Zolfagharian Farzaneh, Razavi Bibi Marjan, Hosseinzadeh Hossein
School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
Targeted Drug Delivery Research Center, Department of Pharmacodynamy and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
Avicenna J Phytomed. 2016 May-Jun;6(3):305-12.
Regarding the anticonvulsant effects of Satureja hortensis (S . hortensis) in Avicenna's book: canon of medicine; the present study was undertaken to evaluate the anti- eplileptic effects of S . hortensis aqueous and ethanolic aerial part extracts. Furthermore, the mechanisms of their anticonvulsant activities were also evaluated.
Seizure was induced by Pentylentetrazol (PTZ) and MES (maximal electroshock) models. Mice were randomly divided into 8 groups; negative control (normal saline, 10ml/Kg), positive control (diazepam, 2 mg/kg), S. hortensis aqueous and ethanolic extracts (200, 400 and 600 mg/kg). In PTZ test, latency to the first minimal clonic seizure (MCS), latency to the first generalized tonic-clonic seizures (GTCS), the total duration of seizures and protection against mortality were evaluated. In MES test, the stretching length of extremities and protection against mortality were recorded.
Aqueous and ethanolic extracts (400 and 600 mg/kg) significantly increased MCS and GTCS latencies in PTZ model. Three doses of the extracts decreased the total duration of seizure. These extracts did not show any protective effects on seizure induced by MES model. In PTZ model, flumazenil, an antagonist of benzodiazepine (BZD) site in the GABAA-BZD receptor complex and 7- nitroindazole (7- NI), a selective nNOS (neuronal nitric oxide synthase) inhibitor, reduced the prolongation of seizure latency.
S. hortensis showed anticonvulsant activity in PTZ model and this effect may be mediated, at least partly, through interacting with nitric oxide and GABAA-BZD receptor complex.
鉴于阿维森纳的《医典》中提及了冬香薄荷(Satureja hortensis)的抗惊厥作用,本研究旨在评估冬香薄荷地上部分水提取物和乙醇提取物的抗癫痫作用。此外,还对其抗惊厥活性机制进行了评估。
采用戊四氮(PTZ)和最大电休克(MES)模型诱导惊厥。将小鼠随机分为8组;阴性对照组(生理盐水,10ml/kg)、阳性对照组(地西泮,2mg/kg)、冬香薄荷水提取物和乙醇提取物组(200、400和600mg/kg)。在PTZ试验中,评估首次轻微阵挛性惊厥(MCS)的潜伏期、首次全身性强直阵挛性惊厥(GTCS)的潜伏期、惊厥总持续时间以及对死亡率的保护作用。在MES试验中,记录四肢伸展长度和对死亡率的保护作用。
水提取物和乙醇提取物(400和600mg/kg)显著延长了PTZ模型中MCS和GTCS的潜伏期。三种剂量的提取物均缩短了惊厥总持续时间。这些提取物对MES模型诱导的惊厥未显示出任何保护作用。在PTZ模型中,氟马西尼(一种GABAA - BZD受体复合物中苯二氮䓬(BZD)位点的拮抗剂)和7 - 硝基吲唑(7 - NI,一种选择性神经元型一氧化氮合酶(nNOS)抑制剂)可缩短惊厥潜伏期的延长。
冬香薄荷在PTZ模型中显示出抗惊厥活性,且这种作用可能至少部分是通过与一氧化氮和GABAA - BZD受体复合物相互作用介导的。