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mu-Opioid receptor in the CA1 involves in tramadol and morphine cross state-dependent memory

机译:CA1中的MU-阿片受体涉及曲马多和吗啡交叉状态依赖记忆

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摘要

In the present study, the effect of tramadol - an opioid painkiller drug with abuse potential- on amnesia and state-dependent memory and its interaction with the opioidergic system was investigated in male Wistar rats. Intra CA-1 administration of tramadol (0.5, 1, and 2 mu g/rat) before training, dose-dependently decreased the learning ability in passive avoidance task. Amnesia induced by pre-train tramadol administration was significantly reversed by pre-test administration of tramadol (1 mu g/rat). Pre-test administration of naltrexone (a mu-opioid receptor (MOR) antagonist) inhibited the effect of tramadol on memory retrieval. In addition, the pre-test administration of morphine (1 mu g/rat, intra-CA1) also reversed memory impairment induced by pre-train tramadol administration. Although, pre-train morphine administration (1 mu g/rat, intra-CA1), induced memory impairment reversed by pre-test tramadol administration (1 mu g/rat, intra-CA1). In addition, the level of MOR in the hippocampus decreased in animals with memory impairment due to using tramadol in the training day. However, state-dependent retrieval using tramadol or cross state-dependent retrieval using morphine enhanced the MOR level in the hippocampus.
机译:在本研究中,在雄性Wistar大鼠中研究了曲马多毒液 - 一种阿片类止痛药药与滥用漏洞和状态依赖性记忆的影响及其与术语的相互作用。 CA-1曲马多(0.5,1和2μg/大鼠)在训练前给药,剂量依赖性降低了被动避免任务中的学习能力。通过火车前曲马多的静脉曲轨诱导的敏捷者通过预测试施用曲马多(1μg/大鼠)显着逆转。纳曲酮的预测试施用(MU-阿片受体(MOR)拮抗剂)抑制曲马多对记忆检索的影响。此外,对吗啡的预测试施用(1μg/大鼠,CA1)也逆转火车前曲马多给药诱导的记忆障碍。虽然火车前吗啡给药(1μg/大鼠,CA1),所诱导的记忆损伤通过预测试曲马多给药(1μg/大鼠,CA1)。此外,由于在训练日中使用曲马多,海马在海马中的莫尔在动物中减少。然而,使用曲马多或交叉状态依赖检索的状态依赖性检索,使用吗啡增强了海马的MOR水平。

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