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Blood Root, ©2008 Todd Caldecott

Botanical Name: Sanguinaria canadensis, Papaveraceae

Common names: Blood root, Puccoon, Red Puccoon, Indian Paint, Redroot, Pauson, Tetterwort, Red Turmeric.

Plant description: Blood root is a herbaceous perennial arising from a creeping rhizome, reaching a height of up to 25 cm.  The rhizome emits an acrid bright orange-colored juice when cut or bruised. The leaves are basal, up to 20 cm wide, usually with only one open leaf, with five to nine lobes, becoming progressively larger as the plant matures through the season.  The flower is solitary, scentless, with 8-16 white petals, sometimes with a purplish or rosy tint.  The stamens are short with oblong yellow anthers, ovary oblong and compressed, style absent, the stigma two-lobed with a yellow center.  The flower gives way to an elongated two-valved capsule with numerous, dark red seeds.

Habitat, ecology and distribution: Blood root is native to North America, found east of the Rocky Mountains in open woods and cleared areas, preferring a rich loamy or clay soil, usually away from water.  It can be locally abundant but for the most part is quite rare.  Although cultivated sources exist overharvesting is common and wild Bloodroot stands are currently designated as "at risk" by United Plant Savers (http://www.unitedplantsavers.org).

Part used: Rhizome, root; best harvested in autumn.

History: The first mention of Bloodroot was made by Jaques Cornuti in his Canadensium Plantarum Historia (1635), which placed it in the genus Chelidonium (Papaveraceae). The genus name Sanguinaria was first applied by the French botanist Pierre Morin in 1651, derived from the Latin term sanguis meaning 'blood,' a name given because the plant exudes a blood-like sap when bruised or cut. Blood root was well known to the First Nations who used it as a dyeing agent and body paint, as well as an alterative, respiratory and digestive remedy.  It attracted the attention of the Europeans early on when local First Nations groups presented a young woman as a bedmate to a colonist in Jamestown, wearing nothing except a coat of Bloodroot paste. According to Felter and Lloyd Bloodroot was first mentioned as a medicine in Schoepf's Materia Medica Americana, a Latin work published in Germany in 1787, used in small doses as an emetic and in the treatment of gonorrhea (1893).

Constituents: Bloodroot is noted for its isoquinoline alkaloids (up to 70,000 ppm), which include sanguinarine (>85%), sanguidaridine, sanguidimerine, sanguirubine, sanguilutine, dihydrosanguilutine, oxysanguinaridine, oxysanguinarine, berberine, coptisine, protopine, chelerythrine, pseudochelerythrine, chelilutine, alpha and beta allocryptopine, beta homochelidonine, chelirubine and porphyroxin.  Other constituents that have been identified included malic acid, a resin and starch (Duke 2003).

