Screening of antiviral effect of Melia Azedarach ( Mahanimba ) leaves extract evaluated by MTS method
Mahanimba- Melia azedarach
Main Synonym
Dreka, ramyaka, vishmushti, nimbala, karmuka, jiva
Regional Name
Bengali : ghoda neem
Gujarati : bakan limdo
Hindi : bakayana
Punjabi : deka, dhareka
Tamil : malaivembu
Telugu : turaka, bevaka
English : the beed tree
Botanical Name
Melia azedarach
Family
Meliaceae
Classification (Gana)
Bhavprakash nighantu : guuchyadi varga.
Kaiyadeva nighantu : aushadhi varga
External Morphology
5-15 meter high tree
Useful Parts
Root, stem bark, leaves, fruit
Important Phytoconstituent
Tannins, azadirechtine, sitosterol, melianone
Rasa Panchak
Rasa : tannins, azadirechtine, sitosterol, melianone
Guna : laghu, ruksha, tikshna
Virya : ushna
Vipaka : katu
Action
Kaphapittahara
Therapeutic Indication
Grahi (reduce excessive secretions), arshoghna (useful in piles), krimighna (anti-helminthic), kusthaghna (useful in skin disorders), mushika-vishhara (useful in rat poison)
Therapeutic Uses
1. Twakavikara - bark and flower paste is given with water for skin disorders.
2. Shirahshoola - flower and leaves paste is applied externally in headaches.
3. Krimi - bark, and leaves are useful to treat worms in children.
Dose
Bark powder - 1-3 gm, flower - 3-5 gm, leaves - 1-3 gm
Formulations
Mahavishgarbha taila, bruhadmanjisthadi kwath
INTRODUCTION
The drugs which are used as analgesic and anti inflammatory agents cause many side effects and
toxic effects. Many medicines of plant origin have been used from many years without any side
effects. In Ayurvedic ancient text named Gada Nigraha, it has been mentioned that Mahanimba (Melia
azedarach Linn.) Moola can be used in the management of Gridhrasi (Sciatica). In Gridhrasi pain
and inflammation of Sciatic nerve is the main cardinal symptoms. So, in this pharmacological study
evaluation of analgesic and anti inflammatory activity of test drug Mahanimba Moola have been
assessed with compare to Standard drug Parijata Patra (Nyctanthes arbortristis)
Antiviral Test
Antiviral activity was tested as described earlier [65, 67]. The final, maximal DMSO concentration in the assay wells with the highest sample input (1%) was well tolerated by the cells. Rupintrivir was used as a positive control. All data were expressed as EC50, CC50, and SI. For cytotoxicity assays, plant extracts (only those that showed antiviral activity) were evaluated by the MTS method. In brief, the same experimental setup was used as for the antiviral assay; except for cytotoxicity determination, uninfected cultures were incubated with a serial dilution of plant extract for three days at 37°C. “The cytotoxic concentration was calculated as CC50 or the concentration of plant extracts required to reduce cell proliferation by 50% relative to the number of cells in the solvent-treated controls. The formula used to calculate cytotoxic activity was % CPE = [ODcc − OD plant extract]/ODcc, where ODcc corresponds to the optical density of the uninfected and untreated cell cultures, and OD plant extract corresponds to the OD of uninfected cultures, treated with the extract. In addition, the selectivity index (SI) was calculated as the ratio of CC50 for cell growth to EC50 (CC50/EC50)”
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