Rappeneau Virginie, Tobinski Ann-Marie, Guevara Leonardo Miguel Caisachana, Meyer Neele, Jüngling Kay, Touma Chadi
Department of Behavioural Biology, Osnabrück University, Osnabrück, Germany.
Department of Behavioural Biology, Osnabrück University, Osnabrück, Germany.
Behav Brain Res. 2025 May 8;485:115530. doi: 10.1016/j.bbr.2025.115530. Epub 2025 Mar 8.
The neuropeptide S (NPS) and its receptor (NPSR1) are involved in various physiological processes, including arousal, sleep, anxiety, memory, and stress responses in rodents. Recent attention has focused on the association between the NPS/NPSR1 system and stress-related disorders, particularly involving a specific single nucleotide polymorphism (SNP) in the NPSR1 gene (rs324981). This SNP causes an amino acid change at position 107 in the protein, reducing NPSR1 signalling potency; however, its effects on behavioural, cognitive, and physiological aspects relevant to stress-related disorders remain unclear. Addressing this topic, we characterized the behavioural phenotype of a gene-editing mouse model, expressing either the murine/ancestral NPSR1-I107 variant or the human NPSR1-N107 variant. Both, male and female mice underwent a comprehensive behavioural test battery assessing arousal, exploratory and anxiety-related behaviour under varying levels of novelty stress. Moreover, cognitive functions were evaluated with a special focus on cognitive flexibility using the Attentional Set Shifting Task (ASST). Additionally, markers of behavioural and endocrine stress reactivity were assessed as well as changes in body weight and body composition. Our results showed that NPSR1-N107 mice displayed increased anxiety-related behaviour compared to NPSR1-I107 mice, with no significant differences in arousal, exploratory behaviour or hormonal stress responses. However, NPSR1-N107 mice also exhibited better rule-reversal learning in the ASST, indicating enhanced cognitive flexibility. These findings provide clear evidence for a role of the NPSR1 rs324981 SNP in regulating emotionality and cognitive flexibility, underscoring the potential of the NPSR1-I107N mouse model for further elucidating the molecular mechanisms underlying stress-related disorders.
神经肽 S(NPS)及其受体(NPSR1)参与多种生理过程,包括啮齿动物的觉醒、睡眠、焦虑、记忆和应激反应。最近的研究重点集中在 NPS/NPSR1 系统与应激相关障碍之间的关联,特别是涉及 NPSR1 基因中的一个特定单核苷酸多态性(SNP)(rs324981)。这种 SNP 导致蛋白质第 107 位的氨基酸发生变化,降低了 NPSR1 的信号传导能力;然而,其对与应激相关障碍相关的行为、认知和生理方面的影响仍不清楚。为了解决这个问题,我们对一种基因编辑小鼠模型的行为表型进行了表征,该模型表达小鼠/祖先 NPSR1-I107 变体或人类 NPSR1-N107 变体。雄性和雌性小鼠都接受了一系列全面的行为测试,以评估在不同程度的新奇应激下的觉醒、探索和焦虑相关行为。此外,使用注意力集转换任务(ASST)特别关注认知灵活性来评估认知功能。此外,还评估了行为和内分泌应激反应性的标志物以及体重和身体成分的变化。我们的结果表明,与 NPSR1-I107 小鼠相比,NPSR1-N107 小鼠表现出增加的焦虑相关行为,在觉醒、探索行为或激素应激反应方面没有显著差异。然而,NPSR1-N107 小鼠在 ASST 中也表现出更好的规则反转学习能力,表明认知灵活性增强