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Docosahexaenoic Acid Is a Potent Inhibitor of Rat Uterine Stromal Cell Proliferation

The effect of different families of fatty acids on the proliferation of rat uterine stromal cells (U III) was studied. Docosahexaenoic acid (DHA) exerted a strong and dose-dependent inhibitory effect (IC 50 ∼ 2 μM), whereas arachidonic acid (AA) stimulated U III cell proliferation at the optimal con...

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Published in:Biochemical and biophysical research communications 1995-02, Vol.207 (3), p.1015-1021
Main Authors: Tessier, C., Fayard, J.M., Cohen, H., Pageaux, J.F., Lagarde, M., Laugier, C.
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container_issue 3
container_start_page 1015
container_title Biochemical and biophysical research communications
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creator Tessier, C.
Fayard, J.M.
Cohen, H.
Pageaux, J.F.
Lagarde, M.
Laugier, C.
description The effect of different families of fatty acids on the proliferation of rat uterine stromal cells (U III) was studied. Docosahexaenoic acid (DHA) exerted a strong and dose-dependent inhibitory effect (IC 50 ∼ 2 μM), whereas arachidonic acid (AA) stimulated U III cell proliferation at the optimal concentration of 10 μM. Oleic, linoleic and linolenic acids were ineffective from 0.1 to 10 μM. The inhibitory effect of DHA was independent of the eicosanoid biosynthesis and lipid peroxidation, since it was not reversed by the addition of the antioxidant BHT and no significant production of oxidized species from DHA occurred in our culture conditions.
doi_str_mv 10.1006/bbrc.1995.1286
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ispartof Biochemical and biophysical research communications, 1995-02, Vol.207 (3), p.1015-1021
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1090-2104
language eng
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source ScienceDirect Journals
subjects Animals
Arachidonic Acid - pharmacology
Butylated Hydroxytoluene - pharmacology
Cell Division - drug effects
Cells, Cultured
DNA - biosynthesis
Docosahexaenoic Acids - administration & dosage
Docosahexaenoic Acids - pharmacology
Dose-Response Relationship, Drug
Fatty Acids - pharmacology
Female
Lipid Peroxidation - drug effects
Rats
Stromal Cells - cytology
Uterus - cytology
title Docosahexaenoic Acid Is a Potent Inhibitor of Rat Uterine Stromal Cell Proliferation
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