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:含丙胺或GABA(B)受体配体对在可卡因自我管理中停止后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:我们测试了如果可卡因自我管理的停药可以导致强迫游泳试验中的抑郁样症状的发展,这是由于大鼠的不动,游泳和攀爬行为的变化表示。一种“Yoked”程序,其中在三组中同时进行大鼠,用两只大鼠接受被动注射可卡因或盐水。后来,我们检查了常规抗抑郁脂钙或GABA(B)受体配体的急性治疗是否可以改变在停止自我施用的可卡因后记录的不动的增加。在停止可卡因(0.5mg / kg /输注/ 2小时)自我施用14天后,我们发现不动时间的显着增加(44%)3天;这种增强类似于在慢性轻度胁迫后的大鼠中观察到的。用含丙胺(15或30mg / kg),GABA(B)受体激动剂Baclofen(0.125mg / kg)和SKF 97541(0.005mg / kg),正变构调制器CGP 7930(0.3mg / kg)或拮抗剂SCH 50911(0.3mg / kg)抵消了可卡因停止诱导的不动度时间增强。在自我给药的可卡因(但没有被赋予Cocaine被动)的大鼠中增强的不可动脉时间可以反映可卡因的增强响应的动机或认知过程,并且可以是本身的成瘾过程的潜在驱动因素。此外,通过它们的配体在非常低剂量中阻断或刺激GABA(B)受体在停止可卡因自我给药后的大鼠中的增强的不可动时间,并且这些发现扩展了临床前研究,证明了GABA(B)受体配体的潜在累及减少可卡因渴望。

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