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首页> 外文期刊>BMC Complementary and Alternative Medicine >Valerenic acid and Valeriana officinalis extracts delay onset of Pentylenetetrazole (PTZ)-Induced seizures in adult Danio rerio (Zebrafish)
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Valerenic acid and Valeriana officinalis extracts delay onset of Pentylenetetrazole (PTZ)-Induced seizures in adult Danio rerio (Zebrafish)

机译:缬草酸和缬草提取物延缓戊四氮(PTZ)诱导的成年达尼奥雷(斑马鱼)癫痫发作

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Background Anticonvulsant properties have been attributed to extracts of the herbal medicine Valeriana officinalis . Our aims were to examine the anticonvulsant properties of valerenic acid and valerian extracts and to determine whether valerian preparations interact with the activity of other anti-epileptic drugs (phenytoin or clonazepam). To achieve these goals, we validated the adult zebrafish, Danio rerio, as an animal model for studying anticonvulsant drugs. Methods All drug treatments were administered by immersion in water containing the drug. For assays of anticonvulsant activity, zebrafish were pretreated with: anti-epileptic drugs, valerenic acid, aqueous or ethanolic valerian extracts, or mixtures (phenytoin or clonazepam with valerenic acid or valerian extracts). Seizures were then induced with pentylenetetrazole (PTZ). A behavioral scale was developed for scoring PTZ-induced seizures in adult zebrafish. The seizure latency was evaluated for all pretreatments and control, untreated fish. Valerenic acid and both aqueous and ethanolic extracts of valerian root were also evaluated for their ability to improve survival after pentylenetetrazole-challenge. The assay was validated by comparison with well-studied anticonvulsant drugs (phenytoin, clonazepam, gabapentin and valproate). One-way ANOVA followed by Tukey post-hoc test was performed, using a p Results After exposure to pentylenetetrazole, zebrafish exhibited a series of stereotypical behaviors prior to the appearance of clonic-like movements—convulsions. Both valerenic acid and valerian extracts (aqueous and ethanolic) significantly extended the latency period to the onset of seizure (convulsion) in adult zebrafish. The ethanolic valerian extract was a more potent anticonvulsant than the aqueous extract. Valerenic acid and both valerian extracts interacted synergistically with clonazepam to extended the latency period to the onset of seizure. Phenytoin showed interaction only with the ethanolic valerian extracts. Conclusions Valerenic acid and valerian extracts have anticonvulsant properties in adult zebrafish. Valerian extracts markedly enhanced the anticonvulsant effect of both clonazepam and phenytoin, and could contribute to therapy of epileptic patients.
机译:背景抗惊厥特性归因于草药缬草的提取物。我们的目的是检查缬草酸和缬草提取物的抗惊厥性质,并确定缬草制剂是否与其他抗癫痫药(苯妥英或氯硝西p)的活性相互作用。为了实现这些目标,我们验证了成年斑马鱼Danio rerio作为研究抗惊厥药物的动物模型。方法所有药物治疗均通过浸入含有药物的水中进行。为了测定抗惊厥活性,斑马鱼用以下药物进行预处理:抗癫痫药,戊戊酸,缬草水提取物或乙醇提取物或混合物(苯妥英钠或氯硝西am与戊烯酸或缬草提取物)。然后用戊四氮(PTZ)诱发癫痫发作。开发了一种行为量表,用于对成年斑马鱼中PTZ诱发的癫痫发作进行评分。对所有预处理和未处理鱼的癫痫发作潜伏期进行了评估。还评估了戊戊烯酸以及缬草根的水提取物和乙醇提取物在戊烯四唑攻击后提高存活率的能力。通过与研究充分的抗惊厥药(苯妥英,氯硝西am,加巴喷丁和丙戊酸盐)进行比较,验证了该测定方法。结果。暴露于戊烯四唑后,斑马鱼在出现阵挛性运动-惊厥之前表现出一系列定型行为。戊烯酸和缬草提取物(水性和乙醇性)均显着延长了成年斑马鱼癫痫发作(惊厥)的潜伏期。乙醇缬草提取物比水性提取物更有效。缬草酸和两种缬草提取物与氯硝西am协同相互作用,从而延长了癫痫发作的潜伏期。苯妥英钠仅与乙醇缬草提取物相互作用。结论缬草酸和缬草提取物对成年斑马鱼具有抗惊厥作用。缬草提取物显着增强了氯硝西am和苯妥英钠的抗惊厥作用,并可能有助于治疗癫痫患者。

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