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Pharmacology and Clinical Use

The genus Aristolochia comprises approximately 200 species, many of which have played important roles in folk medicine for treating sore throat, venomous snakebites, wounds, fevers, and tuberculosis. The chemistry and pharmacology of aristolochic acid, the main active principle, was researched by many scientists. Many worthy achievements in the pharmacology of aristolochic acid have been published. [Pg.54]

Kupchan and Doskotsch (9) found that an alcoholic extract of A. indica possessed reproducible activity against the adenocarcinoma 755 test system. The active principle, aristolochic acid I, was isolated and characterized. Kamatsh and co-workers (97) reported that growth of mouse sarcoma-37 cells incubated with aristolochic acid at concentration of 100-200 p-g/ml for 3 hr was completely inhibited. Treatment of mice with aristolochic acid (1.25-5 mg/kg ip per day) for 3 days after subcutaneous implantation of sarcoma-37 cells inhibited tumor growth in 40-50%. A dose of 2.5-5 mg/kg ip per day for 5 days remarkably prolonged survival. The cytotoxic effect on HeLa cells in culture was observed at a concentration of 25 p-g/ml. [Pg.54]

Aristolochic acid I was used in clinical trials in cancer therapy however, it was abandoned due to liver and kidney toxicity 98). It is interesting that the cytotoxicity of aristolochic acid, not only previously observed in animal cells, has also been confirmed for plant cells (99). Aristoloside (10), isolated from A. manshuriensis, possessed antitumor activity (31). [Pg.54]

Experiments performed in rabbits and guinea pigs showed marked stimulation of leukocyte phagocytosis following application of various dilutions of [Pg.54]

In mice infections with pneumococci were influenced very satisfactorily by aristolochic acid I. Rats with wounds infected with Staphylococcus aureus were treated intraperitoneally or orally with aristolochic acid I compared to controls, the treated animals recovered much faster. Rabbits after intravenous application of aristolochic acid I showed an increased antibactericial action of serum (97). Mice infected with bacteria including Staphylococcus aureus, Diphococcus pneumoniae, and Streptococcus pyogenes could be protected by treatment with 50 xg/kg ip of aristolochic acid I (97). [Pg.55]


W. I. Taylor and N. R. Famswortli, eds., The Catharanthus Alkaloids, Botanj, Chemist, Pharmacology and Clinical Uses, Marcel Dekker, New York, 1973 W. I. Taylor and N. R. Famswortli, eds.. The Uinca Alkaloids, Botanj, Chemistry and Pharmacology, Marcel Dekker, New York, 1973. [Pg.559]

W.I. Taylor and N. R. Farnsworth, eds., Catharanthus Alkaloids Botany, Chemistry, Pharmacology and Clinical Uses. Dekker, New York, 1975. [Pg.69]

Cheer MC, Dunn CJ, Foster R. Tinzaparin sodium. A review of its pharmacology and clinical use in the prophylaxis and treatment of thromboemboUc disease. Drugs 2004 64 1479-1502. [Pg.82]

Dirks. J.H. D/ii fiir, Physiology. Pharmacology and Clinical Use. W.B. Saunders Company, Philadelphia. PA, 1945. [Pg.506]

White CM, Thrombin-directed inhibitors pharmacology and clinical use, Am Heart J 2005 I49 S54-S60. [Pg.91]

Sciulli TM, Mauro VE Pharmacology and clinical use of bivalirudin. Ann Pharmacother 2002 36 1028-1041. [Pg.107]

Scarborough RM, Kleiman NS, Phillips DR. Platelet glycoprotein llb/llla antagonists. What are the relevant issues concerning their pharmacology and clinical use Circulation 1999 100(4) 437-444. [Pg.581]

Furr, and Wakeling, A.E. (1987) Pharmacology and Clinical Uses of Inhibitors of Hormone... [Pg.164]

Sandow, J. (1987) In Pharmacology and Clinical Uses of Inhibitors of Hormone Secretion and Action, Chapter 20 (Furr, B.J.A. and Wakeling, A.E., eds.) pp. 365-384. Bailliere Tindall, Eastbourne, England. [Pg.165]

Lynch JJ, Lucchesi BR. New antiarrhythmic agents. II. The pharmacology and clinical use of encainide. Pract Cardiol 1984 10 109-32. [Pg.1214]


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