Bejunco de Cerca, Butua, Cissampelos pareira, False Pareira, Feuille de Velous, Herbe des Sages-Femmes, Menispermaceae, Pareira, Patacon, Patha, Velvetleaf, Vigne Maronne, Vigne Sauvage, Xi Sheng Teng.
Abuta (Cissampelos pareira) is an herb. People use the root, bark, and other parts that grow above the ground as medicine.
Don't confuse abuta (Cissampelos pareira) with Abuta grandifolia, which is also referred to as abuta and is a South American medicinal plant used by indigenous people for making arrow poison.
People use abuta medicinally for a wide range of conditions. It is used for digestion problems including diarrhea, dysentery, colic, upset stomach, and stomachache; for respiratory tract problems including colds, cough, bronchitis, and asthma; for skin problems including acne, wounds, boils, burns, sores, itching, and a severe rash with fever and vomiting caused by strep bacteria (erysipelas); and for urinary tract problems including bladder and kidney infections.
Other uses include treatment of dog bites, snake bites, chills, cholera, convulsions, delirium, diabetes, fluid retention, fevers, bleeding (hemorrhage), high blood pressure, jaundice, malaria, pounding heart, rabies, arthritis-like pain (rheumatism), toothaches, sexually transmitted diseases, and eye infections.
Abuta is also used to increase urine flow (as a diuretic), to loosen phlegm (as an expectorant), to stop bleeding (as a styptic), to improve sense of well being (as a tonic), and to arouse sexual desire (as an aphrodisiac).
How does it work?
There isn't enough information to know how abuta might work.
Insufficient Evidence to Rate Effectiveness for...
- High blood pressure.
- Menstrual problems.
- Other conditions.
Natural Medicines Comprehensive Database rates effectiveness based on scientific evidence according to the following scale: Effective, Likely Effective, Possibly Effective, Possibly Ineffective, Likely Ineffective, and Insufficient Evidence to Rate (detailed description of each of the ratings).
The appropriate dose of abuta depends on several factors such as the user's age, health, and several other conditions. At this time there is not enough scientific information to determine an appropriate range of doses for abuta. Keep in mind that natural products are not always necessarily safe and dosages can be important. Be sure to follow relevant directions on product labels and consult your pharmacist or physician or other healthcare professional before using.
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Ahmad, R. and Cava, M. P. Grisabine and grisabutine, new bisbenzylisoquinoline alkaloids from Abuta grisebachii. J Org.Chem. 6-24-1977;42(13):2271-2273. View abstract.
Cava, M. P., Saa, J. M., Lakshmikantham, M. V., and Mitchell, M. J. Panurensine and norpanurensine, new bisbenzylisoquinoline alkaloids from Abuta panurensis. J Org.Chem. 9-5-1975;40(18):2647-2649. View abstract.
Galeffi, C., Scarpetti, P., and Marini-Bettolo, G. B. New curare alkaloids. II. New bisbenzylisoquinoline alkaloids from Abuta grisebachii (Menispermaceae). Farmaco [Sci] 1977;32(12):853-865. View abstract.
Kupchan, S. M., Patel, A. C., and Fujita, E. Tumor inhibitors. VI. Cissampareine, new cytotoxic alkaloid from Cissampelos pareira. Cytotoxicity of bisbenzylisoquinoline alkaloids. J.Pharm.Sci. 1965;54(4):580-583. View abstract.
Morita, H., Matsumoto, K., Takeya, K., Itokawa, H., and Iitaka, Y. Structures and solid state tautomeric forms of two novel antileukemic tropoloisoquinoline alkaloids, pareirubrines A and B, from Cissampelos pareira. Chem.Pharm.Bull.(Tokyo) 1993;41(8):1418-1422. View abstract.
Steele, J. C., Simmonds, M. S., Veitch, N. C., and Warhurst, D. C. Evaluation of the anti-plasmodial activity of bisbenzylisoquinoline alkaloids from Abuta grandifolia. Planta Med 1999;65(5):413-416. View abstract.
SUR, R. N. and PRADHAN, S. N. STUDIES ON CISSAMPELOS ALKALOIDS. I. ACTION OF HAYATIN DERIVATIVES ON THE CENTRAL NERVOUS SYSTEM OF CATS AND DOGS. Arch Int Pharmacodyn.Ther. 11-1-1964;152:106-114. View abstract.
Anwer F, Popli SP, Srivastava RM, Khare MP. Studies in medicinal plants. 3. Protoberberine alkaloids from the roots of Cissampelos pareira Linn. Experientia 1968;24:999. View abstract.
Basu DK. Studies on curariform activity of hayatinin methochloride, an alkaloid of Cissampelos pareira. Jpn J Pharmacol 1970;20:246-52. View abstract.
Bhatnagar AK, Popli SP. Chemical examination of the roots of Cissampelos pareira Linn. V. Structure and stereochemistry of hayatidin. Experientia 1967;23:242-3. View abstract.
Raintree tropical plant database, Amazon plants. www.rain-tree.com/plants.htm (Accessed 30 July 1999).
Ramirez I, Carabot A, Melendez P, et al. Cissampeloflavone, a chalcone-flavone dimer from Cissampelos pareira. Phytochemistry 2003;64:645-7. View abstract.
Schultes RE, Raffauf RF. The Healing Forest, Medicinal and Toxic Plants of the Northwest Amazonia. Portland, OR: Dioscorides Press, 1990.