Department of Anatomy, School of Medicine, Jianghan University, Wuhan 430056, Hubei Province, China.
Department of Physiology, School of Medicine, Jianghan University, Wuhan 430056, Hubei Province, China.
Biochem Biophys Res Commun. 2015 Jan 9;456(2):666-9. doi: 10.1016/j.bbrc.2014.12.014. Epub 2014 Dec 12.
Using whole-cell patch clamp recording on medial prefrontal cortical slices of rats aged 17-33 postnatal days, we demonstrated the glycine-induced strychnine-sensitive outward currents. The amplitude of the peak current increased with the concentrations of glycine with an EC50 of 74.7 μM. Application of 1μM strychnine alone to cells caused a slight inward current without blocking the sIPSCs, indicating that GlyRs in the mPFC are activated by an endogenous ligand that can be released tonically. Glycine reversibly depressed firing rate in cells from both layer 6 and layer 3, with significantly greater inhibition on the former than the latter (EC50 12.9 vs 85.6 μM). Glycine hyperpolarized membrane potential in cells of both layer 6 and layer 3 depending on its concentrations, with an IC50 of 99.1 and 207.2 μM, respectively. We propose that GlyRs participate in a novel inhibitory mechanism in mPFC, modulating neuronal activity. This finding further supports an important role of GlyR in cortical function and dysfunction.
使用出生后 17-33 天的大鼠的内侧前额皮质脑片进行全细胞膜片钳记录,我们证明了甘氨酸诱导的士的宁敏感外向电流。峰值电流的幅度随甘氨酸浓度的增加而增加,EC50 为 74.7 μM。单独应用 1μM 士的宁可引起细胞内轻微的内向电流,而不阻断 sIPSCs,表明 mPFC 中的 GlyRs 被一种内源性配体激活,这种配体可以持续释放。甘氨酸可逆地抑制来自第 6 层和第 3 层的细胞的放电率,对前者的抑制作用明显大于后者(EC50 分别为 12.9 和 85.6 μM)。甘氨酸根据其浓度使第 6 层和第 3 层的细胞的膜电位超极化,IC50 分别为 99.1 和 207.2 μM。我们提出,GlyRs 参与 mPFC 中的一种新型抑制机制,调节神经元活动。这一发现进一步支持了 GlyR 在皮质功能和功能障碍中的重要作用。