TY - JOUR
T1 - Dichloroacetic acid accelerates initial development of 2-cell murine embryos in vitro
AU - Penzias, Alan S.
AU - Rossi, Gabriele
AU - Gutmann, Jacqueline N.
AU - Haj-Hassan, Lamia
AU - Leykin, Lucy
AU - Diamond, Michael Peter
N1 - Funding Information:
From the Depurtment of Obstetrics and Gynecology, Division of Reproductive Endocrinology. Yale Universit?; School of Medicine, New Haven, CT. Submitted June 23, 199.2; accepted January 8. 1993. Supported in part by an ACOGlMead Johnson Clinical Research Fellowship (1992-93, A.S.P.) and an lstituto Scientifico S. Raffaele (Milan, Ita&) Research Training Fellowship (G.R.). Presented at the 39th Annual Meeting of the Society for Gynecologic Investigation, San Antonio, TX, March 18-21, 1992 (abstract no. 526). Present address: M. P.D., Vanderbilt University School of Medicine, Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology Nashville, TN. Address reprint requests to Alan S. Penzias, MD, Tufts University School of Medicine. New England Medical Center, Department of Obstetrics and Gynecology, 750 Washington St, Box 36. Boston, MA 02111. Copyright 0 1993 by W.B. Saunders Companv 0026-049.519314209-0001$03,00~0
PY - 1993/9
Y1 - 1993/9
N2 - Preimplantation embryos up to the 8-cell stage of development use lactate and pyruvate but not glucose or Krebs cycle intermediates to support growth, development, and cleavage. The dominant effect of dichloroacetic acid (DCA) is the irreversible stimulation of pyruvate dehydrogenase (PDH) activity, thus accelerating the oxidative metabolism of pyruvate and lactate. To test the hypothesis that early induction of oxidative metabolism in 2-cell murine embryos accelerates preimplantation embryo cleavage rates, female B6C3F1 mice at 6 to 8 weeks of age were superovulated with pregnant mare serum gonadotropin (PMSG) and human chorionic gonadotropin (hCG) and mated. All 2-cell stage embryos were randomly assigned to culture media with or without 130 μg/mL DCA. The developmental stage of all embryos was then noted every 24 hours for a total of 72 hours. Chi-square analysis and the method of average rank sum were used to compare the distribution of embryos at each observation point. At 24 hours, DCA-exposed embryos had achieved an advanced stage of growth and development relative to controls (average rank sum, P = .026; chi-square distribution, P = .047). Subsequently, at 48 and 72 hours, neither the average rank sum nor the chi-square distribution was different. Our data suggest that DCA accelerates early growth and development of murine embryos before implantation, possibly through the early induction of oxidative metabolism.
AB - Preimplantation embryos up to the 8-cell stage of development use lactate and pyruvate but not glucose or Krebs cycle intermediates to support growth, development, and cleavage. The dominant effect of dichloroacetic acid (DCA) is the irreversible stimulation of pyruvate dehydrogenase (PDH) activity, thus accelerating the oxidative metabolism of pyruvate and lactate. To test the hypothesis that early induction of oxidative metabolism in 2-cell murine embryos accelerates preimplantation embryo cleavage rates, female B6C3F1 mice at 6 to 8 weeks of age were superovulated with pregnant mare serum gonadotropin (PMSG) and human chorionic gonadotropin (hCG) and mated. All 2-cell stage embryos were randomly assigned to culture media with or without 130 μg/mL DCA. The developmental stage of all embryos was then noted every 24 hours for a total of 72 hours. Chi-square analysis and the method of average rank sum were used to compare the distribution of embryos at each observation point. At 24 hours, DCA-exposed embryos had achieved an advanced stage of growth and development relative to controls (average rank sum, P = .026; chi-square distribution, P = .047). Subsequently, at 48 and 72 hours, neither the average rank sum nor the chi-square distribution was different. Our data suggest that DCA accelerates early growth and development of murine embryos before implantation, possibly through the early induction of oxidative metabolism.
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U2 - 10.1016/0026-0495(93)90260-U
DO - 10.1016/0026-0495(93)90260-U
M3 - Article
C2 - 8412755
AN - SCOPUS:0027383836
SN - 0026-0495
VL - 42
SP - 1077
EP - 1080
JO - Metabolism: Clinical and Experimental
JF - Metabolism: Clinical and Experimental
IS - 9
ER -