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Neurotropin 刺激脑源性神经营养因子的神经元表达。

Stimulated neuronal expression of brain-derived neurotrophic factor by Neurotropin.

机构信息

Department of Neurology, Fujita Health University School of Medicine, Kutsukake-cho, Toyoake 470-1192, Japan.

出版信息

Mol Cell Neurosci. 2010 Nov;45(3):226-33. doi: 10.1016/j.mcn.2010.06.013. Epub 2010 Jun 28.

Abstract

Expression of brain-derived neurotrophic factor (BDNF) was stimulated in human neuroblastoma SH-SY5Y cells by a nonprotein extract of inflamed rabbit skin inoculated with vaccinia virus (Neurotropin), an analgesic widely used in Japan for treatment of disorders associated with chronic pain, with the optimal dosage at 10mNU/mL. This stimulation was accompanied by activations of p42/44 MAP kinase, CREB and c-Fos expression. Inhibitors of MAP kinases or PI 3-kinase prevented the stimulatory action of Neurotropin, indicating that neuronal TrkB/CREB pathway mediates the action. Repetitive oral administration of Neurotropin (200NU/kg/day, 3months) prevented the age-dependent decline in hippocampal BDNF expression in Ts65Dn mice, a model of Down's syndrome. This effect was associated with the improvement of spatial cognition of the mice. These results open an intriguing new strategy in which Neurotropin may prove beneficial treatment for neurodegenerative disorders.

摘要

神经刺激素(Neurotropin)是一种在日本广泛用于治疗慢性疼痛相关疾病的镇痛药,它由接种牛痘病毒的兔炎性皮肤的非蛋白提取物制成,可刺激人神经母细胞瘤 SH-SY5Y 细胞表达脑源性神经营养因子(BDNF),在 10mNU/mL 的最佳剂量下刺激效果最佳。这种刺激伴随着 p42/44MAP 激酶、CREB 和 c-Fos 表达的激活。MAP 激酶或 PI3-激酶抑制剂可阻止神经刺激素的刺激作用,表明神经元 TrkB/CREB 途径介导了这种作用。重复口服神经刺激素(200NU/kg/天,3 个月)可预防 Ts65Dn 小鼠(唐氏综合征模型)海马 BDNF 表达随年龄增长而下降,这种作用与改善小鼠的空间认知能力有关。这些结果为神经刺激素可能成为治疗神经退行性疾病的有益治疗方法提供了一个有趣的新策略。

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