Picao Preto

Family: Asteraceae
Genus:
Bidens
Species:
pilosa
Common Names:
Picao Preto, Amor Seco, Aceitilla, Cadillo, Chilca, Pacunga, Pirco, Cuambu, Carrapicho, Erva-Picão, Alfiler, Clavelito De Monte, Romerillo, Saltillo, Yema De Huevo, Z'Aiguille, Jarongan, Ketul, Pau-pau pasir
Parts Used:
Aerial parts, Whole herb

DESCRIPTION

Properties/Actions: Antibacterial, Antidysenteric, Anti-inflammatory, Antimicrobial, Astringent, Diuretic, Emmenagogue, Emollient, Hepatoprotective
Phytochemicals: Acetylenes, B-amyrin, B-sitosterol, beta-D-glucopyranosyloxy-3-hydroxy-6(E)- tetradecen-8, 10,12-triyne, Esculetin, Flavoniods, Friedelin, Friedelan-3 beta-ol, Limonene, Linolic acid, Linolenic acid, Lupeol, Phenylheptatriyne, Phytosterin-B, Sterols, Tannins, tridecapentyn-1-ene, trideca-2,12-diene-4, 6,8,10-tetrayne-1-ol, trideca-3,11-diene-5,7,9-triyne-1,2-diol, trideca-5-ene-7,9,11-triyne-3-ol Volatile oil, Xanthophylis



Picao Preto is small erect annual herb growing up to one meter high that is indigenous to the rainforest and other tropical areas of South America, Africa, the Carribean, and the Philippines. Considered a weed in many places, it has bright green leaves with serrated prickly edges and produces small yellow flowers. It is a Southern cousin to Bidens tripartita, the European Bur Marigold, which has an ancient history in European herbal medicine.

Picao Preto has a long history of use by the indigenous people of the Amazon and virtually all parts of the plant are used. In the Peruvian Amazon, Picao Preto is used for aftosa, angina, diabetes, dysentery, dysmenorrhea, edema, hepatitis, jaundice, laryngitis and worms (1). In Piura, a decoction of the toots is used for alcoholic hepatitis and worms (2). The Cuna tribe mixes the crushed leaves with water to treat headaches (3). Near Pucallpa Peru, the leaf is balled up and applied to a toothache and the leaves are also used for headaches (4). In other parts of the Amazon a decoction of the plant is mixed with lemon juice and used for angina, sore throat, water retention, hepatitis, and dropsy (4). The Exuma tribes grind the sun-dried leaves with olive oil to make poultices for sores and lacerations, and in Tonga, an infusion of the flowers is used to treat upset stomach in food poisoning (4). Dr. James Duke reports that "Chewing or gargling may help angina and sores in the mouth: infusions used as emmenagogue, antidysenteric, and to alleviate chills." (4) He also reports that indigenous peoples in Brazil use the plant as a diuretic and to treat jaundice.
In Peruvian herbal medicine today, the plant is called Amor Seco or Cadillo and is considered diuretic, anti-inflammatory, and hepatoprotective; commonly used for hepatitis, conjunctivitis, abscesses, mycosis, urinary infections, as a weight loss aid and to stimulate childbirth (5). In Brazilian herbal medicine, it is called Picao Preto or Cuambu and is considered emollient, astringent, and diuretic being used for fevers, blenorrhagia, leucorrhea, jaundice, diabetes, sore throat, tonsilitis, obstructions in the liver and other liver disorders, urinary infections and vaginal infections (6-8).
Picao Preto has been the subject of recent clinical studies which has explained many of its uses in herbal medicine. It's antibacterial activity against Gram-positive bacteria was demonstrated in a 1997 study (9). New bioactive phytochemicals were discovered in 1996 which showed over growing actions against normal and transformed human cell lines (10). Also in 1996, a Picao Preto extract was shown to possess prostaglandin-synthesis inhibitory activity, a process linked to headaches and inflammatory diseases (11). A research group in Taiwan documented its hepatoprotective (liver protecting) activity, stating that Bidens pilosus can "protect liver injuries from various hepatotoxins and have potential as broad spectrum antihepatic agents." (12). This same research group clinically demonstrated Picao Preto's significant anti-inflammatory activities one year earlier in 1995 (13). In 1991, Swiss scientists isolated several known phytochemical with antimicrobial and anti-inflammatory properties which led them to believe that the presence of these compounds "may rationalize the use of this plant in traditional medicine in the treatment of wounds, against inflammation and against bacterial infection of the gastrointestinal tract (14). During the same year, scientists in Egypt were studying and documenting Bidens pilosa's antimicrobial activity as well. (15) Even as early as 1979 and 1980, scientists demonstrated that specific chemicals found in Picao Preto were phototoxic to bacteria and fungi. (16, 17)


