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Lipoxygenase products of arachidonic acid stimulate LHRH release from rat median eminence.

作者信息

Gerozissis K, Vulliez B, Saavedra J M, Murphy R C, Dray F

出版信息

Neuroendocrinology. 1985 Mar;40(3):272-6. doi: 10.1159/000124084.

DOI:10.1159/000124084
PMID:3921861
Abstract

Exogenous arachidonic acid (AA) incubated in presence of male rat hypothalamus, shows a low rate of conversion (less than 1%) of the substrate with a major product, identified as 12-hydroxyeicosatetraenoic acid (12-HETE) by reverse phase-high performance liquid chromatography (rpHPLC) and gas chromatography-mass spectrometry (GC-MS). Furthermore, immunoreactive 12-HETE estimated after purification on rpHPLC is produced by hypothalamus slices or median eminences (MEs) incubated in absence of any exogenous precursor. The effect of 12-HETE was tested on the release of LHRH from rat MEs after a 30-min incubation and was compared to the effect of another lipoxygenase product, 5-HETE, and to the well-known stimulatory effect of prostaglandin E2 (PGE2). The three AA metabolites stimulate LHRH release. A significant stimulatory effect on LHRH release is obtained with 10(-9) M of 12-HETE and only with 10(-8) M of 5-HETE or PGE2. Furthermore, the effect of higher concentrations is different according to the eicosanoid tested. The maximal response (176% of the control) is reached with 12-HETE at 10(-8) M. No significant change is observed at 10(-7) and 10(-6) M. The response with 5-HETE is also maximal (162% of the control) at 10(-8) M but decreases significantly (only 117% of the control) at 10(-6) M. The amplitude of the response to PGE2 is larger and higher, reaching a plateau (300% of the control) at 10(-6) M. 12-HETE has no effect on somatostatin (SRIF), release, as already known for PGE2.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

相似文献

1
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Neuroendocrinology. 1985 Mar;40(3):272-6. doi: 10.1159/000124084.
2
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引用本文的文献

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Specific delta-opioid antagonists exert an agonist-independent inhibitory effect, similar to the agonist, on the release of GnRH in vitro.特异性δ阿片受体拮抗剂在体外对促性腺激素释放激素(GnRH)的释放发挥与激动剂相似的、不依赖激动剂的抑制作用。
Cell Mol Neurobiol. 1995 Aug;15(4):389-400. doi: 10.1007/BF02071875.
2
Brain 12-HETE formation in different species, brain regions, and in brain microvessels.
Neurochem Res. 1987 Nov;12(11):1029-33. doi: 10.1007/BF00970932.
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Possible involvement of lipoxygenase pathway of arachidonic acid in rat pituitary hormone release in vitro.花生四烯酸的脂氧合酶途径可能参与大鼠垂体激素的体外释放。
J Endocrinol Invest. 1988 Dec;11(11):805-8. doi: 10.1007/BF03350230.