Department of Pharmacology and Division of Brain Korea 21 Biomedical Science, Korea University College of Medicine, Sungbuk-gu, Seoul, Republic of Korea.
Eur J Pharmacol. 2010 Nov 25;647(1-3):110-6. doi: 10.1016/j.ejphar.2010.08.023. Epub 2010 Sep 6.
Cocaine and amphetamine regulated transcript (CART) has been implicated in the regulation of the stress response. Although the forced swimming test (FST), in which rats are forced to swim for 15 min (pretest swim) and then again for 5 min (test swim) 24 h later, has been used to study the effects of antidepressants, there have been few studies examining the effects of antidepressants on FST-induced changes in CART mRNA levels in the brain. To answer this question, we injected reboxetine and citalopram into male Sprague-Dawley rats 1, 5, and 23.5 h before the test swim and then sacrificed rats 2 h after the test swim, at the peak of the FST-induced increase in CART expression. The FST significantly increased CART mRNA levels in the nucleus accumbens, central nucleus of the amygdala, and locus ceruleus 2 h after the test session. Both reboxetine and citalopram pretreatment blocked FST-induced increases in CART mRNA levels in the nucleus accumbens, central nucleus of the amygdala, and locus ceruleus, despite the fact these antidepressants exert their therapeutic effect by different mechanisms. In addition, the FST significantly increased plasma corticosterone levels, and this effect was also blocked by reboxetine and citalopram pretreatment. These results suggest that inhibition of FST-induced increases in CART expression in the nucleus accumbens, central nucleus of the amygdala, and locus ceruleus may be a common mechanism of antidepressant effects during the FST.
可卡因和安非他命调节转录本(CART)被认为与应激反应的调节有关。虽然强迫游泳试验(FST)已被用于研究抗抑郁药的作用,其中大鼠被迫游泳 15 分钟(预测试游泳),然后在 24 小时后再次游泳 5 分钟(测试游泳),但很少有研究检查抗抑郁药对 FST 诱导的大脑 CART mRNA 水平变化的影响。为了回答这个问题,我们在测试游泳前 1、5 和 23.5 小时向雄性 Sprague-Dawley 大鼠注射瑞波西汀和西酞普兰,然后在测试游泳后 2 小时处死大鼠,此时是 FST 诱导的 CART 表达增加的峰值。FST 显著增加了 2 小时后测试期间核仁accumbens、杏仁核中央核和蓝斑中 CART mRNA 水平。尽管这些抗抑郁药通过不同的机制发挥治疗作用,但瑞波西汀和西酞普兰预处理均阻断了核仁accumbens、杏仁核中央核和蓝斑中 FST 诱导的 CART mRNA 水平增加。此外,FST 显著增加了血浆皮质酮水平,而瑞波西汀和西酞普兰预处理也阻断了这种作用。这些结果表明,抑制 FST 诱导的核仁accumbens、杏仁核中央核和蓝斑中 CART 表达的增加可能是 FST 期间抗抑郁作用的共同机制。