Weber E T, Gannon R L, Rea M A
Biological Rhythms and Integrative Neuroscience Research Institute, Armstrong Laboratory, Brooks AFB, TX 78235-5104, USA.
Neurosci Lett. 1995 Sep 15;197(3):227-30. doi: 10.1016/0304-3940(95)11961-u.
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.
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。