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天麻素对N-甲基-D-天冬氨酸兴奋毒性及实验性颞叶癫痫后海马神经元的作用

The Role of Gastrodin on Hippocampal Neurons after N-Methyl-D-Aspartate Excitotoxicity and Experimental Temporal Lobe Seizures.

作者信息

Wong Shi-Bing, Hung Wei-Chen, Min Ming-Yuan

机构信息

Department of Pediatrics, Taipei Tzu Chi General Hospital, Buddhist Tzu Chi Medical Foundation, New Taipei City 23142, Taiwan, Republic of China.

Institute of Zoology, College of Life Science, National Taiwan University, Taipei 10617, Taiwan, Republic of China.

出版信息

Chin J Physiol. 2016 Jun 30;59(3):156-64. doi: 10.4077/CJP.2016.BAE385.

Abstract

Tian ma (Gastrodia elata, GE) is an ancient Chinese herbal medicine that has been suggested to be effective as an anticonvulsant and analgesic, and to have sedative effects against vertigo, general paralysis, epilepsy and tetanus. The primary active ingredient isolated from GE is termed gastrodin, which is the glucoside of 4-hydroxybenzyl alcohol (4-HBA). Gastrodin can abolish hypoxia-, glutamate- and N-methyl-D-aspartate (NMDA) receptor-induced toxicity in primary culture of rat cortical neurons, and reduces seizure severity in seizure-sensitive gerbils. We evaluated the effect of gastrodin on NMDA excitotoxicity in hippocampal slice cultures (HSCs) with propidium iodide (PI) fluorescence measurement. We also evaluated the effects of gastrodin for treating active in vivo temporal lobe seizures induced by lithium/pilocarpine. Seizure severity, time span to seizure onset, mortality rate and hippocampal histology for survivors were compared. The effect of gastrodin was evaluated for treating in vitro seizures induced by Mg²⁺-free medium in hippocampal slices. Frequencies and amplitudes of epileptiform discharges were compared. The effect of gastrodin on synaptic transmission was evaluated on hippocampal CA1 Schaffer collaterals. Application of 25 μM gastrodin significantly suppressed NMDA excitotoxicity in CA3 but not in CA1 hippocampus and dentate gyrus. Intraventricular gastrodin accelerated seizure onset for 12 min after intraperitoneal pilocarpine injection (P = 0.051). Three of five rats (60%) in the gastrodin group, and three of four (75%) in the dimethyl sulfoxide (DMSO) group died within 3 days after status epilepticus (SE). Gastrodin also failed to inhibit epileptiform discharges in hippocampal slices induced by Mg²⁺-free medium, believed to be NMDA receptor-mediated spontaneous activity. The frequencies of the spontaneous epileptiform discharges were similar under treatments with 25 μM gastrodin, 200 μM gastrodin and DMSO. For the evaluation of gastrodin on synaptic transmission, application of DMSO, 25 μM or 200 μM gastrodin had no significant effect on excitatory postsynaptic potential (EPSP) slopes. Gastrodin at 200 μM decreased paired-pulse facilitation (PPF) from 1.23 ± 0.04 to 1.12 ± 0.04 (P = 0.002). In conclusion, gastrodin failed to suppress in vivo and in vitro seizures in our study. Gastrodin showed no effect on hippocampal Schaffer collateral EPSP. These findings suggest that gastrodin does not interact with ionotropic glutamate receptors to inhibit NMDA receptor-facilitated seizures. However, gastrodin showed protective effects against NMDA toxicity on cultured hippocampal slices. Nevertheless, gastrodin is still a potential neuroprotective agent against NMDA excitotoxicity, with potential benefits for stroke and patients with epilepsy.

摘要

天麻(天麻,GE)是一种古老的中药材,被认为具有抗惊厥和镇痛作用,对眩晕、全身麻痹、癫痫和破伤风有镇静作用。从GE中分离出的主要活性成分是天麻素,它是4-羟基苄醇(4-HBA)的糖苷。天麻素可以消除大鼠皮层神经元原代培养中缺氧、谷氨酸和N-甲基-D-天冬氨酸(NMDA)受体诱导的毒性,并降低癫痫敏感沙鼠的癫痫严重程度。我们用碘化丙啶(PI)荧光测量法评估了天麻素对海马切片培养物(HSCs)中NMDA兴奋性毒性的影响。我们还评估了天麻素对锂/匹罗卡品诱导的体内颞叶癫痫发作的治疗效果。比较了癫痫严重程度、癫痫发作开始的时间跨度、死亡率和幸存者的海马组织学。评估了天麻素对海马切片中无镁培养基诱导的体外癫痫发作的治疗效果。比较了癫痫样放电的频率和幅度。在海马CA1区的Schaffer侧支上评估了天麻素对突触传递的影响。应用25μM天麻素可显著抑制CA3区而非CA1区海马和齿状回的NMDA兴奋性毒性。脑室注射天麻素可使腹腔注射匹罗卡品后癫痫发作开始时间提前12分钟(P = 0.051)。天麻素组的5只大鼠中有3只(60%),二甲基亚砜(DMSO)组的4只大鼠中有3只(75%)在癫痫持续状态(SE)后3天内死亡。天麻素也未能抑制无镁培养基诱导的海马切片中的癫痫样放电,这种放电被认为是NMDA受体介导的自发活动。在25μM天麻素、200μM天麻素和DMSO处理下,自发癫痫样放电的频率相似。为了评估天麻素对突触传递的影响,应用DMSO、25μM或200μM天麻素对兴奋性突触后电位(EPSP)斜率没有显著影响。200μM的天麻素使双脉冲易化(PPF)从1.23±0.04降至1.12±0.04(P = 0.002)。总之,在我们的研究中,天麻素未能抑制体内和体外癫痫发作。天麻素对海马Schaffer侧支EPSP没有影响。这些发现表明,天麻素不与离子型谷氨酸受体相互作用以抑制NMDA受体介导的癫痫发作。然而,天麻素对培养的海马切片中的NMDA毒性具有保护作用。尽管如此,天麻素仍然是一种潜在的抗NMDA兴奋性毒性的神经保护剂,对中风和癫痫患者可能有益。

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