COUNTRY

ETHNOBOTANY WORLDWIDE USES

Amazonia Ache(head), Ache(stomach), Ache(tooth), Aftosa, Angina, Chills, Diabetes, Diuretic, Dysentery, Dysmenorrhea, Edema, Emmenagogue, Hepatitis, Jaundice, Laryngitis, Sore(throat), Sore(mouth), Vulnerary, Worms, Wounds
Bahamas Cancer, Carminative, Diuretic, Fever, Heat-Rash Itch, Sore
Brazil Astringent, Blenorrhagia, Diabetes, Diuretic, Emollient, Fever, Jaundice, Leucorrhea, Liver, Liver(Obstructions), Sclerosis(Glands), Throat(Sore), Tonsilitis, Urinary Infections, Vaginal Infections
Dominican Republic Diuretic, Emmenagogue, Lactogogue, Pectoral, Sialogogueue, Toothache
Elsewhere Boil, Cold, Conjunctivitis, Cough, Dysentery, Eye, Food-Poison, Inflammation, Liver, Rheumatism, Stomach, Styptic, Toothache
Ghana Allergy, Ear, Eye, Styptic, Urticaria
Haiti Aftosa, Amygdalitis, Angina, Catarrh, Diabetes, Lactogogue, Stomatitis
Malaya Antidote, Cough, Conjunctivitis
Mexico Diabetes, Diuretic, Pectoral
Peru Abscess, Anti-inflammatory, Childbirth, Conjunctivitis, Diuretic, Hepatitis, Hepatoprotective, Mycosis, Obesity, Urinary Infections, Weightloss
Philippines Boil, Intoxicant
Upper Volta Bite(Snake),Bronchitis, Colic, Cough, Diarrhea, Intestine
Venezuela Dysentery, Vulnerary





Footnotes:

