Ee. Waugh et Rg. Wales, OXIDATIVE UTILIZATION OF GLUCOSE, ACETATE AND LACTATE BY EARLY PREIMPLANTATION SHEEP, MOUSE AND CATTLE EMBRYOS, Reproduction, fertility and development, 5(1), 1993, pp. 123-133
The production of radiolabelled CO2 from [U-C-14]glucose, [1-C-14]lact
ate, and [U-C-14]acetate was used to study the oxidative metabolism of
embryos recovered from sheep, mice and cattle. Sheep embryos showed a
n increasing capacity to oxidize glucose after the 4- to 8-cell stage
and oxidative turnover of this substrate at the blastocyst stage was f
our times that at the early stages. Decarboxylation of carbon-1 of lac
tate followed a pattern similar to that seen for glucose oxidation, bu
t acetate oxidation was tow and did not follow the trends with develop
ment seen for the other substrates. Furthermore, estimates of incorpor
ation of acetate into the macromolecules of sheep embryos were low com
pared with similar estimates for glucose and, unlike glucose, did not
increase with development. Oxidation of all three substrates by mouse
embryos increased with development but the rate Of CO2 production from
acetate was low compared with that from the other substrates. A combi
nation of lactate or glucose with acetate had no influence on the util
ization of acetate by mouse morulae/early blastocysts, nor did acetate
influence utilization of the other substrates. Cattle morulae/early b
lastocysts also produced more CO2 from glucose and lactate than from a
cetate and the incorporation of carbon from acetate into the macromole
cules of these embryos was less than from glucose. Overall, cattle emb
ryos showed the greatest ability to metabolize acetate but were not as
effective in using the other substrates as either sheep or mouse embr
yos at the same stage.