Chemical composition and effects of Ocimum gratissimum essential oil (OGEO) on the expression of mRNA for antioxidant enzymes during in vitro culture of bovine ovarian secondary follicles

References

• C.A. Pereira and J.F. Maia, Study of the antioxidant activity and essential oil from wild basil (Ocimum gratissimum L.) leaf. Food Science and Technology, 27, 624–632 (2007). doi:10.1590/S0101-20612007000300030.
   Google Scholar
• F.B.M. Mohr, C. Lermen, Z.C. Gazim, J.E. Gonçalves and O. Alberton, Antifungal activity, yield, and composition of Ocimum gratissimum essential oil. Genetics and Molecular Research, 16, 1–10 (2017). doi:10.4238/gmr16019542.
   Web of Science ®Google Scholar
• M.T. Trevisan, M.G. Vasconcelos Silva, B. Pfundstein, B. Spiegelhalder and R.W. Owen, Characterization of the volatile pattern and antioxidant capacity of essential oils from different species of the genus Ocimum. Journal of Agriculture and Food Chemistry, 54, 4382–4383 (2006). doi:10.1021/jf060181+.
   Google Scholar
• R.K. Joshi, Chemical composition, in vitro antimicrobial and antioxidant activities of the essential oils of Ocimum gratissimum, O. Sanctum and their major constituents. Indian Journal of Pharmaceutical Sciences, 75, 457–462 (2013). doi:10.4103/0250-474X.119834.
   PubMed Web of Science ®Google Scholar
• S. Bhatt, M. Bisht, G. Tewari, C. Pande, O. Prakash and L. Rana, Evaluation of antioxidant potential and quality of volatile constituents of fresh and sun dried Ocimum gratissimum. Journal of the Indian Chemical Society, 96, 297–304 (2019).
   Web of Science ®Google Scholar
• Y. Ponnusam, T. Louis, V. Madhavachandran, S. Kumar, N. Thoprani, M.R. Hamblin and S. Lakshmanan, Antioxidant activity of the ancient herb, Holy Basil in CCl4-induced liver injury in rats. Ayurvedic, 2, 34–38 (2015). doi:10.14259/av.v2i2.176.
   PubMedGoogle Scholar
• R.H. Kashka, S. Zavareh and T. Lashkarbolouki, Augmenting effect of vitrification on lipid peroxidation in mouse preantral follicle during cultivation: Modulation by coenzyme Q10. Systems Biology in Reproductive Medicine, 62, 404–414 (2016). doi:http://dx.doi.org/10.1080/19396368.2016.1235236.
   PubMed Web of Science ®Google Scholar
• F.J. Martín-Romero, E.M. Miguel-Lasobras, J.A. Domínguez-Arroyo, E. González-Carrera and I.S. Alvarez, Contribution of culture media to oxidative stress and its effect on human oocytes. Reproductive Biomedicine Online, 17, 652–661 (2008). doi:10.1016/s1472-6483(10)60312-4.
   PubMed Web of Science ®Google Scholar
• M. Kala, M.V. Shaikh and M. Nivsarkar, Equilibrium between anti-oxidants and reactive oxygen species: a requisite for oocyte development and maturation. Reproductive Medicine and Biology, 16, 28–35 (2016). doi:10.1002/rmb2.12013.
   PubMed Web of Science ®Google Scholar
• A.B. Fisher, Peroxiredoxin 6: a bifunctional enzyme with glutathione peroxidase and phospholipase A₂ activities. Antioxidants & Redox Signaling, 15, 831–844 (2011). doi:10.1089/ars.2010.3412.
   PubMed Web of Science ®Google Scholar
• L.P. Santos, V.R.P. Barros, A.Y.P. Cavalcante, V.G. Menezes, T.S.J. Macedo and V.R. Araújoet al., Protein localization of epidermal growth factor in sheep ovaries and improvement of follicle survival and antrum formationIn vitro. Reproduction in Domestic Animals, 49, 783–789 (2014). doi:10.1111/rda.12369.
   PubMed Web of Science ®Google Scholar
• M. Farzollahi, H. Tayefi-Nasrabadi, D. Mohammadnejad and A. Abedelahi, Supplementation of culture media with vitamin E improves mouse antral follicle maturation and embryo development from vitrified ovarian tissue. The Journal of Obstetrics and Gynaecology Research, 42, 526–535 (2016). doi:10.1111/jog.12933.
