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首页> 外文期刊>Indian Journal of Experimental Biology >On the sleep promoting effects of BR-16A: Interaction with GABAergic modulators
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On the sleep promoting effects of BR-16A: Interaction with GABAergic modulators

机译:关于BR-16A的促睡眠作用:与GABA能调节剂的相互作用

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摘要

Pentobarbitone-induced hypnosis test was used as an animal model to explore the role of BR-16A, a polyherbal formulation in sleep. Pentobarbitone produces quick sleep latency (onset) and prolongation of total sleep time (duration). Sleep latency and total sleep time were used as a parameters for the evaluation. BR-16A potentiated the effect of triazolam (0.1 mg/kg, ip) and alprazolam (0.25 mg/kg, ip). Melatonin (5.0 mg/kg, ip) and zolpidem (0.5 mg/kg, ip) did not produce any significant effect on sleep parameters. However, alprazolam (0.25mg/kg, ip) potentiated the effect of BR-16A (100 mg/kg, po) in higher dose only. Sleep promoting effect of BR-16A in combination with GABAergic drugs (triazolam and alprazolam,) suggested that these drugs have common mechanism in sleep promoting effect of pentobarbitone and could be used along with other GABAergic hypnotics for the treatment of insomnia. This may reduce the dose of the latter drug(s), BR-16A can be used for the treatment of sleep and sleep-relateddisorders.
机译:戊巴比妥诱导的催眠试验被用作动物模型,以探索BR-16A(一种多草药配方)在睡眠中的作用。戊巴比妥产生快速的睡眠潜伏期(发作)和总睡眠时间延长(持续时间)。睡眠潜伏期和总睡眠时间被用作评估的参数。 BR-16A增强了三唑仑(0.1 mg / kg,ip)和阿普唑仑(0.25 mg / kg,ip)的作用。褪黑激素(5.0 mg / kg,腹膜内)和唑吡坦(0.5 mg / kg,腹膜内)对睡眠参数没有明显影响。但是,阿普唑仑(0.25mg / kg,ip)仅在较高剂量时才增强BR-16A(100 mg / kg,po)的作用。 BR-16A与GABA能药物(三唑仑和阿普唑仑)合用的促睡眠作用表明,这些药物在戊巴比妥的促睡眠作用中具有共同的机制,可与其他GABA催眠药一起用于治疗失眠。这可以减少后一种药物的剂量,BR-16A可用于治疗睡眠和与睡眠有关的疾病。

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