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Diverse effects of intrathecal pituitary adenylate cyclase-activating polypeptide on nociceptive transmission in mice spinal cord.

机译:鞘内垂体腺苷酸环化酶激活多肽对小鼠脊髓伤害性传递的不同作用。

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Pituitary adenylate cyclase-activating polypeptide (PACAP) immunoreactive neural elements have been detected in the mouse spinal cord. The discrepancy of PACAP actions in the role of sensory transmission has been proposed to have potentiation and inhibition on nociceptive responses after intrathecal application of PACAP. The aim of the present study was to assess nociceptive transmission of PACAP in the mouse spinal cord by comparison with that of substance P (SP). The intrathecal injection of PACAP induced licking or scratching behavior similar to that of SP. These PACAP-induced aversive behaviors showed different manner from SP-induced responses in point of time course. SP-induced aversive responses quickly increased and suddenly disappeared almost within 1 min. Meanwhile, following a long latency after the injection, PACAP-induced aversive responses gradually appeared, and then persisted more than 60 min. In the early phase, PACAP produced an increase of tail flick latency. Pretreatment with 6-hydroxydopamine (6-OHDA) which destroys noradrenaline neuron of descending pain inhibitory systems in the spinal cord markedly abridged the latency and augmented the duration of PACAP-induced aversive responses. In this way, PACAP exhibits diverse effects on nociception, such as an analgesic role in early phase of the injection and subsequently lasting algesia. These results suggest that PACAP as a neurotransmitter or neuromodulator might have crucial role in nociceptive transmission system.
机译:在小鼠脊髓中已检测到垂体腺苷酸环化酶激活多肽(PACAP)免疫反应性神经元。有人提出,鞘内应用PACAP后,PACAP作用在感觉传递中的差异可能会增强和抑制伤害感受。本研究的目的是通过与物质P(SP)的比较来评估PACAP在小鼠脊髓中的伤害性传递。鞘内注射PACAP会引起类似于SP的舔lick或抓挠行为。这些PACAP诱导的厌恶行为表现出与SP诱导的反应不同的方式。 SP引起的厌恶反应迅速增加,几乎在1分钟内突然消失。同时,注射后经过长时间潜伏,PACAP引起的厌恶反应逐渐出现,并持续超过60分钟。在早期阶段,PACAP使甩尾潜伏期增加。用6-羟基多巴胺(6-OHDA)预处理可破坏脊髓下行疼痛抑制系统的去甲肾上腺素神经元,从而显着缩短潜伏期并延长PACAP引起的厌恶反应的持续时间。这样,PACAP对伤害感受表现出多种作用,例如在注射初期和随后的持续性痛觉过敏中起镇痛作用。这些结果表明,PACAP作为神经递质或神经调节剂可能在伤害性传递系统中起关键作用。

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