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on rat blastocyst growth and glucose metabolism
Tumour necrosis factor
(TNF-
) synthesis has recently been described in the uterus during the preimplantation phase of pregnancy. The present study was undertaken to determine whether preimplantation embryos are a potential target for TNF-
in rats. First, the expression of TNF-
receptors by blastocysts was demonstrated by ligand binding assay with human 125I-labelled TNF-
and reverse transcription–amplification for the p60 receptor form. The functionality of these receptors was then assessed by incubating blastocysts with 3 nmol mouse TNF-
l–1 in vitro and determining their morphology and the number of cells after 24 h. At that concentration, cell proliferation in blastocysts was inhibited by TNF-
but this was not accompanied by any change in the morphology of the embryos. Similar results were obtained when lower doses of TNF-
(30 and 300 pmol l–1) were tested. The rate of glucose consumption of rat blastocysts exposed to 3 nmol TNF-
l–1 was not altered when they were incubated with the cytokine for 4 h, but the rate of glucose incorporation decreased over the same period. Our data indicate that rat blastocysts are responsive to physiological concentrations of TNF-
and that this cytokine has the potential to influence the preimplantation development of rats.
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