Creighton University, School of Medicine, Department of Pharmacology & Neuroscience, Omaha, NE, 68174, USA.
Creighton University, School of Medicine, Department of Pharmacology & Neuroscience, Omaha, NE, 68174, USA.
Eur J Pharmacol. 2023 Jul 5;950:175763. doi: 10.1016/j.ejphar.2023.175763. Epub 2023 May 3.
Orexin is a neuromodulatory peptide produced by lateral hypothalamic orexin neurons and binds to G-protein-coupled orexin-1 receptor and orexin-2 receptors. Whether orexin modulates learning and memory is not fully understood. Orexin has biphasic effects on learning and memory: promoting learning and memory at homeostatic levels and inhibiting at supra- and sub-homeostatic levels. Hippocampal sharp wave-ripples encode memory information and are essential for memory consolidation and retrieval. The role of orexin on sharp wave-ripples in hippocampal CA1 remains unknown. Here, we used multi-electrode array recordings in acute ex vivo hippocampal slices to determine the effects of orexin receptor antagonists on sharp wave-ripples. Bath-application of either the orexin-1 receptor antagonist N-(2-Methyl-6-benzoxazolyl)-N'-1,5-naphthyridin-4-yl urea (SB-334867) or the orexin-2 receptor antagonist N-Ethyl-2-[(6-methoxy-3-pyridinyl)[(2-methylphenyl)sulfonyl]amino]-N-(3-pyridinylmethyl)-acetamide (EMPA) reduced sharp wave and ripple incidence, sharp wave amplitude, and sharp wave duration. SB-334867 and EMPA effects on sharp wave amplitude and duration were equivalent, whereas EMPA exhibited a greater reduction of sharp wave and ripple incidence. EMPA also increased ripple duration, whereas SB-334867 had no effect. Inhibition of both orexin receptors with a dual orexin receptor antagonist N-[1,1'-Biphenyl]-2-yl-1-[2-[(1-methyl-1H-benzimidazol-2-yl)thio]acetyl-2-pyrrolidinedicarboxamide (TCS-1102) had effects similar to EMPA, however, sharp wave amplitude and duration were unaffected. Region-specific expression of orexin receptors suggests orexin may regulate sharp wave generation in CA3, dentate gyrus-mediated sharp wave modification, sharp wave propagation to CA1, and local ripple emergence in CA1. Our study indicates an orexin contribution to hippocampal sharp wave-ripple complexes and suggests a mechanism by which sub-homeostatic concentrations of orexin may inhibit learning and memory function.
食欲素是一种由外侧下丘脑食欲素神经元产生的神经调节肽,与 G 蛋白偶联的食欲素-1 受体和食欲素-2 受体结合。食欲素是否调节学习和记忆尚不完全清楚。食欲素有双向调节学习和记忆的作用:在稳态水平促进学习和记忆,在超稳态和亚稳态水平抑制学习和记忆。海马体的尖波-涟漪编码记忆信息,对记忆巩固和检索至关重要。食欲素在海马体 CA1 中的尖波-涟漪中的作用尚不清楚。在这里,我们使用急性离体海马切片中的多电极阵列记录来确定食欲素受体拮抗剂对尖波-涟漪的影响。浴应用食欲素-1 受体拮抗剂 N-(2-甲基-6-苯并恶唑基)-N'-1,5-萘啶-4-基脲(SB-334867)或食欲素-2 受体拮抗剂 N-乙基-2-[(6-甲氧基-3-吡啶基)[(2-甲基苯基)磺酰]氨基]-N-(3-吡啶基甲基)-乙酰胺(EMPA)均降低了尖波和涟漪的发生率、尖波幅度和尖波持续时间。SB-334867 和 EMPA 对尖波幅度和持续时间的作用相当,而 EMPA 对尖波和涟漪发生率的抑制作用更大。EMPA 还增加了涟漪持续时间,而 SB-334867 则没有影响。用双重食欲素受体拮抗剂 N-[1,1'-联苯]-2-基-1-[2-[(1-甲基-1H-苯并咪唑-2-基)硫代]乙酰基-2-吡咯烷二羧酸酰胺(TCS-1102)抑制两种食欲素受体的作用类似于 EMPA,但尖波幅度和持续时间不受影响。食欲素受体的区域特异性表达表明,食欲素可能调节 CA3 中的尖波产生、齿状回介导的尖波修饰、尖波传播到 CA1 以及 CA1 中的局部涟漪出现。我们的研究表明,食欲素对海马体尖波-涟漪复合物有贡献,并提出了亚稳态浓度的食欲素可能抑制学习和记忆功能的机制。