首页> 外文期刊>Brain Sciences >l -Carnitine Modulates Epileptic Seizures in Pentylenetetrazole-Kindled Rats via Suppression of Apoptosis and Autophagy and Upregulation of Hsp70
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l -Carnitine Modulates Epileptic Seizures in Pentylenetetrazole-Kindled Rats via Suppression of Apoptosis and Autophagy and Upregulation of Hsp70

机译:l-肉碱通过抑制细胞凋亡,自噬和Hsp70的上调来调节戊四唑点燃的大鼠的癫痫发作。

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l -Carnitine is a unique nutritional supplement for athletes that has been recently studied as a potential treatment for certain neuropsychiatric disorders. However, its efficacy in seizure control has not been investigated. Sprague Dawley rats were randomly assigned to receive either saline (Sal) (negative control) or pentylenetetrazole (PTZ) 40 mg/kg i.p. × 3 times/week × 3 weeks. The PTZ group was further subdivided into two groups, the first received oral l -carnitine ( l -Car) (100 mg/kg/day × 4 weeks) (PTZ + l -Car), while the second group received saline (PTZ + Sal). Daily identification and quantification of seizure scores, time to the first seizure and the duration of seizures were performed in each animal. Molecular oxidative markers were examined in the animal brains. l -Car treatment was associated with marked reduction in seizure score ( p = 0.0002) that was indicated as early as Day 2 of treatment and continued throughout treatment duration. Furthermore, l -Car significantly prolonged the time to the first seizure ( p 0.0001) and shortened seizure duration ( p = 0.028). In addition, l -Car administration for four weeks attenuated PTZ-induced increase in the level of oxidative stress marker malondialdehyde (MDA) ( p 0.0001) and reduced the activity of catalase enzyme ( p = 0.0006) and increased antioxidant GSH activity ( p 0.0001). Moreover, l -Car significantly reduced PTZ-induced elevation in protein expression of caspase-3 ( p 0.0001) and β-catenin ( p 0.0001). Overall, our results suggest a potential therapeutic role of l -Car in seizure control and call for testing these preclinical results in a proof of concept pilot clinical study.
机译:l-肉碱是运动员的独特营养补充剂,最近已被研究作为某些神经精神疾病的潜在疗法。然而,尚未研究其在癫痫发作控制中的功效。将Sprague Dawley大鼠随机分配接受40 mg / kg i.p.的生理盐水(Sal)(阴性对照)或戊四氮(PTZ)。 ×3次/周×3周。 PTZ组又分为两组,第一组口服口服左旋肉碱(l-Car)(100 mg / kg /天×4周)(PTZ + l-Car),第二组接受盐水(PTZ +萨尔)。对每只动物进行每日鉴定和量化癫痫发作分数,第一次发作的时间和癫痫发作的持续时间。在动物脑中检查了分子氧化标记。 l-汽车治疗与癫痫发作分数显着降低有关(p = 0.0002),这在治疗的第2天就已表明,并在整个治疗过程中持续存在。此外,l -Car显着延长了首次发作的时间(p <0.0001)并缩短了发作时间(p = 0.028)。此外,l -Car施用4周可减轻PTZ诱导的氧化应激标志物丙二醛(MDA)水平的升高(p <0.0001)并降低过氧化氢酶的活性(p = 0.0006)和增加的抗氧化剂GSH活性(p <0.0001)。此外,l -Car显着降低了PTZ诱导的caspase-3(p <0.0001)和β-catenin(p <0.0001)蛋白表达的升高。总体而言,我们的结果表明l -Car在癫痫发作控制中的潜在治疗作用,并要求在概念验证的临床试验研究中测试这些临床前结果。

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