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Oxygen uptake and carbohydrate metabolism by in vitro derived bovine embryos

Oxygen uptake and carbohydrate metabolism by in vitro derived bovine embryos
Oxygen uptake and carbohydrate metabolism by in vitro derived bovine embryos
The consumption of oxygen, uptake of pyruvate and glucose and production of lactate were determined for groups of bovine embryos produced in vitro from the one-cell to the blastocyst stage (day 0–6 of culture). Measurements were made in Hepes-buffered synthetic oviduct fluid medium supplemented with 1.0 mmol pyruvate l−1, 10 mmol d,l-lactate l−1 and 1.5 mmol glucose l−1 and also 3 mg BSA ml−1 and, from day 5 of development, 10% (v/v) fetal calf serum. The amount of ATP production was determined from oxygen consumption and the proportion of glucose taken up that could be accounted for by lactate production. The data revealed that oxygen consumption was relatively constant from days 0–4 of culture (0.24–0.27 nl per embryo h−1), but increased with the initiation of compaction (0.39 nl per embryo h−1) and continued to increase with the formation and expansion of the blastocoel (0.9 nl per embryo h−1). Both pyruvate and glucose uptake followed similar patterns. Furthermore, when plotted against oxygen consumption, both pyruvate and glucose uptake increased significantly (P < 0.001) in a linear relationship (R2 = 0.61 and 0.49, respectively). Lactate production also increased with development and accounted for 40% of glucose uptake at day 0 of culture (putative zygotes), increasing to 70% by day 2 (eight-cell stage) and 100% of glucose uptake from day 4 of culture onwards. ATP production followed a similar pattern to that of oxygen consumption (60–85 pmol per embryo h−1 from day 0 to day 4) increasing with compaction (124 pmol per embryo h−1) and blastulation (221 pmol per embryo h−1). For precompaction stages, 93–96% of ATP production was derived from oxidative phosphorylation, decreasing to 82% with compaction. ATP produced by oxidative phosphorylation could be accounted for by the uptake of pyruvate, suggesting that bovine embryos produced in vitro utilize little endogenous substrates when appropriate exogenous substrates are present in the culture medium. The data revealed that bovine embryos were dependent on oxidative phosphorylation for energy (ATP) production at all stages of pre-elongation development, with perhaps a shift in dependence towards glycolysis in conjunction with compaction. It follows that oxidizable substrates, such as pyruvate and certain amino acids, are preferred in embryo culture medium during development in vitro.
299-306
Thompson, J.G.
685d4ca7-6b34-4fa4-a7d2-2f7f52c7aaec
Partridge, R.J.
125ec66c-3117-4945-90b5-516f17b20646
Houghton, F.D.
53946041-127e-45a8-9edb-bf4b3c23005f
Cox, C.I.
35ee0a4a-ecb5-4f9e-b6de-3ab82fd5b8b3
Leese, H.J.
1f369c23-4361-4534-a093-54699ec5eceb
Thompson, J.G.
685d4ca7-6b34-4fa4-a7d2-2f7f52c7aaec
Partridge, R.J.
125ec66c-3117-4945-90b5-516f17b20646
Houghton, F.D.
53946041-127e-45a8-9edb-bf4b3c23005f
Cox, C.I.
35ee0a4a-ecb5-4f9e-b6de-3ab82fd5b8b3
Leese, H.J.
1f369c23-4361-4534-a093-54699ec5eceb

Thompson, J.G., Partridge, R.J., Houghton, F.D., Cox, C.I. and Leese, H.J. (1996) Oxygen uptake and carbohydrate metabolism by in vitro derived bovine embryos. Journal of Reproduction and Fertility, 106 (2), 299-306. (doi:10.1530/jrf.0.1060299).

Record type: Article

Abstract

The consumption of oxygen, uptake of pyruvate and glucose and production of lactate were determined for groups of bovine embryos produced in vitro from the one-cell to the blastocyst stage (day 0–6 of culture). Measurements were made in Hepes-buffered synthetic oviduct fluid medium supplemented with 1.0 mmol pyruvate l−1, 10 mmol d,l-lactate l−1 and 1.5 mmol glucose l−1 and also 3 mg BSA ml−1 and, from day 5 of development, 10% (v/v) fetal calf serum. The amount of ATP production was determined from oxygen consumption and the proportion of glucose taken up that could be accounted for by lactate production. The data revealed that oxygen consumption was relatively constant from days 0–4 of culture (0.24–0.27 nl per embryo h−1), but increased with the initiation of compaction (0.39 nl per embryo h−1) and continued to increase with the formation and expansion of the blastocoel (0.9 nl per embryo h−1). Both pyruvate and glucose uptake followed similar patterns. Furthermore, when plotted against oxygen consumption, both pyruvate and glucose uptake increased significantly (P < 0.001) in a linear relationship (R2 = 0.61 and 0.49, respectively). Lactate production also increased with development and accounted for 40% of glucose uptake at day 0 of culture (putative zygotes), increasing to 70% by day 2 (eight-cell stage) and 100% of glucose uptake from day 4 of culture onwards. ATP production followed a similar pattern to that of oxygen consumption (60–85 pmol per embryo h−1 from day 0 to day 4) increasing with compaction (124 pmol per embryo h−1) and blastulation (221 pmol per embryo h−1). For precompaction stages, 93–96% of ATP production was derived from oxidative phosphorylation, decreasing to 82% with compaction. ATP produced by oxidative phosphorylation could be accounted for by the uptake of pyruvate, suggesting that bovine embryos produced in vitro utilize little endogenous substrates when appropriate exogenous substrates are present in the culture medium. The data revealed that bovine embryos were dependent on oxidative phosphorylation for energy (ATP) production at all stages of pre-elongation development, with perhaps a shift in dependence towards glycolysis in conjunction with compaction. It follows that oxidizable substrates, such as pyruvate and certain amino acids, are preferred in embryo culture medium during development in vitro.

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Published date: 1 March 1996
Additional Information: Copyright: Journals of Reproduction and Fertility Ltd.

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Local EPrints ID: 457881
URI: http://eprints.soton.ac.uk/id/eprint/457881
PURE UUID: 10c414b4-4a45-4cfc-be7b-836965a6ed08
ORCID for F.D. Houghton: ORCID iD orcid.org/0000-0002-5167-1694

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Date deposited: 21 Jun 2022 18:10
Last modified: 17 Mar 2024 03:05

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Contributors

Author: J.G. Thompson
Author: R.J. Partridge
Author: F.D. Houghton ORCID iD
Author: C.I. Cox
Author: H.J. Leese

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