scholarly journals Integrating insulin into single-step culture medium regulates human embryo development in vitro

2017 ◽  
Vol 107 (2) ◽  
pp. 405-412 ◽  
Author(s):  
Mohamed Fawzy ◽  
Mohamed Sabry ◽  
Mohamed Nour ◽  
Mohamed Y. Abdelrahman ◽  
Eman Roshdy ◽  
...  
1998 ◽  
Vol 13 (5) ◽  
pp. 1325-1330 ◽  
Author(s):  
A. M. Wetzels ◽  
B. A. Bastiaans ◽  
J. C. Hendriks ◽  
H. J. Goverde ◽  
A. P. Punt-van der Zalm ◽  
...  

1993 ◽  
Vol 8 (12) ◽  
pp. 2133-2140 ◽  
Author(s):  
Michelle Plachot ◽  
J.M. Antoine ◽  
Sylvia Alvarez ◽  
C. Firmin ◽  
A. Pfister ◽  
...  

1997 ◽  
Vol 12 (Suppl_2) ◽  
pp. 292-293
Author(s):  
A.M.M. Wetzels ◽  
L.A. Bastiaans ◽  
H.J.M. Goverde ◽  
A.P.E.M. Punt ◽  
J. Verbeet ◽  
...  

1999 ◽  
Vol 14 (9) ◽  
pp. 2350-2356 ◽  
Author(s):  
F. Devreker ◽  
M. Van den Bergh ◽  
J. Biramane ◽  
RM.L. Winston ◽  
Y. Englert ◽  
...  

2020 ◽  
Author(s):  
Ricardo Josue Acuña-González ◽  
Fela Vanesa Morales-Hernández ◽  
Jorge Skiold López-Canales ◽  
Jair Lozano-Cuenca ◽  
Mauricio Osorio-Caballero ◽  
...  

Abstract Background: Morphologic features are the most common criteria for selecting human embryo to be transferred to the receptive uterine cavity. However, such characteristics are not valid for embryos in cellular arrest. The aim of this study was to quantify the expression profile of hsa-miR-21-3p, -24-1-5p, -191-5p, and -372-5p on day 3 of culture media from in vitro fertilization (IVF) embryo that were implanted or failed to be implanted in patients (n=25 pregnant and 25, non-pregnant patients). Methods: Fifty patients were accepted in the Department of Reproductive Biology of a Hospital in México City, based on the Institutional inclusion criteria for in vitro fertilization. On day 3 of development, embryos were transferred to women, and the culture medium was collected from implanted embryos (n=25, pregnant patients) and non-implanted embryos (n=25, non-pregnant). In the culture medium, RNA was isolated using TRIzol reagent. MiRNA expression was detected through RT-PCR with specific primers. Expression bands were quantified using an optic density.Results: The expression profiles were compared between pregnant and non-pregnant patients revealing a significant 5.2-fold greater expression of hsa-miR-191-5p in the former group (p ≤0.001) and a significantly higher expression of hsa-miR-24-1-5p (p =0.043) in the latter. No significant difference was found between the two groups in regard hsa-miR-21-3p or hsa-miR-372-5p (p =0.41). Conclusions: According to the results, has-miR-191-5p could possibly be a possible biomarker of adequate human embryo development. This miRNA modulated IGF2BP-1 and IGF2R, which are associated with the implantation window. On the other hand, hsa-miR-24-1-5p may be related to a poor prognosis of human embryo development.


1985 ◽  
Vol 442 (1 In Vitro Fert) ◽  
pp. 336-341 ◽  
Author(s):  
MICHELLE PLACHOT ◽  
JACQUELINE MANDELBAUM ◽  
ANNE-MARIE JUNCA ◽  
JACQUES SALAT-BAROUX ◽  
JEAN COHEN

1996 ◽  
Vol 8 (5) ◽  
pp. 835 ◽  
Author(s):  
T Pinyopummintr ◽  
BD Bavister

Effects of amino acids on early bovine embryo development in vitro were examined using a chemically-defined, protein-free culture medium. Bovine embryos produced in vitro were cultured from 18 h to 72 h post insemination in a simple medium containing lactate as the only energy source except for the amino acid treatments. Subsequently, embryos were transferred to TCM-199 supplemented with serum for blastocyst development to substantiate their developmental competence. Treatments were: (1) non-essential amino acids from TCM-199 (NEA); (2) essential amino acids from TCM-199 (EA); (3) NEA+EA; (4) Eagle's minimum essential medium amino acids (MEM AA); (5) 11 amino acids present in HECM-6 (11 AA); and (6) 0.2 mM glutamine (GLN). A higher proportion of embryos (percentage of inseminated ova) cleaved to the > or = 8-cell stage by 72 h post insemination in NEA (56.7%), EA (41.2%), 11 AA (40.3%) and GLN (51.1%) than in either NEA+EA (30.0%) or MEM AA (33.1%). However, after transfer to complex medium, embryos that had developed in EA, as well as those in MEM AA or NEA+EA, produced significantly fewer blastocysts (37.1%, 34.4% and 25.6% respectively) than those in NEA (56.7%), GLN (48.9%) or 11 AA (37.7%). The ability of blastocysts to hatch from their zonae pellucidae was also affected by amino acid treatment during cleavage stages. The present study indicated that the addition of NEA or GLN or 11 AA to a chemically-defined culture medium during the cleavage phase of bovine embryo development increases their subsequent ability to reach the blastocyst stage. These data have implications for understanding the nutritional needs of bovine embryos produced in vitro and for optimizing the composition of culture media to support their development.


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