阿索卡-萨拉卡-阿索卡(saraca asoca roxb.DE (WILDE.)

Asha S Raj, Sara Monsy Oommen
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引用次数: 0

摘要

阿育吠陀将 "治疗--获得健康的方式"(chikitsa)解释为 "四肢"(chatushpada)的组合。我们可以从《查拉卡三集》(Charaka Samhita)的《Shadvirechana Shatasriteeya Adhyaya》中首次探索药物的药理分类。Asoka - Saraca asoca [Roxb] de Wilde 已被列入阿查里亚-查拉卡(Acharya Charaka)提到的 Vedanasthapana mahakashaya(缓解特定感觉的一组药物),Nighantukaara 将其解释为 streenam uchrokanashanaya。soka 的词源是 chittavikalatha,是药物作用于 "manasika bhava's "的 "引线"。根据临床经验,除了疼痛外,恶心、呕吐、谵妄、失眠、情绪不稳定、紧张、易怒、愤怒和恐惧等相关症状也会因使用该药物而得到缓解。迄今为止,Asoka 对 "manasika bhava's "的药理作用仍未得到研究。因此,我们进行了一项初步的反向药理实验研究,以评估这种药物对中枢神经系统的作用。药物对中枢神经系统的抑制作用是通过神经和激素机制介导的。自发运动活动的即刻减弱是通过神经机制实现的,而持久作用则是通过激素作用实现的。该药物具有苦味原理。苦味受体 T2R 在脑细胞中表达功能性苦味。T2R-4、T2R-107 和 T2R-38 转录本存在于脑干、大脑皮层和小脑中。该药物是一种有效的植物雌激素来源,具有模拟雌激素的作用。在所有评估日的中枢神经系统抑制活动研究中,该药物都能明显降低自发运动活动,p 值为。
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CNS DEPRESSANT ACTIVITY OF KASHAYA OF ASOKA – SARACA ASOCA ROXB. DE (WILDE.)
Ayurveda explains chikitsa (treatment – mode to attain health) as a conglomeration of chatushpada’s (four limbs). Pharmacological categorization of drugs can be explored for the first time from the Charaka Samhita, Shadvirechana Shatasriteeya Adhyaya. Asoka - Saraca asoca [Roxb] de Wilde has been included in the Vedanasthapana mahakashaya (group of drugs which alleviates a specific sensation) mentioned by Acharya Charaka, which is explained as streenam uchrokanashanaya by the Nighantukaara’s. The etymology of soka is chittavikalatha, which is a ‘lead’ to the action of a drug on “manasika bhava’s”. In clinical experience, apart from the pain, associated symptoms like nausea, vomiting, delirium, insomnia, emotional instability, nervousness, irritability, anger, and fear are also relieved by its usage. Till now, the pharmacological action of Asoka on “manasika bhava’s” remains unexplored. Hence, a preliminary experimental study has been undertaken on the reverse pharmacological aspect to assess the action of this drug on CNS. The depressant action of drugs on CNS is mediated through both neural and hormonal mechanisms. The immediate reduction in spontaneous motor activity was achieved through the neural mechanism, and the prolonged effect was achieved through the hormonal action. The drug possesses bitter principles. The functional bitter taste is expressed in brain cells by bitter taste receptors T2R’s. T2R-4, T2R-107, and T2R-38 transcripts are found in the brain stem, cerebral cortex and cerebellum. The drug is a potent source of phytoestrogen, which has oestrogen-mimicking action. The drug significantly reduces spontaneous motor activity in the CNS depressant activity study on all assessment days, with a p-value.
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