Bogdan Rebecca, Kayumova Rukhshona, Schwarting Rainer K W, Wöhr Markus, Kisko Theresa M
Behavioral Neuroscience, Experimental and Biological Psychology, Faculty of Psychology, Philipps-University Marburg, Marburg, Germany.
Centre for Mind, Brain, and Behavior (CMBB), Philipps-University Marburg, Marburg, Germany.
Front Behav Neurosci. 2023 Aug 3;17:1190272. doi: 10.3389/fnbeh.2023.1190272. eCollection 2023.
Healthy brain development depends on early social practices and experiences. The risk gene is implicated in numerous neuropsychiatric disorders, in which key characteristics include deficits in social functioning and communication. Recently, we reported sex-dependent impairments in social behavior and ultrasonic vocalizations (USV) in juvenile heterozygous (HET) rats. Specifically, HET females displayed increases in rough-and-tumble play that eliminated the typically observed sex difference between male and female rats. Interestingly, female wild-type (WT) pairs also showed a similar increase in social play when housed with HET females, suggesting their behavior may be influenced by HET cage mates. This indicates that the genetic makeup of the social environment related to can influence social play, yet systematic studies are lacking.
In the present study, we housed juvenile females in MIXED- or SAME-genotype cages and tested them in a social play paradigm with a same- and opposite-genotype partner.
The results show that the early social environment and the genotype of the play partner influence social play and 50-kHz USV emission. Experience with a WT play partner appears necessary for HET females to show comparable levels of play and 50-kHz USV emission. Same-genotype HET pairs played less and emitted fewer 50-kHz USV than same-genotype WT or opposite-genotype pairs; however, we found that the decrease in social play and 50-kHz USV in HET pairs can be rescued by playing with a WT partner. The effect was particularly prominent when the first play partner was WT, as we found it increased play and 50-kHz USV emission in all subsequent interactions with ensuing partners.
These findings suggest that the genetic makeup related to the social environment and/or social peers influences social play in haploinsufficient rats. Specifically, our results show that WT peers can rescue behavior and communication alterations in female rats. Our findings have important implications because they show that the genetic makeup of the social environment can divulge phenotypic changes in genetic rat models of neuropsychiatric disorders.
健康的大脑发育依赖于早期的社交行为和经历。该风险基因与多种神经精神疾病有关,这些疾病的关键特征包括社交功能和沟通缺陷。最近,我们报道了幼年杂合(HET)大鼠在社交行为和超声波发声(USV)方面存在性别依赖性损伤。具体而言,HET雌性大鼠的混战玩耍增加,消除了通常观察到的雄性和雌性大鼠之间的性别差异。有趣的是,当与HET雌性大鼠饲养在一起时,雌性野生型(WT)配对的社交玩耍也出现了类似的增加,这表明它们的行为可能受到HET笼伴的影响。这表明与该基因相关的社交环境的基因组成可以影响社交玩耍,但缺乏系统性研究。
在本研究中,我们将幼年雌性大鼠饲养在混合基因型或同基因型笼子中,并在与同基因型和异基因型伙伴的社交玩耍范式中对它们进行测试。
结果表明,早期社交环境和玩耍伙伴的基因型会影响社交玩耍和50kHz USV发射。对于HET雌性大鼠来说,与WT玩耍伙伴的经历似乎是表现出 comparable levels of play and 50-kHz USV emission所必需的。同基因型HET配对比同基因型WT或异基因型配对玩耍更少,发出的50kHz USV也更少;然而,我们发现与WT伙伴玩耍可以挽救HET配对中社交玩耍和50kHz USV的减少。当第一个玩耍伙伴是WT时,这种效果尤为突出,因为我们发现它增加了在所有后续与后续伙伴的互动中的玩耍和50kHz USV发射。
这些发现表明,与社交环境和/或社交同伴相关的基因组成会影响单倍体不足大鼠的社交玩耍。具体而言,我们的结果表明WT同伴可以挽救雌性大鼠的行为和沟通改变。我们的发现具有重要意义,因为它们表明社交环境的基因组成可以揭示神经精神疾病基因大鼠模型中的表型变化。