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双相情感障碍:源于心境稳定剂的分子和细胞作用机制。

Bipolar disorder: leads from the molecular and cellular mechanisms of action of mood stabilizers.

作者信息

Manji H K, Moore G J, Chen G

机构信息

Laboratory of Molecular Pathophysiology, Wayne State University School of Medicine, Detroit, Michigan, USA.

出版信息

Br J Psychiatry Suppl. 2001 Jun;41:s107-19.

Abstract

BACKGROUND

New research is dramatically altering our understanding of the molecular mechanisms underlying neuronal communication.

AIM

To elucidate the molecular mechanisms underlying the therapeutic effects of mood stabilizers.

METHOD

Results from integrated clinical and laboratory studies are reviewed.

RESULTS

Chronic administration of lithium and valproate produced a striking reduction in protein kinase C (PKC) isozymes in rat frontal cortex and hippocampus. In a small study, tamoxifen (also a PKC inhibitor) had marked antimanic efficacy. Both lithium and valproate regulate the DNA binding activity of the activator protein I family of transcription factors. Using mRNA differential display, it was also shown that chronic administration of lithium and valproate modulates expression of several genes. An exciting finding is that of a robust elevation in the levels of the cytoprotective protein, bcl-2.

CONCLUSIONS

The results suggest that regulation of signalling pathways may play a major part in the long-term actions of mood stabilizers. Additionally, mood stabilizers may exert underappreciated neuroprotective effects.

摘要

背景

新的研究正在极大地改变我们对神经元通讯潜在分子机制的理解。

目的

阐明心境稳定剂治疗作用的潜在分子机制。

方法

综述综合临床和实验室研究的结果。

结果

长期给予锂盐和丙戊酸盐可使大鼠额叶皮质和海马中的蛋白激酶C(PKC)同工酶显著减少。在一项小型研究中,他莫昔芬(也是一种PKC抑制剂)具有显著的抗躁狂疗效。锂盐和丙戊酸盐均可调节转录因子激活蛋白I家族的DNA结合活性。利用mRNA差异显示技术还表明,长期给予锂盐和丙戊酸盐可调节多个基因的表达。一个令人兴奋的发现是细胞保护蛋白bcl-2水平显著升高。

结论

结果表明,信号通路的调节可能在心境稳定剂的长期作用中起主要作用。此外,心境稳定剂可能具有未被充分认识的神经保护作用。

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