Vaughan P F, Murphy M G, Ball S G
Department of Cardiovascular Studies, University of Leeds, England.
J Neurochem. 1993 Apr;60(4):1365-71. doi: 10.1111/j.1471-4159.1993.tb03297.x.
Nordihydroguaiaretic acid (NDGA; a lipoxygenase inhibitor), LY-270766 (an inhibitor of 5-lipoxygenase), and the diacylglycerol lipase inhibitor RG 80267 completely eliminated potassium-evoked release of [3H]-noradrenaline ([3H]NA) from the human neuroblastoma clone SH-SY5Y with IC50 values of 10, 15, and 30 microM, respectively. In contrast, these inhibitors only partially inhibited carbachol-evoked release and had little effect on the calcium ionophore A23187-evoked release of NA in this cell line. Arachidonic acid partially inhibited potassium- and A23187-evoked release but did not reverse the inhibition of potassium-evoked release observed in the presence of RG 80267. These studies suggest that arachidonic acid (or its lipoxygenase products) are not important intermediates in the regulation of exocytosis in SH-SY5Y. This conclusion is strengthened by our studies in which SH-SY5Y cells were grown in medium supplemented with bovine serum albumin-linoleic acid (50 microM). Under these conditions there was a selective increase in content of membrane polyunsaturated fatty acids of the omega 6 series, including arachidonic acid; however, these changes did not effect potassium-, veratridine-, carbachol-, or calcium ionophore-evoked release of [3H]NA.
去甲二氢愈创木酸(NDGA;一种脂氧合酶抑制剂)、LY-270766(一种5-脂氧合酶抑制剂)和二酰甘油脂肪酶抑制剂RG 80267可完全消除钾离子诱发的人神经母细胞瘤克隆SH-SY5Y细胞释放[3H]-去甲肾上腺素([3H]NA),其IC50值分别为10、15和30微摩尔。相比之下,这些抑制剂仅部分抑制卡巴胆碱诱发的释放,对该细胞系中钙离子载体A23187诱发的NA释放几乎没有影响。花生四烯酸部分抑制钾离子和A23187诱发的释放,但不能逆转在RG 80267存在下观察到的对钾离子诱发释放的抑制作用。这些研究表明,花生四烯酸(或其脂氧合酶产物)在SH-SY5Y细胞胞吐作用调节中不是重要的中间体。我们的研究进一步支持了这一结论,即在补充了牛血清白蛋白-亚油酸(50微摩尔)的培养基中培养SH-SY5Y细胞。在这些条件下,包括花生四烯酸在内的ω6系列膜多不饱和脂肪酸含量选择性增加;然而,这些变化并未影响钾离子、藜芦碱、卡巴胆碱或钙离子载体诱发的[3H]NA释放。