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首页> 外文期刊>Journal of pharmacological sciences. >Basic and Translational Research on Proteinase-Activated Receptors: Regulation of Nicotine Reward by the Tissue Plasminogen Activator (tPA) – Plasmin System via Proteinase-Activated Receptor 1
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Basic and Translational Research on Proteinase-Activated Receptors: Regulation of Nicotine Reward by the Tissue Plasminogen Activator (tPA) – Plasmin System via Proteinase-Activated Receptor 1

机译:蛋白酶激活受体的基础研究和转化研究:组织纤溶酶原激活物(tPA)–通过蛋白酶激活受体的纤溶酶系统调节烟碱奖励1

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References(50) Cited-By(5) Nicotine, a primary component of tobacco, is one of the most abused drugs worldwide. Mesolimbic dopaminergic neurons mediate the rewarding effects of abused drugs, including nicotine. We show that the tissue plasminogen activator (tPA) – plasmin system regulates nicotine-induced reward and dopamine release in the nucleus accumbens (NAc) by activating proteinase-activated receptor 1 (PAR1). Nicotine-induced conditioned place preference and dopamine release in the NAc are diminished in tPA knockout (tPA−/−) mice. The defect of nicotine-induced dopamine release in tPA−/− mice is reversed by microinjection of either exogenous tPA or plasmin into the NAc. Acute nicotine treatment increases tPA protein levels and promoted the release of tPA into the extracellular space. The expression of PAR1 on dopaminergic neurons is evident and the activation of PAR1 by plasmin is demonstrated by assaying GTP-γS binding. Finally, nicotine-induced conditioned place preference and dopamine release are diminished in PAR1−/− mice. These findings suggest that targeting the tPA-plasmin–PAR1 system would provide new therapeutic approaches for the treatment of nicotine dependence.
机译:参考文献(50)被引用的(5)尼古丁是烟草的主要成分,是世界上滥用最严重的药物之一。中脑边缘多巴胺能神经元介导滥用药物(包括尼古丁)的有益作用。我们表明,组织纤溶酶原激活物(tPA)–纤溶酶系统通过激活蛋白酶激活受体1(PAR1)调节尼古丁诱导的伏击核素(NAc)中的奖励和多巴胺释放。在tPA基因敲除(tPA-/-)小鼠中,烟碱诱导的NAc条件性位置偏好和多巴胺释放减少。通过将外源性tPA或纤溶酶微注射到NAc中,可以逆转tPA-/-小鼠中尼古丁引起的多巴胺释放的缺陷。急性尼古丁治疗可增加tPA蛋白质水平,并促进tPA释放到细胞外空间。 PAR1在多巴胺能神经元上的表达是明显的,并且通过测定GTP-γS结合证明了纤溶酶对PAR1的激活。最后,在PAR1-/-小鼠中,烟碱诱导的条件性位置偏好和多巴胺释放减少。这些发现表明,靶向tPA-纤溶酶-PAR1系统将为尼古丁依赖性治疗提供新的治疗方法。

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