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钙拮抗剂对体外培养的大鼠脑内脂质过氧化或花生四烯酸诱导的线粒体肿胀的抑制作用。

Inhibitory effects of calcium antagonists on mitochondrial swelling induced by lipid peroxidation or arachidonic acid in the rat brain in vitro.

作者信息

Takei M, Hiramatsu M, Mori A

机构信息

Department of Neuroscience, Okayama University Medical School, Japan.

出版信息

Neurochem Res. 1994 Sep;19(9):1199-206. doi: 10.1007/BF00965156.

Abstract

Inhibitory effects of calcium antagonists, efonidipine (NZ-105), nicardipine, nifedipine, nimodipine and flunarizine, on mitochondrial swelling induced by lipid peroxidation or arachidonic acid in the rat brain in vitro were investigated. Mitochondrial swelling and lipid peroxidation induced by FeSO4 and ascorbic acid system showed a close and significant relationship. Mitochondrial swelling and lipid peroxidation induced by FeSO4 and ascorbic acid were inhibited by all of calcium antagonists tested. The order of inhibition was: flunarizine > nicardipine > efonidipine > nimodipine > nifedipine. This result suggests that calcium antagonists tested have anti-peroxidant activities resulting in protection of mitochondrial membrane damage and that each moiety of these structures would play an important role in appearance of anti-peroxidant activities. Furthermore, flunarizine and efonidipine inhibited mitochondrial swelling induced by arachidonic acid, which is not associated with lipid peroxidation. In contrast, nicardipine, nifedipine, and nimodipine did not inhibited this swelling. It is possible that flunarizine and efonidipine could directly interact with mitochondrial membrane. In conclusion, it is capable that calcium antagonists tested may protect from the membrane damage induced by lipid peroxidation and that flunarizine and efonidipine could stabilize the membrane, which is attributed to a direct interaction with the membrane.

摘要

研究了钙拮抗剂依福地平(NZ - 105)、尼卡地平、硝苯地平、尼莫地平和氟桂利嗪对体外大鼠脑内脂质过氧化或花生四烯酸诱导的线粒体肿胀的抑制作用。由硫酸亚铁和抗坏血酸系统诱导的线粒体肿胀与脂质过氧化呈现密切且显著的关系。所有测试的钙拮抗剂均抑制了由硫酸亚铁和抗坏血酸诱导的线粒体肿胀和脂质过氧化。抑制顺序为:氟桂利嗪>尼卡地平>依福地平>尼莫地平>硝苯地平。该结果表明,所测试的钙拮抗剂具有抗过氧化活性,从而保护线粒体膜免受损伤,并且这些结构的每个部分在抗过氧化活性的表现中都发挥着重要作用。此外,氟桂利嗪和依福地平抑制了由花生四烯酸诱导的线粒体肿胀,这与脂质过氧化无关。相反,尼卡地平、硝苯地平和尼莫地平并未抑制这种肿胀。氟桂利嗪和依福地平有可能直接与线粒体膜相互作用。总之,所测试的钙拮抗剂有可能保护免受脂质过氧化诱导的膜损伤,并且氟桂利嗪和依福地平可以稳定膜,这归因于它们与膜的直接相互作用。

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