Animal Reproduction (AR)
https://www.animal-reproduction.org/article/doi/10.21451/1984-3143-AR885
Animal Reproduction (AR)
Original Article

Effects of chlorogenic acid on the maturation and fertilisation of bovine oocytes and their embryonic development with a comparative bovine granulosa cell co-culture

Hélder Patrício Nunes, Selma Furnas, Marleen Dinis, Alfredo Borba, Joaquim Moreira da Silva

Downloads: 0
Views: 843

Abstract

Chlorogenic acid (CGA) plays several biological roles, but lacks studies that demonstrate how this phenolic compound affects animal reproduction. The aim of the present study was to evaluate the effects of different CGA concentrations on bovine oocyte maturation and embryo development in vitro. This study also evaluates co-culture systems involving bovine granulosa cells (BGC) from fed with CGA containing plant, Pittosporum Undulatum. The ovaries were recovered after slaughter and the oocytes were removed, maturated, in vitro fertilized and cultured in medium containing CGA in 5 different concentrations 1.25; 2.5; 5; 10; 20 µm and a control group (0 µm) for seven days. Selected oocytes (n = 1040) were maturated in any of the 5 treatment or control groups. Significantly lower (P < 0.05) maturation rates were observed for the highest CGA concentrations 10 µm, and 20 µm, compared to the control group (Control = 93.4 ± 2.1% vs. 10 µm = 80.9 ± 2.2%; 20 µm 77.9 ± 3.3%). We observed that the higher the concentration of CGA present, the lower the rate of cleavage and development after 3 and 7 days, respectively. It was observed that the significant difference recorded in regards to embryonic development were evident between control and group (20; 51.1 ±5.6 vs. 19.4 ± 2.2%). In respects to the study involving co-culture of embryos with BGC the only difference recorded involved the block rate. No differences (P > 0.05) were identified between control and experimental groups in relation to the progesterone production by BGC. These results suggest that CGA may affect oocyte maturation and inhibit the progression of meiosis and consequently the entire embryo development in vitro.

Keywords

blastocysts, bovine, chlorogenic acid, IVF, IVM, P. undulatum; progesterone.

References

Calder MD, Caveney AN, Westhusin ME, Watson AJ. 2001. Cyclooxygenase-2 and prostaglandin E2(PGE2) receptor messenger RNAs are affected by bovine oocyte maturation time and cumulus-oocyte complex quality, and PGE2 induces moderate expansion of the bovine cumulus in vitro. Biol Reprod, 65:135- 140.

Faheem MS, Carvalhais I, Chaveiro A, Moreira da Silva F. 2011. In vitro oocyte fertilization and subsequent embryonic development after cryopreservation of bovine ovarian tissue, using an effective approach for oocyte collection. Anim Reprod Sci, 125:49-55.

Gordon MH, Wishart K. 2010. Effects of chlorogenic acid and bovine serum albumin on the oxidative stability of low density lipoproteins in vitro. J Agric Food Chem, 58:5828-5833.

Gugliucci A, Bastos DHM, Schulze J, Souza MFF. 2009. Caffeic and chlorogenic acids in Ilex paraguariensis extracts are the main inhibitors of AGE generation by methylglyoxal in model proteins. Fitoterapia, 80:339-344.

Hao Y, Gao R, Liu D, He G, Tang Y, Guo Z. 2016. Selective extraction and determination of chlorogenic acid in fruit juices using hydrophilic magnetic imprinted nanoparticles. Food Chem, 200:215-222. Kang NJ, Shin SH, Lee HJ, Lee KW. 2011.

Polyphenols as small molecular inhibitors of signaling cascades in carcinogenesis. Pharmacol Ther, 130:310- 324.

Katz M, Amit I, Yarden Y. 2007. Regulation of MAPKs by growth factors and receptor tyrosine kinases. Biochim Biophys Acta, 1773:1161-1176.

Liu Q, Zhao Y, Pan J, Van der Bruggen B, Shen J. 2016. A novel chitosan base molecularly imprinted membrane for selective separation of chlorogenic acid. Sep Purif Technol, 164:70-80.

Lourenço P, Medeiros V, Gil A, Silva L. 2011. Distribution, habitat and biomass of Pittosporum undulatum, the most important woody plant invader in the Azores Archipelago. For Ecol Manage, 262:178- 187.

Madan P, Calder MD, Watson AJ. 2005. Mitogenactivated protein kinase (MAPK) blockade of bovine preimplantation embryogenesis requires inhibition of both p38 and extracellular signal-regulated kinase (ERK) pathways. Reproduction, 130:41-51.

Meinecke B, Janas U, Podhajsky E, MeineckeTillmann S. 2001. Histone H1 and MAP kinase activities in bovine oocytes following protein synthesis inhibition. Reprod Domest Anim, 36:183-188.

Nunes H, Falé PL, Duarte MF, Serralheiro ML, Borba Alfredo ES, Silva JFM. 2014. Pittosporum undulatum and hedychium gardnerianum nutritive value and secondary metabolites on cattle reproductive performances. Int J Pure Appl Sci Technol, 22:1-9.

Oliveira DM, Bastos DHM. 2011. Biodisponibilidade de ácidos fenólicos. Quím Nova, 34:1051-1056.

Pakrasi PL, AK Jain. 2008. Cyclooxygenase-2-derived endogenous prostacyclin reduces apoptosis and enhances embryo viability in mouse. Prostaglandins, Leukotrienes and Essential Fatty Acids, 79: 27-33.

Santos P, Chaveiro A, Simões N, Moreira da Silva F. 2008. Bovine oocyte quality in relation to ultrastructural characteristics of zona pellucida, polyspermic penetration and developmental competence. Reprod Domest Anim, 43:685-689.

Shan J, Fu J, Zhao Z, Kong X, Huang H, Luo L, Yin Z. 2009. Chlorogenic acid inhibits lipopolysaccharideinduced cyclooxygenase-2 expression in RAW264.7 cells through suppressing NF-κB and JNK/AP-1 activation. Int Immunopharmacol, 9:1042-1048.

Thatcher WW, Wolfenson D, Curl JS, Rico LE, Knickerbocker JJ, Bazer FW, Drost M. 1984.

Prostaglandin dynamics associated with development of the bovine conceptus. Anim Reprod Sci, 7:149-176.

Tian XC, Lonergan P, Jeong B-S, Evans ACO, Yang X. 2002. Association of MPF, MAPK, and nuclear progression dynamics during activation of young and aged bovine oocytes. Mol Reprod Dev, 62:132-138.

5b7319740e8825d9188068a8 animreprod Articles
Links & Downloads

Anim Reprod

Share this page
Page Sections