Medical Research: The vast majority of research on Sanguinaria concerns a proprietary toothpaste and mouthrinse marketed under the name Viadent, that at one time contained sanguinarine and zinc chloride.  In 2001 Allen et al reported an association between the use of Viadent toothpaste and/or mouthwash and the development of potentially preneoplastic leukoplakia oral mucosal lesions, and since this time the manufacturers of Viadent removed these constituents from the products.
•Antimycobacterial: Based on the traditional usage of Sanguinaria canadensis in tuberculosis and leprosy, researchers examined the efficacy of a methanolic extract of the roots in an in vitro screening assay using two model species of mycobacteria, M. aurum and M. smegmatis. The crude methanolic extract of S. canadensis was found to have significant antimycobacterial activity against M. aurum.  A bioassay guided fractionation of this extract led to the isolation of two benzophenanthridine alkaloids, sanguinarine and chelerythrine, the latter being the most active against both Mycobacteria aurum and M. smegmatis (Newton et al 2002).
•Gingivitis and periodontal disease: A 14-week controlled clinical trial of sixty patients diagnosed with adult periodontitis assessed the efficacy of a toothpaste and oral rinse containing Sanguinaria extract, after scaling, root planing and a chlorhexidine regimen. The results showed that sanguinarine-containing toothpaste and oral rinse significantly inhibited the redevelopment of gingivitis through the 12 weeks following the chlorhexidine phase compared to the control toothpaste and rinse, with 26% fewer bleeding sites at 8 weeks, and 32% fewer at 14 weeks (Tenenbaum et al 1999). A randomized double-blind parallel study of 34 subjects examined the efficacy of a dentifrice and oral rinse containing Sanguinaria extract and zinc chloride in gingival inflammation following initial hygiene and scaling therapy. Results demonstrated that the use of a dentifrice and oral rinse containing Sanguinaria did not improve the efficacy of initial therapy (Cullinan et al 1997).  A 6-month, double-blind, placebo-controlled, parallel investigation involving 120 subjects examined the efficacy of Sanguinaria-containing dental hygiene regimens with and without fluoride. Test subjects were divided into four groups: group 1 received a dentifrice containing 0.075% Sanguinaria extract (SaE) and 2.0% zinc chloride (ZnCl2) in a dicalcium phosphate base, plus an oral rinse containing 0.03% SaE and 0.2% ZnCl2; group 2 received identical products without SaE or ZnCl2; group 3 received a dentifrice containing 0.8% sodium monofluorophosphate, 0.075% SaE, and 0.05% ZnCl2 in a silica base, plus an oral rinse containing 0.03% SaE and 0.2% ZnCl2; group 4 products were identical to those of Group 3 but without SaE and ZnCl2. Supragingival plaque and gingival inflammation were scored at 0, 1, 2, 1.5, 3, 4.5, and 6 months; bleeding upon probing was measured at 1, 1.5, 3, and 6 months. Microbiological samples were taken from plaque, tongue, and cheek areas. The active products produced statistically significantly lower scores than the placebo agents for all indices.  Six-month plaque scores were 13.1% lower for Group 1 and 17.4% lower for Group 3 compared to placebo products. When the Plaque Severity Index was applied, the percentage reductions were 33% for Group 1 and 41% for Group 3 compared to placebos. Gingival inflammation scores were 16.7% lower for Group 1 and 18.1% lower for Group 3 at 6 months compared to placebo scores (Kopczyk et al 1991).  Researchers examined the of twice daily brushing with a dentifrice containing 0.075% Sanguinaria extract and 2% zinc chloride, followed by use of a mouthrinse containing 0.03% Sanguinaria extract and 0.2% zinc chloride upon the oral flora. Sixty subjects were randomly assigned to treatment or placebo groups and monitored in a 6-month double-blind clinical trial. Total Gram-negative counts in supragingival plaque samples decreased 83% in the active group compared to a 232% increase for the control group. Populations of Bacteroides intermedius in supragingival plaque were significantly lower in the active group at 3 months.  Significantly lower counts of Fusobacterium spp. were observed at 3 and 6 months. Results indicate that use of the test products did not promote opportunistic overgrowth of pathogens in the oral flora (Harper et al 1990a).  The efficacy of combined use of toothpaste and oral rinse containing Sanguinaria extract and zinc chloride was compared to placebo products in a 6-month clinical trial. Sixty subjects with moderate levels of plaque and gingivitis were randomly assigned to active and placebo groups. Noninvasive measures of plaque and gingivitis were assessed at baseline and at 2, 6, 8, 14, 20, and 28 weeks. Bleeding on probing was measured at baseline and 6, 14, and 28 weeks. Active group scores were significantly lower than placebo scores at each post-baseline time point for all indices, with the exception of plaque at 2 weeks. The 28 week active group scores were 21% lower than the placebo group for plaque, 25% lower for gingivitis, and 43% lower for bleeding on probing. No dental staining or taste alteration was reported in the active group. Three of 30 active group subjects exhibited minor soft tissue irritations that resolved spontaneously without discontinuation of product use (Harper et al 1990b).  In vitro studies indicate that the anti-plaque action of Sanguinaria is due to its ability to inhibit bacterial adherence to newly formed pellicle (a clear, thin covering containing proteins and lipids found in saliva).  Long term use of Sanguinaria-containing toothpaste and oral rinse products does not predispose users to detrimental shifts in oral flora (Godowski 1989).

Toxicity: Reproductive and developmental toxicology studies were conducted with orally administered Sanguinaria extract in rats and rabbits. Researchers concluded that the oral intake of Sanguinaria extract has no selective effect on fertility, reproduction or fetal and neonatal development in rats or rabbits (Keller and Meyer et al 1989).  The acute oral LD50 in rats for sanguinarine was calculated to be 1658 mg/kg.  No toxic effects were observed in rats fed up to 150 ppm sanguinarine in the diet for 14 days and in rats treated by gavage with up to 0.6 mg/kg body weight for 30 days. The acute dermal LD50 in rabbits was found to be greater than 200 mg/kg (Becci et al 1987).  Recent concern about the association of Sanguinaria and oral leukoplakia is somewhat suspect, considering that all the studies that looked at the potential association of Bloodroot and leukoplakia concerned the usage of a Sanguinaria and zinc chloride formulation (Viadent).  The 1968 edition of the Merck Index however describes zinc chloride (butter of zinc) as a caustic, with moderately irritating effects on the skin and mucus membranes.  Nonetheless, Bloodroot does have a history of usage as an escharotic and should be used in smaller doses and under professional supervision.

