Departamento de Fisiología, Facultad de Medicina, Universidad de la República, Gral. Flores 2125, Montevideo ZP11800, Uruguay.
UGC Salud Mental, Instituto de Investigación Biomédica de Málaga (IBIMA), Hospital Regional Universitario de Málaga, Universidad de Málaga, Av. Carlos Haya 82, Málaga 29010, Spain.
Prog Neuropsychopharmacol Biol Psychiatry. 2023 Apr 20;123:110703. doi: 10.1016/j.pnpbp.2022.110703. Epub 2022 Dec 21.
Interest in the role of melanin-concentrating hormone (MCH) in memory processes has increased in recent years, with some studies reporting memory-enhancing effects, while others report deleterious effects. Due to these discrepancies, this study seeks to provide new evidence about the role of MCH in memory consolidation and its relation with BDNF/TrkB system. To this end, in the first experiment, increased doses of MCH were acutely administered in both hippocampi to groups of male rats (25, 50, 200, and 500 ng). Microinjections were carried out immediately after finishing the sample trial of two hippocampal-dependent behavioral tasks: the Novel Object Recognition Test (NORT) and the modified Elevated Plus Maze (mEPM) test. Results indicated that a dose of 200 ng of MCH or higher impaired memory consolidation in both tasks. A second experiment was performed in which a dose of 200 ng of MCH was administered alone or co-administered with the MCHR-1 antagonist ATC-0175 at the end of the sample trial in the NORT. Results showed that MCH impaired memory consolidation, while the co-administration with ATC-0175 reverted this detrimental effect. Moreover, MCH induced a significant decrease in hippocampal MCHR-1 and TrkB expression with no modification in the expression of BDNF and NMDA receptor subunits NR1, NR2A, and NR2B. These results suggest that MCH in vivo elicits pro-amnesic effects in the rat hippocampus by decreasing the availability of its receptor and TrkB receptors, thus linking both endogenous systems to memory processes.
近年来,人们对黑色素浓缩激素 (MCH) 在记忆过程中的作用产生了浓厚的兴趣,一些研究报告称其具有增强记忆的作用,而另一些研究则报告称其具有有害作用。由于这些差异,本研究旨在提供关于 MCH 在记忆巩固中的作用及其与 BDNF/TrkB 系统的关系的新证据。为此,在第一个实验中,将不同剂量的 MCH 急性注入两组雄性大鼠的海马体中(25、50、200 和 500ng)。微注射在完成两个海马依赖性行为任务(新颖物体识别测试 (NORT) 和改良高架十字迷宫 (mEPM) 测试)的样本试验后立即进行。结果表明,200ng 或更高剂量的 MCH 会损害两种任务的记忆巩固。第二个实验中,在 NORT 的样本试验结束时,单独给予或共同给予 MCHR-1 拮抗剂 ATC-0175 200ng 的 MCH。结果表明,MCH 损害了记忆巩固,而与 ATC-0175 共同给药则逆转了这种有害作用。此外,MCH 诱导海马体中 MCHR-1 和 TrkB 表达显著下降,而 BDNF 和 NMDA 受体亚单位 NR1、NR2A 和 NR2B 的表达没有改变。这些结果表明,体内 MCH 通过降低其受体和 TrkB 受体的可用性,在大鼠海马体中引发促健忘作用,从而将这两个内源性系统与记忆过程联系起来。