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Journal of reproduction and fertility1994; 102(2); 371-378; doi: 10.1530/jrf.0.1020371

In vitro development of day 2 embryos obtained from young, fertile mares and aged, subfertile mares.

Abstract: This study was designed to investigate the development of day 2 embryos obtained from young and aged mares, co-cultured with oviductal epithelial cells obtained from mares in each age group in a 2 x 2 crossover design. Young, fertile mares (n = 19; 2-7 years of age) and aged, subfertile, mares (n = 16; 17-24 years of age) were used as embryo and oviductal epithelial cell donors. Embryos (n = 37) were collected from the oviducts 2 days after ovulation and were paired (embryos obtained from young mares with embryos obtained from aged mares) so that eight pairs were co-cultured with young mare oviductal epithelial cells and eight pairs were co-cultured with aged mare oviductal epithelial cells. Five additional embryos obtained from young mares were co-cultured with oviductal epithelial cells from either young mares or aged mares but were not paired. Embryos were co-cultured for 7 days at 38.5 degrees C in 5% CO2 or until morphological degeneration was detected. The proportions of paired embryos that reached the blastocyst stage were similar for embryos obtained from young mares and embryos obtained from aged mares after co-culture with oviductal epithelial cells from young mares (6 of 8 versus 5 of 8) or from aged mares (6 of 8 versus 5 of 8), respectively. Although the overall rate of development of embryos to blastocyst from both young mares and aged mares was similar, blastocysts developing from embryos obtained from aged mares were inferior to blastocysts obtained from young mares in terms of number of cell nuclei, quality score, and diameter at day 7.(ABSTRACT TRUNCATED AT 250 WORDS)
Publication Date: 1994-11-01 PubMed ID: 7861390DOI: 10.1530/jrf.0.1020371Google Scholar: Lookup
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  • Comparative Study
  • Journal Article
  • Research Support
  • Non-U.S. Gov't
  • Research Support
  • U.S. Gov't
  • Non-P.H.S.

Summary

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The research focuses on comparing the development of early-stage embryos from young, fertile mares and aged, subfertile mares. The embryos were co-cultured with oviductal epithelial cells from both age groups, manifesting similar development rates, but the blastocysts from aged mares appeared inferior in various aspects.

Objective of the Research

  • This study aims to investigate the development of day-2 embryos obtained from young fertile mares and aged subfertile mares. The investigation also evaluates how these embryos develop when co-cultured with oviductal epithelial cells procured from utilized mares. The embryo and epithelial cell donors varied in their age and fertility condition.

Methodology Employed

  • The researchers leveraged a 2 x 2 crossover design for the study. The embryo and oviductal epithelial cell donors were young, fertile mares aged between 2 and 7 years old, and aged, subfertile mares aged between 17 and 24 years old.
  • The embryos were collected from the oviducts two days post ovulation and were paired, with embryos procured from young mares grouped with embryos taken from aged ones. Eight pairs of these embryos were co-cultured on young mare oviductal epithelial cells, and another eight pairs were co-cultured on aged mare oviductal epithelial cells.
  • A group of five additional embryos obtained from young mares were co-cultured with oviductal epithelial cells from either young or aged mares but were not paired.
  • Co-culturing lasted for seven days at a temperature of 38.5 degrees Celsius in a 5% CO2 environment or until morphological degeneration was observed.

Research Findings

  • The researchers found that the proportions of paired embryos that matured to the blastocyst stage did not show a significant difference for embryos sourced from both young and aged mares when co-cultured with either young or aged mare oviductal epithelial cells.
  • However, despite the overall development rate of embryos to the blastocyst stage being similar between the two groups, it was observed that blastocysts derived from embryos obtained from aged mares were inferior in certain parameters, such as the number of cell nuclei, quality score, and diameter at day 7, when compared to blastocysts obtained from young mares.

Cite This Article

APA
Brinsko SP, Ball BA, Miller PG, Thomas PG, Ellington JE. (1994). In vitro development of day 2 embryos obtained from young, fertile mares and aged, subfertile mares. J Reprod Fertil, 102(2), 371-378. https://doi.org/10.1530/jrf.0.1020371

Publication

ISSN: 0022-4251
NlmUniqueID: 0376367
Country: England
Language: English
Volume: 102
Issue: 2
Pages: 371-378

Researcher Affiliations

Brinsko, S P
  • Department of Clinical Sciences, New York State College of Veterinary Medicine, Cornell University, Ithaca 14853.
Ball, B A
    Miller, P G
      Thomas, P G
        Ellington, J E

          MeSH Terms

          • Aging / physiology
          • Animals
          • Blastocyst / cytology
          • Blastocyst / physiology
          • Cells, Cultured
          • Embryo, Mammalian / physiology
          • Embryonic and Fetal Development / physiology
          • Female
          • Fertility
          • Horses / physiology
          • Infertility, Female / embryology
          • Microscopy, Fluorescence

          Citations

          This article has been cited 3 times.
          1. Ashraf R, Rashid S, Rasheed I, Asif S. Early embryonic death in equines and camelids.. Open Vet J 2022 Nov-Dec;12(6):903-909.
            doi: 10.5455/OVJ.2022.v12.i6.16pubmed: 36777062google scholar: lookup
          2. Derisoud E, Jouneau L, Dubois C, Archilla C, Jaszczyszyn Y, Legendre R, Daniel N, Peynot N, Dahirel M, Auclair-Ronzaud J, Wimel L, Duranthon V, Chavatte-Palmer P. Maternal age affects equine day 8 embryo gene expression both in trophoblast and inner cell mass.. BMC Genomics 2022 Jun 15;23(1):443.
            doi: 10.1186/s12864-022-08593-7pubmed: 35705916google scholar: lookup
          3. Sadraie SH, Saito H, Kaneko T, Saito T, Hiroi M. Effects of aging on ovarian fecundity in terms of the incidence of apoptotic granulosa cells.. J Assist Reprod Genet 2000 Mar;17(3):168-73.
            doi: 10.1023/a:1009422323306pubmed: 10911578google scholar: lookup