Δ9-Tetrahydrocannabivarin suppresses in vitro epileptiform and in vivo seizure activity in adult rats

被引:83
作者
Hill, Andrew J. [1 ,2 ]
Weston, Samantha E. [1 ]
Jones, Nicholas A. [1 ,2 ]
Smith, Imogen [1 ]
Bevan, Sarah A. [1 ]
Williamson, Elizabeth M. [1 ]
Stephens, Gary J. [1 ]
Williams, Claire M. [2 ]
Whalley, Benjamin J. [1 ]
机构
[1] Univ Reading, Sch Pharm, Reading, Berks, England
[2] Univ Reading, Sch Psychol & Clin Language Sci, Reading, Berks, England
关键词
Epilepsy; Anticonvulsant; Cannabinoid; Pentylenetetrazole; Piriform cortex; PENTYLENETETRAZOLE-INDUCED SEIZURE; ENDOCANNABINOID SYSTEM; CANNABINOID RECEPTOR; PIRIFORM CORTEX; ANTICONVULSANT PROPERTIES; CB1; CANNABIDIOL; EPILEPSY; AGONIST; MODEL;
D O I
10.1111/j.1528-1167.2010.02523.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
P>Purpose: We assessed the anticonvulsant potential of the phytocannabinoid Delta 9-tetrahydrocannabivarin (Delta 9-THCV) by investigating its effects in an in vitro piriform cortex (PC) brain slice model of epileptiform activity, on cannabinoid CB1 receptor radioligand-binding assays and in a generalized seizure model in rats. Methods: Delta 9-THCV was applied before (10 mu m Delta 9-THCV) or during (10-50 mu m Delta 9-THCV) epileptiform activity induced by Mg2+-free extracellular media in adult rat PC slices and measured using multielectrode array (MEA) extracellular electrophysiologic techniques. The actions of Delta 9-THCV on CB1 receptors were examined using [3H]SR141716A competition binding and [35S]GTP gamma S assays in rat cortical membranes. Effects of Delta 9-THCV (0.025-2.5 mg/kg) on pentylenetetrazole (PTZ)-induced seizures in adult rats were also assessed. Results: After induction of stable spontaneous epileptiform activity, acute Delta 9-THCV application (>= 20 mu m) significantly reduced burst complex incidence and the amplitude and frequency of paroxysmal depolarizing shifts (PDSs). Furthermore, slices pretreated with 10 mu m Delta 9-THCV prior to induction of epileptiform activity exhibited significantly reduced burst complex incidence and PDS peak amplitude. In radioligand-binding experiments, Delta 9-THCV acted as a CB1 receptor ligand, displacing 0.5 nm [3H]SR141716A with a Ki similar to 290 nm, but exerted no agonist stimulation of [35S]GTP gamma S binding. In PTZ-induced seizures in vivo, 0.25 mg/kg Delta 9-THCV significantly reduced seizure incidence. Discussion: These data demonstrate that Delta 9-THCV exerts antiepileptiform and anticonvulsant properties, actions that are consistent with a CB1 receptor-mediated mechanism and suggest possible therapeutic application in the treatment of pathophysiologic hyperexcitability states.
引用
收藏
页码:1522 / 1532
页数:11
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