  1. Rutter, R.A. 1990. Catalogo de Plantas Utiles de la Amazonia Peruana. Instituto Linguistico de Verano. Yarinacocha, Peru.
  2. de Feo, V. 1992. Medicinal and magical plants in the northern Peruvian Andes. Fitoterapia 63: 417-440
  3. Vasquez, M. R., 1990 Useful Plants of Amazonian Peru. Second Draft. Filed with USDA's National Agricultural Library. USA
  4. Duke, James & Vasquez, Rudolfo, 1994 Amazonian Ethnobotanical Dictionary, CRC Press Inc.: Boca Raton, FL )
  5. Kember Mejia and Elsa Reng, 1995. Plantas medicinales de uso popular en la Amazonia Peruana. AECI and IIAP: Lima, Peru.
  6. de Almeida, E.R., 1993. Plantas Medicinais Brasileiras, Conhecimentos Populares E Cientificos. Hemus Editora Ltda.: Sau Paulo, Brazil.
  7. Coimbra, Raul, 1994. Manual de Fitoterapia 2 nd Ed., Editora Cejup: Belem, Brazil.
  8. Neves, J.L., et al, 1982. Contribuicao ao Estudo de "Biden pilosa", VII Simposio de Plantas Medicinais do Brasil, p. 90, September 1-3, 1982, Belo Horizonte-MG, Brazil
  9. Rabe T, 1997., Antibacterial activity of South African plants used for medicinal purposes. J Ethnopharmacol 56(1), 81-87
  10. Alvarez L, et.al., 1996. Bioactive polyacetylenes from Bidens pilosa. Planta Med 62(4), 355-357
  11. Jager AK et al., 1996. Screening of Zulu medicinal plants for prostaglandin-synthesis inhibitors. J Ethnopharmacol 52(2), 95-100
  12. Chin HW, et.al., 1996. The hepatoprotective effects of Taiwan folk medicine ham-hong-chho in rats. Am J Chin Med 24(3-4), 231-240
  13. Chih HW, et.al., 1995. Anti-inflammatory activity of Taiwan folk medicine "ham-hong-chho" in rats. Am J Chin Med 23(3-4), 273-278
  14. Geissberger P, et al., 1991. Constituents of Bidens pilosa L.: do the components found so far explain the use of this plant in traditional medicine? Acta Trop 48(4), 251-261
  15. Sarg TM, et.al., 1991. Constituents and biological activity of Bidens pilosa L. grown in Egypt.Acta Pharm Hung 61(6), 317-323
  16. Wat CK, et.al. 1979., Ultraviolet-mediated cytotoxic activity of phenylheptatriyne from Bidens pilosa L. J Nat Prod 42(1), 103-111
  17. Arnason T, et.al., 1980. Photosensitization of Escherichia coli and Saccharomyces cerevisiae by phenylheptatriyne from Bidens pilosa. Can J Microbiol 26(6), 698-705




Clinical References

  1. Rabe T, 1997., Antibacterial activity of South African plants used for medicinal purposes. J Ethnopharmacol 56(1), 81-87 (1997)
  2. Alvarez L, 1996., Bioactive polyacetylenes from Bidens pilosa. Planta Med 62(4), 355-357 (1996)
  3. Jager AK, 1996 Screening of Zulu medicinal plants for prostaglandin-synthesis inhibitors. J Ethnopharmacol 52(2), 95-100 (1996)
  4. Vian A, 1996 Is membrane potential involved in calmodulin gene expression after external stimulation in plants? FEBS Lett 380(1-2), 93-96 (1996)
  5. Chin HW, 1996 The hepatoprotective effects of Taiwan folk medicine ham-hong-chho in rats. Am J Chin Med 24(3-4), 231-240 (1996)
  6. Rivera D, 1995 The ethnopharmacology of Madeira and Porto Santo Islands, a review. J Ethnopharmacol 46(2), 73-93 (1995)
  7. Chih HW, 1995 Anti-inflammatory activity of Taiwan folk medicine "ham-hong-chho" in rats. Am J Chin Med 23(3-4), 273-278 (1995)
  8. Sarg TM, 1991 Constituents and biological activity of Bidens pilosa L. grown in Egypt. Acta Pharm Hung 61(6), 317-323 (1991)
  9. Geissberger P, 1991 Constituents of Bidens pilosa L.: do the components found so far explain the use of this plant in traditional medicine? Acta Trop 48(4), 251-261 (1991)
  10. Desbiez MO, 1989 The role of mineral ions in controlling morphogenesis in plants: a case of the inhibition of growth of the hypocotyle of Bidens pilosa L. C R Seances Soc Biol Fil 183(6), 493-506 (1989)
  11. Mirvish SS, 1985 Test of catechol, tannic acid, Bidens pilosa, croton oil, and phorbol for cocarcinogenesis of esophageal tumors induced in rats by methyl-n-amylnitrosamine. J Natl Cancer Inst 74(6), 1283-1290 (1985)
  12. Arnason T, 1980 Photosensitization of Escherichia coli and Saccharomyces cerevisiae by phenylheptatriyne from Bidens pilosa. Can J Microbiol 26(6), 698-705 (1980)
  13. Mirvish SS, 1979., Studies on the esophagus. II. Enhancement of [3H]thymidine incorporation in the rat esophagus by Bidens pilosa (a plant eaten in South Africa) and by croton oil. Cancer Lett 6(3), 159-165 (1979)
  14. Wat CK, 1979., Ultraviolet-mediated cytotoxic activity of phenylheptatriyne from Bidens pilosa L. J Nat Prod 42(1), 103-111 (1979)


Clinical Abstracts


J Ethnopharmacol 1997 Mar;56(1):81-87
Antibacterial activity of South African plants used for medicinal purposes.

