Ver registro no DEDALUS
Exportar registro bibliográfico

Metrics


Metrics:

The periovulatory endocrine milieu affects the uterine redox environment in beef cows (2015)

  • Authors:
  • USP affiliated authors: BINELLI, MARIO - FMVZ
  • USP Schools: FMVZ
  • DOI: 10.1186/s12958-015-0036-x
  • Subjects: BOVINOS DE CORTE (REPRODUÇÃO); CICLO ESTRAL ANIMAL; ESTRADIOL (CONCENTRAÇÃO); PROGESTERONA (CONCENTRAÇÃO)
  • Language: Inglês
  • Imprenta:
  • Source:
  • Acesso online ao documento

    Online accessDOI or search this record in
    Informações sobre o DOI: 10.1186/s12958-015-0036-x (Fonte: oaDOI API)
    • Este periódico é de acesso aberto
    • Este artigo é de acesso aberto
    • URL de acesso aberto
    • Cor do Acesso Aberto: hybrid
    • Licença: cc-by
    Versões disponíveis em Acesso Aberto do: 10.1186/s12958-015-0036-x (Fonte: Unpaywall API)

    Título do periódico: Reproductive Biology and Endocrinology

    ISSN: 1477-7827

    • Melhor URL em Acesso Aberto:


    • Outras alternativas de URLs em Acesso Aberto:


        • Página do artigo
        • Evidência: oa journal (via doaj)
        • Licença: cc-by
        • Versão: publishedVersion
        • Tipo de hospedagem: publisher




        • Página do artigo
        • Link para o PDF
        • Evidência: oa repository (via OAI-PMH title and first author match)
        • Licença: cc-by
        • Versão: publishedVersion
        • Tipo de hospedagem: repository


        • Página do artigo
        • Evidência: oa repository (via pmcid lookup)
        • Licença:
        • Versão: publishedVersion
        • Tipo de hospedagem: repository


    Informações sobre o Citescore
  • Título: Reproductive Biology and Endocrinology

    ISSN: 1477-7827

    Citescore - 2017: 3.33

    SJR - 2017: 1.203

    SNIP - 2017: 1.21


  • Exemplares físicos disponíveis nas Bibliotecas da USP
    BibliotecaCód. de barrasNúm. de chamada
    FMVZ2688488-10BIN - 176
    How to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas

    • ABNT

      RAMOS, Roney dos Santos; OLIVEIRA, Milena L; IZAGUIRRY, Aryele P; et al. The periovulatory endocrine milieu affects the uterine redox environment in beef cows. Reproductive Biology and Endocrinology, London, BioMed Central Ltd, v. 13, p. 1-10, 2015. Disponível em: < http://dx.doi.org/10.1186/s12958-015-0036-x > DOI: 10.1186/s12958-015-0036-x.
    • APA

      Ramos, R. dos S., Oliveira, M. L., Izaguirry, A. P., Vargas, L. M., Soares, M. B., Mesquita, F. S., et al. (2015). The periovulatory endocrine milieu affects the uterine redox environment in beef cows. Reproductive Biology and Endocrinology, 13, 1-10. doi:10.1186/s12958-015-0036-x
    • NLM

      Ramos R dos S, Oliveira ML, Izaguirry AP, Vargas LM, Soares MB, Mesquita FS, Santos FW, Binelli M. The periovulatory endocrine milieu affects the uterine redox environment in beef cows [Internet]. Reproductive Biology and Endocrinology. 2015 ; 13 1-10.Available from: http://dx.doi.org/10.1186/s12958-015-0036-x
    • Vancouver

      Ramos R dos S, Oliveira ML, Izaguirry AP, Vargas LM, Soares MB, Mesquita FS, Santos FW, Binelli M. The periovulatory endocrine milieu affects the uterine redox environment in beef cows [Internet]. Reproductive Biology and Endocrinology. 2015 ; 13 1-10.Available from: http://dx.doi.org/10.1186/s12958-015-0036-x

