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环磷酸腺苷对大鼠大脑皮质神经元原代培养物中即刻早期基因的诱导作用。

Induction of immediate early genes by cyclic AMP in primary cultures of neurons from rat cerebral cortex.

作者信息

Vaccarino F M, Hayward M D, Le H N, Hartigan D J, Duman R S, Nestler E J

机构信息

Department of Psychiatry, Yale University School of Medicine, New Haven, CT 06508.

出版信息

Brain Res Mol Brain Res. 1993 Jul;19(1-2):76-82. doi: 10.1016/0169-328x(93)90151-e.

Abstract

In this paper, we tested whether physiological activators of the cAMP second messenger pathway in primary cultures of neurons from rat cerebral cortex directly induce c-fos and other immediate early gene (IEG) transcription factors. We have found that brief (30 s to 2 min) stimulation of neurons with vasoactive intestinal peptide (VIP) and SKF-38393, a D1-dopaminergic receptor agonist, potently increased mRNA levels for the IEGs c-fos, jun-B, and NGFI-A, with weaker increases for c-jun. This action was mimicked by forskolin and dibutyryl cAMP. IEG induction by VIP and dibutyryl cAMP was not blocked by excitatory amino acid receptor antagonists or by blockers of dihydropyridine-sensitive calcium channels. Moreover, calcium-free medium did not modify IEG induction by dibutyryl cAMP, suggesting that cAMP can directly regulate IEG expression in differentiated neurons independently of calcium.

摘要

在本文中,我们测试了大鼠大脑皮层神经元原代培养物中cAMP第二信使途径的生理激活剂是否直接诱导c-fos和其他即刻早期基因(IEG)转录因子。我们发现,用血管活性肠肽(VIP)和D1-多巴胺能受体激动剂SKF-38393对神经元进行短暂(30秒至2分钟)刺激,可显著提高IEG c-fos、jun-B和NGFI-A的mRNA水平,而c-jun的增加则较弱。这种作用可被福斯可林和二丁酰环磷腺苷模仿。VIP和二丁酰环磷腺苷对IEG的诱导作用不受兴奋性氨基酸受体拮抗剂或二氢吡啶敏感性钙通道阻滞剂的阻断。此外,无钙培养基不会改变二丁酰环磷腺苷对IEG的诱导作用,这表明cAMP可以独立于钙直接调节分化神经元中IEG的表达。

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