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Antiepileptic activity of total triterpenes isolated from Poria cocos is mediated by suppression of aspartic and glutamic acids in the brain

机译:从茯苓中分离的分离的分三萜烯的抗癫痫活性是通过抑制大脑中的天冬氨酸和谷氨酸的介导

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Context: Triterpenes from Poria cocos Wolf (Polyporaceae) have been used to treat various diseases in traditional Chinese medicine. However, the antiepileptic effects and mechanism are not fully understood.Objective: The objective of this study is to investigate the antiepileptic properties of total triterpenes (TTP) from the whole P. cocos.Materials and methods: The ethanol extract TTP was identified by HPLC fingerprint analysis. Male ICR mice were gavaged (i.g.) with TTP (5, 20, 80 or 160mg/kg) or reference drugs twice a day for 7 d. Antiepileptic activities of TTP were evaluated by maximal electroshock (MES)- and pentylenetetrazole (PTZ)-induced seizures in mice for 30 and 60min, respectively. Locomotor activity and Rota-rod tests were performed for 60min and 5min, respectively. The levels of glutamic acid (Glu), aspartic acid (Asp), -aminobutyric acid (GABA) and glycine (Gly) in convulsive mice were estimated. The chronic epileptic model of Wistar rats was built to measure expressions of glutamate decarboxylase 65 (GAD65) and GABA(A) in rat brain after TTP treatment.Results: The LC50 of TTP (i.g.) was above 6g/kg. TTP (5-160mg/kg) protected mice against MES- and PTZ-induced convulsions at 65.0% and 62.5%, respectively, but have no effect on rota-rod treadmill; TTP (20-160mg/kg) significantly reduced the locomotor activities, shortened the onset of pentobarbital sodium-induced sleep; TTP decreased Glu and Asp levels in convulsive mice, but increased the GAD65 and GABA(A) expressions in chronic epileptic rats at doses usage.Discussion and conclusion: TTP extracted from P. cocos possessed potential antiepileptic properties and is a candidate for further antiepileptic drug development.
机译:背景:来自Poria Cocos Wolf(Polyporaceae)的Triterpenes已被用于治疗中药中的各种疾病。然而,抗癫痫效应和机制尚未完全理解。目的:本研究的目的是研究来自整个P. Cocos.Materials和方法的总三萜(TTP)的抗癫痫特性:通过HPLC鉴定乙醇提取物TTP指纹分析。雄性ICR小鼠胃肠(即)与TTP(5,20,80或160mg / kg)或参考药物每天两次,7天。通过最大电孔(MES) - 和五苯乙烯四唑(PTZ) - 在小鼠中诱导30分钟的癫痫发作,评估TTP的抗癫痫活性。运动活性和旋转杆试验分别进行60min和5min。估计谷氨酸(Glu),天冬氨酸(ASP), - 氨基丁酸(GABA)和甘氨酸(GLY)在抽搐小鼠中的水平估计。 Wistar大鼠的慢性癫痫模型是为了在TTP治疗后测量大鼠脑中谷氨酸脱羧酶65(GAD65)和GABA(A)的表达。结果:TTP的LC50(即,I.g)高于6g / kg。 TTP(5-160mg / kg)在65.0%和62.5%以65.0%和62.5%的痉挛保护小鼠,但对罗拉杆跑步机没有影响; TTP(20-160mg / kg)显着降低了运动活动,缩短了戊巴比妥钠诱导的睡眠的发作; TTP降低了痉挛小鼠的Glu和Asp水平,但是在剂量使用的慢性癫痫大鼠中增加了GAD65和GABA(A)表达。分数和结论:从P.Cocos提取的TTP具有潜在的抗癫痫特性,是进一步抗癫痫药物的候选者发展。

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