    Referências citadas na obra
    Peres RF, Claro I, Sá Filho OG, Nogueira GP, Vasconcelos JL. Strategies to improve fertility in Bos indicus postpubertal heifers and nonlactating cows submitted to fixed-time artificial insemination. Theriogenology. 2009;72:681–9.
    Meneghetti M, Sá Filho OG, Peres RF, Lamb GC, Vasconcelos JL. Fixed-time artificial insemination with estradiol and progesterone for Bos indicus cows I: basis for development of protocols. Theriogenology. 2009;72:179–89.
    Dadarwal D, Mapletoft RJ, Adams GP, Pfeifer LF, Creelman C, Singh J. Effect of progesterone concentration and duration of proestrus on fertility in beef cattle after fixed-time artificial insemination. Theriogenology. 2013;79:859–66.
    Bridges GA, Mussard ML, Burke CR, Day ML. Influence of the length of proestrus on fertility and endocrine function in female cattle. Anim Reprod Sci. 2010;117:208–15.
    Perry GA, Smith MF, Roberts AJ, MacNeil MD, Geary TW. Relationship between size of the ovulatory follicle and pregnancy success in beef heifers. J Anim Sci. 2007;85:684–9.
    McNeill RE, Diskin MG, Sreenan JM, Morris DG. Associations between milk progesterone concentration on different days and with embryo survival during the early luteal phase in dairy cows. Theriogenology. 2006;65:1435–41.
    Binelli M, Hampton J, Buhi WC, Thatcher WW. Persistent dominant follicle alters pattern of oviductal secretory proteins from cows at estrus. Biol Reprod. 1999;61:127–34.
    Bauersachs S, Rehfeld S, Ulbrich SE, Mallok S, Prelle K, Wenigerkind H, et al. Monitoring gene expression changes in bovine oviduct epithelial cells during the oestrous cycle. J Mol Endocrinol. 2004;32:449–66.
    Bauersachs S, Ulbrich SE, Gross K, Schmidt SE, Meyer HH, Einspanier R, et al. Gene expression profiling of bovine endometrium during the oestrous cycle: detection of molecular pathways involved in functional changes. J Mol Endocrinol. 2005;34:889–908.
    Bridges GA, Mussard ML, Pate JL, Ott TL, Hansen TR, Day ML. Impact of preovulatory estradiol concentrations on conceptus development and uterine gene expression. Anim Reprod Sci. 2012;133:16–26.
    Forde N, Beltman ME, Duffy GB, Duffy P, Mehta JP, O'Gaora P, et al. Changes in the endometrial transcriptome during the bovine estrous cycle: effect of low circulating progesterone and consequences for conceptus elongation. Biol Reprod. 2011;84:266–78.
    Forde N, Carter F, Fair T, Crowe MA, Evans AC, Spencer TE, et al. Progesterone-regulated changes in endometrial gene expression contribute to advanced conceptus development in cattle. Biol Reprod. 2009;81:784–94.
    Schafer FQ, Buettner GR. Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple. Free Radic Biol Med. 2001;30:1191–212.
    Thannickal VJ, Fanburg BL. Reactive oxygen species in cell signaling. Am J Physiol Lung Cell Mol Physiol. 2000;279:L1005–28.
    Agarwal A, Gupta S, Sharma RK. Role of oxidative stress in female reproduction. Reprod Biol Endocrinol. 2005;3:28.
    Fujii J, Iuchi Y, Okada F. Fundamental roles of reactive oxygen species and protective mechanisms in the female reproductive system. Reprod Biol Endocrinol. 2005;3:43.
    Ohwada M, Suzuki M, Sato I, Tsukamoto H, Watanabe K. Glutathione peroxidase activity in endometrium: effects of sex hormones and cancer. Gynecol Oncol. 1996;60:277–82.
    Lyttle CR, DeSombre ER. Uterine peroxidase as a marker for estrogen action. Proc Natl Acad Sci U S A. 1977;74:3162–6.
    Díaz-Flores M, Baiza-Gutman LA, Pedrón NN, Hicks JJ. Uterine glutathione reductase activity: modulation by estrogens and progesterone. Life Sci. 1999;65:2481–8.
    Al-Gubory KH, Bolifraud P, Garrel C. Regulation of key antioxidant enzymatic systems in the sheep endometrium by ovarian steroids. Endocrinology. 2008;149:4428–34.
    Mesquita FS, Pugliesi G, Scolari SC, Franca MR, Ramos RS, Oliveira ML, et al. Manipulation of the periovulatory sex steroidal milieu affects endometrial but not luteal gene expression in early diestrus Nelore cows. Theriogenology. 2014;81:861–9.
    Siddiqui MA, Gastal EL, Gastal MO, Almamun M, Beg MA, Ginther OJ. Relationship of vascular perfusion of the wall of the preovulatory follicle to in vitro fertilisation and embryo development in heifers. Reproduction. 2009;137:689–97.
    Garbarino EJ, Hernandez JA, Shearer JK, Risco CA, Thatcher WW. Effect of lameness on ovarian activity in postpartum Holstein cows. J Dairy Sci. 2004;87:4123–31.
    Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976;72:248–54.
