Maia Luciana Maria Silva de Seixas, Amancio-Dos-Santos Angela, Germano Paula Catirina Pereira da Silva, Falcão Anna Carolina Santos Marinho, Duda-de-Oliveira Desirré, Guedes Rubem Carlos Araújo
Departamento de Histologia e Embriologia, Centro de Biociências, UFPE, 50740-600, Recife PE, Brazil.
Departamento de Fisiologia e Farmacologia, Centro de Biociências, UFPE, 50740-600, Recife PE, Brazil.
Neurosci Lett. 2017 May 22;650:134-138. doi: 10.1016/j.neulet.2017.04.044. Epub 2017 Apr 25.
In the rat, we previously demonstrated that serotonin-enhancing drugs impair cortical spreading depression (CSD) and that l-arginine (arginine) treatment enhances CSD. Here, we investigated the interaction between topical application of the serotonin uptake enhancer tianeptine and systemic arginine administration on CSD. From postnatal day 7-28, female Wistar rats (n=40) received by gavage 300mg/Kg/day arginine (n=20) or water (n=20). Half of the arginine- or water-treated rats underwent CSD recording at 30-40days of age (young), while the other half was recorded at 90-120days (adult). Following baseline recording (four episodes of CSD), we applied tianeptine solution (10mg/ml) to a rectangular portion of the intact dura mater for 10-min and then elicited CSD. This procedure was repeated three times. Compared to baseline values, CSD velocities and amplitudes following tianeptine application increased, and CSD duration decreased significantly (p<0.05) in both young and adult rats, regardless of treatment group. CSD acceleration caused by systemic treatment with arginine is in agreement with previous findings. Topical cortical application of tianeptine replicated the effect of systemic application, suggesting a cortically based mechanism for tianeptine's action. However, the absence of interaction between arginine and tianeptine treatments suggests that they probably act through separate mechanisms.
在大鼠中,我们之前已证明,增强血清素的药物会损害皮质扩散性抑制(CSD),而L-精氨酸治疗可增强CSD。在此,我们研究了血清素摄取增强剂噻奈普汀局部应用与全身性精氨酸给药对CSD的相互作用。从出生后第7天至28天,雌性Wistar大鼠(n = 40)通过灌胃给予300mg/kg/天的精氨酸(n = 20)或水(n = 20)。精氨酸或水处理的大鼠中有一半在30 - 40日龄(幼年)时进行CSD记录,而另一半在90 - 120日龄(成年)时进行记录。在基线记录(四组CSD)后,我们将噻奈普汀溶液(10mg/ml)应用于完整硬脑膜的矩形区域10分钟,然后引发CSD。此过程重复三次。与基线值相比,无论治疗组如何,幼年和成年大鼠在应用噻奈普汀后CSD速度和幅度均增加,而CSD持续时间显著缩短(p<0.05)。全身性精氨酸治疗引起的CSD加速与先前的研究结果一致。噻奈普汀局部应用于皮质再现了全身应用的效果,表明噻奈普汀的作用存在基于皮质的机制。然而,精氨酸和噻奈普汀治疗之间不存在相互作用,这表明它们可能通过不同的机制起作用。