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Intravenous self‐administration of benzydamine, a non‐steroidal anti‐inflammatory drug with a central cannabinoidergic mechanism of action

机译:苯霉素的静脉内酰胺,一种非甾体抗炎药,具有中央大麻的作用机制

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Abstract Benzydamine (BZY) is a non‐steroidal anti‐inflammatory drug used for the topical treatment of inflammations of the oral and vaginal mucosae. Virtually nothing is known about the central pharmacological actions of BZY. Yet there are reports of voluntary systemic overdosage of BZY in drug addicts, resulting in a euphoric, hallucinatory state. In the present study, we investigated the reinforcing properties of BZY in a rat self‐administration paradigm. We found that BZY has a powerful reinforcing effect and that this effect is greatly facilitated in animals that already had substance experience, having previously self‐administered heroin and cocaine, indicating cross sensitization between BZY and other common drugs of abuse. We then assessed the effect of BZY on prelimbic cortex‐to‐nucleus accumbens glutamatergic transmission, using field recordings in rat parasagittal brain slices. BZY dose‐dependently reduced both field excitatory post synaptic potential amplitude and paired pulse ratio, suggesting a presynaptic mechanism of action. Similarly to the in vivo paradigm, also the electrophysiological effects of BZY were potentiated in slices from animals that had undergone cocaine and heroin self‐administration. Furthermore, BZY‐induced Long Term Depression (LTD)‐like responses in the prelimbic cortex‐to‐nucleus accumbens circuitry were significantly reduced in the presence of the CB1 receptor antagonist AM251. These findings provide firm evidence of the abuse liability of BZY and suggest a possible cannabinoidergic mechanism of action. Further research is needed in order to give insights into the molecular mechanism underlying BZY psychoactive and reinforcing effects, to better understand its abuse potential.
机译:摘要苯并胺(BZY)是一种非甾体抗炎药,用于局部治疗口腔和阴道粘膜的炎症。几乎没有任何关于BZY的中央药理学作用所知的。然而,有报道有关于吸毒成瘾者的BZY自愿全身过量的报道,导致欣快,幻觉状态。在本研究中,我们研究了在大鼠自我管理范式中的BZY的增强性质。我们发现BZY具有强大的增强效果,并且这种效果在已经有物质经验的动物中大大促进,具有先前自我管理的海洛因和可卡因,表明BZY和其他滥用常见药物之间的交叉敏化。然后,我们评估了BZY对前列腺皮质到核的作用,使用大鼠促进脑切片的现场记录。 BZY剂量依赖性地减少了突触后突触潜在幅度和配对脉冲比的两种兴奋性突起,暗示了突触前的作用机制。类似于体内范式,BZY的电生理学效应也被从未助成的动物和海洛因自我给药的动物的切片中加强。此外,在CB1受体拮抗剂AM251存在下显着降低了BZY诱导的长期凹陷(LTD) - 在前列腺皮质 - 核抵抗电路中的反应。这些调查结果提供了坚定的证据表明BZY的滥用责任,并提出了可能的加盟机制的行动机制。需要进一步的研究,以便在BZY精神活性和增强效果下面的分子机制深入了解,以更好地了解其滥用潜力。

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