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反义寡脱氧核苷酸灌注对大鼠脊髓中c-Fos蛋白表达的抑制作用。

Inhibition of c-Fos protein expression in rat spinal cord by antisense oligodeoxynucleotide superfusion.

作者信息

Gillardon F, Beck H, Uhlmann E, Herdegen T, Sandkühler J, Peyman A, Zimmermann M

机构信息

II. Physiologisches Institut, Universität Heidelberg, Germany.

出版信息

Eur J Neurosci. 1994 May 1;6(5):880-4. doi: 10.1111/j.1460-9568.1994.tb00999.x.

DOI:10.1111/j.1460-9568.1994.tb00999.x
PMID:8075829
Abstract

Peripheral noxious stimulation leads to a rapid and transient expression of c-fos, c-jun and other immediate-early genes (IEGs) in the spinal cord. However, the role of IEG encoded transcription factors in plasticity of spinal neurons remains speculative. In the present study we have shown that superfusion of rat spinal cord with antisense oligodeoxynucleotides complementary to c-fos mRNA suppresses heat-induced c-Fos protein expression without affecting other members of the Fos and Jun family, thus providing a technique to determine the function of IEGs in vivo.

摘要

外周伤害性刺激可导致脊髓中c-fos、c-jun和其他即刻早期基因(IEGs)快速短暂表达。然而,IEG编码的转录因子在脊髓神经元可塑性中的作用仍具有推测性。在本研究中,我们发现用与c-fos mRNA互补的反义寡脱氧核苷酸灌注大鼠脊髓,可抑制热诱导的c-Fos蛋白表达,而不影响Fos和Jun家族的其他成员,从而提供了一种在体内确定IEGs功能的技术。

相似文献

1
Inhibition of c-Fos protein expression in rat spinal cord by antisense oligodeoxynucleotide superfusion.反义寡脱氧核苷酸灌注对大鼠脊髓中c-Fos蛋白表达的抑制作用。
Eur J Neurosci. 1994 May 1;6(5):880-4. doi: 10.1111/j.1460-9568.1994.tb00999.x.
2
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Application of morphine prior to noxious stimulation differentially modulates expression of Fos, Jun and Krox-24 proteins in rat spinal cord neurons.在有害刺激之前应用吗啡可不同程度地调节大鼠脊髓神经元中Fos、Jun和Krox-24蛋白的表达。
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Immediate early genes in blood pressure regulation.血压调节中的即刻早期基因。
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Induction and suppression of immediate-early genes in the rat brain by a selective alpha-2-adrenoceptor agonist and antagonist following noxious peripheral stimulation.选择性α-2-肾上腺素能受体激动剂和拮抗剂在有害外周刺激后对大鼠脑内即刻早期基因的诱导和抑制作用。
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The neurotrophic peptide Org 2766 does not influence the expression of the immediate early gene c-fos following sciatic nerve crush in the rat.神经营养肽Org 2766不影响大鼠坐骨神经损伤后即刻早期基因c-fos的表达。
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引用本文的文献

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Preclinical and clinical pharmacology of antisense oligonucleotides.反义寡核苷酸的临床前和临床药理学
Mol Biotechnol. 1999 Aug;12(1):1-11. doi: 10.1385/MB:12:1:1.
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Antibodies and antisense oligodeoxynucleotides to mu-opioid receptors, selectively block the effects of mu-opioid agonists on intestinal transit and permeability in mice.
针对μ-阿片受体的抗体和反义寡脱氧核苷酸可选择性阻断μ-阿片激动剂对小鼠肠道转运和通透性的影响。
Br J Pharmacol. 1999 May;127(2):397-404. doi: 10.1038/sj.bjp.0702570.
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Intrastriatally injected c-fos antisense oligonucleotide interferes with striatonigral but not striatopallidal gamma-aminobutyric acid transmission in the conscious rat.纹状体内注射c-fos反义寡核苷酸可干扰清醒大鼠纹状体黑质而非纹状体苍白球的γ-氨基丁酸传递。
Proc Natl Acad Sci U S A. 1996 Nov 26;93(24):14134-9. doi: 10.1073/pnas.93.24.14134.
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Cell Mol Neurobiol. 1994 Oct;14(5):487-505. doi: 10.1007/BF02088833.