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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Combined melatonin and adrenocorticotropic hormone treatment attenuates N-methyl-D-aspartate-induced infantile spasms in a rat model by regulating activation of the HPA axis
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Combined melatonin and adrenocorticotropic hormone treatment attenuates N-methyl-D-aspartate-induced infantile spasms in a rat model by regulating activation of the HPA axis

机译:结合的褪黑激素和肾上腺皮质激素治疗通过调节HPA轴的激活,通过调节对大鼠模型中的N-甲基-D-天冬氨酸诱导的婴儿痉挛

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摘要

Infantile spasms (IS) is a serious epileptic syndrome that frequently occurs in infancy. Adrenocorticotropic hormone (ACTH) is generally the first-line treatment for IS; however, side effects limit its application. Melatonin (MT) has been used in clinical treatment for sleep disorders with only minor side effects. Further, MT was shown to be a powerful anticonvulsant in an animal model of epilepsy. In this research, we aimed to compare the anticonvulsant efficacy of ACTH and/or MT for treatment of IS and explore the mechanisms underlying the anticonvulsant activity of MT, using an N-methyl-D-aspartate (NMDA)-induced IS model in neonatal rats following exposure to prenatal stress. Latency to the onset of spasms and the total number of spasms were recorded to assess spasm severity. Treatment with ACTH and/or MT significantly reduced the number of spasms and prolonged the latency period. Additionally, expression of GR-alpha, HDAC2, BNDF, TrkB, and C-Cbl were significantly increased by induction with NMDA, and this effect was reversed by ACTH and/or MT treatment. Hence, our data suggest that combined ACTH and MT treatment is effective for reducing the number of spasms and increasing the latency period in NMDA rats, by restoring dysregulation of the HPA axis. These findings have the potential to provide a new strategy for the treatment of IS.
机译:婴儿痉挛(IS)是一种严重的癫痫综合征,经常发生在婴儿期。促肾上腺皮质激素(ACTH)通常是is的一线治疗;然而,副作用限制了其应用。褪黑素(MT)已用于临床治疗睡眠障碍,但副作用很小。此外,MT在癫痫动物模型中被证明是一种强大的抗惊厥剂。在这项研究中,我们旨在比较ACTH和/或MT治疗IS的抗惊厥效果,并在暴露于产前应激的新生大鼠中使用N-甲基-D-天冬氨酸(NMDA)诱导的IS模型,探索MT抗惊厥活性的机制。记录痉挛发作的潜伏期和痉挛总数,以评估痉挛的严重程度。ACTH和/或MT治疗显著减少痉挛次数,延长潜伏期。此外,通过NMDA诱导,GRα、HDAC2、BNDF、TrkB和C-Cbl的表达显著增加,ACTH和/或MT治疗可逆转这种效应。因此,我们的数据表明,ACTH和MT联合治疗可通过恢复HPA轴的失调,有效减少NMDA大鼠的痉挛次数,延长潜伏期。这些发现有可能为IS的治疗提供新的策略。

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