Hooked on benzodiazepines: GABAA receptor subtypes and addiction

被引:228
作者
Tan, Kelly R. [1 ]
Rudolph, Uwe [2 ,3 ]
Luescher, Christian [1 ,4 ]
机构
[1] Univ Geneva, Fac Med, Dept Basic Neurosci, CH-1211 Geneva, Switzerland
[2] Harvard Univ, Sch Med, McLean Hosp, Lab Genet Neuropharmacol, Belmont, MA 02478 USA
[3] Harvard Univ, Sch Med, Dept Psychiat, Belmont, MA 02478 USA
[4] Univ Hosp Geneva, Neurol Clin, Dept Clin Neurosci, CH-1211 Geneva, Switzerland
基金
瑞士国家科学基金会;
关键词
VENTRAL TEGMENTAL AREA; MESOLIMBIC DOPAMINE SYSTEM; AMINOBUTYRIC ACID(A) RECEPTORS; EVOKED SYNAPTIC PLASTICITY; CEREBELLAR GRANULE CELLS; LONG-TERM POTENTIATION; IN-VIVO MICRODIALYSIS; NUCLEUS-ACCUMBENS; BINDING-SITE; A RECEPTORS;
D O I
10.1016/j.tins.2011.01.004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Benzodiazepines are widely used clinically to treat anxiety and insomnia. They also induce muscle relaxation, control epileptic seizures, and can produce amnesia. Moreover, benzodiazepines are often abused after chronic clinical treatment and also for recreational purposes. Within weeks, tolerance to the pharmacological effects can develop as a sign of dependence. In vulnerable individuals with compulsive drug use, addiction will be diagnosed. Here we review recent observations from animal models regarding the cellular and molecular basis that might underlie the addictive properties of benzodiazepines. These data reveal how benzodiazepines, acting through specific GABA(A) receptor subtypes, activate midbrain dopamine neurons, and how this could hijack the mesolimbic reward system. Such findings have important implications for the future design of benzodiazepines with reduced or even absent addiction liability.
引用
收藏
页码:188 / 197
页数:10
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