首页> 外文期刊>European Journal of Pharmacology: An International Journal >Effects of imipramine or GABA(B) receptor ligands on the immobility, swimming and climbing in the forced swim test in rats following discontinuation of cocaine self-administration.
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Effects of imipramine or GABA(B) receptor ligands on the immobility, swimming and climbing in the forced swim test in rats following discontinuation of cocaine self-administration.

机译:可卡因自我给药中断后,丙咪嗪或GABA(B)受体配体对大鼠强制游泳试验中的不动,游泳和攀爬的影响。

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We tested if discontinuation of cocaine self-administration can lead to the development of depressive-like symptoms in the forced swim test expressed as changes in immobility, swimming and climbing behaviors in rats. A "yoked" procedure in which rats were run simultaneously in groups of three, with two rats received the passive injection of cocaine or saline, was employed. Later, we examined whether acute treatment with the classical antidepressant imipramine or GABA(B) receptor ligands could alter the increases in immobility recorded after discontinuation of self-administered cocaine. We found a significant increase (44%) in the immobility time 3 days following discontinuation of cocaine (0.5mg/kg/infusion/2h daily) self-administration for 14 days; such enhancement resembled that observed in rats following the chronic mild stress. Acute administration with imipramine (15 or 30 mg/kg), the GABA(B) receptor agonists baclofen (0.125 mg/kg) and SKF 97541 (0.005 mg/kg), the positive allosteric modulator CGP 7930 (0.3mg/kg) or the antagonist SCH 50911 (0.3mg/kg) counteracted the cocaine discontinuation-induced enhancement in the immobility time. The enhanced immobility time in rats that self-administered cocaine (but not given cocaine passively) may reflect the motivated or cognitive processes of reinforced responding of cocaine and could be a potential driver of the addiction process per se. Moreover, either blockade or stimulation of GABA(B) receptors by their ligands in very low doses attenuated the enhanced immobility time in rats after discontinuation of cocaine self-administration and these findings extend preclinical studies demonstrating the potential involvement of GABA(B) receptor ligands to reduce cocaine craving.
机译:我们测试了可卡因自我给药的中断是否会导致强迫游泳试验中抑郁样症状的发展,这种症状表现为大鼠不动,游泳和攀爬行为的变化。采用“叉腰”程序,其中大鼠每三只一组同时奔跑,两只大鼠被动注射可卡因或盐水。后来,我们检查了用经典抗抑郁药丙咪嗪或GABA(B)受体配体进行的急性治疗是否可以改变中止自行服用可卡因后记录的固定性增加。我们发现,停用可卡因(每天0.5mg / kg /输注2h)连续14天后3天的不动时间显着增加(44%);这种增强类似于慢性轻度应激后在大鼠中观察到的增强。急性用丙咪嗪(15或30 mg / kg),GABA(B)受体激动剂巴氯芬(0.125 mg / kg)和SKF 97541(0.005 mg / kg),正变构调节剂CGP 7930(0.3mg / kg)或拮抗剂SCH 50911(0.3mg / kg)抵消了可卡因停药引起的固定时间延长。自行服用可卡因(而不是被动给予可卡因)的大鼠不动时间增加,可能反映了可卡因反应增强的动机或认知过程,并且可能是成瘾过程本身的潜在驱动因素。此外,可卡因自我给药中断后,配体以极低的剂量阻断或刺激GABA(B)受体可减弱大鼠固定时间的延长,这些发现扩展了临床前研究,证明了GABA(B)受体配体的潜在参与减少可卡因的渴望。

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