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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Antidepressant drug treatments induce glial cell line-derived neurotrophic factor (GDNF) synthesis and release in rat C6 glioblastoma cells.
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Antidepressant drug treatments induce glial cell line-derived neurotrophic factor (GDNF) synthesis and release in rat C6 glioblastoma cells.

机译:抗抑郁药治疗可诱导胶质细胞源性神经营养因子(GDNF)合成并在大鼠C6胶质母细胞瘤细胞中释放。

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摘要

Modulation of neurotrophic factors to protect neurons from damage is proposed as a novel mechanism for the action of antidepressants. However, the effect of antidepressants on modulation of glial cell line-derived neurotrophic factor (GDNF), which has potent and widespread effects, remains unknown. Here, we demonstrated that long-term use of antidepressant treatment significantly increased GDNF mRNA expression and GDNF release in time- and concentration-dependent manners in rat C6 glioblastoma cells. Amitriptyline treatment also increased GDNF mRNA expression in rat astrocytes. GDNF release continued for 24 h following withdrawal of amitriptyline. Furthermore, following treatment with antidepressants belonging to several different classes (amitriptyline, clomipramine, mianserin, fluoxetine and paroxetine) significantly increased GDNF release, but which did not occur after treatment with non-antidepressant psychotropic drugs (haloperidol, diazepam and diphenhydramine). Amitriptyline-induced GDNF release was inhibited by U0126 (10 microM), a mitogen-activated protein kinase (MAPK)-extracellular signal-related kinase (ERK) kinase (MEK) inhibitor, but was not inhibited by H-89 (1 microM), a protein kinase A inhibitor, calphostin C (100 nM), a protein kinase C inhibitor and PD 169316 (10 microM), a p38 mitogen-activated protein kinase inhibitor. These results suggested that amitriptyline-induced GDNF synthesis and release occurred at the transcriptional level, and may be regulated by MEK/MAPK signalling. The enhanced and prolonged induction of GDNF by antidepressants could promote neuronal survival, and protect neurons from the damaging effects of stress. This may contribute to explain therapeutic action of antidepressants and suggest new strategies of pharmacological intervention.
机译:提出了调节神经营养因子以保护神经元不受损害的方法,作为抗抑郁药作用的新机制。然而,抗抑郁药对神经胶质细胞系神经营养因子(GDNF)的调节作用,具有有效和广泛的作用,仍然是未知的。在这里,我们证明了长期使用抗抑郁药可以显着提高大鼠C6胶质母细胞瘤细胞中GDNF mRNA的表达和GDNF的释放,呈时间和浓度依赖性。阿米替林治疗还增加了大鼠星形胶质细胞中GDNF mRNA的表达。停用阿米替林后,GDNF释放持续24小时。此外,在用属于几种不同类别的抗抑郁药(阿米替林,氯米帕明,米安色林,氟西汀和帕罗西汀)治疗后,GDNF的释放显着增加,但在使用非抗精神病药物(氟哌啶醇,地西and和苯海拉明)治疗后并未发生。阿米替林诱导的GDNF释放被有丝分裂原激活的蛋白激酶(MAPK)-细胞外信号相关激酶(ERK)激酶(MEK)抑制剂U0126(10 microM)抑制,但不受H-89(1 microM)抑制。 ,蛋白激酶A抑制剂,钙磷蛋白C(100 nM),蛋白激酶C抑制剂和PD 169316(10 microM),p38丝裂原活化蛋白激酶抑制剂。这些结果表明,阿米替林诱导的GDNF合成和释放发生在转录水平,并且可能受MEK / MAPK信号传导的调节。抗抑郁药增强和延长GDNF的诱导可以促进神经元存活,并保护神经元免受压力的破坏作用。这可能有助于解释抗抑郁药的治疗作用,并提出新的药理干预策略。

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