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环磷酸鸟苷依赖性蛋白激酶抑制剂可阻断体内昼夜节律的光诱导相位提前。

cGMP-dependent protein kinase inhibitor blocks light-induced phase advances of circadian rhythms in vivo.

作者信息

Weber E T, Gannon R L, Rea M A

机构信息

Biological Rhythms and Integrative Neuroscience Research Institute, Armstrong Laboratory, Brooks AFB, TX 78235-5104, USA.

出版信息

Neurosci Lett. 1995 Sep 15;197(3):227-30. doi: 10.1016/0304-3940(95)11961-u.

Abstract

The suprachiasmatic nucleus (SCN) contains the primary mammalian circadian clock. Light synchronizes these circadian rhythms through a mechanism involving the release of excitatory amino acids (EAA) and synthesis of nitric oxide (NO) in the SCN. In the current study, we investigated whether cGMP-mediated activation of cGMP-dependent protein kinase (PKG) is associated with light-induced phase shifts of the circadian oscillator. Local administration of the specific PKG inhibitor, KT-5823, significantly attenuated light-induced advances in the phase of activity rhythms when administered during late subjective night (CT 19). Similar treatment at CT 14 had no significant effect on light-induced phase delays. These results are the first to implicate PKG in the biochemical pathway(s) responsible for photic phase advances, and suggest a divergence in biochemical pathways involved in photic phase shifts.

摘要

视交叉上核(SCN)包含主要的哺乳动物昼夜节律时钟。光通过一种机制使这些昼夜节律同步,该机制涉及视交叉上核中兴奋性氨基酸(EAA)的释放和一氧化氮(NO)的合成。在本研究中,我们调查了cGMP介导的cGMP依赖性蛋白激酶(PKG)激活是否与昼夜振荡器的光诱导相移有关。当在主观夜后期(CT 19)给予特异性PKG抑制剂KT-5823局部给药时,显著减弱了活动节律相位的光诱导提前。在CT 14进行类似处理对光诱导的相位延迟没有显著影响。这些结果首次表明PKG参与了负责光诱导相位提前的生化途径,并提示在光诱导相移所涉及的生化途径中存在差异。

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