   PubMed Web of Science ®Google Scholar
• N.A.R. Sá, J.B. Bruno, D.D. Guerreiro, J. Cadenas, B.G. Alves and F.W.S. Cibinet al., Anethole reduces oxidative stress and improves in vitro survival and activation of primordial follicles. Brazilian Journal of Medical and Biological Research, 51, 1–8 (2018). doi:10.1590/1414-431x20187129.
   Web of Science ®Google Scholar
• J.H. Britt, Impacts of early postpartum metabolism on follicular development and fertility. The Bovine Practitioner Proceeding, 24, 39–43 (1991).
   Google Scholar
• M.J. O’-Brien, J.K. Pendola and J.J. Eppig, A revised protocol for in vitro development of mouse oocytes from primordial follicles dramatically improves their developmental competence. Biology of Reproduction, 68, 1682–1686 (2002). doi:10.1095/biolreprod.102.013029.
   PubMed Web of Science ®Google Scholar
• J.R. Silva, R. Van Den Hurk and J.R. Figueiredo, Ovarian follicle development in vitro and oocyte competence: advances and challenges for farm animals. Domestic Animal Endocrinology, 55, 123–135 (2016). doi:10.1016/j.domaniend.2015.12.006.
   PubMed Web of Science ®Google Scholar
• V.R. Araújo, M.O. Gastal, A. Wischral, J.R.F. A and E.L. Gastal, Long-Term in vitro culture of bovine preantral follicles: Effect of base medium and medium replacement methods. Animal Reproduction Science, 161, 23–31 (2015). doi:10.1016/j.anireprosci.2015.07.006.
   PubMed Web of Science ®Google Scholar
• R. Fabbri, G. Pasquinelli, I. Parazza, M. Macciocca, V. Magnani and C. Battagliaet al., Effects of cyclic increase in gonadotropins on the in vitro development of primordial follicles to antral stage. Ultrastructural Pathology, 36, 356–361 (2012). doi:10.3109/01913123.2012.679353.
   PubMed Web of Science ®Google Scholar
• R.P. Adams, Identification of Essential Oils by Gas Chromatography Quadrupole Mass Spectrometry. Allured Publ. Corp., Carol Stream, IL (2007).
   Google Scholar
• H. Van den Dool and P.D.A. Kratz, A generalization of the retention index system including linear temperature programmed gas-liquid partition chromatography. Journal of Chromatography, 11, 463–471 (1963). doi:10.1016/S0021-9673(01)80947-X.
   PubMed Web of Science ®Google Scholar
• R. Van Den Hurk, E.R. Spek, W.J. Hage, T. Fair, J.H. Ralph and K. Schotanus, Ultrastructure and viability of isolated bovine preantral follicles. Human Reproduction Update, 4, 833–8416.833 (1998). doi:10.1093/humupd/4.
   PubMed Web of Science ®Google Scholar
• K.J. Livak and T.D. Schmittgen, Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods, 25, 402–408 (2001). doi:10.1006/meth.2001.1262.
   PubMed Web of Science ®Google Scholar
• R.S. Melo, Á.M.A. Azevedo, A.M.G. Pereira, R.R. Rocha, R.M.B. Cavalcante and M.N.C. Matoset al., Chemical composition and antimicrobial effectiveness of Ocimum gratissimum L. Essential oil against multidrug-resistant isolates of Staphylococcus aureus and Escherichia coli. Moleculares, 24, 2–17 (2019). doi:10.3390/molecules24213864.
   Web of Science ®Google Scholar
• L. Gobbo-Neto and N.P.L. Lopes, Medicinal plants: factors of influence on the content of secondary metabolites. Quimica Nova, 30, 374–381 (2007). doi:10.1590/S0100-40422007000200026.
   Web of Science ®Google Scholar
• G. Leyens, B. Knoops and I. Donnay, Expression of peroxiredoxins in bovine oocytes and embryos produced in vitro. Molecular Reproduction and Development, 69, 243–251 (2004). doi:10.1002/mrd.20145.
   PubMed Web of Science ®Google Scholar
• A.J. Harvey, K.L. Kind and J.G. Thompson, REDOX regulation of early embryo development. Reproduction, 123, 479–486 (2002). doi:10.1530/rep.0.1230479.
   PubMed Web of Science ®Google Scholar
• D.G. De Matos, C.C. Furnus and D.F. Moses, Glutathione synthesis during in vitro maturation of bovine oocytes: role of cumulus cells. Biology of Reproduction, 57, 1420–1425 (1997). doi:10.1095/biolreprod57.6.1420.
   PubMed Web of Science ®Google Scholar
• J.A. Arevalo and J.P. Vázquez-Medina, The role of peroxiredoxin 6 in cell signaling. Antioxidants, 24, 1–13 (2018).
