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Protection of flunarizine on cerebral mitochondria injury induced by cortical spreading depression under hypoxic conditions

机译:氟尿利嗪对低氧条件下皮质扩散抑制所致脑线粒体损伤的保护

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摘要

A rat cortical spreading depression (CSD) model was established to explore whether cerebral mitochondria injury was induced by CSD under both normoxic and hypoxic conditions and whether flunarizine had a protective effect on cerebral mitochondria. SD rats, which were divided into seven groups, received treatment as follows: no intervention (control Group I); 1 M NaCl injections (Group II); 1 M KCl injections (Group III); intraperitoneal flunarizine (3 mg/kg) 30 min before KCl injections (Group IV); 14% O2 inhalation before NaCl injections (Group V); 14% O2 inhalation followed by KCl injections (Group VI); 14% O2 inhalation and intraperitoneal flunarizine followed by KCl injections (Group VII). Following treatment, brains were removed for the analysis of mitochondria transmembrane potential (MMP) and oxidative respiratory function after recording the number, amplitude and duration of CSD. The duration of CSD was significantly longer in Group VI than that in Group III. The number and duration of CSD in Group VII was significantly lower than that in Group VI. MMP in Group VI was significantly lower than that in Group III, and MMP in Group VII was significantly higher than that in Group VI. State 4 respiration in Group VI was significantly higher than that in Group III, and state 3 respiration in Group VII was significantly higher than that in Group VI. Respiration control of rate in Group VII was also significantly higher than that in Group VI. Thus, we concluded that aggravated cerebral mitochondria injury might be attributed to CSD under hypoxic conditions. Flunarizine can alleviate such cerebral mitochondria injury under both normoxic and hypoxic conditions.
机译:建立了大鼠皮层扩展抑郁症(CSD)模型,以探讨在缺氧和缺氧条件下CSD是否均可诱发脑线粒体损伤,氟纳利嗪是否对脑线粒体具有保护作用。分为7组的SD大鼠接受以下治疗:不干预(对照组I); 1 M NaCl注射液(II组); 1 M KCl注射液(III组);注射氯化钾前30分钟腹腔内注射氟那利嗪(3 mg / kg)(第IV组);注射NaCl之前吸入14%的O2(V组);吸入14%的氧气,然后注射氯化钾(VI组);吸入14%O2并腹膜内注射氟硝嗪,然后注射氯化钾(第VII组)。治疗后,在记录CSD的数量,幅度和持续时间后,取出大脑以分析线粒体跨膜电位(MMP)和氧化呼吸功能。 VI组的CSD持续时间明显长于III组。 VII组的CSD数量和持续时间显着低于VI组。第六组的MMP显着低于第三组,第七组的MMP显着高于第六组。第六组的状态4呼吸显着高于第三组,第七组的状态3呼吸显着高于第六组。第七组的呼吸控制率也显着高于第六组。因此,我们得出的结论是,在缺氧条件下,脑线粒体损伤加剧可能归因于CSD。在正常氧和缺氧条件下,氟硝利嗪可以减轻这种脑线粒体损伤。

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