Rabe T, van Staden J
Department of Botany, University of Natal Pietermaritzburg, Scotsville, South Africa.
Crude extracts from 21 South African medicinal plants, traditionally used for ailments of an infectious or septic nature, were screened for in vitro antibacterial activity using the agar diffusion and dilution methods. Almost all the activity exhibited was against Gram-positive bacteria, with 12 of the 21 plant species tested showing some activity against Bacillus subtilis. Only the Warburgia salutaris methanol extract inhibited the growth of Escherichia coli. None of the extracts had any activity against Klebsiella pneumoniae. The highest activity was found in the methanol extracts from Bidens pilosa, Psidium guajava, Artemisia afra and Warburgia salutaris. The majority of the antibacterial activity was present in the methanolic, rather than the aqueous extracts.



Planta Med 1996 Aug;62(4):355-357
Bioactive polyacetylenes from Bidens pilosa.
Alvarez L, Marquina S, Villarreal ML, Alonso D, Aranda E, Delgado G
From the methanolic extract of the whole plants of Bidens pilosa the new beta-D-glucopyranosyloxy-3-hydroxy-6(E)-tetradecen-8, 10,12-triyne besides a known polyine has been isolated and identified mainly by IR and NMR methods. The new compound showed overgrowing action against normal and transformed human cell lines in culture.



J Ethnopharmacol 1996 Jun;52(2):95-100
Screening of Zulu medicinal plants for prostaglandin-synthesis inhibitors.
Jager AK, Hutchings A, van Staden J
Department of Botany, University of Natal Pietermarizburg, Scottsville, South Africa.
Aqueous and ethanolic extracts of 39 plants used in traditional Zulu medicine to treat headache or inflammatory diseases were screened for prostaglandin-synthesis inhibitors. Extracts were tested in an in vitro assay for cyclooxygenase inhibitors. In general, ethanolic extracts caused higher inhibition than aqueous extracts. Two-thirds of the plants screened had high inhibitory activity. The highest inhibition was obtained with ethanolic extracts of Bidens pilosa, Eucomis autumnalis, Harpephyllum caffrum, Helichrysum nudifolium, Leonotis intermedia, L. leonorus, Ocotea bullata, Rumex saggitatus, Solanum mauritianum, Synadenium cupulare and Trichilia dregeana.



Am J Chin Med 1996;24(3-4):231-240
The hepatoprotective effects of Taiwan folk medicine ham-hong-chho in rats.
Chin HW, Lin CC, Tang KS
Foo Yin College of Nursing & Medical Technology, Kaohsiung, Taiwan.
Bidens pilosa L. var minor (Blume) Sherff, B. pilosa L. and B. chilensis DC (compositae), commonly known as "Ham-hong-chho" in Taiwan, have been traditionally used for medicinal purposes. To clarify and compare the hepatoprotective effects of these three plants, we evaluated their potential effectiveness on CCl4- and acetaminophen-induced acute hepatic lesions in rats. The results indicated that the increase in SGOT and SGPT activities caused by CCl4 (3.0 ml/kg, s.c.) and acetaminophen administration (600 mg/kg, i.p.) could be significantly reduced by treating with the extracts of all the three kinds of "Ham-hong-chho" and the extract of B. chilensis exhibited the greatest hepatoprotective effects. These phenomena were also confirmed by histological observation. Liver damage induced by CCl4 and acetaminophen was markedly improved in the extract of B. chilensis treated groups, while groups treated with the extracts of B. pilosa var minor and B. pilosa demonstrated only moderate protective effects. The pharmacological and pathological effects of these three crude groups were compared with Bupleurum chinense, which has been reported previously as a treatment criteria in the CCl4 model, and with silymarin as a standard reference medicine in the acetaminophen model. The results suggest that B. pilosa var minor, B. pilosa and B. chilensis can protect liver injuries from various hepatotoxins and have potential as broad spectrum antihepatic agents.



