Kaster Manuella Pinto, Raupp Inara, Binfaré Ricardo Wabner, Andreatini Roberto, Rodrigues Ana Lúcia S
Departamento de Bioquímica, Centro de Ciências Biológicas, Universidade Federal de Santa Catarina, Campus Universitário, Trindade - 88040-900, Florianópolis-SC, Brazil.
Eur J Pharmacol. 2007 Jun 22;565(1-3):119-24. doi: 10.1016/j.ejphar.2007.03.003. Epub 2007 Mar 19.
Lamotrigine is an anticonvulsant drug that is also effective in the treatment of mood disorders, especially bipolar disorder. However, few studies have been conducted in animal models of depression to evaluate its mechanism of action. The present study investigated the effect of lamotrigine in the forced swimming test in mice and the involvement of the noradrenergic system in this effect. Lamotrigine (20-30 mg/kg, i.p.) decreased the immobility time in the forced swimming test and the number of crossings in the open-field test. In addition, the pretreatment of mice with the inhibitor of the enzyme tyrosine hydroxylase, alpha-methyl-p-tyrosine (100 or 250 mg/kg), prevented the antidepressant-like effect of lamotrigine (30 mg/kg, i.p.) in the forced swimming test. Besides that, the pretreatment of mice with prazosin (1 mg/kg, i.p., an alpha1-adrenoceptor antagonist) or yohimbine (1 mg/kg, i.p., an alpha2-adrenoceptor antagonist) also prevented the anti-immobility effect of lamotrigine (30 mg/kg, i.p.). Moreover, the administration of subeffective doses of phenylephrine (5 mg/kg, i.p., an alpha1-adrenoceptor agonist) or clonidine (0.06 mg/kg, i.p., an alpha2-adrenoceptor agonist) was able to potentiate the action of a subeffective dose of lamotrigine (10 mg/kg, i.p.) in the forced swimming test. Thus, the present study suggests that the antidepressant-like effect of lamotrigine in the forced swimming test is related to the noradrenergic system, likely due to an activation of alpha1- and alpha2-postsynaptic adrenoceptors.
拉莫三嗪是一种抗惊厥药物,对治疗情绪障碍尤其是双相情感障碍也有效。然而,在抑郁症动物模型中评估其作用机制的研究较少。本研究调查了拉莫三嗪在小鼠强迫游泳试验中的作用以及去甲肾上腺素能系统在该作用中的参与情况。拉莫三嗪(20 - 30毫克/千克,腹腔注射)减少了强迫游泳试验中的不动时间以及旷场试验中的穿越次数。此外,用酪氨酸羟化酶抑制剂α-甲基-对酪氨酸(100或250毫克/千克)预处理小鼠,可阻止拉莫三嗪(30毫克/千克,腹腔注射)在强迫游泳试验中的抗抑郁样作用。除此之外,用哌唑嗪(1毫克/千克,腹腔注射,一种α1肾上腺素能受体拮抗剂)或育亨宾(1毫克/千克,腹腔注射,一种α2肾上腺素能受体拮抗剂)预处理小鼠,也可阻止拉莫三嗪(30毫克/千克,腹腔注射)的抗不动作用。此外,给予亚有效剂量的去氧肾上腺素(5毫克/千克,腹腔注射,一种α1肾上腺素能受体激动剂)或可乐定(0.06毫克/千克,腹腔注射,一种α2肾上腺素能受体激动剂)能够增强亚有效剂量的拉莫三嗪(10毫克/千克,腹腔注射)在强迫游泳试验中的作用。因此,本研究表明拉莫三嗪在强迫游泳试验中的抗抑郁样作用与去甲肾上腺素能系统有关,可能是由于α1和α2突触后肾上腺素能受体的激活。