    Wendel A. Glutathione peroxidase. Methods Enzymol. 1981;77:325–33.
    Hissin PJ, Hilf R. A fluorometric method for determination of oxidized and reduced glutathione in tissues. Anal Biochem. 1976;74:214–26.
    Loetchutinat C, Kothan S, Dechsupa S, Meesungnoen J, Jay-Gerin J-P, Mankhetkorn S. Spectrofluorometric determination of intracellular levels of reactive oxygen species in drug-sensitive and drug-resistant cancer cells using the 2′,7′-dichlorofluorescein diacetate assay. Radiat Phys Chem. 2005;72:323–31.
    Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979;95:351–8.
    Misra HP, Fridovich I. The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. J Biol Chem. 1972;247:3170–5.
    Aebi H. Catalase in vitro. Methods Enzymol. 1984;105:121–6.
    Ramakers C, Ruijter JM, Deprez RH, Moorman AF. Assumption-free analysis of quantitative real-time polymerase chain reaction (PCR) data. Neurosci Lett. 2003;339:62–6.
    Vandesompele J, De Preter K, Pattyn F, Poppe B, Van Roy N, De Paepe A, et al. Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol. 2002;3:RESEARCH0034.
    Mullen MP, Elia G, Hilliard M, Parr MH, Diskin MG, Evans AC, et al. Proteomic characterization of histotroph during the preimplantation phase of the estrous cycle in cattle. J Proteome Res. 2012;11:3004–18.
    Yoon SB, Choi SA, Sim BW, Kim JS, Mun SE, Jeong PS, et al. Developmental competence of bovine early embryos depends on the coupled response between oxidative and endoplasmic reticulum stress. Biol Reprod. 2014;90:104.
    Ayala A, Muñoz MF, Argüelles S. Lipid peroxidation: production, metabolism, and signaling mechanisms of malondialdehyde and 4-hydroxy-2-nonenal. Oxid Med Cell Longev. 2014;2014:360438.
    Jamieson DJ, Stephen DW, Terrière EC. Analysis of the adaptive oxidative stress response of Candida albicans. FEMS Microbiol Lett. 1996;138:83–8.
    González-Párraga P, Hernández JA, Argüelles JC. Role of antioxidant enzymatic defenses against oxidative stress H(2)O(2) and the acquisition of oxidative tolerance in Candida albicans. Yeast. 2003;20:1161–9.
    Khassaf M, McArdle A, Esanu C, Vasilaki A, McArdle F, Griffiths RD, et al. Effect of vitamin C supplements on antioxidant defense and stress proteins in human lymphocytes and skeletal muscle. J Physiol. 2003;549:645–52.
    Sugino N, Karube-Harada A, Kashida S, Takiguchi S, Kato H. Differential regulation of copper-zinc superoxide dismutase and manganese superoxide dismutase by progesterone withdrawal in human endometrial stromal cells. Mol Hum Reprod. 2002;8:68–74.
    Ponsuksili S, Murani E, Schwerin M, Schellander K, Tesfaye D, Wimmers K. Gene expression and DNA-methylation of bovine pretransfer endometrium depending on its receptivity after in vitro-produced embryo transfer. PLoS One. 2012;7:e42402.
    Al-Gubory KH, Garrel C. Antioxidative signaling pathways regulate the level of reactive oxygen species at the endometrial-extraembryonic membranes interface during early pregnancy. Int J Biochem Cell Biol. 2012;44:1511–8.
    Al-Gubory KH, Arianmanesh M, Garrel C, Bhattacharya S, Cash P, Fowler PA. Proteomic analysis of the sheep caruncular and intercaruncular endometrium reveals changes in functional proteins crucial for the establishment of pregnancy. Reproduction. 2014;147:599–614.
    Sordillo LM, Aitken SL. Impact of oxidative stress on the health and immune function of dairy cattle. Vet Immunol Immunopathol. 2009;128:104–9.
    Murdoch WJ. Inhibition by oestradiol of oxidative stress-induced apoptosis in pig ovarian tissues. J Reprod Fertil. 1998;114:127–30.
    Jain S, Saxena D, Kumar PG, Koide SS, Laloraya M. Effect of estradiol and selected antiestrogens on pro- and antioxidant pathways in mammalian uterus. Contraception. 1999;60:111–8.
    Laloraya M. Fluidity of the phospholipid bilayer of the endometrium at the time of implantation of the blastocyst–a spin label study. Biochem Biophys Res Commun. 1990;167:561–7.
    Lazzari G, Colleoni S, Duchi R, Galli A, Houghton FD, Galli C. Embryonic genotype and inbreeding affect preimplantation development in cattle. Reproduction. 2011;141:625–32.
    Bettegowda A, Patel OV, Ireland JJ, Smith GW. Quantitative analysis of messenger RNA abundance for ribosomal protein L-15, cyclophilin-A, phosphoglycerokinase, beta-glucuronidase, glyceraldehyde 3-phosphate dehydrogenase, beta-actin, and histone H2A during bovine oocyte maturation and early embryogenesis in vitro. Mol Reprod Dev. 2006;73:267–78.