EVALUATION OF VEDANASTHAPANA (ANALGESIC) EFFECT OF MOCARASA: SHALMALI NIRYASA (SALMALIA MALABARICA – GUM DC)

Huddar Shreedevi, Anup Kumar Elleri, Devaraj C
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Abstract

Pain, said to be one of nature’s earliest signs of morbidity and is also one of the most typical presentations seen in medical practice, brings disturbance in the equilibrium state of a person. In order to manage such conditions, several drugs are available in the present era. Among them, some are expensive, and some have side effects such as dyspepsia and gastrointestinal bleeding, burning sensations, etc. For relieving pain, Acharya Charaka mentioned Vedanasthapana Daseimani Gana (Group of 10 Drugs), of which Mocarasa (Salmalia malabarica Dc.) is one among them. This study is taken up to evaluate the Vedanasthapana (Analgesic) karma of Mocarasa on albino mice using Eddy’s hot plate method. The Eddy’s Hot plate method is followed with three groups of Albino mice (6 mice in each group) as control group, standard drug group and trial drug group. Distilled water is fed to the control group, Mocarasa kwatha (decoction) for the trial drug group and Diclofenac sodium for the standard drug group. Statistically, the analgesic effect in the trial drug started gradually at 60 min and continued up to 120 min. Meanwhile, the standard group showed immediate onset of action at 15 min duration and progressively increased up to 120 min. The trial drug and the standard drug showed insignificant differences, which reveals that both have similar analgesic activity.
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评估 mocarasa:shalmali niryasa(salmalia malabarica - 树胶 DC)的 Vedanasthapana(镇痛)效果
据说,疼痛是自然界最早的发病迹象之一,也是医疗实践中最典型的表现之一,它扰乱了人的平衡状态。为了控制这种情况,当今时代有多种药物可供选择。其中,有些药物价格昂贵,有些药物有副作用,如消化不良和胃肠道出血、灼烧感等。为了缓解疼痛,阿查里亚-查拉卡(Acharya Charaka)提到了 Vedanasthapana Daseimani Gana(10 种药物组),Mocarasa(Salmalia malabarica Dc.)就是其中之一。本研究采用艾迪热板法评估 Mocarasa 对白化小鼠的 Vedanasthapana(镇痛)作用。埃迪热板法使用三组白化小鼠(每组 6 只),分别为对照组、标准药物组和试验药物组。给对照组喂蒸馏水,给试验药物组喂莫卡拉沙水煎剂,给标准药物组喂双氯芬酸钠。据统计,试验药物的镇痛效果从 60 分钟开始逐渐显现,一直持续到 120 分钟。与此同时,标准药物组在 15 分钟时立即起效,并在 120 分钟时逐渐增强。试验药物和标准药物的差异不明显,这表明两者具有相似的镇痛活性。
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