Building better strategies to develop new medications in Alcohol Use Disorder: Learning from past success and failure to shape a brighter future

被引:9
|
作者
Cannella, Nazzareno [1 ]
Ubaldi, Massimo [1 ]
Masi, Alessio [1 ]
Bramucci, Massimo [1 ]
Roberto, Marisa [2 ]
Bifone, Angelo [3 ,4 ]
Ciccocioppo, Roberto [1 ]
机构
[1] Univ Camerino, Sch Pharm, Pharmacol Unit, Via Madonna delle Carceri 9, I-62032 Camerino, MC, Italy
[2] Scripps Res Inst, Dept Neurosci, La Jolla, CA 92037 USA
[3] Ist Italian Tecnol, Ctr Neurosci & Cognit Syst UniTn, Corso Bettini 31, I-38068 Rovereto, Italy
[4] Univ Torino, Dept Mol Biotechnol & Hlth Sci, Turin, Italy
来源
基金
美国国家卫生研究院;
关键词
Alcoholism; Ethanol; Opioids; Brain imaging; CRF; PET; fMRI; CORTICOTROPIN-RELEASING-FACTOR; POSITIVE ALLOSTERIC MODULATOR; PLACEBO-CONTROLLED TRIAL; GAMMA-HYDROXYBUTYRIC ACID; STATE FUNCTIONAL CONNECTIVITY; ETHANOL-SEEKING BEHAVIOR; VENTRAL TEGMENTAL AREA; OPIOID RECEPTOR GENE; FREE-CHOICE DRINKING; PREFERRING MSP RATS;
D O I
10.1016/j.neubiorev.2019.05.014
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Alcohol Use Disorder (AUD) is a chronic disease that develops over the years. The complexity of the neurobiological processes contributing to the emergence of AUD and the neuroadaptive changes occurring during disease progression make it difficult to improve treatments. On the other hand, this complexity offers researchers the possibility to explore new targets. Over years of intense research several molecules were tested in AUD; in most cases, despite promising preclinical data, the clinical efficacy appeared insufficient to justify futher development. A prototypical example is that of corticotropin releasing factor type 1 receptor (CRF1R) antagonists that showed significant effectiveness in animal models of AUD but were largely ineffective in humans. The present article attempts to analyze the most recent venues in the development of new medications in AUD with a focus on the most promising drug targets under current exploration. Moreover, we delineate the importance of using a more integrated translational framework approach to correlate preclinical findings and early clinical data to enhance the probability to validate biological targets of interest.
引用
收藏
页码:384 / 398
页数:15
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