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Embryotrophic effects of ethylenediaminetetraacetic acid and hemoglobin on in vitro porcine embryos development
This study investigated the embryotrophic effects of ethylenediaminetetraacetic acid (EDTA) and hemoglobin (Hb) on porcine preimplantation embryo development. Porcine embryos produced by in vitro maturation/fertilization were cultured for 6 days in modified North Carolina State University-23 medium...
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Published in: | Theriogenology 2006-07, Vol.66 (2), p.449-455 |
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Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | This study investigated the embryotrophic effects of ethylenediaminetetraacetic acid (EDTA) and hemoglobin (Hb) on porcine preimplantation embryo development. Porcine embryos produced by in vitro maturation/fertilization were cultured for 6 days in modified North Carolina State University-23 medium (mNCSU-23) supplemented with EDTA and/or Hb. In Exp. 1, culturing porcine zygotes with 100
μM EDTA significantly increased cleavage frequencies (85.3%) at 48
h post insemination and the number of inner cell mass (ICM) (9.6
±
5.5) compared to the control (7.0
±
2.8). However, 100
μM EDTA did not improve blastocyst formation compared to 0, 1 or 10
μM EDTA. In Exp. 2, in vitro fertilized oocytes were cultured with 0, 1 or 10
μg/ml Hb. Culturing with Hb did not promote porcine embryo development, but significantly increased the cell numbers of blastocysts in 1
μg/ml Hb compared to 0 or 10
μg/ml Hb. In Exp. 3, culturing embryos with 100
μM EDTA
+
1
μg/ml Hb significantly improved frequencies of cleavage, blastocyst formation, and total cell numbers in blastocysts compared to the control. Moreover, 100
μM EDTA, 1
μg/ml Hb and their combination reduced reactive oxygen species (ROS) accumulation and decreased the incidence of apoptosis. In conclusion, the present study clearly demonstrated that the combining treatment of EDTA and Hb improved IVF porcine embryo development. |
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ISSN: | 0093-691X 1879-3231 |
DOI: | 10.1016/j.theriogenology.2005.12.008 |