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提取物抑制大鼠海马体中的兴奋性突触传递和化学诱导的癫痫发作。

Extract Depresses Excitatory Synaptic Transmission and Chemically-Induced Seizures in the Rat Hippocampus.

作者信息

Amoateng Patrick, Tagoe Thomas A, Karikari Thomas K, Kukuia Kennedy K E, Osei-Safo Dorcas, Woode Eric, Frenguelli Bruno G, Kombian Samuel B

机构信息

Department of Pharmacology and Toxicology, School of Pharmacy, College of Health Sciences, University of Ghana, Accra, Ghana.

Department of Physiology, UG Medical School, College of Health Sciences, University of Ghana, Accra, Ghana.

出版信息

Front Pharmacol. 2021 Mar 8;12:610025. doi: 10.3389/fphar.2021.610025. eCollection 2021.

Abstract

Extracts of the tropical Cinderella plant are used traditionally to manage convulsive conditions in the West African sub-region. This study sought to determine the neuronal basis of the effectiveness of these plant extracts to suppress seizure activity. Using the hippocampal slice preparation from rats, the ability of the extract to depress excitatory synaptic transmission and seizure activity were investigated. Bath perfusion of the hydro-ethanolic extract of (SNE) caused a concentration-dependent depression of evoked field excitatory postsynaptic potentials (fEPSPs) recorded extracellularly in the CA1 region of the hippocampus with maximal depression of about 80% and an estimated IC of 0.06 mg/ml. The SNE-induced fEPSP depression was accompanied by an increase in paired pulse facilitation. The fEPSP depression only recovered partially after 20 min washing out. The effect of SNE was not stimulus dependent as it was present even in the absence of synaptic stimulation. Furthermore, it did not show desensitization as repeat application after 10 min washout produced the same level of fEPSP depression as the first application. The SNE effect on fEPSPs was not via adenosine release as it was neither blocked nor reversed by 8-CPT, an adenosine A receptor antagonist. In addition, SNE depressed seizures induced by zero Mg and high K -containing artificial cerebrospinal fluid (aCSF) in a concentration-dependent manner. The results show that SNE depresses fEPSPs and spontaneous bursting activity in hippocampal neurons that may underlie its ability to abort convulsive activity in persons with epilepsy.

摘要

在西非次区域,热带灰姑娘植物的提取物传统上用于治疗惊厥病症。本研究旨在确定这些植物提取物抑制癫痫活动有效性的神经元基础。利用大鼠海马脑片标本,研究了该提取物抑制兴奋性突触传递和癫痫活动的能力。对海马CA1区细胞外记录的诱发场兴奋性突触后电位(fEPSPs)进行细胞外浴灌流(SNE)的水乙醇提取物,可引起浓度依赖性抑制,最大抑制率约为80%,估计IC为0.06mg/ml。SNE诱导的fEPSP抑制伴随着双脉冲易化的增加。洗脱20分钟后,fEPSP抑制仅部分恢复。SNE的作用不依赖于刺激,因为即使在没有突触刺激的情况下也存在。此外,它没有表现出脱敏现象,因为洗脱10分钟后重复应用产生的fEPSP抑制水平与第一次应用相同。SNE对fEPSPs的作用不是通过腺苷释放,因为它既不被腺苷A受体拮抗剂8-CPT阻断也不被其逆转。此外,SNE以浓度依赖性方式抑制由零镁和高钾人工脑脊液(aCSF)诱导的癫痫发作。结果表明,SNE抑制海马神经元中的fEPSPs和自发爆发活动,这可能是其终止癫痫患者惊厥活动能力的基础。

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