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Interactions of the opioid and cannabinoid systems in reward: Insights from knockout studies

机译:阿片类药物和大麻素系统在奖励中的相互作用:淘汰赛研究中的见解

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The opioid system consists of three receptors, mu, delta, and kappa, which are activated by endogenous opioid peptides (enkephalins, endorphins, and dynorphins). The endogenous cannabinoid system comprises lipid neuromodulators (endocannabinoids), enzymes for their synthesis and their degradation and two well-characterized receptors, cannabinoid receptors CB1 and CB2. These systems play a major role in the control of pain as well as in mood regulation, reward processing and the development of addiction. Both opioid and cannabinoid receptors are coupled to G proteins and are expressed throughout the brain reinforcement circuitry. Extending classical pharmacology, research using genetically modified mice has provided important progress in the identification of the specific contribution of each component of these endogenous systems in vivo on reward process. This review will summarize available genetic tools and our present knowledge on the consequences of gene knockout on reinforced behaviors in both systems, with a focus on their potential interactions. A better understanding of opioid–cannabinoid interactions may provide novel strategies for therapies in addicted individuals.
机译:阿片类药物由三个受体,亩,三角洲和κ,由内源性阿片类药物(Enkephalins,内啡肽和染月藻)激活。内源性大麻素体系包括脂质神经调节剂(Endocannabinoids),其合成的酶及其降解和两个良好表征的受体,大麻素受体CB1和CB2。这些系统在控制疼痛以及情绪调节方面发挥了重要作用,奖励加工和成瘾的发展。阿片类药物和大麻素受体偶联至G蛋白,在整个脑加强电路中表达。延伸古典药理学,使用遗传修饰小鼠的研究在鉴定了这些内源系统在体内对奖励过程中的每个组分的具体贡献提供了重要进展。本综述将总结有可用的遗传工具和我们对基因敲除对两个系统中加强行为的后果的看法,重点关注其潜在的互动。更好地了解阿片类药物相互作用可以为上瘾的人提供新的疗法策略。

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