Dept of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behaviour, Nijmegen, the Netherlands; Dept of Psychiatry, Radboud University Medical Centre, Nijmegen, the Netherlands.
Dept of Behavioural Neurobiology, Groningen Institute for Evolutionary Life Sciences, Groningen, the Netherlands.
Neuropharmacology. 2019 Jul 15;153:134-141. doi: 10.1016/j.neuropharm.2019.05.004. Epub 2019 May 9.
Brain serotonin (5-HT) plays a key role in aggressive behaviours and related psychopathologies, but its precise mechanism of action remains elusive. Genetic animal models may provide a tool to elucidate the relationship between aggression and serotonin. The present study showed that tryptophan hydroxylase 2 (Tph2) knockout (KO) rats, which exhibit profoundly diminished extracellular serotonin levels, display increased aggressiveness compared to their Tph2 wildtype (WT) counterparts. However, the level of aggression in Tph2 KO rats did not equal that of feral wild type Groningen (WTG) rats. To investigate whether enhanced 5-HT receptor functionality may be present in Tph2 KO rats, we tested the acute anti-aggressive potency of the highly selective 5-HT receptor full agonist NLX-112 (a.k.a. befiradol or F13640). Data show that compared to Tph2 WT and WTG rats, the NLX-112 dose-effect curve was shifted to the right in Tph2 KO animals. These results suggest that, unlike previous reports in Tph2 KO mice, Tph2 KO rats have a decreased 5-HT receptor sensitivity compared to both Tph2 WT and WTG animals.
大脑中的 5-羟色胺(5-HT)在攻击性行为和相关的精神病理学中起着关键作用,但它的确切作用机制仍难以捉摸。遗传动物模型可能为阐明攻击行为与 5-HT 之间的关系提供工具。本研究表明,色氨酸羟化酶 2(Tph2)敲除(KO)大鼠表现出明显降低的细胞外 5-HT 水平,与 Tph2 野生型(WT)大鼠相比,其攻击性增加。然而,Tph2 KO 大鼠的攻击性水平并不等同于野生型格罗宁根(WTG)大鼠。为了研究 Tph2 KO 大鼠是否存在增强的 5-HT 受体功能,我们测试了高度选择性 5-HT 受体完全激动剂 NLX-112(又名 befiradol 或 F13640)的急性抗攻击性效力。数据表明,与 Tph2 WT 和 WTG 大鼠相比,NLX-112 在 Tph2 KO 动物中的剂量-效应曲线向右移位。这些结果表明,与 Tph2 KO 小鼠的先前报告不同,与 Tph2 WT 和 WTG 动物相比,Tph2 KO 大鼠的 5-HT 受体敏感性降低。