G protein-coupled receptor kinase/β-arrestin systems and drugs of abuse -: Psychostimulant and opiate studies in knockout mice

被引:31
作者
Bohn, LM
Gainetdinov, RR
Caron, MG [1 ]
机构
[1] Ohio State Univ, Coll Med & Publ Hlth, Dept Pharmacol, Columbus, OH 43210 USA
[2] Duke Univ, Med Ctr, Dept Cell Biol, Howard Hughes Med Inst Labs, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
关键词
GPCR kinase (GRK); G protein-coupled receptor (GPCR); desensitization; arrestin; morphine; cocaine; amphetamine; knockout mice; drug abuse; addiction;
D O I
10.1385/NMM:5:1:041
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
G protein-coupled receptors (GPCRs) currently represent pharmaceutical targets for numerous medicinal compounds that are used to treat conditions ranging from blood pressure dysregulation to depression to pain, demonstrating the wide range of functions mediated by this receptor family. GPCR activation is determined not only by the initiation of signaling cascades but also by regulatory mechanisms that control the extent and duration of their signals. The balance of activation and desensitization dictate the ultimate physiological response to both endogenous and exogenous receptor stimuli. Therefore, these mechanisms may play a particularly relevant role during chronic exposure to agonists such as in conditions when drugs are abused. Two major classes of drugs of abuse, opiates and psychostimulants, both use either direct or indirect GPCR signaling mechanisms to mediate their effects. Therefore, the regulation of GPCRs may have bearing on the neuronal adaptations that underlie the reinforcing properties of drugs of abuse.
引用
收藏
页码:41 / 50
页数:10
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