Herbal action: alterative, antitumor, antimicrobial, expectorant, cholalgogue, emmenagogue

Indications: atonic dyspepsia, chronic hepatitis, coughs, laryngitis, pharyngitis, chronic catarrh, bronchitis, asthma, hayfever, nasal polyps, male and female reproductive deficiency, skin cancer

Contraindications and cautions: Large doses promote nausea and emesis, vertigo, gastritis, cardiac excitiation soon followed by depression and irregularity, pupil dilation and paralysis of the spinal nerves (Felter and Lloyd 1893).  Despite no indication of any kind of toxic effects in pregnant experimental animals, tradition states that Bloodroot is strictly avoided in pregnancy.

Medicinal uses: Based on the doctrine of signatures, and inferred from its name, Bloodroot is particularly suited to problems with the blood, as is one the most important alteratives in the materia medica, indicated in particular by states of irritation and inflammation, with signs of redness and heat, characterized by bleeding and acrid mucosal discharges.  As a fresh plant remedy, Cook states that Bloodroot is rather acrid and harsh, but in dried form acts as a "slow relaxant and stimulant, influencing the mucous membranes, gall-ducts, and secreting organs in general" (1869).  Bloodroot has long been considered to be an important remedy for the lungs, stated to be somewhat similar to Lobelia in effect, with a similar acrid sensations noticed upon ingestion.  It was used as a stimulating expectorant, more often in atonic conditions to normalize bronchial secretions, but is used equally in states of irritation and inflammation.  It is especially indicated in irritation and inflammation of the throat and larynx, and in irritative, tickling coughs, bronchitis and in chronic nasal catarrh.  Similarly, it was used in allergic reactions such as hayfever to control the inflammatory response and alleviate itching or tickling sensations in the ear and Eustachian tubes.  Combined with Bayberry and applied as an errhine or snuff, Bloodroot was traditionally used to treat chronic catarrhal afflictions as well as to destroy nasal polyps, but only if the secretions were free and abundant.  In digestive disorders, Bloodroot is used in small doses as a cholagogue, used in congestive states and chronic hepatitis, especially with cold extremities and nauseating headaches. As a stomachic Bloodroot is similarly used in drop doses to enhance gastric secretion and improve the appetite, useful in atonic dyspepsia.  In reproductive disorders Bloodroot is stated as being useful in seminal weakness, impotence, with seminal incontinence, and is was considered equally useful in gynecological disorders such as amenorrhea and dysmenorrhea, particularly when associated with debility and anxiety.  Bloodroot is stated to be an efficacious remedy in a variety of skin diseases, applied topically as an antisyphilitic remedy in chancres, as well as ringworm, eczema and warts. Bloodroot was at one time extensively used in the treatment of cancer and ulcerous conditions as an escharotic paste.  Herbalist Donald Yance states that alkaloids of Bloodroot possesses antitumor, antiviral and antimicrobial properties, and have been shown to be effective in Ehrlich carcinoma and sarcoma 37 (in mice) (1999, 129).  Eli Jones mentions Bloodroot internally as a specific for cancer of rectum.  Jones also used Bloodroot as an escharotic paste on occasion, along with internal therapies, in the treatment of skin cancer.  In his text, Cancer: It's Causes, Symptoms and Treatment (1911), Jones offers several escharotic formulas, some of these pastes use containing Bloodroot in combination with zinc chloride.  A typical escharotic paste can be prepared by mixing equal parts finely sieved Bloodroot powder, zinc chloride and some kind of paste, an ointment, or a little hypoallergenic flour (e.g. rice, arrowroot) mixed with water.  The paste should be thoroughly mixed with a spatula.  Adhesive strips should then be laid around the tumor to protect the healthy adjacent tissue, and the paste is spread on a piece of sterile cotton sheet and placed over the tumor.  Over this adhesive strips are laid to keep the paste in place.  The paste is retained for 24 hours, after which it is removed and then reapplied, after washing the tumor clean with warm water.  Jones counsels that the treatment should be repeated until "Šthe patient tells you that the growth feels heavy, like a dead weight," adding further that the growth should feel hard when pressing down on it, "like the sole of your shoe."  Yance states that this treatment should not exceed two applications, or it may cause scarring (1999, 173).  Once the escharotic paste is discontinued, Jones recommends the application of a poultice comprised of equal parts of ground Slippery Elm, Flaxseed, Lobelia seed and Bayberry bark mixed smooth with warm water, applied onto a piece of clean cloth, and changed every two hours, cleaning the tumor with equal parts of distilled extract of Witch Hazel and warm water. After this Jones states that the growth should eventually break loose, on its own, after which he typically applied his "Yellow Healing salve," comprised of Burgundy pitch (Abies excelsa), White Pine (Pinus monticola) turpentine, beeswax, mutton tallow, and Olive oil to heal the tissues and draw out the remaining necrotic tissue.  To this end any healing and drawing salve can be used.  This salve is applied thrice daily on the wound until it has healed well.

