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Inhibitory action of brotizolam on circadian and light-induced Per1 and Per2 expression in the hamster suprachiasmatic nucleus

机译:布替唑仑对昼夜节律和光诱导仓鼠超视神经核中Per1和Per2表达的抑制作用

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摘要

Triazolam reportedly causes phase advances in hamster wheel-running rhythm after injection during subjective daytime. However, it is unclear whether benzodiazepine affects the Per gene expression accompanying a behavioural phase shift.Brotizolam (0.5–10 mg kg−1) induced large phase advances in hamster rhythm when injected during mid-subjective daytime (circadian time 6 or 9), but not at circadian time 0, 3 or 15.Brotizolam (5 mg kg−1) significantly reduced the expression of Per1 and Per2 in the suprachiasmatic nucleus 1 and 2 h after injection at circadian time 6, and slightly reduced them at circadian time 20.Injection of 8-OH-DPAT (5 mg kg−1) at subjective daytime induced similar phase advances with a reduction of Per1 and Per2 expression. Co-administration of brotizolam with 8-OH DPAT failed to potentiate the 8-OH DPAT-induced phase advances and reduced Per expression.Both phase advance and rapid induction of Per1 and Per2 in the suprachiasmatic nucleus after light exposure (5 lux, 15 min) at circadian time 20 was strongly attenuated by co-treatment with brotizolam 5 mg kg−1.The present results strongly suggest that reduction of Per1 and/or Per2 expression during subjective daytime by brotizolam may be an important step in causing a behavioural phase advance. The co-administration experiment suggests that common mechanism(s) are involved in brotizolam- or 8-OH DPAT-induced phase advances and the reduction of Per gene expression.These results suggest that brotizolam is not only a good drug for insomnia but also a drug capable of facilitating re-entrainment like melatonin.
机译:据报道,三唑仑在主观白天在注射后引起仓鼠车轮运转节奏的相移。然而,尚不清楚苯并二氮杂whether是否会伴随行为相移而影响Per基因表达。当在主观白天(昼夜节律时间6或9)注射时,Brotizolam(0.5–10 mg kg-1)引起仓鼠节律的大幅提前,但在昼夜节律时间6注射后,Brotizolam(5 mg kg-1)显着降低了视交叉上核1和2 h中Per1和Per2的表达,但在昼夜节律时间6、20略有减少。在主观的白天注射8-OH-DPAT(5 mg kg-1)诱导相似的相进展,但Per1和Per2表达减少。溴替唑仑与8-OH DPAT的共同给药未能增强8-OH DPAT诱导的相进展并降低了Per表达。光照后(5 lux,15 min),两相进展和视交叉上核中Per1和Per2的快速诱导。 )在昼夜节律时间20与溴硝唑仑5 mg kg-1共同处理可大大减弱。目前的结果强烈表明,溴硝唑仑在主观白天减少Per1和/或Per2表达可能是导致行为相进展的重要步骤。共同给药实验表明,溴丁唑仑或8-OH DPAT诱导的相进展和Per基因表达的降低均涉及共同的机制。这些结果表明,溴丁唑仑不仅是治疗失眠的好药,而且是一种失眠的药物。褪黑素这样的能够促进再夹带的药物。

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