- •Contents
- •Preface to the Third Edition
- •About the Authors
- •How to Use Herbal Medicines
- •Introduction
- •General References
- •Agnus Castus
- •Agrimony
- •Alfalfa
- •Aloe Vera
- •Aloes
- •Angelica
- •Aniseed
- •Apricot
- •Arnica
- •Artichoke
- •Asafoetida
- •Avens
- •Bayberry
- •Bilberry
- •Bloodroot
- •Blue Flag
- •Bogbean
- •Boldo
- •Boneset
- •Borage
- •Broom
- •Buchu
- •Burdock
- •Burnet
- •Butterbur
- •Calamus
- •Calendula
- •Capsicum
- •Cascara
- •Cassia
- •Cat’s Claw
- •Celandine, Greater
- •Celery
- •Centaury
- •Cereus
- •Chamomile, German
- •Chamomile, Roman
- •Chaparral
- •Cinnamon
- •Clivers
- •Clove
- •Cohosh, Black
- •Cohosh, Blue
- •Cola
- •Coltsfoot
- •Comfrey
- •Corn Silk
- •Couchgrass
- •Cowslip
- •Cranberry
- •Damiana
- •Dandelion
- •Devil’s Claw
- •Drosera
- •Echinacea
- •Elder
- •Elecampane
- •Ephedra
- •Eucalyptus
- •Euphorbia
- •Evening Primrose
- •Eyebright
- •False Unicorn
- •Fenugreek
- •Feverfew
- •Figwort
- •Frangula
- •Fucus
- •Fumitory
- •Garlic
- •Gentian
- •Ginger
- •Ginkgo
- •Ginseng, Eleutherococcus
- •Ginseng, Panax
- •Golden Seal
- •Gravel Root
- •Ground Ivy
- •Guaiacum
- •Hawthorn
- •Holy Thistle
- •Hops
- •Horehound, Black
- •Horehound, White
- •Horse-chestnut
- •Horseradish
- •Hydrangea
- •Hydrocotyle
- •Ispaghula
- •Jamaica Dogwood
- •Java Tea
- •Juniper
- •Kava
- •Lady’s Slipper
- •Lemon Verbena
- •Liferoot
- •Lime Flower
- •Liquorice
- •Lobelia
- •Marshmallow
- •Meadowsweet
- •Melissa
- •Milk Thistle
- •Mistletoe
- •Motherwort
- •Myrrh
- •Nettle
- •Parsley
- •Parsley Piert
- •Passionflower
- •Pennyroyal
- •Pilewort
- •Plantain
- •Pleurisy Root
- •Pokeroot
- •Poplar
- •Prickly Ash, Northern
- •Prickly Ash, Southern
- •Pulsatilla
- •Quassia
- •Queen’s Delight
- •Raspberry
- •Red Clover
- •Rhodiola
- •Rhubarb
- •Rosemary
- •Sage
- •Sarsaparilla
- •Sassafras
- •Saw Palmetto
- •Scullcap
- •Senega
- •Senna
- •Shepherd’s Purse
- •Skunk Cabbage
- •Slippery Elm
- •Squill
- •St John’s Wort
- •Stone Root
- •Tansy
- •Thyme
- •Uva-Ursi
- •Valerian
- •Vervain
- •Wild Carrot
- •Wild Lettuce
- •Willow
- •Witch Hazel
- •Yarrow
- •Yellow Dock
- •Yucca
- •1 Potential Drug–Herb Interactions
- •4 Preparations Directory
- •5 Suppliers Directory
- •Index
Fucus
Summary and Pharmaceutical Comment
Kelp is a generic term that strictly speaking refers to Laminaria and Macrocystis species of brown seaweeds, although in practice it may be used in reference to other species of brown algae including Nereocystis and Fucus. The species Fucus vesiculosus is reported to be commonly used in the preparation of kelp products.(G60) The principal constituents of seaweeds are polysaccharides. For brown seaweeds the major polysaccharide is alginic acid (algin). Fucoidan, present in all brown algae, is thought to refer to a number of related polysaccharide esters whose main sugar component is fucose. The traditional uses of kelp in obesity and goitre are presumably attributable to the iodine content, although the self-diagnosis and treatment of these conditions with a herbal remedy is not suitable. There have been no documented studies supporting the traditional use of kelp in rheumatic conditions. In view of the iodine content and potential accumulation of toxic elements, excessive ingestion of kelp is inadvisable. Doubt over the quality of commercial seaweed preparations has been reported.
Species (Family)
Fucus vesiculosus L. and other Fucus species (Fucaceae)
Synonym(s)
Black Tang, Bladderwrack, Kelp, Kelpware, Rockweed, Seawrack Brown seaweeds refer to species of Fucus, Ascophyllum,
Laminaria and Macrocystis. 'Kelps' refer to species of Laminaria and Macrocystis, although kelp is often used in reference to species of Fucus.
Part(s) Used
Thallus (whole plant)
Pharmacopoeial and Other Monographs
BHC 1992(G6)
BHP 1996(G9)
BP 2007 (kelp)(G84)
Martindale 35th edition(G85)
Ph Eur 2007 (kelp)(G81)
Legal Category (Licensed Products)
GSL(G37)
Constituents
The following is compiled from several sources, including General References G2 and G6.
