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首页> 外文期刊>Behavioural Brain Research: An International Journal >Glucocorticoid receptors in the basolateral amygdala mediated the restraint stress-induced reinstatement of methamphetamine-seeking behaviors in rats
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Glucocorticoid receptors in the basolateral amygdala mediated the restraint stress-induced reinstatement of methamphetamine-seeking behaviors in rats

机译:基底外侧杏仁糖膜的糖皮质激素受体介导约束应激诱导大鼠甲基苯丙胺寻求行为的恢复

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Methamphetamine (METH) addiction is a growing epidemic worldwide. It is a common psychiatric disease and stress has an important role in the drug seeking and relapse behaviors. The involvement of the basolateral amygdala (BLA) in effects of stress on the reward pathway has been discussed in several studies. In this study, we tried to find out the involvement of glucocorticoid receptors (GRs) in the BLA in stress-induced reinstatement of the extinguished METH-induced conditioned place preference (CPP) in rats. The CPP paradigm was done in eighty-one adult male Wistar rats weighing 220-250 g. The animals received a daily injection of methamphetamine (0.5 mg/kg), during the conditioning phase. In extinction phase, the rats were put in the CPP box for 30 min per day for 8 days. After the extinction, the animals were exposed to acute restraint stress (ARS), 3h before subcutaneous administration of sub-threshold dose of methamphetamine (0.125 mg/kg), based on our previous study, in reinstatement phase. In separated groups, the rats were exposed to chronic restraint stress (CRS) for 1 h each day during the extinction phase. To block the GRs in BLA, the animals unilaterally received RU38486 as GRs antagonist (10, 30 and 90 ng/0.3 mu l DMSO) in all ARS groups on reinstatement day. In separated experiments, RU38486 (3, 10 and 30 ng/0.3 mu l DMSO) was microinjected into the BLA in CRS groups prior to exposure to stress every day in extinction phase. The results revealed that intra-BLA RU38486 in ARS (90 ng) and CRS (10 and 30 ng) groups significantly prevented the stress-induced reinstatement. It can be proposed that stress partially exerts its effect on the reward pathway via GRs in the BLA. This effect was not quite similar in acute and chronic stress conditions.
机译:甲基苯丙胺(甲基)成瘾是全球生长的流行病。它是一种常见的精神疾病,压力在药物寻求和复发行为中具有重要作用。在几项研究中讨论了基石运动amygdala(BLA)对压力对奖励途径的影响。在这项研究中,我们试图找出糖皮质激素受体(GRS)在BLA中的应激诱导的大鼠熄灭的甲状腺诱导条件偏好(CPP)的恢复方案中的参与。 CPP范例是在八十一成年男性Wistar大鼠中进行的,重220-250克。在调理相期间,动物每天注射甲基苯丙胺(0.5mg / kg)。在消灭阶段,将大鼠置于CPP盒中每天30分钟,持续8天。消失后,将动物暴露于急性约束应激(ARS),3h在皮下施用甲基苯丙胺(0.125mg / kg)的甲基戊酮(0.125mg / kg)的恢复阶段。在分离的基团中,在消光相期间每天暴露于慢性约束应激(CRS)1小时。为了阻断BLA中的GR,动物在恢复日的所有ARS组中,动物单侧地接受RU38486作为GRS拮抗剂(10,30和90ng /0.3μldmso)。在分离的实验中,在暴露在消光相中每天暴露于应力之前,将Ru38486(3,10和30ng /0.3μg/0.3μmLdmso)在CRS基团中微量注射到BLA中。结果表明,ARS(90ng)和Crs(10和30ng)组中的BLA内部ru38486显着阻止了应力诱导的恢复。可以提出,应力部分地施加对BLA中的奖励途径的影响。这种效果在急性和慢性胁迫条件下并不相似。

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