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Oxygen consumption and energy metabolism of the early mouse embryo

Oxygen consumption and energy metabolism of the early mouse embryo
Oxygen consumption and energy metabolism of the early mouse embryo
Oxygen consumption of preimplantation and early postimplantation mouse embryos has been measured using a novel noninvasive ultramicrofluorescence technique, based on an oil-soluble, nontoxic quaternary benzoid compound pyrene, whose fluorescence is quenched in the presence of oxygen. Pyruvate and glucose consumption, lactate production, and glycogen formation from glucose were also measured. Preimplantation mouse embryos of the strain CBA/Ca × C57BL/6 were cultured in groups of 10–30 in 2 μl of modified M2 medium containing 1 mmol l−1 glucose, 0 mmol l−1 lactate, and 0.33 mmol l−1 pyruvate, for between 4–6 hr. Day 6.5 and 7.5 embryos were cultured singly in 40 μl M2 medium for between 2–3 hr. Oxygen consumption was detected at all stages of development, including, for the first time, in the early postimplantation embryo. Consumption remained relatively constant from zygote to morula stages before increasing in the blastocyst and day 6.5–7.5 stages. When expressed as QO2 (μl/mg dry weight/hr), oxygen consumption was relatively constant from the one-cell to morula stages before increasing sharply at the blastocyst stage and declining to preblastocyst levels on days 6.5 and 7.5. Pyruvate was consumed during preimplantation stages, with glucose uptake undetectable until the blastocyst stage. Glucose was the main substrate consumed by the 6.5 and 7.5 day embryo. The proportions of glucose accounted for by lactate appearance were 81%, 86%, and 119% at blastocyst, day 6.5, and day 7.5 stages, respectively. The equivalent figures for glucose incorporated into glycogen were 10.36%, 0.21%, and 0.19%, respectively. The data are consistent with a switch from a metabolism dependent on aerobic respiration during early preimplantation stages to one dependent on both oxidative phosphorylation and aerobic glycolysis at the blastocyst stage, a pattern which is maintained on days 6.5 and 7.5. Our technique for measuring oxygen consumption may have diagnostic potential for selecting viable embryos for transfer following assisted conception techniques in man and domestic animals.
1040-452X
476-485
Houghton, F.D.
53946041-127e-45a8-9edb-bf4b3c23005f
Thompson, J.G.
685d4ca7-6b34-4fa4-a7d2-2f7f52c7aaec
Kennedy, C.J.
2837c7d9-48fa-488b-9685-19a21b36de8d
Leese, H.J.
1f369c23-4361-4534-a093-54699ec5eceb
Houghton, F.D.
53946041-127e-45a8-9edb-bf4b3c23005f
Thompson, J.G.
685d4ca7-6b34-4fa4-a7d2-2f7f52c7aaec
Kennedy, C.J.
2837c7d9-48fa-488b-9685-19a21b36de8d
Leese, H.J.
1f369c23-4361-4534-a093-54699ec5eceb

Houghton, F.D., Thompson, J.G., Kennedy, C.J. and Leese, H.J. (1996) Oxygen consumption and energy metabolism of the early mouse embryo. Molecular Reproduction and Development, 44 (4), 476-485. (doi:10.1002/(SICI)1098-2795(199608)44:4<476::AID-MRD7>3.0.CO;2-I).

Record type: Article

Abstract

Oxygen consumption of preimplantation and early postimplantation mouse embryos has been measured using a novel noninvasive ultramicrofluorescence technique, based on an oil-soluble, nontoxic quaternary benzoid compound pyrene, whose fluorescence is quenched in the presence of oxygen. Pyruvate and glucose consumption, lactate production, and glycogen formation from glucose were also measured. Preimplantation mouse embryos of the strain CBA/Ca × C57BL/6 were cultured in groups of 10–30 in 2 μl of modified M2 medium containing 1 mmol l−1 glucose, 0 mmol l−1 lactate, and 0.33 mmol l−1 pyruvate, for between 4–6 hr. Day 6.5 and 7.5 embryos were cultured singly in 40 μl M2 medium for between 2–3 hr. Oxygen consumption was detected at all stages of development, including, for the first time, in the early postimplantation embryo. Consumption remained relatively constant from zygote to morula stages before increasing in the blastocyst and day 6.5–7.5 stages. When expressed as QO2 (μl/mg dry weight/hr), oxygen consumption was relatively constant from the one-cell to morula stages before increasing sharply at the blastocyst stage and declining to preblastocyst levels on days 6.5 and 7.5. Pyruvate was consumed during preimplantation stages, with glucose uptake undetectable until the blastocyst stage. Glucose was the main substrate consumed by the 6.5 and 7.5 day embryo. The proportions of glucose accounted for by lactate appearance were 81%, 86%, and 119% at blastocyst, day 6.5, and day 7.5 stages, respectively. The equivalent figures for glucose incorporated into glycogen were 10.36%, 0.21%, and 0.19%, respectively. The data are consistent with a switch from a metabolism dependent on aerobic respiration during early preimplantation stages to one dependent on both oxidative phosphorylation and aerobic glycolysis at the blastocyst stage, a pattern which is maintained on days 6.5 and 7.5. Our technique for measuring oxygen consumption may have diagnostic potential for selecting viable embryos for transfer following assisted conception techniques in man and domestic animals.

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Published date: 1 August 1996
Additional Information: © 1996 Wiley-Liss, Inc.

Identifiers

Local EPrints ID: 457878
URI: http://eprints.soton.ac.uk/id/eprint/457878
ISSN: 1040-452X
PURE UUID: 990bbf12-443b-411a-92b8-08551213df21
ORCID for F.D. Houghton: ORCID iD orcid.org/0000-0002-5167-1694

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Date deposited: 21 Jun 2022 18:09
Last modified: 17 Mar 2024 03:05

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Contributors

Author: F.D. Houghton ORCID iD
Author: J.G. Thompson
Author: C.J. Kennedy
Author: H.J. Leese

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