We hypothesized that neonatal seizures lead to increased Ca(2+) influx (nCa(2+)I) in neuronal nuclei of newborn rats and that such increase is nitric-oxide mediated. Neuronal nuclear (45)Ca(2+) influx (nCa(2+)I) was measured in neuronal nuclei of 25 10-day-old male rat-pups newborn brains. They were divided into five groups (n = 5/group). (I) control; (II) hypoxia without seizures; (III) hypoxia with seizures; (IV) kainate, 2 mg/kg intraperitoneal (i.p.)-induced seizures and (V) 7-nitroindazole (7-NINA), 1 mg/kg i.p. pretreated, kainate-induced seizures. nCa(2+)I was significantly (P < 0.05) increased following hypoxia or seizures (hypoxic- or kainate-induced). Post-hypoxic seizures further enhanced nCa(2+)I increase induced by hypoxia (P < 0.05). 7-NINA abated the nCa(2+)I increase induced by kainate. We conclude that (1) kainate or hypoxia-induced seizures in newborn rats modify the neuronal nuclear membrane function, resulting in increased nCa(2+)I, (2) seizures exacerbate the hypoxia-induced increased nCa(2+)I incurred after hypoxia and (3) intranuclear calcium surges during kainate-induced neonatal seizures are nitric oxide-mediated.

译文

:我们假设新生儿癫痫发作可导致新生大鼠神经核中Ca(2)内流(nCa(2)I)增加,并且这种增加是由一氧化氮介导的。神经元的核(45)Ca(2)涌入(nCa(2)I)在25个10天大的雄性大鼠幼崽的新生大脑的神经元核中进行了测量。他们分为五组(n = 5 /组)。 (I)控制; (II)缺氧而无癫痫发作; (III)缺氧伴癫痫发作; (IV)海藻酸盐,2 mg / kg腹膜内(i.p.)诱发的癫痫发作;(V)7-硝基吲唑(7-NINA),1 mg / kg i.p.预处理,海藻酸盐诱发的癫痫发作。缺氧或癫痫发作(缺氧或海因酸盐诱导)后,nCa(2)I显着升高(P <0.05)。缺氧后癫痫发作进一步增强了缺氧诱导的nCa(2)I增加(P <0.05)。 7-NINA抑制了海藻酸盐诱导的nCa(2)I增加。我们得出的结论是:(1)新生大鼠的海藻酸盐或低氧诱导的癫痫发作会改变神经元核膜功能,从而导致nCa(2)I升高,(2)癫痫发作会加剧低氧引起的低氧诱导的nCa(2)I升高,并且(3)在海藻酸盐诱发的新生儿癫痫发作期间,核内钙激增是由一氧化氮介导的。

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