Postgraduate Program in Health Sciences, National Institute for Translational Medicine, University of Southern Santa Catarina, Criciúma, SC, Brazil.
J Neural Transm (Vienna). 2010 Mar;117(3):309-16. doi: 10.1007/s00702-010-0373-z. Epub 2010 Feb 4.
Previous studies have suggested that bipolar disorder may be associated with oxidative stress. Administration of D: -amphetamine (AMPH) has been put forward as an animal model of mania, and has shown to increase oxidative stress parameters in the rat brain. Thus, we have used the gastrin-releasing peptide receptor antagonist [D-Tpi(6)Leu(13)psi (CH(2)NH)-Leu(14)] bombesin (RC-3095) as a pharmacological tool to investigate the role of bombesin-like peptides in the redox balance in the hippocampus and cortex of rats treated with AMPH. Rats were given a single 10 ml/kg intraperitoneal (i.p.) injection of saline (SAL) or RC-3095 (0.1, 1.0 or 10.0 mg/kg) followed by an i.p. injection of SAL or amphetamine (AMPH 2.0 mg/kg) 30 min later. Locomotor activity was evaluated 2 h after the last drug injection. The thiobarbituric acid reactive substances (TBARS), protein carbonyl formation, superoxide dismutase and catalase (CAT) activity were measured in hippocampus, striatum and cortex as markers of oxidative stress. The results show that RC-3095 blocks AMPH-induced hyperlocomotion. Moreover, specific doses of RC-3095 alone increased the levels of oxidative stress in the dorsal hippocampus and cortex. However, when AMPH was subsequently administrated, RC-3095 decreased TBARS and protein carbonyls formation and increased the superoxide dismutase and CAT activity in the hippocampus, striatum and cortex. The effects of GRPR antagonist seemed to be region and dose specific. In conclusion, the results suggest that GRPR antagonists might display antioxidant properties in the brain.
先前的研究表明,双相情感障碍可能与氧化应激有关。D: -苯丙胺(AMPH)的给药已被提出作为躁狂的动物模型,并已显示出增加大鼠大脑中的氧化应激参数。因此,我们使用胃泌素释放肽受体拮抗剂[D-Tpi(6)Leu(13)psi(CH(2)NH)-Leu(14)]蛙皮素(RC-3095)作为一种药理学工具来研究蛙皮素样肽在 AMPH 处理的大鼠海马体和皮质中的氧化还原平衡中的作用。大鼠给予单次 10ml/kg 腹膜内(i.p.)注射生理盐水(SAL)或 RC-3095(0.1、1.0 或 10.0mg/kg),30 分钟后再给予 SAL 或安非他命(AMPH 2.0mg/kg)腹膜内注射。最后一次药物注射后 2 小时评估运动活动。以海马体、纹状体和皮质中的硫代巴比妥酸反应性物质(TBARS)、蛋白质羰基形成、超氧化物歧化酶和过氧化氢酶(CAT)活性作为氧化应激的标志物进行测量。结果表明,RC-3095 阻断 AMPH 诱导的过度活跃。此外,RC-3095 单独的特定剂量增加了背侧海马体和皮质中的氧化应激水平。然而,当随后给予 AMPH 时,RC-3095 降低了 TBARS 和蛋白质羰基的形成,并增加了海马体、纹状体和皮质中的超氧化物歧化酶和 CAT 活性。GRPR 拮抗剂的作用似乎具有区域和剂量特异性。总之,结果表明 GRPR 拮抗剂在大脑中可能具有抗氧化特性。