Carbohydrates Polysaccharides: alginic acid (algin) as the major
component; fucoidan and laminarin (sulfated polysaccharide esters).(1)
Iodine Content of various Laminaria species has been reported as 0.07–0.76% of dry weight.(2)
Other constituents Various vitamins and minerals, particularly ascorbic acid (vitamin C) (0.013–0.077% of fresh material).(2)
Food Use |
F |
Seaweeds are commonly included in the diet of certain populations. The gelling properties of alginic acid, the major polysaccharide in brown seaweeds, including fucus, are extensively utilised in the dairy and baking industries to improve texture, body and smoothness of products.(1) Fucus is listed by the Council of Europe as a natural source of food flavouring (category N2). This category indicates that fucus can be added to foodstuffs in
small quantities, with a possible limitation of an active principle (as yet unspecified) in the final product.(G16)
Herbal Use
Fucus is stated to possess antihypothyroid, anti-obesity and antirheumatic properties. Traditionally, it has been used for
lymphadenoid goitre, myxoedema, obesity, arthritis and rheuma-
tism.(G2, G6, G7, G8, G64)
Figure 1 Selected constituents of fucus.
273
274 Fucus
F
Figure 2 Fucus (Fucus vesiculosus).
Dosage
Dosages for oral administration (adults) for traditional uses recommended in standard herbal reference texts are given below.
Dried thallus 5–10 g as an infusion three times daily.(G6, G7)
Liquid extract 4–8 mL (1 : 1 in 25% alcohol) three times
daily.(G6, G7)
Pharmacological Actions
There is a paucity of information documented specifically for Fucus vesiculosus, although pharmacological activities are recognised for individual constituents and other brown seaweed species.
Alginic acid is a hydrophilic colloidal substance that swells to approximately 25–35 times its original bulk in an alkaline environment and as such exerts a bulk laxative action.(3) It is stated to compare favourably with the carboxylic type of cation exchange resins. The colloidal properties of alginates have been utilised in wound dressings and skin grafts.(3)
Anticoagulant properties have been documented for brown seaweeds.(3) The glucose polymer laminarin has been identified as the anticoagulant principle in a Laminaria species.(4) A fucoidan fraction has been isolated from Fucus vesiculosus with 40–50% blood anticoagulant activity of heparin.(5)
The iodine content of seaweeds is well recognised. The low incidence of goitre amongst maritime people has been attributed to the inclusion of seaweeds in their diet.(3, 4) Similarly, the traditional use of Fucus vesiculosus in 'slimming teas' is thought to be attributable to the effect of iodine on hypothyroidism.(4)
Extracts of various brown seaweeds including Ascophyllum nodosum and Fucus vesiculosus have been reported to exhibit a high in vitro inhibitory activity towards mammalian digestive enzymes (a-amylase, trypsin and lipase) isolated from the porcine pancreas.(6) Activity was attributed to high molecular weight (30 000–100 000) polyphenols.(6)
Inhibitory effects of laminarin sulfate on lipidaemia and atherosclerosis (in vivo, rabbit) have been partially attributed to the in vitro inhibition of lipid synthesis observed in cultured chick aortic cells.(7)
Hypotensive activity observed in rats intravenously administered extracts of commercial seaweed (Laminaria species) preparations has been attributed to their histamine content.(8) However, histamine concentrations varied considerably between
preparations, and authentic specimens of the Laminaria species were devoid of histamine.
Kelp extracts have antiviral activity(9) and laminarin is reported to have exhibited some tumour-inhibiting actions.(1)
Clinical studies
There is a lack of clinical research assessing the effects of fucus and rigorous randomised controlled clinical trials are required.
Side-effects, Toxicity
There is a lack of clinical safety and toxicity data for fucus preparations and further investigation of these aspects is required.
Hyperthyroidism has been associated with the ingestion of kelp and is attributable to the iodine content in the plant.(10, 11) Typical symptoms of hyperthyroidism (weight loss, sweating, fatigue, frequent soft stools) were exhibited by a 72-year-old woman following ingestion of a commercial kelp product for six months.(10) Laboratory tests confirmed the hyperthyroidism although no pre-existing evidence of thyroid disease was found and the condition resolved in six months following discontinuation of the tablets. Analysis of the kelp tablets reported an iodine content of 0.7 mg/tablet representing a daily intake of 2.8–4.2 mg iodine.(10) Clinically evident hyperthyroidism developed in an otherwise healthy woman following the daily ingestion of six 200mg kelp tablets.(11) Symptoms gradually resolved on cessation of therapy.
The association between halogen salts and acneiform eruptions is well established.(12) Ingestion of kelp products has been
associated with the worsening of pre-existing acne and the development of acneiform eruptions, which improved following withdrawal of the tablets.(12)
The ability of marine plants to accumulate heavy metals and other toxic elements is recognised, and the uptake of various radioactive compounds by seaweeds has been reported.(3, 13, 14) Fifteen samples of kelp-containing dietary supplements have been analysed for their iodine and arsenic contents.(15) The levels of arsenic were low in all but one product. The iodine levels varied widely, even between different samples of the same product, and in some products the iodine levels were high in relation to safe daily intake.
