Ray M, Mediratta P K, Reeta Kh, Mahajan P, Sharma K K
Department of Pharmacology, University College of Medical Sciences and GTB Hospital, Delhi, India.
Methods Find Exp Clin Pharmacol. 2004 Apr;26(3):177-81. doi: 10.1358/mf.2004.26.3.809723.
The present study investigates the mechanisms involved in the anticonvulsant effect of melatonin in maximum electroshock (MES) seizures. Melatonin (25-100 mg/kg) dose-dependently decreased the duration of tonic hindlimb extension (THLE). The anticonvulsant effect of melatonin was blocked by bicuculline, a GABA(A) receptor antagonist, and luzindole, an ML(1) receptor antagonist, while prazosin, an ML(2) receptor antagonist, enhanced the anticonvulsant actions of melatonin in this seizure model. Administration of serotonergic agents, mianserin and ondansetron, along with melatonin, increased the antiseizurogenic activity of melatonin, while buspirone had no effect. Pretreating the animals with diazepam, carbamazepine or lamotrigine enhanced the anticonvulsant effect of melatonin. Melatonin thus appears to be an effective anticonvulsant, and melatonin ML(1) receptors, GABAergic and serotonergic mechanisms may play an important role in mediating the anticonvulsant activity of melatonin in electroshock seizures.
本研究探讨褪黑素在最大电休克(MES)惊厥中抗惊厥作用的相关机制。褪黑素(25 - 100毫克/千克)剂量依赖性地缩短了强直性后肢伸展(THLE)的持续时间。褪黑素的抗惊厥作用被GABA(A)受体拮抗剂荷包牡丹碱和褪黑素(1)(ML(1))受体拮抗剂鲁辛朵尔阻断,而ML(2)受体拮抗剂哌唑嗪在该惊厥模型中增强了褪黑素的抗惊厥作用。给予血清素能药物米安色林和昂丹司琼与褪黑素联合使用,增强了褪黑素的抗致惊厥活性,而丁螺环酮则无作用。用苯二氮䓬、卡马西平或拉莫三嗪预处理动物增强了褪黑素的抗惊厥作用。因此,褪黑素似乎是一种有效的抗惊厥药,且褪黑素ML(1)受体、GABA能和血清素能机制可能在介导褪黑素在电休克惊厥中的抗惊厥活性方面发挥重要作用。