Department of Integrative Physiology and Neuroscience, Washington State University Vancouver, Washington, 98686, USA.
Dow Neurobiology, Legacy Research Institute, 1225 NE 2nd Ave, Portland, OR, 97232, USA.
Brain Struct Funct. 2021 May;226(4):1135-1153. doi: 10.1007/s00429-021-02229-4. Epub 2021 Feb 14.
Perineuronal nets (PNNs) surrounding fast-spiking, parvalbumin (PV) interneurons provide excitatory:inhibitory balance, which is impaired in several disorders associated with altered diurnal rhythms, yet few studies have examined diurnal rhythms of PNNs or PV cells. We measured the intensity and number of PV cells and PNNs labeled with Wisteria floribunda agglutinin (WFA) and also the oxidative stress marker 8-oxo-deoxyguanosine (8-oxo-dG) in rat prelimbic medial prefrontal cortex (mPFC) at Zeitgeber times (ZT) ZT0 (lights-on, inactive phase), ZT6 (mid-inactive phase), ZT12 (lights-off, active phase), and ZT18 (mid-active phase). Relative to ZT0, the intensities of PNN and PV labeling were increased in the dark (active) phase compared with the light (inactive) phase. The intensity of 8-oxo-dG was decreased from ZT0 at all times (ZT6,12,18). We also measured GAD 65/67 and vGLUT1 puncta apposed to PV cells with and without PNNs. There were more excitatory puncta on PV cells with PNNs at ZT18 vs. ZT6, but no changes in PV cells without PNNs and no changes in inhibitory puncta. Whole-cell slice recordings in fast-spiking (PV) cells with PNNs showed an increased ratio of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor:N-methyl-D-aspartate receptor (AMPA: NMDA) at ZT18 vs. ZT6. The number of PV cells and PV/PNN cells containing orthodenticle homeobox 2 (OTX2), which maintains PNNs, showed a strong trend toward an increase from ZT6 to ZT18. Diurnal fluctuations in PNNs and PV cells are expected to alter cortical excitatory:inhibitory balance and provide new insights into treatments for diseases impacted by disturbances in sleep and circadian rhythms.
周围快速放电、巴氨丁肽(PV)中间神经元的神经周细胞网络(PNNs)提供了兴奋抑制平衡,这种平衡在几种与昼夜节律改变相关的疾病中受到损害,但很少有研究检查 PNNs 或 PV 细胞的昼夜节律。我们测量了 Wisteria floribunda agglutinin(WFA)标记的 PV 细胞和 PNNs 的强度和数量,以及大鼠前额叶皮层(mPFC)内侧前额叶的氧化应激标志物 8-氧代脱氧鸟苷(8-oxo-dG)在 Zeitgeber 时间(ZT)ZT0(灯亮,不活动期)、ZT6(中不活动期)、ZT12(灯关,活动期)和 ZT18(中活动期)的时间点。与 ZT0 相比,PNN 和 PV 标记的强度在黑暗(活动)期比在光照(不活动)期增加。8-oxo-dG 的强度从所有时间点(ZT6、12、18)的 ZT0 开始降低。我们还测量了与有和没有 PNN 的 PV 细胞相对应的 GAD 65/67 和 vGLUT1 点状结构。在 ZT18 与 ZT6 相比,有 PNN 的 PV 细胞上的兴奋性点状结构更多,但在没有 PNN 的 PV 细胞中没有变化,抑制性点状结构也没有变化。在有 PNN 的快速放电(PV)细胞的全细胞切片记录中,与 ZT6 相比,在 ZT18 时,α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体:N-甲基-D-天冬氨酸受体(AMPA:NMDA)的比值增加。含有同源异型盒 2(OTX2)的 PV 细胞和含有 PNN 的 PV/PNN 细胞的数量显示出从 ZT6 到 ZT18 增加的强烈趋势。PNNs 和 PV 细胞的昼夜波动预计会改变皮质兴奋性抑制平衡,并为受睡眠和昼夜节律紊乱影响的疾病的治疗提供新的见解。