5-hydroxy-6-8-11-14-eicosatetraenoic-acid has been researched along with 5-6-epoxy-8-11-14-eicosatrienoic-acid* in 2 studies
2 other study(ies) available for 5-hydroxy-6-8-11-14-eicosatetraenoic-acid and 5-6-epoxy-8-11-14-eicosatrienoic-acid
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5,6-Epoxyeicosatrienoic acid stimulates growth hormone release in rat anterior pituitary cells.
The effect of arachidonic acid and some of its metabolites have been examined in rat anterior pituitary cells for their ability to release growth hormone. The cytochrome P-450 metabolite, 5,6-epoxyeicosatrienoic acid is a much more effective growth-hormone releasing agent than 15-hydroxyeicosatetraenoic acid, 15-hydroxyeicosatetraenoic acid methyl ester, 5-hydroxyeicosatetraenoic acid or arachidonic acid. The release of growth hormone is rapid, dose-dependent and reaches an apparent saturation after eight minutes. These studies described herein provide evidence that lipoxygenase and cyclooxygenase products of arachidonic acid are less potent while cytochrome P-450 products are more potent in the release of growth hormone from anterior pituitary cells. Topics: 8,11,14-Eicosatrienoic Acid; Animals; Arachidonic Acids; Cells, Cultured; Fatty Acids, Unsaturated; Female; Growth Hormone; Hydroxyeicosatetraenoic Acids; Kinetics; Pituitary Gland, Anterior; Rats; Rats, Inbred F344 | 1989 |
Epoxy derivatives of arachidonic acid are potent stimulators of prolactin secretion.
Arachidonic acid is metabolized to three distinct classes of metabolites: cyclooxygenase produces prostaglandins, prostacyclins, and thromboxanes; lipoxygenase produces hydroperoxyeicosatetraenoic acids and, epoxygenase, a NADPH-dependent cytochrome P-450 enzyme, produces epoxyeicosatrienoic acids. Addition of 5,6-epoxyeicosatrienoic acid (5,6-EET) to GH3 cells, a rat anterior pituitary cell line, produces a rapid, dose-dependent stimulation of prolactin (PRL) release. Incubation with arachidonic acid (AA) was ineffective at increasing PRL release. The lipoxygenase metabolite 5-hydroxyeicosatetraenoic acid (5-HETE), however, increased PRL release from GH3 cells but with a much lower maximal response than 5,6-EET. We examined the role of metabolism inhibitors in 5,6-EET-mediated PRL release. Microsomal and cytosolic epoxide hydrolase (EH) inhibitors do not alter 5,6-EET-induced PRL release, suggesting that EH does not play a significant role in 5,6-EET mediated PRL release from GH3 cells. A chemical analog of 5,6-EET wherein the epoxide oxygen is replaced with a sulfur to afford 5,6-thioepoxyeicosatrienoic acid was also tested and found to stimulate the release of PRL, although not to the same extent as 5,6-EET. Although 5-HETE tends to increase PRL release from GH3 cells, 5,6-EET is significantly more potent at the stimulation of PRL release from GH3 cells. Topics: 8,11,14-Eicosatrienoic Acid; Animals; Arachidonic Acids; Cell Line; Epoxide Hydrolases; Epoxy Compounds; Hydroxyeicosatetraenoic Acids; Pituitary Gland, Anterior; Prolactin; Rats | 1987 |