首页> 美国卫生研究院文献>Oxidative Medicine and Cellular Longevity >Clarified Açaí (Euterpe oleracea) Juice as an Anticonvulsant Agent: In Vitro Mechanistic Study of GABAergic Targets
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Clarified Açaí (Euterpe oleracea) Juice as an Anticonvulsant Agent: In Vitro Mechanistic Study of GABAergic Targets

机译:澄清的Açaí(Euterpe oleracea)果汁作为抗惊厥药:GABA能靶标的体外机制研究

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摘要

Seizures affect about 50 million people around the world. Approximately 30% of seizures are refractory to the current pharmacological arsenal, so, the pursuit of new therapeutic alternatives is essential. Clarified Euterpe oleracea (EO) juice showed anticonvulsant properties similar to diazepam in an in vivo model with pentylenetetrazol, a GABAA receptor blocker. This study investigated the effects of EO on the main GABAergic targets for anticonvulsant drugs, analyzing the effect on the GABA receptor's benzodiazepine and picrotoxinin binding sites and the GABA uptake. Primary cultures of cortical neurons and astrocytes were treated with EO (0–25%) for up to 90 min. [3H]Flunitrazepam and [3H]TBOB binding, [3H]GABA uptake, cell viability, and morphology were assayed. Nonlethal concentrations of EO increased agonist binding and decreased antagonist binding in cortical neurons. Low concentrations significantly inhibited GABA uptake, especially in astrocytes, suggesting an accumulation of endogenous GABA in the synaptic cleft. The results demonstrate, for the first time, that EO can improve GABAergic neurotransmission via interactions with GABAA receptor and modulation of GABA uptake. Understanding these molecular mechanisms will help in the treatment of seizures and epilepsy, especially in developing countries where geographic isolation and low purchasing power are the main barriers to access to adequate treatment.
机译:癫痫发作影响全球约5000万人。大约30%的癫痫发作对目前的药理武库是难治的,因此,寻求新的治疗方法至关重要。澄清的Euterpe oleracea(EO)汁在体内模型中与地西epa相似,使用戊烯四唑(一种GABAA受体阻滞剂)具有抗惊厥作用。这项研究调查了EO对抗惊厥药物主要GABA能靶标的作用,分析了对GABA受体的苯二氮卓和微毒素的结合位点以及GABA吸收的影响。皮层神经元和星形胶质细胞的原代培养物用EO(0–25%)处理长达90分钟。测定了[ 3 H]氟尼西epa和[ 3 H] TBOB的结合,[ 3 H] GABA的摄取,细胞活力和形态。非致死浓度的EO增加了皮质神经元中激动剂的结合并降低了拮抗剂的结合。低浓度会明显抑制GABA的摄取,尤其是在星形胶质细胞中,表明内源性GABA在突触间隙中积累。结果首次证明,EO可通过与GABAA受体相互作用和调节GABA吸收来改善GABA能神经传递。理解这些分子机制将有助于治疗癫痫和癫痫病,尤其是在地理隔离和购买力低是获得适当治疗的主要障碍的发展中国家。

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