Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary.
PLoS One. 2011;6(11):e27196. doi: 10.1371/journal.pone.0027196. Epub 2011 Nov 4.
The endocannabinoid system plays a central role in retrograde synaptic communication and may control the spread of activity in an epileptic network. Using the pilocarpine model of temporal lobe epilepsy we examined the expression pattern of the Type 1 cannabinoid receptor (CB1-R) in the hippocampi of CD1 mice at survival times of 2 hours, 1 day, 3 days and 2 months (acute, latent and chronic phases). Based on the behavioral signs of the acute seizures, animals were classified as "weakly" or "strongly" epileptic using the modified Racine scale. Mice of the weak group had mild seizures, whereas seizures in the strong group were frequent with intense motor symptoms and the majority of these animals developed sclerosis in the chronic phase. In control samples the most intense staining of CB1-R-positive fibers was found in the molecular layer of the dentate gyrus and in str. pyramidale of the cornu Ammonis. In weak animals no significant changes were seen at any survival time compared to controls. In strong animals, however, in the acute phase, a massive reduction in CB1-R-stained terminals occurred in the hippocampus. In the latent phase CB1-R immunoreactivity gradually recovered. In the chronic phase, CB1-immunostaining in sclerotic samples was stronger throughout the hippocampus. Quantitative electron microscopic analysis showed an increase in the number of CB1-R-positive terminals in the dentate gyrus. Moreover, the number of immunogold particles significantly increased in GABAergic terminals. Our results suggest a proconvulsive downregulation of CB1 receptors in the acute phase most probably due to receptor internalization, followed by compensatory upregulation and sprouting in the chronic phase of epilepsy. In conclusion, the changes in CB1 receptor expression pattern revealed in this study are associated with the severity of hippocampal injury initiated by acute seizures that ultimately leads to sclerosis in the vulnerable regions in the chronic phase.
内源性大麻素系统在逆行突触通讯中发挥核心作用,可能控制癫痫网络中活动的扩散。我们使用匹罗卡品颞叶癫痫模型,在 2 小时、1 天、3 天和 2 个月的存活时间(急性、潜伏和慢性期)检查了 CD1 小鼠海马中的 1 型大麻素受体(CB1-R)的表达模式。根据急性发作的行为迹象,使用改良 Racine 量表将动物分为“弱”或“强”癫痫。弱组的小鼠有轻度癫痫发作,而强组的癫痫发作频繁,伴有强烈的运动症状,大多数动物在慢性期发展为硬化。在对照样本中,CB1-R 阳性纤维的最强染色出现在齿状回的分子层和角状回的 pyramidale 层。在弱动物中,与对照组相比,任何存活时间都没有明显变化。然而,在强动物中,在急性期,海马中 CB1-R 染色末端大量减少。在潜伏期中,CB1-R 免疫反应逐渐恢复。在慢性期,硬化样本中的 CB1 免疫染色在整个海马中更强。定量电子显微镜分析显示齿状回中 CB1-R 阳性末端数量增加。此外,GABA 能末端的免疫金颗粒数量显著增加。我们的结果表明,在急性期,CB1 受体的促惊厥下调最可能是由于受体内化,随后在癫痫的慢性期代偿性上调和发芽。总之,本研究中揭示的 CB1 受体表达模式的变化与急性发作引发的海马损伤的严重程度相关,最终导致慢性期脆弱区域的硬化。