. Ann. Endocrinol., 77, 67–74.Codoñer-Franch, P., Valls-Bellés, V., Arilla-Codoñer, A., Alonso-Iglesias, E., 2011. Oxidant mechanisms in childhood obesity: the link between inflammation and oxidative stress. Transl. Res., 158(6), 369-84. Constant, F., Camous, S., Chavatte-Palmer, P., Heyman, Y., De Sousa, N., Richard, C., Beckers, J.F., Guillomot, M., 2011. Altered secretion of pregnancy-associated glycoproteins during gestation in bovine somatic clones. Theriogenology, 76, 1006–1021. Dosogne, H., Burvenich, C., Freeman, A.E., Kehrli, M.E.Jr., Detilleux, J.C., Sulon, J., Beckers, J.F., Hoeben, D., 1999. Pregnancy-associated glycoprotein and decreased polymorphonuclear leukocyte function in early post-partum dairy cows. Vet. Immunol. Immunopathol., 67(1), 47–54. Dosogne, H., Massart-Leen, A.M., Bervenich, C., 2000. Immunological aspects of pregnancy associated glycoproteins. Adv. Exp. Cell Biol., 480, 295−305. Fainaru, O., Almog, B., Pinchuk, I., Kupferminc, M.J., Lichtenberg, D., Many, A., 2002. Active labour is associated with increased oxidisibility of serum lipids ex vivo. B.J.O.G., 109 (9), 938-941.Friedrich, M., Holtz, W., 2010. Establishment of an ELISA for measuring bovine pregnancy associated glycoprotein in serum or milk and its application for early pregnancy detection. Reprod. Dom. Anim., 45, 142–146. Gajewski, Z., Petrajtis-Golobow, M., De Sousa, N.M., Beckers, J.F., Pawlinski, B., Wehrend, A., 2014. Comparison of accuracy of pregnancy-associated glycoprotein (PAG) concentration in blood and milk for early pregnancy diagnosis in cows. Schweiz. Arch. Tierh., 156, 585-590. García-Ispierto, I., Rosselló-Visa, M.A., Serrano-Pérez, B., Mur-Novales, R., De Sousa, N.M.,, Beckers, J.F., López-Gatius, F., 2015. Plasma concentrations of pregnancy-associated glycoproteins I and II and progesterone on day 28 post-AI as markers of twin pregnancy in dairy cattle. Livestock Sciences,192, 44–47. Garrel, C., Fowler, P.A., Al-Gubory, K.H., 2010. Developmental changes in antioxidant enzymatic defences against oxidative stress in sheep placentomes. J. Endocrinol., 205, 107–116. Gilbert, R.O., 2011.The effects of endometritis on the establishment of pregnancy in cattle. Reprod. Fertil. Dev., 24, 252–257. Green, J.A., Parks, T.E., Avalle, M.P., Telugu, B.P., McLain, A.L., Peterson, A.J., McMillan, W., Mathialagan, N., Hook, R.R., Xie, S., Roberts, R.M., 2005. The establishment of an ELISA for the detection of pregnancy-associated glycoproteins (PAGs) in the serum of pregnant cows and heifers. Theriogenology, 63, 1481–1503. Green, L.E., Huxley, J.N., Banks, C., Green, M.J., 2014. Temporal associations between low body condition, lameness and milk yield in a UK dairy herd. Prev. Vet.y Med., 113 (1), 63-71. Gupta, S., Agarwal, A., Banerjee, J., Alvarez, J.G., 2007. The role of oxidative stress in spontaneous abortion and recurrent pregnancy loss: A systematic review. Obstet. Gynecol. Sur., 62, 335-347. Hoeben, D., Monfardini, E., Opsomer, G., Burvenich, C., Dosogne, H., De Kruif, A., Beckers, J.F., 2000. Chemiluminescence of bovine polymorphonuclear leucocytes during the periparturient period and relation with metabolic markers and bovine pregnancy-associated glycoprotein. J. Dairy Res., 67, 249–59. Jauniaux, E., Gulbis, B., Burton, G.J., 2003. The human first trimester gestational sac limits rather than facilities oxygen transfer to the foetus: a review. Placenta, 24, S86–S93. Karen, A., Bajcsy, Á. C., Minoia, R., Kovács, R., De Sousa, N.M., Beckers, J.F., Tibold, J.,Mádl, I.,Szenci, O., 2014. Relationship of progesterone, bovine pregnancy-associated glycoprotein-1 and nitric oxide with late embryonic and early fetal mortalities in dairy cows. J. Reprod. Dev., 60 (2), 162-167. Kindahl, H., Kornmatitsuk, B., Gustafsson, H., 2004. The cow in endocrine focus before and after calving. Reprod. Dom. Anim., 39, 217–221. Ledezma-Torres, R.A., Beckers, J.F., Holtz, W., 2006. Assessment of plasma profile of pregnancy-associated glycoprotein (PAG) in sheep with a heterologous (anti-caPAG55+59) RIA and its potential for diagnosing pregnancy. Theriogenology, 66 (4), 906-912. Liu, A.X., Jin, F., Zhang, W.W., Zhou, T.H., Zhou, C.Y., Yao, W.M., Qian, Y.L., Huang, H.F., 