Okuda S, Saito H, Katsuki H
Department of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, University of Tokyo, Japan.
Neuroscience. 1994 Dec;63(3):691-9. doi: 10.1016/0306-4522(94)90515-0.
Arachidonic acid (20:4) is a component of membrane lipids that has been implicated as a messenger both in physiological and pathophysiological processes, including ischemic injury and synaptic plasticity. In order to clarify direct trophic or toxic effects of arachidonic acid on central neurons, primary cultures of rat hippocampal neurons were exposed to arachidonic acid under chemically-defined conditions. Arachidonic acid present in the culture medium at concentrations over 5 x 10(-6) M showed profound toxicity, whereas at lower concentrations (10(-6) M) it significantly supported the survival of hippocampal neurons. These effects were not mimicked by oleic acid (18:1) or palmitic acid (16:0). The toxic action of 10(-5) M arachidonic acid was markedly and significantly prevented by a lipoxygenase inhibitor nordihydroguaiaretic acid (10(-6) M). AA861 and baicalein (each at 10(-6) M), a selective inhibitor for 5- and 12-lipoxygenase, respectively, also showed a significant protective effect, whereas cyclooxygenase inhibitor indomethacin (10(-5) M) had no effect. The toxic action was also prevented by an antioxidant alpha-tocopherol (10(-6) M), but not by superoxide dismutase (100 U/ml) or catalase (200 U/ml). The trophic effect of 10(-6) M arachidonic acid was not suppressed by the treatments listed above. At lower concentrations (10(-7)-10(-6) M), arachidonic acid promoted neurite elongation, which was not inhibited by nordihydroguaiaretic acid or indomethacin. Overall, arachidonic acid has both trophic and toxic actions on cultured hippocampal neurons, part of which involves its metabolism by lipoxygenases. The mechanisms and the physiological significance of these effects are discussed.
花生四烯酸(20:4)是膜脂的一种成分,在生理和病理生理过程中均被认为是一种信使,包括缺血性损伤和突触可塑性。为了阐明花生四烯酸对中枢神经元的直接营养或毒性作用,在化学定义的条件下,将大鼠海马神经元的原代培养物暴露于花生四烯酸中。培养基中浓度超过5×10(-6)M的花生四烯酸显示出显著的毒性,而在较低浓度(10(-6)M)时,它能显著支持海马神经元的存活。油酸(18:1)或棕榈酸(16:0)未表现出类似作用。10(-5)M花生四烯酸的毒性作用被脂氧合酶抑制剂去甲二氢愈创木酸(10(-6)M)显著且明显地抑制。AA861和黄芩素(均为10(-6)M),分别是5-和12-脂氧合酶的选择性抑制剂,也显示出显著的保护作用,而环氧合酶抑制剂吲哚美辛(10(-5)M)则无作用。抗氧化剂α-生育酚(10(-6)M)也能阻止毒性作用,但超氧化物歧化酶(100 U/ml)或过氧化氢酶(200 U/ml)则不能。上述处理并未抑制10(-6)M花生四烯酸的营养作用。在较低浓度(10(-7)-10(-6)M)时,花生四烯酸促进神经突伸长,这不受去甲二氢愈创木酸或吲哚美辛的抑制。总体而言,花生四烯酸对培养的海马神经元具有营养和毒性作用,其中部分作用涉及脂氧合酶对其的代谢。本文讨论了这些作用的机制和生理意义。