Differential involvement of GABAA and GABAB receptors in propofol self-administration in rats

被引:12
|
作者
Yang, Bo [2 ,3 ]
Wang, Ben-fu [2 ,3 ]
Lai, Miao-jun [1 ]
Zhang, Fu-qiang [1 ]
Yang, Xiao-wei [2 ,3 ]
Zhou, Wen-hua [1 ]
Lian, Qing-quan [2 ,3 ]
机构
[1] Ningbo Univ, Sch Med, Ningbo Addict Res & Treatment Ctr, Ningbo 315010, Zhejiang, Peoples R China
[2] Wenzhou Med Coll, Affiliated Hosp 2, Dept Anesthesiol, Wenzhou 325000, Peoples R China
[3] Wenzhou Med Coll, Inst Neuroendocrinol, Wenzhou 325000, Peoples R China
基金
中国国家自然科学基金;
关键词
addiction; propofol; drug abuse; GABA receptors; baclofen; bicuculline; ventral tegmental area (VTA); locomotor activity; VENTRAL TEGMENTAL AREA; NUCLEUS-ACCUMBENS; DOPAMINE RELEASE; AFFECTIVE STATE; REINFORCEMENT; LOCALIZATION; AGONISTS; NEURONS; BRAIN; ABUSE;
D O I
10.1038/aps.2011.123
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Aim: Propofol has shown abuse potential. The aim of the present study is to investigate the effects of GABA(A) antagonist and GABA(B) agonist on propofol reinforcement. Methods: Sprague-Dawley rats were trained to self-administer propofol at a dose of 1.7 mg/kg per infusion under a fixed ratio (FR1) schedule of reinforcement for 14 d. In a separate set of experiments, food-maintained self-administration under a fixed ratio (FR5) schedule and locomotor activities of Sprague-Dawley rats were examined. Results: GABA(A) receptor antagonist bicuculline (0.25 mg/kg, ip) significantly increased the number of injections and active responses. Pretreatment with GABA(B) receptor agonist baclofen (3 mg/kg, ip) significantly decreased the number of active responses and total infusions of propofol during the training session. Moreover, microinjection of baclofen (50 and 100 ng/side) into the ventral tegmental area (VTA) significantly decreased the number of active responses and total infusions of propofol. Neither baclofen (1-3 mg/kg, ip) nor bicuculline (0.25-1 mg/kg, ip) affected food-maintained responses or motor activities. Conclusion: Propofol maintains its reward properties partially through GABA(A) receptor activation. Stimulation of GABA(B) receptors in VTA may counteract the reinforcing properties of propofol.
引用
收藏
页码:1460 / 1465
页数:6
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