2006. Proteomic analysis on the alteration of protein expression in the placental villous tissue of early pregnancy loss. Biol. Reprod., 75, 414–420. Lobago, F., Bekana, M., Gustafsson, H., Beckers, J.F., Yohannes, G., Aster, Y., Kindahl, H., 2009. Serum profiles of pregnancy‐associated glycoprotein, oestrone sulphate and progesterone during gestation and some factors influencing the profiles in Ethiopian Borana and crossbred cattle. Reprod. Dom. Anim., 44 (4), 685-692. Lopez-Gatius, F., Garbayo, J.M., Santolaria, P., Yaniz, J., Ayad, A., De Sousa, N.M., Beckers, J.F., 2007. Milk production correlates negatively with plasma levels of pregnancy-associated glycoprotein (PAG) to plasma pregnancy-associated glycoprotein (PAG) during the early fetal period in high producing dairy cows with live fetuses. Dom. Anim. Endocrinol., 32 (1), 29-42. Mocatta, T.J., Winterbourn, C.C., Inder, T.E., Darlow, B.A., 2004. The effect of gestational age and labour on markers of lipid and protein oxidation in cord plasma. Free Radical Res., 38, 185–191. Mohanty, S., Sahu, P.K., Mandal, M.K., Mohapatra, P.C., Panda, A., 2006. Evaluation of oxidative stress in pregnancy induced hypertension. Indian J. Clin. Biochem., 21 (1), 101-105. Nathan, C., Cunningham-Bussel, A., 2013. Beyond oxidative stress: an immunologist's guide to reactive oxygen species. Nat. Rev. Immunol., 13(5), 349. Nemmar, A., Raza, H., Yuvaraju, P., Beegam, S., John, A., Yasin, J., Hameed, R.S., Adeghate, E., Ali, B.H., 2013. Nose-only water-pipe smoking effects on airway resistance, inflammation, and oxidative stress in mice. J. Appl. Physiol., 115(9), 1316-1323. Ness, R.B., 2004. The consequences for human reproduction of a robust inflammatory response. Q. Rev. Biol., 79(4), 383–393. Piechotta, M., Bollwein, J., Friedrich, M., Heilkenbrinker, T., Passavant, C., Branen, J., Bollwein, H., 2011. Comparison of commercial ELISA blood tests for early pregnancy detection in dairy cows. J. Reprod. Dev., 57(1), 72-75. Poston, L., Igosheva, N., Mistry, H.D., Seed, P.T., Shennan, A.H., Rana, S., Karumanchi, S.A., Chappell, L.C., 2011. Role of oxidative stress and antioxidant supplementation in pregnancy disorders. Am. J. Clin. Nutr., 94, 1980S-5S. Qanungo, S., Mukherjea, M., 2000. Ontogenic profile of some antioxidants and lipid peroxidation in human placental and fetal tissues. Mol. Cell. Biochem., 215, 11–19. Smith, S.K., Charnock-Jones, D.S., Sharkey, A.M., 1998. The role of leukemia inhibitory factor and interleukin-6 in human reproduction. Hum. Reprod., 13(3), 237–43. Soehnlein, O., Weber, C., Lindbom, L., 2009. Neutrophil granule proteins tune monocytic cell function. Trends Immunol., 30, 538–46. Sordillo, L.M., Aitken, S.L., 2009. Impact of oxidative stress on thehealthandimmune function of dairy cattle. Vet. Immunol. Immunopathol., 128(1-3), 104-9. Sorg, O., 2004. Oxidative stress: a theoretical model or a biological reality?. C. R. Biol., 327, 649–662. Sousa, N.M., Ayad, A., Beckers, J.F., Gajewski, Z., 2006. Pregnancy-associated glycoproteins (PAG) as pregnancy markers in the ruminants. J. Physiol. Pharmacol., 57(8), 153-71.Talukder, S., Kerrisk, K.L., Ingenhoff, L., Gabai, G., Garcia, S.C., Celi, P., 2014. Changes in plasma oxidative stress biomarkers in dairy cows after oestrussynchronisation with controlled internal drug release (CIDR) and prostaglandin F2α (PGF2α). Anim. Product. Sci., 54(9), 1490–6.Trevisan, M., Browne, R., Ram, M., Muti, P., Freudenheim, J., Carosella, A.N., Armstrong, D., 2001. Correlates of markers of oxi- dative status in the general population. Am. J. Epidemiol., 154, 348–356. Tuuli, M.G., Longtine, M.S., Nelson, D.M., 2011. Review: oxygen and trophoblast biology—a source of controversy. Placenta, 32 (2), S109–18. Wall, P.D., Pressman, E.K., Woods, J.R.Jr., 2002. Preterm premature rupture of the membranes and antioxidants: the free radical connection. J. Perinat. Med., 30, 447–457. Wallace, D.C., 2005. A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine. Ann. Rev. Gen., 39, 359–407. Wilde, D., 2006. Influence of macro and micro minerals in the peri- parturient period on fertility in dairy cattle. 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Details

