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Barberry |
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Barberry/Barberry Bark/Barberry
Root/Barberry Root Bark (English) Berberis vulgaris
(Botanical) Berberidaceae (Plant Family) Berberis vulgaris/Berberidis
cortex/Berberidis radix/Berberidis radicis
cortex (Pharmacopeial)
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Overview |
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In traditional folk medicine, barberry soothes sore throats, treats diarrhea
or constipation, and eases inflammation and infection of the urinary,
gastrointestinal, and respiratory tracts. It may reduce the discomfort of
arthritis and rheumatism, soothe psoriasis, and treat chronic yeast infections.
These uses reflect barberry's reputation as an herbal antibiotic.
Sought after as an alternative to goldenseal (a once-endangered botanical
regarded as "king" of herbal antibiotics by some individuals), barberry and
other herbs with similar constituents (e.g., berberine) and actions are termed
mucous membrane tonics and adaptogens by herbalists. Mucous membrane tonics
regulate the flow of mucus; they may increase or decrease mucus secretion.
Adaptogens also allow immune factors already present within the body to
stimulate antibacterial responses during illness.
The study of barberry's isoquinoline alkaloid constituents has overshadowed
study of the plant as a whole. These constituents are potentially therapeutic,
with bactericidal, smooth muscle, and cardiovascular effects.
Barberry was used in ancient Egypt to prevent the plague, during the middle
ages in Europe as a purgative and antiseptic, and by Native Americans as tea to
stimulate the appetite. It has other uses as well; the yellow color of the root
and inner bark provide a semi-colorfast clothing dye, and the berries can be
made into jam or sugared for cake decorations. |

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Macro Description |
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Deciduous shrub grows to nine feet. Branches, gray, bear thorns. Leaves
alternate or in rosette formation, can be various colors, spiny teeth, four to
five leaves per branch. Flowers, bright yellow, in 21/2 inch racemes,
bloom April to June. The berries are red and grow in drooping bunches. Inner
bark is yellow.
The bark of the stem and root, and the root itself, are used medicinally.
Traditionally, the berries were also used as a tonic in tea, but they do not
contain isoquinoline alkaloids and are more closely associated with culinary
use. Barberry grows in the northeastern United States, particularly in New
England, and is native to Europe. |

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Part Used/Pharmaceutical
Designations |
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- Roots
- Berry
- Root bark
- Stem bark
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Constituents/Composition |
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Isoquinoline alkaloids berberine, berbamine, oxyacanthine, jatrorrhizine,
columbamine, palmatine, magnoflorine; also, resin, tannins |

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Commercial
Preparations |
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Crude bark for tea or powdered in capsules; aqueous alcohol or alcohol
extracts available as 1:5 tinctures or standardized fluid extracts (standardized
to 8% to 12% isoquinoline alkaloids); ointment |

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Medicinal
Uses/Indications |
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- Traditional: Berry as tea, diuretic, expectorant, laxative, appetite
stimulant; root bark and bark as tea, anti-inflammatory, diaphoretic,
astringent, antiseptic, laxative, bitter tonic, alterative (blood purifier),
cholagogue (liver stimulant that promotes bile excretion)
- Conditions: chronic diarrhea, dysentery, indigestion, eye ailments,
mouth sores, jaundice, hepatitis, fever, hemorrhage, arthritis, rheumatism, low
back pain, stomach bacterial infections, H. pylori
- Clinical applications (listed as "unapproved" in German Commission E
monograph): Inflammation/infection of the kidneys and urinary, bronchial, and
gastrointestinal tracts; liver, spleen, and circulatory disorders; spasms; and
chronic candidiasis
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Pharmacology |
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Herbalists provide much of the information available on the usage and effects
of whole barberry rootbark and bark preparations. While these sources often
corroborate empirical results of barberry use, scientific study tends to focus
on determining the scope and application of the bactericidal activity of the
isoquinoline alkaloid constituents. At least one study demonstrated superior
anti-inflammatory actions of whole barberry extract, compared to single
constituents. By using tissue or bacterial cultures and single alkaloid
preparations, researchers have determined antimicrobial, bactericidal,
anti-inflammatory, immune-stimulant, hypotensive, antifibrillatory,
antiarrhythmic, sedative, anticonvulsant and smooth muscle effects.
Berberine has in vitro antibacterial activity. Actions against
Staphylococcus spp., Streptomyces spp., Chlamydia spp., Corynebacterium
diphtheria, Escherichia coli, Salmonella typhi, Vibrio cholerae, Diplococcus
pneumoniae, Pseudomonas spp., Shigella dysenteriae, Entamoeba histolytica,
Trichomonas vaginalis, Neisseria gonorrhoeae, N. meningitidis, Treponema
pallidum, Giardia lamblia, Leishmania donovani, and Candida albicans
may be due to adhesion blockage of the streptococci to host cells through
the depletion of lipoteichoic acid and fibronectin. In other studies berberine
raised blood flow to the spleen; reduced fever, possibly by altering interferon
response to microorganisms; stimulated bile secretion; altered bilirubin levels;
inhibited brain tumor cells in rats; and was superior to sulfacetamide against
Chlamydia trachomatis.
In vitro studies demonstrate that oxyacanthine dilates blood vessels,
modulates adrenaline, and is bactericidal to Bacillus subtilis, Colpidium
colpoda. Palmatine is antiarrhythmic, adrenocorticotrophic, analgesic, and
bactericidal. Jatrorrhizine is sedating, hypotensive, and fungicidal. In animal
studies, one experiment showed a berbamine-induced immune response in mice with
influenza.
These actions have not been scientifically demonstrated to occur in the human
body. Berberine absorption in the small intestine is poor, and large doses
obtained through excess intake of berberine-containing plant preparations cause
negative side effects on the stomach and small intestines. However, because it
is excreted through the urine, it may have antibiotic actions specific to that
area of the body. This remains to be proven, but concurs with traditional use.
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Dosage Ranges and Duration of
Administration |
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For throat, urinary, gastrointestinal, respiratory inflammation or infection,
including chronic candidiasis, any of the following can be taken for five to
seven days.
- Tea: 2 to 4 g steeped dried root tid
- Tincture (1:5): 3 to 6 ml tid
- Dry extracts: 250 to 500 mg tid
For skin disorders: 10% extract of barberry in ointment, applied topically
tid |