   Google Scholar
• J.A. Elvin, C. Yan and M.M. Matzuk, Growth differentiation factor-9 stim- ulates progesterone synthesis in granulosa cells via a prostaglandin E2/EP2 receptor pathway. Proceedings of the National Academy of Sciences of the United States of America, 97, 10288–10293 (2000). doi:10.1073/pnas.180295197
   Google Scholar
• M.D. Calder, A.N. Caveney, M.E. Westhusin and A.J. Watson, Cyclooxygen-Ase-2 and prostaglandin E(2)(PGE(2)) receptor messenger RNAs are affected by bovine oocyte maturation time and cumulus-oocyte com- plex quality, and PGE(2) induces moderate expansion of the bovine cumulus in vitro. Biology of Reproduction, 65, 135–140 (2001). doi:10.1095/biolreprod65.1.135.
   PubMed Web of Science ®Google Scholar
• C.A. Gallelli, S. Calcagnini, A. Romano, J.B. Koczwara, M. De Ceglia and D. Dante, Modulation of the oxidative stress and lipid peroxidation by endocannabinoids and their lipid analogues. Antioxidants, 7, 2–44 (2018). doi:10.3390/antiox7070093.
   Web of Science ®Google Scholar
• Q.K. Alabi, R.O. Akomolafe, J.G. Omole, M.A. Adefisayo, O.L. Ogundipe, A.S. Aturamu and J.O. Sanya, Polyphenol-Rich extract of Ocimum gratissimum leaves ameliorates colitis via attenuating colonic mucosa injury and regulating pro-inflammatory cytokines production and oxidative stress. Biomedicine & Pharmacotherapy, 103, 812–818 (2018). doi:10.1016/j.biopha.2018.04.071.
   PubMed Web of Science ®Google Scholar
• Y.S. Park, S.Y. You, S. Cho, H.J. Jeon, S. Lee and D.H. Choet al., Eccentric localization of catalase to protect chromosomes from oxidative damages during meiotic maturation in mouse oocytes. Histochemistry and Cell Biology, 146, 281–288 (2016). doi:10.1007/s00418-016-1446-3.
   PubMed Web of Science ®Google Scholar
• L. Yang, Q. Wang, M. Cui, Q. Li and Z. Zhao, Effect of melatonin on the in vitro maturation of Porcine oocytes, development of parthenogenetically activated embryos, and expression of genes related to the oocyte developmental capability. Animals, 209, 2–13 (2020). doi:10.3390/ani10020209.
   Google Scholar
• M. Kala and M. Nivsarkar, Role of cortisol and superoxide dismutase in psychological stress induced anovulation. General and Comparative Endocrinology, 225, 117–124 (2016). doi:10.1016/j.ygcen.2015.09.010.
   PubMed Web of Science ®Google Scholar
• R.G. Torres, L. Casanova, J. Carvalho, M.C. Marcondes, S.S. Costa, M. Sola-Penna and P. Zancan, Ocimum basilicum but not Ocimum gratissimum present cytotoxic effects on human breast cancer cell line MCF-7, inducing apoptosis and triggering mTor/akt/p70s6k pathway. Journal of Bioeneratics and Biomembranes, 50, 93–105 (2018). doi:10.1007/s10863-018-9750-3.
   PubMed Web of Science ®Google Scholar
• I.I. Ijeh, O.D. Omodamiro and I.J. Nwanna, Antimicrobial effects of aqueous and ethanolic fractions of two spices, Ocimum gratissimum and Xylopia aethiopica. African Journal of Biotecnology, 4, 953–956 (2005). doi:10.5897/AJB2005.000-3193.
   Web of Science ®Google Scholar
• A. De Araújo Lopes, F.N. Da Fonseca, T.M. Rocha, L.B. De Freitas, E.V.O. Araújo and D.V.T. Wong et al., Eugenol as a promising molecule for the treatment of dermatitis: antioxidant and anti-inflammatory activities and its nanoformulation. Oxidative Medicine and Cellular Longevity, 1–13 (2018). doi:10.1155/2018/8194849.
   Web of Science ®Google Scholar
• L.B.S. Oliveira, A.H.M. Batista, F.C. Fernandes, G.W.P. Sales and N.A.P. Nogueira, Atividade antifúngica e possível mecanismo de ação do óleo essencial de folhas de Ocimum gratissimum (Linn.) sobre espécies de Candida. Revista Brasileira de Plantas Medicinais, 18, 511–523 (2016). doi:10.1590/1983-084X/15_222.
   Google Scholar