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Nalini Sofia, H∗, Thomas M.Walter∗∗ Liquorice has been used in medicine for more than 4000 years. The earliest record of its use in medicine is found in ‘code Humnubari’ (2100 BC). It was also one of the important plants mentioned in Assyrian herbal (2000BC). Hippocrates (400BC) mentioned its use as a remedy of ulcers and quenching of thirds. The drug was also mentioned by Theophrastus and Dioscorides. In traditional Siddha system of medicine, liquorice is used as a demulcent, expectorant, anti.tussive, laxative and sweetener. Loquiritae officinalis Mo ench Plantae Angiospermae Dicotyledoneae Rosales ! Leguminosae " Glycyrrhiza glabra Linn # $ % Jashtimadhu, Jaishbomodhu & ' ( Yashti.madhuh. Madhuka Jethimadhu Jothi.madh, Mulhatti Yastimadhuka, atimaddhura ∗ Siddha Physician, Chennai, India. dr.nalinisofia@gmail.com Asst. Lecturer (Selection Grade), P.G. Dept of Gunapadam (Pharmacology), Govt. Siddha Medical College, Palayamkottai, Tamilnadu, India. dr.thomaswalter@gmail.com ∗∗ ) ) Iratimadhuram Jeshtamadha ! Jatimadhu * Atimaduram * Atimadhuranu, Yashtimadhukam + Licorice, Liquorice, Sweet wood , " Aslussiesa Ausareha mahaka Boisdoux Sussholz # Native to central and south western Asia and the Mediterranean region. It is cultivated in the Mediterranean is basin of Africa, in South Europe and in India. Glycyrrhiza glabra is a diploid with 2n=16. ( Glycyrrhiza glabra is a hard herb or under shrub attaining a height up to 6ft; leaves multifoliate, imparipinnate, flowers in axillary spikes, papilinaceous, lavender to violet in colour, pods compressed, and containing reniform seeds. The dried, peeled or un peeled underground stems and roots constitute the drug, known in the trade as Liquorice. Flowers in March and fruits in August. Root and Rhizomes The major bio.active constituent of rhizomes is a triterpenoids saponin glycyrrhizin, glycyrrhizinic acid, glabrin A&B, glycyrrhetol, glabrolide, isoglabrolide, isoflavones,coumarins, triterpene sterols etc. - # # Total ash Not more than 7% Acid insoluble ash Not more than 2% Sulfated ash Not more than 10% Water soluble extractive Not less than 20% Diluted alcohol.soluble extractive Not less than 25% Moisture 5.25% Ether extracts 16.85% Albuminoids 37.00 %( containing nitrogen5.92%) Soluble carbohydrates 31.00% Woody fiber 5.05% Ash 4.80 %( containing sand 0.25%) Manchurian licorice is obtained from glycyrrhiza uralensis. Being a substitute it dose contain glycyrrhizin the active principle but very little of free sugars. The common adulterant is wild licorice also called Indian licorice, derived from the roots of Abrus precatorious (leguminosae). Microscopically the adulterant is characterized by stone cells. , Tonic, demulcent, expectorant, diuretic, mild laxative, anti.arthritic, anti. inflammatory, anti.biotic, anti.viral, anti.ulcer, memory stimulant (being MAO inhibitor), anti.tussive, aphrodisiac, anti.mytotic, estrogenic, anti.oxidant, anti.caries agent, anti.neoplastic, anti.cholinergic, anti.diuretic, hypolipidemic activity, etc. - % The bio availability of glycyrrhizin was much decreased when given in extract form with equivalent amount of compound, when compared to giving pure compound. The decoction of the dried rhizome, taken orally by 5 normal adults at a concentration of 5%, reached maximum serum concentration of glycyrrhetic glycoside at 4 hours post ingestion and was eliminated with in 72 hours. Glycyrrhetic acid reached maximum serum concentration, 24 hours post ingestion. The highest concentration was 30ng/ml and excreation was not completed after 96 hours in two of the subjects. In two cases if pseudo aldosteronism the serum glycyrrhetic acid levels were as high as 70.80ng/ml while glycosides were quite low. Water extracts of the dried root, administered intra gastrically to rats at a dose of 6.278gm/kg, was excreted in the bile, reaching maximum by 8hours after dosing. * • A decoction of madhuka or its powder was prescribed with honey in anaemia. • Yashti mixed with cow’s milk was prescribed for promoting lactation. • 10g madhuka powder mixed with 10g sugar, pounded with rice water was prescribed in men.metrorrhagia. • A confection of rice.milk, prepared with yashtimadhu, was prescribed in hoarseness of voice. • Charaka prescribed 10g madhuka powder mixed with honey, followed by intake of milk, as an aphrodisiac and as an intellect.promoting tonic. • Charaka also percribed a paste of liquorice and picrorrhiza kurroa with sugar.water as a cardiac tonic. • Charaka datta prescribed yashtimadhu and santalum album, powdered with milk, in haematemisis. • Sushruta prescribed the paste of yashtimadhu 10g, in intrinsic haemorrhage. • In oedema, the paste of licorice, sesamum indicum and milk mixed with butter was prescribed. • Warm clarified butter mixed with licorice, was applied topically on wounds, bruises and burns. • A decoction of madhuka was applied on erysipelas. • Yashti is an important ingredient in Narikelanjana (IMCOPS) eye.drops, prescribed in both acute and chronic conjunctivitis, and also in blepharitis. • +.