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     FOREVER NIRGUNDI

Vitex negundo

Sanskrit

:

Nirgundi

English

:

Five leaved chaste tree

Latin name

:

Vitex negundo

Family

:

Verbanaceae

 

Morphology: Large shrub, tender parts grey pubescent. Leaf: Opposite, digitately 3-5 foliolate, leaflets lanceolate, acuminate tip, entire margin, green above, grey pubescent beneath. Flower: Blue in terminal thyrosoid, grey pubescent panicle; Fruit: Ovoid drupes, 1 cm long black when ripe.

Ayurvedic Pharmacodynamic properties:

Rasa

:

Katu (pungent), Tikta (bitter)

Guna

:

Laghu (Ruksha), Ruksha (dry)

Virya

:

Ushna (Hot)

Vipaka

:

Katu (pungent)

Doshakarma

:

Kapha-Vata Shamaka

 

 

Useful parts

:

Leaves, seeds and root bark.

Medicinal uses

:

It is acrid, bitter, heating, astringent, stomachic, cephalic, anthelmintic and useful in treatment of leucoderma, consumption, inflammations, eye diseases, spleen enlargement, bronchitis, asthma, biliousness, painful teething of children etc. It has germicidal properties. It is easily digestible and can cure morbid vata and kapha and used in arthritis, cephalgia, otalgia, inflammatory, glandular and rheumatic swellings, intestinal worms, fever, ulcers, skin diseases, nervous disorders and leprosy.

Dose

:

Swarasa (juice) 10-20 ml; churna (powder) 3-6 gm

Important formulations

:

Nirgundi Taila.

Home remedies:

  1. In cold, its decoction 20ml should be used along with 1 gm Pippali and 250 mg Vacha.
  2. In pneumonitis, Swarasa of its leaves 10 ml is so beneficial along with    gm Pippali.
  3. Its paste on affected site is painkiller and anti-inflammatory.

 

Recent studies:

1: Indian J Med Res. 2006 Oct;124(4):447-50. Vitex negundo Linn (VN) leaf extract as an adjuvant therapy to standard anti-inflammatory drugs. Tandon VR, Gupta RK. Postgraduate Department of Pharmacology & Therapeutics, Government Medical College, Jammu, India.

The sub-effective dose of VN potentiated anti-inflammatory activity of phenlbutazone and ibuprofen significantly in carrageenin induced hind paw oedema and cotton pellet granuloma models. The potentiation of anti-inflammatory activities phenlbutazone and ibuprofen by VN indicates that it may be useful as an adjuvant therapy along with standard antiinflammatory drugs. PMID: 17159267 [PubMed - indexed for MEDLINE]

 

2: Bioorg Med Chem Lett. 2007 Jan 1;17(1):239-42. Epub 2006 Oct 5. New antifungal flavonoid glycoside from Vitex negundo. Sathiamoorthy B, Gupta P, Kumar M, Chaturvedi AK, Shukla PK, Maurya R. Medicinal and Process Chemistry Division, Central Drug Research Institute, Lucknow 226 001, India.

Flavonoids are ubiquitous in photosynthesizing cells and are common part of human diet. For centuries, preparations containing these compounds as the principal physiologically active constituents have been used to treat human diseases. Increasingly, this class of natural products is becoming the subject of anti-infective research. Our bioactivity guided fractionation of ethanolic extract of leaves of Vitex negundo resulted in the isolation of new flavone glycoside (4) along with five known compounds 1-3, 5 and 6. All the isolated compounds were evaluated for their antimicrobial activities. The new flavone glycoside 4 and compound 5 were found to have significant antifungal activity against Trichophyton mentagrophytes and Cryptococcus neoformans at MIC 6.25 microg/ml. PMID: 17027268 [PubMed - indexed for MEDLINE]

 

3: J Ethnopharmacol. 2006 Mar 8;104(1-2):129-31. Epub 2005 Oct 25. Comparative anti-hyperglycemic potentials of medicinal plants. Villasenor IM, Lamadrid MR. Natural Products Research Laboratory, Institute of Chemistry, University of the Philippines, Diliman, Quezon City 1101, Philippines. irene.villasenor@up.edu.ph

Validation of the ethnobotanical use of the leaves of Artemisia vulgaris Linn. (Compositae), Eucalyptus tereticornis Sm. (Myrtaceae), Solanum nigrum Linn. (Solanaceae), and Vitex negundo Linn. (Verbenaceae); stems of Nopalea cochinellifera (Linn.) Salm-Dyck (Cactaceae); roots of Imperata cylindrica Beauv. (Gramineae); dried bark of Syzygium cumini (Linn.) Skeels (Myrtaceae) as anti-diabetic agents using the oral glucose tolerance test showed that only the bark of Syzygium cumini and the leaves of Vitex negundo and Eucalyptus tereticornis exhibited anti-hyperglycemic activities when fed simultaneously with glucose. At the same dosages of 5 mg/20 g mouse, Syzygium cumini-treated mice showed a significant decrease in blood glucose levels (BGLs) at 30 min (alpha=0.10) and from 45 min onwards at alpha=0.05. Vitex negundo exhibited greater anti-hyperglycemic activity than Eucalyptus tereticornis. Both showed a significant decrease in BGLs at 60 min but at alpha=0.05 for Vitex negundo and at alpha=0.07 for Eucalyptus tereticornis. There was no significant lowering in BGLs for Imperata cylindrica and Solanum nigrum while there was even an increase in BGLs for Nopalea cochinellifera and Artemisia vulgaris. PMID: 16253452 [PubMed - indexed for MEDLINE]

