Nucleus accumbens AGS3 expression drives ethanol seeking through Gβγ

被引:68
作者
Bowers, M. Scott [1 ]
Hopf, F. Woodward [1 ]
Chou, Jonathan K. [1 ]
Guillory, Anitra M. [1 ]
Chang, Shao-Ju [1 ]
Janak, Patricia H. [1 ,2 ]
Bonci, Antonello [1 ,2 ]
Diamond, Ivan
机构
[1] Univ Calif San Francisco, Dept Neurol, Ernest Gallo Clin & Res Ctr, Emeryville, CA 94608 USA
[2] Univ Calif San Francisco, Wheeler Ctr Neurobiol Addict, San Francisco, CA 94143 USA
关键词
self-administration; reinstatement; alcohol deprivation effect; Gi alpha; G protein;
D O I
10.1073/pnas.0706999105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
Approximately 90% of alcoholics relapse within 4 years, in part because of an enhanced motivation to seek alcohol (EtOH). A novel G protein modulator (Gpsm1/AGS3) was up-regulated in the rat nucleus accumbens core (NAcore) but not in other limbic nuclei during abstinence from operant EtOH self-administration. Furthermore, NAcore AGS3 knockdown reduced EtOH seeking to pre-abstinence levels in a novel rat model of compulsive, human EtOH seeking. AGS3 can both inhibit G protein Gi alpha-mediated signaling and stimulate G beta gamma-mediated signaling. Accordingly, sequestration of G beta gamma, but not Gi alpha knockdown, significantly reduced EtOH seeking to pre-abstinence levels. Thus, AGS3 and G beta gamma are hypothesized to gate the uncontrolled motivation to seek EtOH during abstinence. AGS3 up-regulation during abstinence may be a key determinant of the transition from social consumption to compulsion-like seeking during relapse.
引用
收藏
页码:12533 / 12538
页数:6
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