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食欲抑制剂、心脏瓣膜病与联合药物治疗

Appetite suppressants, cardiac valve disease and combination pharmacotherapy.

作者信息

Rothman Richard B, Baumann Michael H

机构信息

Clinical Psychopharmacology Section, Intramural Research Program, National Institutes of Health, National Institute on Drug Abuse, Department of Health and Human Services, Baltimore, MD 21224, USA.

出版信息

Am J Ther. 2009 Jul-Aug;16(4):354-64. doi: 10.1097/MJT.0b013e31817fde95.

Abstract

The prevalence of obesity in the United States is a major health problem associated with significant morbidity, mortality, and economic burden. Although obesity and drug addiction are typically considered distinct clinical entities, both diseases involve dysregulation of biogenic amine neuron systems in the brain. Thus, research efforts to develop medications for treating drug addiction can contribute insights into the pharmacotherapy for obesity. Here, we review the neurochemical mechanisms of selected stimulant medications used in the treatment of obesity and issues related to fenfluramine-associated cardiac valvulopathy. In particular, we discuss the evidence that cardiac valve disease involves activation of mitogenic serotonin 2B (5-HT2B) receptors by norfenfluramine, the major metabolite of fenfluramine. Advances in medication discovery suggest that novel molecular entities that target 2 different neurochemical mechanisms, that is, "combination pharmacotherapy," will yield efficacious antiobesity medications with reduced adverse side effects.

摘要

美国肥胖症的流行是一个重大的健康问题,与显著的发病率、死亡率及经济负担相关。尽管肥胖症和药物成瘾通常被视为不同的临床病症,但这两种疾病都涉及大脑中生物胺神经元系统的调节异常。因此,开发治疗药物成瘾的药物的研究工作可为肥胖症的药物治疗提供见解。在此,我们综述了用于治疗肥胖症的某些刺激性药物的神经化学机制以及与芬氟拉明相关的心脏瓣膜病的相关问题。特别是,我们讨论了心脏瓣膜疾病涉及去甲芬氟拉明(芬氟拉明的主要代谢产物)激活有丝分裂原性血清素2B(5-HT2B)受体的证据。药物研发的进展表明,针对两种不同神经化学机制的新型分子实体,即“联合药物疗法”,将产生具有减少副作用的有效抗肥胖药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88b0/2713386/3f25ab8e364a/nihms-85810-f0001.jpg

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