Stemmelin Jeanne, Lukovic Ludovit, Salome Nicolas, Griebel Guy
Sanofi-Synthélabo Research, Department of Psychopharmacology, CNS Research Department, Bagneux, France.
Neuropsychopharmacology. 2005 Jan;30(1):35-42. doi: 10.1038/sj.npp.1300562.
Previous experiments with the first selective nonpeptide vasopressin V1b receptor antagonist SSR149415 ((2S, 4R)-1-[5-chloro-1-[(2,4-dimethoxyphenyl)sulfonyl]-3-(2-methoxyphenyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-4-hydroxy-N,N-dimethyl-2-pyrrolidinecarboxamide) have shown that the drug elicits anxiolytic- and antidepressant-like effects following systemic administration. Extrahypothalamic V1b receptors have been suggested to be involved in these effects as evidenced by the findings that hypophysectomized rats were still sensitive to the antistress action of SSR149415. The first objective of the present work aimed at locating V1b receptors in the rat limbic brain using anti-V1b receptor immunohistochemistry. The immunolabeling revealed high densities of V1b receptors in the lateral septum, the amygdala, the bed nucleus of the stria terminalis, the hippocampal formation, and in several cortical areas. Since the lateral septum is well known to participate in the modulation of emotional processes, the second objective of this study went on to evaluate the behavioral effects of an infusion of SSR149415 into the lateral septum and to determine whether its behavioral effects are mediated by this structure. Animals were tested in models classically used for the screening of anxiolytics (ie the punished drinking and elevated plus-maze tests) and antidepressants (ie the forced-swimming test). Bilateral intraseptal infusion of SSR149415 (10 and 100 ng) produced a decrease in immobility time in the forced-swimming test, indicating antidepressant-like effects. In contrast, the behavior of rats in the punished drinking procedure or in the elevated plus-maze test was not modified by intraseptal infusion of SSR149415. These findings suggest that V1b receptors located in the lateral septum participate in the antidepressant- but not the anxiolytic-like action of SSR149415 in rats.
先前使用首个选择性非肽类血管加压素V1b受体拮抗剂SSR149415((2S, 4R)-1-[5-氯-1-[(2,4-二甲氧基苯基)磺酰基]-3-(2-甲氧基苯基)-2-氧代-2,3-二氢-1H-吲哚-3-基]-4-羟基-N,N-二甲基-2-吡咯烷甲酰胺)所做的实验表明,该药物经全身给药后可产生抗焦虑和抗抑郁样效应。垂体切除的大鼠对SSR149415的抗应激作用仍敏感,这一发现证明,下丘脑外V1b受体可能参与了这些效应。本研究的首要目标是利用抗V1b受体免疫组织化学方法在大鼠边缘脑区定位V1b受体。免疫标记显示,外侧隔区、杏仁核、终纹床核、海马结构以及几个皮质区域中V1b受体密度很高。由于外侧隔区参与情绪过程的调节是众所周知的,因此本研究的第二个目标是评估向外侧隔区注射SSR149415的行为效应,并确定其行为效应是否由该结构介导。在经典的抗焦虑药物筛选模型(即罚饮试验和高架十字迷宫试验)和抗抑郁药物筛选模型(即强迫游泳试验)中对动物进行测试。双侧隔区内注射SSR149415(10和100 ng)可使强迫游泳试验中的不动时间减少,表明具有抗抑郁样效应。相比之下,隔区内注射SSR149415并未改变大鼠在罚饮试验或高架十字迷宫试验中的行为。这些发现表明,位于外侧隔区的V1b受体参与了SSR149415对大鼠的抗抑郁而非抗焦虑样作用。