首页> 外文期刊>Indian Journal of Experimental Biology >Neuropharmacological actions of Panchagavya formulation containing Emblica officinalis Gaerth and Glycyrrhiza glabra Linn in mice
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Neuropharmacological actions of Panchagavya formulation containing Emblica officinalis Gaerth and Glycyrrhiza glabra Linn in mice

机译:Panchagavya制剂,含Emblica officinalis Gaerth和Glycyrrhiza glabra Linn在小鼠中的神经药理作用

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摘要

A panchagavya Ayurvedic formulation containing E. officinalis, G. glabra, and cow's ghee was evaluated for its effect on pentobarbital-induced sleeping time, pentylenetetrazol-induced seizures, maximal electroshock-induced seizures, spontaneous motoractivity, rota-rod performance (motor coordination) and antagonism to amphetamine in mice. The formulation (300, 500 mg/kg, po) produced a significant prolongation of pentobarbital-induced sleeping time and reduced spontaneous locomotor activity. The formulation also significantly antagonised the amphetamine induced hyper-locomotor activity (500, 750 mg/kg, po) and protected mice against tonic convulsions induced by maximal electroshock (500, 750 mg/kg, po). The formulation slightly prolonged the phasesof seizure activity but did not protect mice against lethality induced by pentylenetetrazole. The formulation did not show neurotoxicity. The results suggest that the panchagavya formulation is sedative in nature.
机译:评估了含有厚皮大肠埃希菌,G。glabra和牛油的Panchagavya阿育吠陀制剂对戊巴比妥诱发的睡眠时间,戊四唑诱发的癫痫发作,最大电击诱发的癫痫发作,自发运动能力,旋转棒性能(运动协调)的影响和对苯丙胺的拮抗作用。该制剂(300、500 mg / kg,口服)可大大延长戊巴比妥诱导的睡眠时间,并降低自发运动能力。该制剂还显着拮抗苯丙胺诱导的运动过度活性(500、750 mg / kg,口服),并保护小鼠免受最大电击引起的强直性惊厥(500、750 mg / kg,口服)。该制剂稍微延长了癫痫发作活动的阶段,但不能保护小鼠免受戊四氮诱导的致死性。该制剂未显示神经毒性。结果表明,panchagavya制剂本质上是镇静剂。

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