J Ethnopharmacol 1995 May;46(2):73-93
The ethnopharmacology of Madeira and Porto Santo Islands, a review.
Rivera D, Obon C
Departamento de Biologia Vegetal, Facultad de Biologia, Universidad de Murcia, Spain.
The ethnopharmacology of Madeira and Porto Santo Islands is extremely interesting because of the cultural and biogeographic features of this region, which make it a centre of medicinal plant diversity (richness of endemic flora, geographical isolation in the Atlantic sea, crosscultural influences, and past abundance of local healers). The medicinal flora of Madeira is composed of 259 species. Some noteworthy medicinal taxa, endemic or locally relevant, are: Acanthus mollis, Aeonium glandulosum, Aeonium glutinosum, Bidens pilosa, Borago officinalis, Chamaemelum nobile var. discoideum, Culcita macrocarpa, Echium nervosum, Euphorbia platiphylla, Helichrysum melaleucum, Helichrysum obconicum, Hypericum glandulosum, Hypericum humifussum, Kleinia repens, Laurus azorica, Monizia edulis, Ocotea foetens, Psoralea bituminosa, Rubus bollei, Rumex maderensis, Sambucus lanceolata, Scilla maderensis, Sedum brissemoretii, Sedum farinosum, Sedum nudum, Sibthorpia peregrina, Teucrium betonicum, Thymus caespititius, Trifolium squamosum and Vaccinium padifolium...

Am J Chin Med 1995;23(3-4):273-278
Anti-inflammatory activity of Taiwan folk medicine "ham-hong-chho" in rats.
Chih HW, Lin CC, Tang KS
Foo Yin Junior College of Nursing and Medical Technology, Kaohsiung, Taiwan. "Ham-Hong-Chho" is a folk medicine in Taiwan, derived from the entire plants of Bidens pilosa L. var. minor (Blume) Sherff (Compositae), B. pilosa L. and B. chilensis DC. The anti-inflammatory effect of aqueous extracts of the three plants against paw edema induced by carrageenan and chronic arthritis induced by complete Freund's adjuvant were determined in rats. The results indicated that paw edema induced by carrageenan was significantly decreased by treatment with aqueous extracts (150 or 300 mg/kg) of all three plants (p < 0.05) and that the effect of Bidens pilosa var. minor was the most potent. However, only extracts (500 mg/kg) of B. pilosa L. var. minor and B. pilosa L. significantly decreased the paw edema induced by complete Freund's adjuvant (p < 0.05).



Acta Pharm Hung 1991 Nov;61(6):317-323
Constituents and biological activity of Bidens pilosa L. grown in Egypt.
Sarg TM, Ateya AM, Farrag NM, Abbas FA
Department of Pharmacognosy, Faculty of Pharmacy, University of Zagazig, Egypt.
Column chromotography and preparative TLC of the light petroleum-diethyl ether extract from Bidens pilosa L. afforded tridecapentyn-1-ene, trideca-2,12-diene-4,6,8,10-tetrayne-1-ol, trideca-3,11-diene-5,7,9-triyne-1,2-diol and trideca-5-ene-7,9,11-triyne-3-ol. The compounds were identified on the bases of UV, 1H-NMR spectra and comparison with reported data. The chloroform extract was chromatographed to yield B-amyrin, phytosterin-B, esculetin and B-sitosterol glucoside. The petroleum ether extract afforded long chain ester, saturated hydrocarbon, long chain alcohol, B-amyrin, phytosterin-B, lupeol and lupeol acetate. GLC analysis of the fatty acids indicated the presence of 5 acids. The antimicrobial test was carried out to indicate an evident activity. The antidiabetic activity showed non significant decrease of blood glucose.



