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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Circadian phase-dependent effect of nitric oxide on L-type voltage-gated calcium channels in avian cone photoreceptors
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Circadian phase-dependent effect of nitric oxide on L-type voltage-gated calcium channels in avian cone photoreceptors

机译:一氧化氮对鸟类视锥细胞中L型电压门控钙通道的昼夜节律依赖性

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Nitric oxide (NO) plays an important role in phase-shifting of circadian neuronal activities in the suprachiasmatic nucleus and circadian behavior activity rhythms. In the retina, NO production is increased in a light-dependent manner. While endogenous circadian oscillators in retinal photoreceptors regulate their physiological states, it is not clear whether NO also participates in the circadian regulation of photoreceptors. In this study, we demonstrate that NO is involved in the circadian phase-dependent regulation of L-type voltage-gated calcium channels (L-VGCCs). In chick cone photoreceptors, the L-VGCCα1 subunit expression and the maximal L-VGCC currents are higher at night, and both Ras-mitogen-activated protein kinase (MAPK)-extracellular signal-regulated kinase (Erk) and Ras-phosphatidylinositol 3 kinase (PI3K)-protein kinase B (Akt) are part of the circadian output pathways regulating L-VGCCs. The NO-cGMP-protein kinase G (PKG) pathway decreases L-VGCCα1 subunit expression and L-VGCC currents at night, but not during the day, and exogenous NO donor or cGMP decreases the phosphorylation of Erk and Akt at night. The protein expression of neural NO synthase (nNOS) is also under circadian control, with both nNOS and NO production being higher during the day. Taken together, NO/cGMP/PKG signaling is involved as part of the circadian output pathway to regulate L-VGCCs in cone photoreceptors.
机译:一氧化氮(NO)在视交叉上核中昼夜节律神经元活动的相移和昼夜节律行为活动节律中起重要作用。在视网膜中,NO的产生以光依赖的方式增加。虽然视网膜感光器中的内源性昼夜节律振荡器调节其生理状态,但尚不清楚NO是否也参与感光器的昼夜节律调节。在这项研究中,我们证明NO参与了L型电压门控钙通道(L-VGCC)的昼夜节律依赖性调节。在鸡锥状感光细胞中,L-VGCCα1亚基表达和最大L-VGCC电流在夜间较高,并且Ras促分裂原激活蛋白激酶(MAPK)-细胞外信号调节激酶(Erk)和Ras-磷脂酰肌醇3激酶(PI3K)-蛋白激酶B(Akt)是调节L-VGCC的昼夜节律输出途径的一部分。 NO-cGMP-蛋白激酶G(PKG)途径在夜间(而非白天)降低L-VGCCα1亚基表达和L-VGCC电流,而外源NO供体或cGMP在夜间降低Erk和Akt的磷酸化。神经NO合酶(nNOS)的蛋白质表达也处于昼夜节律控制下,白天nNOS和NO产生均较高。综上所述,NO / cGMP / PKG信号传导是昼夜节律输出途径的一部分,以调节视锥细胞感光器中的L-VGCC。

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