Hanuska Adrienn, Ribiczey Polett, Kató Erzsébet, Papp Zsolt Tamás, Varga Zoltán V, Giricz Zoltán, Tóth Zsuzsanna E, Könczöl Katalin, Zsembery Ákos, Zelles Tibor, Harsing Laszlo G, Köles László
Department of Oral Biology, Semmelweis University, H-1089 Budapest, Hungary.
Department of Pharmacology and Pharmacotherapy, Semmelweis University, H-1089 Budapest, Hungary.
Int J Mol Sci. 2024 Nov 25;25(23):12644. doi: 10.3390/ijms252312644.
NMDA receptors in the prefrontal cortex (PFC) play a crucial role in cognitive functions. Previous research has indicated that angiotensin II (Ang II) affects learning and memory. This study aimed to examine how Ang II impacts NMDA receptor activity in layer V pyramidal cells of the rat PFC. Whole-cell patch-clamp experiments were performed in pyramidal cells in brain slices of 9-12-day-old rats. NMDA (30 μM) induced inward currents. Ang II (0.001-1 µM) significantly enhanced NMDA currents in about 40% of pyramidal cells. This enhancement was reversed by the AT antagonist eprosartan (1 µM), but not by the AT receptor antagonist PD 123319 (5 μM). When pyramidal neurons were synaptically isolated, the increase in NMDA currents due to Ang II was eliminated. Additionally, the dopamine D1 receptor antagonist SCH 23390 (10 μM) reversed the Ang II-induced enhancement, whereas the D2 receptor antagonist sulpiride (20 μM) had no effect. The potentiation of NMDA currents in a subpopulation of layer V pyramidal neurons by Ang II, involving AT1 receptor activation and dopaminergic signaling, may serve as an underlying mechanism for the effects of the renin-angiotensin system (RAS) elements on neuronal functions.
前额叶皮质(PFC)中的N-甲基-D-天冬氨酸(NMDA)受体在认知功能中起着至关重要的作用。先前的研究表明,血管紧张素II(Ang II)会影响学习和记忆。本研究旨在探讨Ang II如何影响大鼠PFC第V层锥体细胞中NMDA受体的活性。对9至12日龄大鼠脑片的锥体细胞进行全细胞膜片钳实验。NMDA(30 μM)诱导内向电流。Ang II(0.001 - 1 μM)在约40%的锥体细胞中显著增强了NMDA电流。这种增强作用可被AT拮抗剂依普罗沙坦(1 μM)逆转,但不能被AT受体拮抗剂PD 123319(5 μM)逆转。当锥体细胞被突触分离时,Ang II引起的NMDA电流增加被消除。此外,多巴胺D1受体拮抗剂SCH 23390(10 μM)可逆转Ang II诱导的增强作用,而D2受体拮抗剂舒必利(20 μM)则无作用。Ang II对第V层锥体细胞亚群中NMDA电流的增强作用,涉及AT1受体激活和多巴胺能信号传导,可能是肾素-血管紧张素系统(RAS)成分对神经元功能产生影响的潜在机制。