Intracerebroventricular infusion of the selective orexin 1 receptor antagonist SB-334867 impairs cognitive flexibility in a sex-dependent manner

增食欲素 认知灵活性 食欲素-A 食欲素受体 心理学 内分泌学 内科学 敌手 认知 神经肽 神经科学 受体 医学
作者
Archana Durairaja,Ceylan-Scarlett Steinecke,Markus Fendt
出处
期刊:Behavioural Brain Research [Elsevier BV]
卷期号:424: 113791-113791 被引量:12
标识
DOI:10.1016/j.bbr.2022.113791
摘要

Orexin neuropeptides are well known for their role in sleep/wake cycle, feeding behavior and motivation-related behaviors. However, their role in cognition is not clearly understood. We recently published that orexin deficiency impairs intra-dimensional set shifting in female homozygous orexin-deficient mice but improves the first reversal phase in male homozygous orexin-deficient mice in the attentional set shifting task (ASST), a well-established rodent test for cognitive flexibility. In the present study, we tested if intracerebroventricular injections of the selective orexin 1 receptor antagonist SB-334867 (4 µg/2 µL) affects cognitive flexibility in the different phases of ASST. We found that SB-334867 injections impaired the first and second reversal phases in female C57BL/6J mice but not in males. In addition, we also showed that at this particular dose of SB-334867, the consumption of the reward that was used in the ASST was not affected in both males and females. Our findings indicate that cognitive flexibility is impaired by orexin 1 receptor antagonism in a sex-dependent manner and reiterates the sexually dimorphic role of orexin in cognitive flexibility. • Blocking orexin 1 receptor (icv) impaired reversal phases only in female C57BL/6J mice in attentional set shifting task. • Reward consumption was not affected by blocking orexin 1 receptor in both sexes. • Orexin plays a sexually dimorphic role in regulating cognitive flexibility.
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