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dc.creatorDovolou, E.en
dc.creatorPeriquesta, E.en
dc.creatorMessinis, I. E.en
dc.creatorTsiligianni, T.en
dc.creatorDafopoulos, K.en
dc.creatorGutierrez-Adan, A.en
dc.creatorAmiridis, G. S.en
dc.date.accessioned2015-11-23T10:25:57Z
dc.date.available2015-11-23T10:25:57Z
dc.date.issued2014
dc.identifier10.1016/j.theriogenology.2013.11.009
dc.identifier.issn0093-691X
dc.identifier.urihttp://hdl.handle.net/11615/27231
dc.description.abstractGhrelin is a gastric peptide having regulatory role in the reproductive system functionality, acting mainly at central level. Because the expression of ghrelin system (ghrelin and its receptor) has been detected in the bovine ovary, the objectives of the present study were to investigate whether ghrelin can affect the developmental potential of in vitro-produced embryos, and to test their quality in terms of relative abundance of various genes related to metabolism, apoptosis and oxidation. In the first experiment, in vitro-produced zygotes were cultured in the absence (control [C]) and in the presence of three concentrations of acylated ghrelin (200 pg/mL [Ghr200], 800 pg/mL [Ghr8001; and 2000 pg/mL [Ghr2000]); blastocyst formation rates were examined on Days 7, 8, and 9. In the second experiment, only the 800 pg/mL dose of ghrelin was used. Zygotes were produced as in experiment 1 and 24 hours post insemination they were divided into 4 groups; in two groups (C; without ghrelin; Ghr800 with ghrelin), embryos were cultured without medium replacement; in the remaining two groups (Control N and GhrN), the culture medium was daily renewed. A pool of Day-7 blastocysts were snap frozen for relative mRNA abundance of various genes related to metabolism, oxidation, implantation, and apoptosis. In experiment 3, embryos were produced as in experiment 2, but in the absence of serum (semi-defined culture medium). In experiment 1, no differences were detected between C, Ghr200, and Ghr2000, although fewer blastocysts were produced in group Ghr800 compared with C. In experiment 2, the lowest blastocysts yield was found in Ghr800, whereas daily renewal of ghrelin (Ghr800N) resulted to increased blastocysts formation rate, which on Day 7 was the highest among groups (P < 0.05). In experiment 3, ghrelin significantly suppressed blastocysts yield. Significant differences were detected in various relative mRNA abundance, giving an overall final notion that embryos produced in the presence of ghrelin were of better quality than controls. Our results imply a specific role of ghrelin in early embryonic development; however, the specific mode of its action needs further investigation. (C) 2014 Elsevier Inc. All rights reserved.en
dc.sourceTheriogenologyen
dc.source.uri<Go to ISI>://WOS:000331772100007
dc.subjectGhrelinen
dc.subjectBovine blastocystsen
dc.subjectIn vitro cultureen
dc.subjectIGF2Ren
dc.subjectDNMT3Aen
dc.subjectDEVELOPMENTALLY RELATED CHANGESen
dc.subjectMESSENGER-RNA EXPRESSIONen
dc.subjectNEGATIVE-ENERGY BALANCEen
dc.subjectPREIMPLANTATION EMBRYOSen
dc.subjectOXIDATIVE STRESSen
dc.subjectCULTUREen
dc.subjectMETABOLISMen
dc.subjectGLUCOSEen
dc.subjectCELLSen
dc.subjectPROLIFERATIONen
dc.subjectReproductive Biologyen
dc.subjectVeterinary Sciencesen
dc.titleDaily supplementation with ghrelin improves in vitro bovine blastocysts formation rate and alters gene expression related to embryo qualityen
dc.typejournalArticleen


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