Primary Language English
Journal Section 2020 Volume 4 Number 1
Authors

Abdelhanine Ayad

Priya Yuvaraju This is me

Sumaya Beegam This is me

Abderrahim Nemmar This is me

Publication Date March 10, 2020
Submission Date October 13, 2019
Published in Issue Year 2020 Volume: 4 Issue: 1

Cite

APA Ayad, A., Yuvaraju, P., Beegam, S., Nemmar, A. (2020). Relationship between oxidative stress status and glycoprotein-associated pregnancy concentrations during the early pregnancy period in dairy cows. Turkish Journal of Veterinary Research, 4(1), 1-8.
AMA Ayad A, Yuvaraju P, Beegam S, Nemmar A. Relationship between oxidative stress status and glycoprotein-associated pregnancy concentrations during the early pregnancy period in dairy cows. TJVR. March 2020;4(1):1-8.
Chicago Ayad, Abdelhanine, Priya Yuvaraju, Sumaya Beegam, and Abderrahim Nemmar. “Relationship Between Oxidative Stress Status and Glycoprotein-Associated Pregnancy Concentrations During the Early Pregnancy Period in Dairy Cows”. Turkish Journal of Veterinary Research 4, no. 1 (March 2020): 1-8.
EndNote Ayad A, Yuvaraju P, Beegam S, Nemmar A (March 1, 2020) Relationship between oxidative stress status and glycoprotein-associated pregnancy concentrations during the early pregnancy period in dairy cows. Turkish Journal of Veterinary Research 4 1 1–8.
IEEE A. Ayad, P. Yuvaraju, S. Beegam, and A. Nemmar, “Relationship between oxidative stress status and glycoprotein-associated pregnancy concentrations during the early pregnancy period in dairy cows”, TJVR, vol. 4, no. 1, pp. 1–8, 2020.
ISNAD Ayad, Abdelhanine et al. “Relationship Between Oxidative Stress Status and Glycoprotein-Associated Pregnancy Concentrations During the Early Pregnancy Period in Dairy Cows”. Turkish Journal of Veterinary Research 4/1 (March 2020), 1-8.
JAMA Ayad A, Yuvaraju P, Beegam S, Nemmar A. Relationship between oxidative stress status and glycoprotein-associated pregnancy concentrations during the early pregnancy period in dairy cows. TJVR. 2020;4:1–8.
MLA Ayad, Abdelhanine et al. “Relationship Between Oxidative Stress Status and Glycoprotein-Associated Pregnancy Concentrations During the Early Pregnancy Period in Dairy Cows”. Turkish Journal of Veterinary Research, vol. 4, no. 1, 2020, pp. 1-8.
Vancouver Ayad A, Yuvaraju P, Beegam S, Nemmar A. Relationship between oxidative stress status and glycoprotein-associated pregnancy concentrations during the early pregnancy period in dairy cows. TJVR. 2020;4(1):1-8.