Acta Trop 1991 Feb;48(4):251-261
Constituents of Bidens pilosa L.: do the components found so far explain the use of this plant in traditional medicine?
Geissberger P, Sequin U
Institute for Organic Chemistry, University of Basel, Switzerland.
The dried aerial parts of Bidens pilosa L. were extracted with petrol ether, chloroform, methanol, and methanol/water. The petrol ether and the methanol/water extracts showed some antimicrobial activity. Fractionation of the extracts yielded well known substances, most of which have, however, not yet been described as constituents of Bidens pilosa. Several of these substances have previously been shown to be biologically active. Thus, phenylheptatriyne, linolic acid and linolenic acid have antimicrobial activities. On the other hand, friedelin and friedelan-3 beta-ol, as well as several of the flavonoids found are anti-inflammatory agents. The detection of these compounds in extracts from B. pilosa may rationalize the use of this plant in traditional medicine in the treatment of wounds, against inflammations and against bacterial infections of the gastrointestinal tract.



J Natl Cancer Inst 1985 Jun;74(6):1283-1290
Test of catechol, tannic acid, Bidens pilosa, croton oil, and phorbol for cocarcinogenesis of esophageal tumors induced in rats by methyl-n-amylnitrosamine.
Mirvish SS, Salmasi S, Lawson TA, Pour P, Sutherland D
Catechol (CAS: 120-80-9), given in drinking water to rats, was the most effective of 5 phenols in enhancing [3H]thymidine incorporation [( 3H]dThd-l) into esophageal DNA. To test for esophageal cocarcinogenesis, groups of 30 male MRC-Wistar rats received 3 weekly ip injections of 25 mg methyl-n-amylnitrosamine [(MNAN) CAS: 13256-07-0]/kg. From the time of the first MNAN injection, each group also received catechol, tannic acid (CAS: 1401-55-4), dried leaves of Bidens pilosa L., or croton oil (CAS: 8001-28-3) (respectively, 2, 10, 50, and 2 g/kg semipurified diet), or were given 20 ip injections of 6 mg phorbol (CAS: 17673-25-5)/rat. The rats were killed after 20-45, 46-52, or 53-72 weeks (subgroups A, B, and C). In the group given MNAN alone, most esophageal papillomas developed during the first 45 weeks. Both catechol and B. pilosa significantly increased the esophageal papilloma multiplicity (No. of papillomas/rat) induced by MNAN, with a maximum tumor yield of 2.2 times that in the corresponding subgroup treated with MNAN alone. Papilloma multiplicity increased from subgroup A to subgroup C in the MNAN plus B. pilosa group but not in the MNAN plus catechol group. No tumors were induced by the test cocarcinogens given without MNAN. We concluded that a) an increased esophageal [3H]dThd-I indicates potential cocarcinogenicity and b) catechol and B. pilosa were weak esophageal cocarcinogens. These results support the view that catechol in cigarette smoke and B. pilosa as eaten in South Africa contribute to the etiology of human esophageal cancer.



J Nat Prod 1979 Jan;42(1):103-111
Ultraviolet-mediated cytotoxic activity of phenylheptatriyne from Bidens pilosa L.
Wat CK, Biswas RK, Graham EA, Bohm L, Towers GH, Waygood ER
The tropical weed Bidens pilosa L. (Asteraceae) contains a number of polyacetylenes which are phototoxic to bacteria, fungi, and human fibroblast cells in the presence of sunlight, artificial sources of long-wave ultraviolet light, or cool-white fluorescent light. The principle photoactive compound in the leaf, phenylheptatriyne, is present in the cuticle as well as in the underlying cells. Experiments with calf thymus DNA indicate that, unlike photoactive furanocoumarins, phenylheptatriyne does not form interstrand cross linkages with DNA in ultraviolet light.

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