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Showing 2 results for Diazepam

A Rezaie, M Pashazadeh, Ch Ahmadizadeh, B Jafari , Hm Jalilzadeh,
year 9, Issue 36 (12-2010)
Abstract

Background: Due to sedation, anticonvulsant and anti-pain effects, Nardostachys jatamansi has had a special place in traditional medicine of China, India and Iran. Regarding Alkaloid, Organic acid esters, valeric acid and isovalerates this plant has always been used to reduce nervous pressure and the treatment depression and chronic insomnia. Objective: Considering the importance of sedative and anxiolytic effects of this plant's we decided to have a comparative study of this plant with chemical drugs. Methods: In this study, first, the rhizome of N. jatamansi was extracted by hydromethanolic (70%) solvent and then, the presence of valporoates, in total extract was revealed by GC-MS analysis of its n-Hexane fraction. For studying the effectiveness of sedative and anxiolytic of N. jatamansi in compraison with diazepam different groups of female wistar rats received N. jatamansi (100, 200, 400 mg/kg, ip), diazepam (1.2 mg/kg, ip), di-metyl solphoxid (DMSO) with equal volume, and 15 min after assessing the relif/sleep inducing effect (induced sleep duration by ketamine, 40 mg/kg, ip) and anxiolytic effects (using Elevated plus were done). Results: The GC-MS analysis of the n-hexan fraction of extract led to identification and quantification of fifteen compounds, the main components were a - Aristolen-1-alpha-ol (31.1%), valerenal (31%) and valerenic acid (26.5%). Pharmacological results showed that herbal extract of N. jatamansi with the maximum inhibition was observed at the does of 200 mg/kg of sedative and anxiolytic effect. Conclusion: Obtained resultes indicated that extract of N. jatamansi gives sedative and anxiolytic effects.

H Hosseinzadeh , M Ramezani , Z Afarin ,
year 11, Issue 41 (2-2012)
Abstract

 Background: Ocimum basilicum showed antinociceptive activity. The antinociceptive effect was inhibited by naloxone in hot-plate test.

 Objective: As O. basilicum antinociceptive activity was inhibited by an opioid antagonist, activity-guided fractionation of methanol extract of this plant was carried out to investigate the isolation of the active component(s) responsible for the alleviation of morphine withdrawal syndrome induced by naloxone.

 Methods: Dependence was induced using subcutaneous injections of morphine daily for three days (50, 50 and 75 mg/kg). On the fourth day, morphine was injected two hours prior to the intraperitoneal injection of naloxone. The number of jumps during the 30 minute period after naloxone injection was considered as measure of the withdrawal syndrome. The extract and fractions were injected 30 min prior to morphine injection. The methanol extract of plant was suspended in water and extracted with chloroform. The active chloroform layer was concentrated and partitioned between methanol-water (9:1) and petroleum ether. The extract or fraction was injected intraperitoneally at doses 0.15 - 1.46 g/kg.

Results: The methanol, chloroform and petroleum ether extracts decreased the jumping numbers more than the aqueous and hydro-alcohol extracts. Further fractionation on silica gel column chromatography yielded a fraction, which was 4 times as effective as the crude extract.

Conclusion: The results of this study indicated that the plant extracts and fractions containing non- polar component (s) could be useful for the alleviation of morphine withdrawal syndrome


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