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内皮细胞增殖可能通过内源性脂氧合酶代谢产物的产生来介导。

Endothelial cell proliferation may be mediated via the production of endogenous lipoxygenase metabolites.

作者信息

Setty B N, Dubowy R L, Stuart M J

出版信息

Biochem Biophys Res Commun. 1987 Apr 14;144(1):345-51. doi: 10.1016/s0006-291x(87)80516-8.

Abstract

Endogenous regulators of endothelial cell proliferation have not been clearly defined. We investigated whether the cyclooxygenase and/or lipoxygenase metabolites are involved in this process, and report that lipoxygenase products can modulate endothelial cell growth. Nordihydroguaiaretic acid--a lipoxygenase inhibitor, inhibited endothelial cell proliferation as well as DNA synthesis. 5,8,11,14-Eicosatetraynoic acid--an inhibitor of both lipoxygenase and cyclooxygenase also inhibited endothelial cell DNA synthesis, while indomethacin--a selective cyclooxygenase inhibitor did not affect cell proliferation or DNA synthesis. While arachidonic acid stimulated DNA synthesis, this effect was completely abolished by nordihydroguaiaretic acid. These results demonstrate that products of the lipoxygenase pathway can affect endothelial cell proliferation.

摘要

内皮细胞增殖的内源性调节因子尚未明确界定。我们研究了环氧化酶和/或脂氧化酶代谢产物是否参与这一过程,并报告脂氧化酶产物可调节内皮细胞生长。去甲二氢愈创木酸——一种脂氧化酶抑制剂,抑制内皮细胞增殖以及DNA合成。5,8,11,14-二十碳四炔酸——一种脂氧化酶和环氧化酶的抑制剂,也抑制内皮细胞DNA合成,而吲哚美辛——一种选择性环氧化酶抑制剂,并不影响细胞增殖或DNA合成。虽然花生四烯酸刺激DNA合成,但这种作用被去甲二氢愈创木酸完全消除。这些结果表明,脂氧化酶途径的产物可影响内皮细胞增殖。

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