Pharmacy and dosage:
•Dry Plant Tincture: dried root, 1:5, 60% alcohol, 5-10 gtt; 1:10, up to 20 gtt.
•Powder: finely sieved, 60-500 mg

 

REFERENCES

Allen CL, Loudon J, Mascarenhas A. 2001. Sanguinaria-related leukoplakia: epidemiologic and clinicopathologic features of a recently described entity. Gen Dent. 2001 Nov-Dec;49(6):608-14.
Becci PJ, Schwartz H, Barnes HH, Southard GL. 1987. Short-term toxicity studies of sanguinarine and of two alkaloid extracts of Sanguinaria canadensis L. J Toxicol Environ Health 20(1-2):199-208
Cook, WM. H. 1869. The Physiomedical Dispensatory.  Cincinnati: self-published.  Digitized version available from http://medherb.com/cook/home.htm.
Cullinan MP, Powell RN, Faddy MJ, Seymour GJ. 1997. Efficacy of a dentifrice and oral rinse containing sanguinaria extract in conjunction with initial periodontal therapy. Aust Dent J Feb;42(1):47-51
Damm DD, Curran A, White DK, Drummond JF. 1999. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1999 Jan;87(1):61-6
Duke, James. 2003. Dr. Duke's Phytochemical and Ethnobotanical Databases. Agricultural Research Services. Available from http://www.ars-grin.gov/duke/
Felter, HW and JU Lloyd. 1893. King's American Dispensatory. Digitized version available from http://www.ibiblio.org/herbmed/eclectic/kings/main.html.
Godowski KC. 1989. Antimicrobial action of sanguinarine. J Clin Dent. Spring;1(4):96-101
Harper DS, Mueller LJ, Fine JB, Gordon J, Laster LL. 1990a. Effect of 6 months use of a dentifrice and oral rinse containing sanguinaria extract and zinc chloride upon the microflora of the dental plaque and oral soft tissues. J Periodontol Jun;61(6):359-63
Harper DS, Mueller LJ, Fine JB, Gordon J, Laster LL. 1990b. Clinical efficacy of a dentifrice and oral rinse containing sanguinaria extract and zinc chloride during 6 months of use. J Periodontol Jun;61(6):352-8
Jones, Eli G. (date n/a). Cancer: It's Causes, Symptoms and Treatment. Online version available from: http://www.planetherbs.com
Keller KA, Meyer DL. 1989. Reproductive and developmental toxicological evaluation of sanguinaria extract. J Clin Dent Winter;1(3):59-66
Kopczyk RA, Abrams H, Brown AT, Matheny JL, Kaplan AL. 1991. Clinical and microbiological effects of a sanguinaria-containing mouthrinse and dentifrice with and without fluoride during 6 months of use. J Periodontol. Oct;62(10):617-22
Newton SM, Lau C, Gurcha SS, Besra GS, Wright CW. 2002. The evaluation of forty-three plant species for in vitro antimycobacterial activities; isolation of active constituents from Psoralea corylifolia and Sanguinaria canadensis.  J Ethnopharmacol. Jan;79(1):57-6
Tenenbaum H, Dahan M, Soell M. 1999. Effectiveness of a sanguinarine regimen after scaling and root planing. J Periodontol. Mar;70(3):307-11
Yance, Donald. 1999. Herbal Medicine, Healing and Cancer.  Chicago: Keats.

 

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