Dragunow M, Goddard G V, Laverty R
Epilepsia. 1985 Sep-Oct;26(5):480-7. doi: 10.1111/j.1528-1157.1985.tb05684.x.
The anticonvulsant properties of adenosine were tested pharmacologically on amygdala-kindled seizure activity in rats. The adenosine analogue 2-chloroadenosine and the adenosine uptake blocker papaverine both increased the latency to behavioral clonus as well as reduced the duration and severity of the clonic motor convulsion. Both drugs, however, failed to alter the postkindling afterdischarge (AD) threshold. Theophylline, an adenosine antagonist, had the opposite effects, prolonging the AD and motor seizure durations and facilitating partially kindled seizures, but again not altering the prekindling or postkindling AD thresholds of amygdala-elicited seizures. In contrast, carbamazepine raised AD thresholds, suggesting that it does not produce its anticonvulsant effects through adenosine systems. Since endogenous adenosine can impede seizure spread and seizure continuation, but does not affect seizure initiation from the amygdala, perhaps endogenous adenosine has the special property of being brought into play as an anticonvulsant only by the seizure itself.
在大鼠杏仁核点燃癫痫发作活动中,对腺苷的抗惊厥特性进行了药理学测试。腺苷类似物2-氯腺苷和腺苷摄取阻滞剂罂粟碱均延长了行为阵挛的潜伏期,并缩短了阵挛性运动惊厥的持续时间和减轻了其严重程度。然而,这两种药物均未能改变点燃后的放电(AD)阈值。腺苷拮抗剂茶碱则产生相反的效果,延长了AD和运动性癫痫发作的持续时间,并促进了部分点燃的癫痫发作,但同样未改变杏仁核诱发癫痫发作的点燃前或点燃后AD阈值。相比之下,卡马西平提高了AD阈值,表明其抗惊厥作用并非通过腺苷系统产生。由于内源性腺苷可阻碍癫痫发作的扩散和持续,但不影响杏仁核引发的癫痫发作起始,或许内源性腺苷具有仅在癫痫发作本身时才发挥抗惊厥作用的特殊性质。