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Side
Effects/Toxicology |
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American Herbal Products Association safety rating: 2b. Safe with appropriate
use, but do not use during pregnancy. Due to a lack of scientific documentation
of barberry's purported therapeutic uses, the German Commission E monograph
lists barberry as an unapproved herb.
Barberry root and root bark preparations have not caused any of the toxic
effects noted with excessive or lethal doses of berberine. (At doses higher than
0.5 g, berberine causes lethargy, nose bleeds, difficulty breathing, skin and
eye irritation, kidney irritation, nausea, vomiting, and diarrhea. Small doses
stimulate respiratory system; large doses lead to respiratory paralysis. Lethal
doses cause hemorrhagic nephritis.) |

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Warnings/Contraindications/Precautions |
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Over-consumption of berberine-containing plant medicines may irritate mucous
membranes, particularly in the stomach. Do not use during pregnancy.
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Interactions |
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No clinically significant interactions between barberry and conventional
medications are known to have been reported in the literature to date, including
the German Commission E monograph (Blumenthal 1998). |

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Regulatory and Compendial
Status |
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In the United States, barberry is a dietary supplement; in Germany the
Commission E does not approve therapeutic use due to lack of scientific
documentation of effects. |

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References |
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Amin AH, Subbaiah, TV, Abbasi KM. Berberine sulfate: antimicrobial activity,
bioassay, and mode of action. Can J Microbiol. 1969;15:1067-1076.
Bergner P. Goldenseal and the common cold; goldenseal substitutes. Medical
Herbalism: A Journal for the Clinical Practitioner. Winter
1996–1997;8:1.
Blumenthal M, ed. The Complete German Commission E Monographs Therapeutic
Guide to Herbal Medicines. Boston: Integrative Medicine Communications;
1998: 309-310.
Foster S, Duke JA. A Field Guide to Medicinal Plants: Eastern and Central
North America. Boston, Mass: Houghton Mifflin; 1990.
Harborn, J, Baxter H. Phytochemical Dictionary: A Handbook of Bioactive
Compounds from Plants. Washington, DC: Taylor & Francis; 1993.
Ivanovska N, Philipov S. Study on the antiinflammatory action of Berberis
vulgaris root extract, alkaloid fractions, and pure alkaloids. Int J
Immunopharmacol. 1996;18:552-561.
Kowalchik C, Hylton W, eds. Rodale's Illustrated Encyclopedia of Herbs.
Emmaus, Pa: Rodale Press; 1998.
Leung A, Foster S. Encyclopedia of Common Natural Ingredients Used in
Food, Drugs, and Cosmetics. 2nd ed. New York, NY: John Wiley & Sons;
1996.
McGuffin M, Hobbs C, Upton R, Goldberg A, eds. American Herbal Products
Association's Botanical Safety Handbook. Boca Raton, Fla: CRC Press;
1996.
Muller K, et al. The antipsoriatic Mahonia aquifolium and its active
constituents; I. Pro- and antioxidant properties and inhibition of
5-lipoxygenase. Planta Med. 1994;60:421-424.
Murray M. The Healing Power of Herbs: The Enlightened Person's Guide to
the Wonders of Medicinal Plants. Rocklin, Calif: Prima Publishing; 1995.
Murray M, Pizzorno J. Encyclopedia of Natural Medicine. 2nd ed.
Rocklin, Calif: Prima Publishing; 1998:310.
Shamsa F, et al. Antihistaminic and anticholinergic activity of barberry
fruit (Berberis vulgaris) in the guinea-pig ileum. J Ethnopharmacol.
1999;64:161-166.
Sotnikova R, et al. Relaxant properties of some aporphine alkaloids from
Mahonia aquifolium. Methods Find Exp Clin Pharmacol. 1997;19:589-597.
Sun D, Courtney HS, Beachey EH. Berberine sulfate blocks adherence of
Streptococcus pyogenes to epithelial cells, fibronectin, and hexadecane.
Antimicrob Agents Chemother.
1988;32:1370-1374. |

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Copyright © 2000 Integrative Medicine
Communications This publication contains
information relating to general principles
of medical care that should not in any event be construed as specific
instructions for individual patients. The publisher does not accept any
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is made in regard to the contents of this material. No claims or endorsements
are made for any drugs or compounds currently marketed or in investigative use.
The reader is advised to check product information (including package inserts)
for changes and new information regarding dosage, precautions, warnings,
interactions, and contraindications before administering any drug, herb, or
supplement discussed herein. | |