Naderi Nima, Aziz Ahari Farzad, Shafaghi Bijan, Najarkolaei Azadeh Hosseini, Motamedi Fereshteh
Neuroscience Research Center, Shahid Beheshti University MC, Tehran, Iran.
J Neural Transm (Vienna). 2008 Nov;115(11):1501-11. doi: 10.1007/s00702-008-0076-x. Epub 2008 Jun 25.
Several studies have shown that cannabinoids have anticonvulsant properties that are mediated through activation of the cannabinoid CB1 receptors. In addition, endogenous cannabinoid compounds (endocannabinoids) regulate synaptic transmission and dampen seizure activity via activation of the same receptors. The aim of this study was to evaluate the possible interactions between antiepileptic effects of cannabinoid compounds and diazepam using electroshock-induced model of seizure in mice. Electroconvulsions were produced by means of an alternating current (ear-clip electrodes, fixed current intensity 35 mA, stimulus duration 0.2 s) and tonic hindlimb extension was taken as the endpoint. All experiments were performed on groups of ten mice and the number of animals who did not display seizure reported as percent protection. Intraperitoneal (i.p.) administration of diazepam (0.25-2 mg/kg) and CB1 receptor agonist WIN55212-2 (0.5-4 mg/kg) dose dependently produced an antiepileptic effect evaluated in terms of increased percentage of protection against electroshock-induced seizure. Logistic regression analysis indicated synergistic interactions in anticonvulsant action after co-administration of diazepam and WIN55212-2 in fixed-ratio combination of 3:1 (diazepam:WIN55212-2), while an additive effect was resulted after co-administration of 1:1 and 1:3 fixed-ratio combinations. Administration of various doses of the endocannabinoid reuptake inhibitor, AM404, did not produce any effect on electroshock-induced seizure. Moreover, co-administration of AM404 and diazepam did not produce significant interaction in antiepileptic properties of these compounds. Administration of the fatty acid amide hydrolase inhibitor, URB597, produced significant antiepileptic effect. Co-administration of URB597 and diazepam led to an antagonistic interaction in protection against shock-induced seizure. Co-administration of different doses of the cannabinoid CB1 receptor antagonist, AM251 did not alter the antiepileptic effect of diazepam in the electroshock-induced seizure test. These results demonstrate that endocannabinoid system participates in the modulation of seizure and combination of small doses of exogenous CB1 receptor agonists with diazepam may have effective consequences in seizure control. Furthermore, inhibiting the endocannabinoid degradation could be more efficacious in modulating seizure than preventing their uptake. This study also suggests that the effects of cannabinoids on epilepsy depend on the relative cannabinoid responsiveness of GABAergic and glutamatergic neurotransmission. While, the antiepileptic effects of cannabinoid compounds are likely by affecting excitatory glutamate neurotransmission, the antagonistic interaction between cannabinoid compounds and diazepam to protect seizure is due to the cannabinoid action on inhibitory GABAergic system.
多项研究表明,大麻素具有抗惊厥特性,这是通过激活大麻素CB1受体介导的。此外,内源性大麻素化合物(内源性大麻素)通过激活相同的受体来调节突触传递并抑制癫痫发作活动。本研究的目的是使用小鼠电休克诱导的癫痫模型评估大麻素化合物与地西泮的抗癫痫作用之间可能的相互作用。通过交流电(耳夹电极,固定电流强度35 mA,刺激持续时间0.2 s)产生电惊厥,并将强直性后肢伸展作为终点。所有实验均在每组十只小鼠上进行,未出现癫痫发作的动物数量报告为保护百分比。腹腔注射(i.p.)地西泮(0.25 - 2 mg/kg)和CB1受体激动剂WIN55212 - 2(0.5 - 4 mg/kg)剂量依赖性地产生抗癫痫作用,根据对电休克诱导癫痫的保护百分比增加来评估。逻辑回归分析表明,以3:(地西泮:WIN55212 - 2)的固定比例联合使用地西泮和WIN55212 - 2后,抗惊厥作用具有协同相互作用,而以1:1和1:3固定比例联合使用后产生相加作用。给予不同剂量的内源性大麻素再摄取抑制剂AM404对电休克诱导的癫痫没有产生任何影响。此外,AM404与地西泮联合使用在这些化合物的抗癫痫特性方面没有产生显著相互作用。给予脂肪酸酰胺水解酶抑制剂URB597产生了显著的抗癫痫作用。URB597与地西泮联合使用导致在预防休克诱导癫痫方面产生拮抗相互作用。给予不同剂量的大麻素CB1受体拮抗剂AM251在电休克诱导癫痫试验中没有改变地西泮的抗癫痫作用。这些结果表明,内源性大麻素系统参与癫痫发作的调节,小剂量外源性CB1受体激动剂与地西泮联合使用可能对癫痫控制产生有效结果。此外,抑制内源性大麻素降解在调节癫痫发作方面可能比阻止其摄取更有效。本研究还表明,大麻素对癫痫的影响取决于GABA能和谷氨酸能神经传递的相对大麻素反应性。虽然大麻素化合物的抗癫痫作用可能是通过影响兴奋性谷氨酸神经传递,但大麻素化合物与地西泮在预防癫痫发作方面的拮抗相互作用是由于大麻素对抑制性GABA能系统的作用。