Section on Clinical Psychoneuroendocrinology and Neuropsychopharmacology, Laboratory of Clinical and Translational Studies, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD 20892, USA.
Alcohol Clin Exp Res. 2013 Feb;37(2):191-3. doi: 10.1111/acer.12064. Epub 2012 Dec 27.
Recent preclinical and clinical evidence using prazosin indicates that α(1) -blockade may represent a new approach to treat alcohol dependence (AD). While most of the alcohol research on α(1) -blockade has been conducted testing prazosin, O'Neil and colleagues recently performed a set of preclinical experiments testing another α(1) -blocker, doxazosin, which has a longer half-life that may enhance clinical utility. Doxazosin and prazosin share the same chemical structure, in which the central element is a piperazine ring. O'Neil and colleagues' main results are that doxazosin significantly reduced alcohol intake without affecting locomotor activity. As such, O'Neil and colleagues provide the first preclinical evidence of the possible role of doxazosin in AD. Additional translational research is needed to further test this hypothesis.
最近使用哌唑嗪的临床前和临床证据表明,α(1) 受体阻滞剂可能代表了治疗酒精依赖(AD)的一种新方法。虽然大多数关于α(1) 受体阻滞剂的酒精研究都是针对哌唑嗪进行的,但 O'Neil 及其同事最近进行了一组使用另一种α(1) 受体阻滞剂多沙唑嗪的临床前实验,其半衰期更长,可能增强临床实用性。多沙唑嗪和哌唑嗪具有相同的化学结构,其中中央元素是哌嗪环。O'Neil 及其同事的主要结果是,多沙唑嗪可显著减少酒精摄入量,而不影响运动活动。因此,O'Neil 及其同事提供了多沙唑嗪在 AD 中可能作用的第一个临床前证据。需要进一步的转化研究来进一步测试这一假设。