黑种草籽主要成分百里醌对小鼠的抗惊厥作用。

Anticonvulsant effects of thymoquinone, the major constituent of Nigella sativa seeds, in mice.

作者信息

Hosseinzadeh H, Parvardeh S

机构信息

Pharmaceutical Research Center, Department of Pharmacodynamy and Toxicology, Faculty of Pharmacy, Mashhad University of Medical Sciences, Mashhad, IR Iran.

出版信息

Phytomedicine. 2004 Jan;11(1):56-64. doi: 10.1078/0944-7113-00376.

Abstract

The anticonvulsant effects of thymoquinone, the major constituent of Nigella sativa seeds, were investigated using pentylenetetrazole (PTZ)- and maximal electroshock (MES)-induced seizure models. We also studied the effect of thymoquinone on pentobarbital-induced hypnosis, locomotor activity, and motor coordination. In PTZ-induced seizure, the intraperitoneally injection of thymoquinone with doses of 40 and 80 mg/kg, prolonged the onset of seizures and reduced the duration of myoclonic seizures. The protective effect of thymoquinone against mortality was 71.4% and 100% in the mentioned doses, respectively. In MES model, thymoquinone failed to reduce the duration of seizure, whereas exhibited a complete protection against mortality. In PTZ model, flumazenil (10 mg/kg, i.p.), an antagonist of benzodiazepine (BZD) site in the GABAA-BZD receptor complex, inhibited the prolongation of seizure latency, but did not show any effect on the duration of myoclonic seizures. Also, pretreatment with naloxone (0.1 and 03 mg/kg, i.p.) inhibited the prolongation of myoclonic seizure latency and antagonized the reduction of myoclonic seizure duration induced by thymoquinone (40 and 80 mg/kg) in the PTZ model. Moreover, thymoquinone (40 and 80 mg/kg) did not have any hypnosis effect in the pentobarbital-induced hypnosis, but impaired the motor coordination and reduced the locomotor activity. These results indicate that thymoquinone may have anticonvulsant activity in the petit mal epilepsy probably through an opioid receptor-mediated increase in GABAergic tone.

摘要

使用戊四氮(PTZ)和最大电休克(MES)诱导的癫痫模型,研究了黑种草籽主要成分百里醌的抗惊厥作用。我们还研究了百里醌对戊巴比妥诱导的催眠、运动活性和运动协调性的影响。在PTZ诱导的癫痫发作中,腹腔注射40和80mg/kg剂量的百里醌可延长癫痫发作的起始时间,并缩短肌阵挛性癫痫发作的持续时间。在上述剂量下,百里醌对死亡率的保护作用分别为71.4%和100%。在MES模型中,百里醌未能缩短癫痫发作的持续时间,但对死亡率表现出完全的保护作用。在PTZ模型中,氟马西尼(10mg/kg,腹腔注射),一种GABAA - BZD受体复合物中苯二氮卓(BZD)位点的拮抗剂,抑制了癫痫发作潜伏期的延长,但对肌阵挛性癫痫发作的持续时间没有任何影响。此外,在PTZ模型中,用纳洛酮(0.1和0.3mg/kg,腹腔注射)预处理可抑制肌阵挛性癫痫发作潜伏期的延长,并拮抗百里醌(40和80mg/kg)诱导的肌阵挛性癫痫发作持续时间的缩短。此外,百里醌(40和80mg/kg)在戊巴比妥诱导的催眠中没有任何催眠作用,但损害了运动协调性并降低了运动活性。这些结果表明,百里醌可能通过阿片受体介导的GABA能张力增加,在失神性癫痫中具有抗惊厥活性。

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