4: Indian J Physiol Pharmacol. 2005 Apr;49(2):199-205. An experimental evaluation of anticonvulsant activity of Vitex-negundo. Tandon VR, Gupta RK. Post Graduate Department of Pharmacology & Therapeutics, Govt. Medical College, Jammu 180 001. dr_vishaltandon@yahoo.com

Maximal electroshock seizures (MES) in albino rats and pentylenetetarazole (PTZ) induced seizures in albino mice were used to study anticonvulsant activity of Vitex-negundo leaf extract. The ethanolic leaf extract of Vitex-negundo was administered orally in graded doses (250, 500 and 1000 mg/kg p.o) in both the experimental models and the effects were compared with diphenylhydantoin in MES method and valporic acid in PTZ induced seizures method as standard control respectively. The Vitex-negundo in the doses (250, 500 and 1000 mg/kg, p.o) did not show protection against MES to any significant extent but significant post-ictal depression was observed in the dose of 1000 mg/kg body weight in comparison to control. However, sub-protective dose of test drug (100 mg/ kg, p.o) potentiated the anticonvulsant action of diphenylhydantoin. The test drug in the dose (1000 mg/kg, po) showed 50% protection in clonic seizures and 24-hour mortality against PTZ induced seizures. It also decreased number and duration of convulsions significantly. Vitex-negundo potentiated anticonvulsant activity of valporic acid. The anticonvulsant activity of Vitex-negundo has not been found equi-effective with standard drugs. These findings suggest that Vitex-negundo possesses anticonvulsant activity particularly against PTZ induced convulsions. Moreover, the potentiation of diphenylhydantoin and valporic acid by Vitex-negundo indicates that it may be useful as an adjuvant therapy along with standard anticonvulsants and can possibly lower the requirement of diphenylhydantoin and valporic acid. PMID: 16170989 [PubMed - indexed for MEDLINE]

5: Indian J Physiol Pharmacol. 2005 Apr;49(2):163-70. Antinociceptive activity of Vitex-negundo Linn leaf extract. Gupta RK, Tandon VR. Department of Pharmacology, M.G.I.M.S. (Sevagram), Wardha 442 102.

Tail flick test in rats and acetic acid induced writhing in mice were employed to study the antinociceptive activity of ethanolic leaf extract of Vitex-negundo (VN) (100, 250 and 500 mg/kg, p.o). The effect was compared with meperidine (40 mg/kg, sc) in tail flick method and aspirin (50 mg/kg, p.o) in writhing test as a standard control respectively. An interaction with naloxone hydrochloride was also studied in tail flick method for its mechanism of central analgesic action. The test drug showed significant analgesic activity in dose dependant manner in both the experimental models. In comparison to standard drug (meperidine), more than ten times dose of VN extract was required to produce comparable significant antinociceptive activity. The sub-effective dose (5 mg/kg, po) of VN potentiated the analgesic activity of meperidine (4 mg/kg, sc) and aspirin (25 mg/kg, po). Naloxone (1 mg/kg, sc) did not reverse the analgesic effect of VN extract. Our observations suggest that VN possesses both central and peripheral analgesic activity. The central analgesic action does not seem to be mediated through opioid receptors. It, may prove to be a useful adjuvant therapy along with standard analgesic drug. PMID: 16170984 [PubMed - indexed for MEDLINE]

6: Phytother Res. 2004 Jan;18(1):8-13. Reproduction in male rats is vulnerable to treatment with the flavonoid-rich seed extracts of Vitex negundo. Das S, Parveen S, Kundra CP, Pereira BM. Department of Biotechnology, Indian Institute of Technology Roorkee, Roorkee - 247 667, Uttaranchal, India.

A partially purified flavonoid-rich extract was prepared from the seed of Vitex negundo. The effect of this extract on the reproductive system of male rats was investigated at four different concentrations. All the major accessory sex organs shed weight when the preparation was administered at doses of >or=15 mg/rat/day after 15 days of treatment. The drop in weight was also reflected in disturbed tissue biochemistry. Secretory products such as citric acid in the prostate, fructose in seminal vesicles and epididymal alpha-glucosidase activity, indices of accessory sex organ function in males, diminished. Microscopic examination of the sperm derived from the cauda epididymides of treated animals showed only a marginal change in vitality. However, sperm numbers dwindled and slackness in their motility was observed, factors that may impede fertility. Toxicity testing in blood did not point to distress in any of the vital organs. Taken together, it is inferred that the seed extracts of V. negundo interfere with male reproductive function without producing adverse toxicity in other vital organs. Copyright 2004 John Wiley & Sons, Ltd. PMID: 14750193 [PubMed - indexed for MEDLINE]

Summary:

Recent studies show that nirgundi has thermogenic, anthelmithitic, expectorant, carminative, anticonvulsant, anti-hyperglycemic and analgesic properties. It is also evaluated for its anitinflammatory activity and the potentiation of anti-inflammatory activities phenlbutazone and ibuprofen by V. Negundo indicates that it may be useful as an adjuvant therapy along with standard antiinflammatory drugs. In other study the new flavone glycosides were found to have significant antifungal activity.


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