Hahn Elizabeth, Burrell Brian
Division of Basic Biomedical Sciences, Sanford School of Medicine, University South Dakota, Vermillion, SD, 57069, USA.
Invert Neurosci. 2015;15(1):177. doi: 10.1007/s10158-014-0177-1. Epub 2015 Jan 9.
This study examined the capacity of a known pro-epileptic drug, pentylenetetrazol (PTZ), to elicit seizure-like activity in the medicinal leech, Hirudo verbana. During in vivo experiments, PTZ elicited increased motor activity in a concentration-dependent manner with the highest concentration (10 mM) eliciting episodes of highly uncoordinated exploratory and swimming behavior. Co-application of the anti-epileptic drug, phenytoin, failed to reduce the absolute amount of PTZ-induced motor behavior, but was able to prevent expression of abnormal exploratory and swimming behaviors. During in vitro experiments in which extracellular recordings of connective nerve activity were made, bath application of 1 μM PTZ in Mg(2+)-free saline elicited a significant increase in spontaneous activity. This PTZ-induced increase in activity was completely inhibited by phenytoin. Interestingly, PTZ-induced hyperactivity was also blocked by co-application of the endocannabinoid 2-arachidonoyl glycerol and the selective serotonin re-uptake inhibitor (SSRI) fluoxetine. These findings suggest that the leech can be a useful system in which to study potential anti-epileptic treatments.
本研究检测了一种已知的促癫痫药物戊四氮(PTZ)诱发药用蚂蟥(宽体金线蛭)癫痫样活动的能力。在体内实验中,PTZ以浓度依赖性方式诱发运动活性增加,最高浓度(10 mM)诱发高度不协调的探索和游泳行为发作。抗癫痫药物苯妥英钠联合应用未能降低PTZ诱导的运动行为的绝对量,但能够阻止异常探索和游泳行为的表现。在进行结缔神经活动细胞外记录的体外实验中,在无镁盐溶液中浴加1 μM PTZ可诱发自发活动显著增加。苯妥英钠完全抑制了这种PTZ诱导的活动增加。有趣的是,内源性大麻素2-花生四烯酸甘油酯和选择性5-羟色胺再摄取抑制剂(SSRI)氟西汀联合应用也阻断了PTZ诱导的多动。这些发现表明,蚂蟥可能是研究潜在抗癫痫治疗方法的有用系统。