# A decoction of the root is a good wash for falling and greying of hair. # Glycrrhiza has the following, experimentally proved activities: • Anti.bacterial activity • Anti hepato toxic activity • Estrogenic activity • Anti fungal activity • Anti hemorrhoido activity • Anti hyper glycemic activity • Anti malarial activity • Anti oxidant activity • Immuno stimulatory& Anti viral activity • Anti ulcer activity # Glycrrhiza has the following, clinically proved Pharmacological activities: • Anti ulcer activity • Anti asthmatic activity • Anti diuretic activity • Anti hepato toxic activity • Eczema and psoriasis • Herpes simplex The use of liquorice extract in the treatment of peptic ulcer sometimes appeared to invoke oedema and other side effects. Many investigations were carried out and it was shown that glycyrrhizin and glycyrrhetetinic acid decreased the out put of ACTH, reduced urinary excretion of sodium and chloride, increased potassium excretion, reduced rennin activity and serum aldosterone, elevated blood pressure and induce metabolic alkalosis with severe hypokalaemia and hypernatremia, capable of causing cardiac arrest. Clinical investigations revealed sodium retention to be connected to an aberration in cortisol metabolism in the kidneys, which interferes with 11.β.hydroxy steroid dehydrogenase. Consumption of licorice or glycyrrhizin in excessive amounts and over a long period produces pseudo aldostronism leading to oedemo, hypertention, and weight gain. The intake of higher doses (above50g/day) over an extened period (>6weeks) may cause sodium retention, potassium depletion, hyper tension, cardiac complaints, kidney disease, obesity, disorders associated with pregnancy and hypo kalaemic alkalosis. It should not be taken concurrently with cortico steroid treatment. The drug is contra indicated in patients with a history of hyper tension, renal failure and using digitalis preparations. It should not be used for longer than 4.6 weeks with out medical advice. Because it increases potassium loss, it should not be administered for prolonged use with thiazide and loop diuretics or cardiac glycosides. Because it reduces sodium and water excretion, the effectiveness of drugs used in the treatment of hypertention may be reduced. It should not be administered in conjunction with spiranolactone or amiloride. * . Ethanol (30%) extract of the root, administered orally to mice of both sexes, produced LD50 32.0ml/kg. Water extract of the dried root (48.58% glycyrrhizin), administered intra peritoneally, orally and subcutaneously to mice and rats, produced LD50 1.5gm/kg, 16.0gm/kg, and 4.2gm/kg, respectively. 1. Materia Medica, vol I, 3rd edition, A.K. Nadkarni, Popular prakashan pvt. Ltd. Bombay. 2. Encyclopedia of Indian medicinal plants, 1st edition, C.P. Khare, Springer.verlag Berlin Heidelberg New York. 3. The Wealth of India, Raw materials, IV F.G, 1st edition, Council of Scientific and Industrial Research. New Delhi. 4. Text book of Natural medicine, vol.I, Joseph E. Pizzorno Jr, Michael T.Murray. Harcourt publisher ltd, Edinburg. 5. WHO monograph on selected medicinal plants, vol.I, Aitbs publishers, India. 6. Indian Herbal Pharmacopoeia, vol.I, 1998, Regional research laboratory & Indian drug manufacture association, Mumbai. 7. Medicinal plants of the world, vol2, Ivan A. Ross, Human press Inc. Totowa, New Jersey. 8. Pharmaco dynamic basis of herbal medicine, Manuchair Ebadi, CRC press, USA. 9. Status Reports on medicinal plants, For NAM countries Dec1992, Dr. Akhtar Husain, Publications and Information Directorate, New Delhi. 10. The useful plants of India, National Institute of science communication, CSIR, 4th reprint 2000, Shri. S.P, Ambasta, New Delhi. //0 Indian medicinal plants, A compendium of 500 species, vol.3, Orient Longman P.Ltd, reprint 2002, P.K.Warrier, V.P.C. Nambiar, C.Ramankutty, Chennai.2.