Beis D, Holzwarth K, Flinders M, Bader M, Wöhr M, Alenina N
Max-Delbrück-Center for Molecular Medicine (MDC), Berlin, Germany.
Behavioral Neuroscience, Philipps-University of Marburg, Marburg, Germany
Biol Lett. 2015 Mar;11(3). doi: 10.1098/rsbl.2015.0057.
A deficit in brain serotonin is thought to be associated with deteriorated stress coping behaviour, affective disorders and exaggerated violence. We challenged this hypothesis in mice with a brain-specific serotonin depletion caused by a tryptophan hydroxylase 2 (TPH2) deficiency. We tested TPH2-deficient (Tph2(-/-)) animals in two social situations. As juveniles, Tph2(-/-) mice displayed reduced social contacts, whereas ultrasonic vocalizations (USVs) were unchanged within same-sex same-genotype pairings. Interestingly, juvenile females vocalized more than males across genotypes. Sexually naive adult males were exposed to fresh male or female urine, followed by an interaction with a conspecific, and re-exposed to urine. Although Tph2(-/-) mice showed normal sexual preference, they were hyper-aggressive towards their interaction partners and did not vocalize in response to sexual cues. These results highlight that central serotonin is essential for prosocial behaviour, especially USV production in adulthood, but not for sexual preference.
大脑血清素缺乏被认为与应激应对行为恶化、情感障碍和过度暴力有关。我们通过色氨酸羟化酶2(TPH2)缺乏导致的大脑特异性血清素耗竭来在小鼠中验证这一假设。我们在两种社交情境中测试了TPH2缺陷(Tph2(-/-))动物。作为幼崽,Tph2(-/-)小鼠的社交接触减少,而在同性同基因型配对中超声发声(USV)没有变化。有趣的是,跨基因型的幼年雌性比雄性发声更多。性成熟前的成年雄性暴露于新鲜的雄性或雌性尿液中,随后与同种个体互动,然后再次暴露于尿液中。尽管Tph2(-/-)小鼠表现出正常的性偏好,但它们对互动伙伴具有过度攻击性,并且对性暗示没有发声反应。这些结果表明,中枢血清素对于亲社会行为至关重要,尤其是成年期的超声发声,但对性偏好并非如此。