Brown algae (Ascophyllum nodosum and Fucus vesiculosus) have been found to be capable of synthesising volatile halogenated organic compounds (VHOCs).(16) VHOCs are considered to be troublesome pollutants because land plants and animals have difficulty in degrading the compounds which consequently persist in terrestrial ecosystems.(16) VHOCs released into the seawater predominantly contain bromine with iodine-containing compounds showing a slower rate of turnover.(16) Concentration of iron by brown seaweeds has been attributed to fucoidan, and alginic acid exhibits a high specificity for the binding of strontium.(13) Elevated urinary arsenic concentrations (138 and 293 mg/24 hour) in two female patients have been associated with the ingestion of kelp tablets. Subsequent analysis of the arsenic
content of various kelp preparations revealed concentrations ranging from 16 to 58 mg/g product.(17, 18) The botanical source of the kelp in the products was not stated.(18)
Ascophyllum nodosum is commonly added to animal foodstuffs as a source of vitamin and minerals, with beneficial results reported for dairy cattle, sheep, pigs and poultry.(13) Feeding
studies using A. nodosum have highlighted an atypical toxic response for rabbits compared with that of rats and pigs.(13, 19)
Addition of A. nodosum to the diet of rabbits (at 5–10%) caused a
severe drop in haemoglobin content, serum iron concentrations and packed cell volume, leading to weight loss and death in twothirds of the animals.(13) No differences in renal and liver function,
and in lipid metabolism were found between test and control animals.(13) Similar, but much milder, toxicity has also been
observed in rabbits fed Fucus serratus.(19) Subsequent studies incorporating A. nodosum into the feed of rats and pigs failed to demonstrate the toxic effects observed in rabbits.(19) The toxic components in A. nodosum have been reported to be nonextractable with chloroform, ethanol, water and 20% sodium carbonate solution, remaining in the insoluble residue.(19)
Contra-indications, Warnings
The iodine content in kelp may cause hyperor hypothyroidism. In view of this, ingestion of kelp preparations by children is inadvisable. The iodine content in kelp has also been associated with acneiform eruptions and aggravation of pre-existing acne. In general, brown seaweeds are known to concentrate various heavy metals and other toxic elements. Elevated urinary arsenic concentrations have been traced to the ingestion of kelp tablets. Prolonged ingestion of kelp may reduce gastrointestinal iron absorption (binding properties of fucoidan), resulting in a slow reduction in haemoglobin, packed cell volume and serum iron concentrations. Prolonged ingestion may also affect absorption of sodium and potassium ions (alginic acid) and cause diarrhoea.
Drug interactions None documented. However, the potential for preparations of fucus to interact with other medicines administered concurrently, particularly those with similar or opposing effects, should be considered. Because of its iodine content, fucus should be used with caution in individuals receiving treatment for existing abnormal thyroid function.
Pregnancy and lactation The safe use of kelp products during pregnancy and lactation has not been established. In view of the potential actions on the thyroid gland and possible contamination with toxic elements, the use of kelp should be avoided.
Preparations
Proprietary multi-ingredient preparations
UK: Fenneherb Slim Aid; Napiers Slimming Tablets; Reducing
(Slimming) Tablets.
Fucus 275
References
1Wood CG. Seaweed extracts. A unique ocean resource. J Chem Ed 1974; 51: 449–452.
2Algae as food for man. In: Chapman VJ, ed. Seaweeds and their Uses. London: Methuen, 1970: 115.
3Whistler RL, ed. Industrial Gums, 2nd edn. New York: Academic Press, 1973: 13.
4 Burkholder PR. Drugs from the sea. Armed Forces Chem J 1963; 17: 6, 8, 10, 12–16.
5Doner LW. Fucoidan. In: Whistler RL, ed. Industrial Gums, 2nd edn. New York: Academic Press, 1973: 115–121.
6 |
Barwell CJ et al. Inhibitors of mammalian digestive enzymes in some |
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species of marine brown algae. Br Phycol J 1983; 18: 200. |
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Murata K. Suppression of lipid synthesis in cultured aortic cells by |
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laminaran sulfate. J Atheroscl Res 1969; 10: 371–378. |
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8 |
Funayama S, Hikino H. Hypotensive principle of Laminaria and allied |
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seaweeds. Planta Med 1981; 41: 29–33. |
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9Kathan RH. Kelp extracts as antiviral substances. Ann N Y Acad Sci 1965; 130: 390–397.
10Shilo S, Hirsch HJ. Iodine-induced hyperthyroidism in a patient with a normal thyroid gland. Postgrad Med J 1986; 62: 661–662.
11Smet PAGM de et al. Kelp in herbal medicines: hyperthyroidism. Ned Tijdschr Geneeskd 1990; 134: 1058–1059.
12Harrell BL, Rudolph AH. Kelp diet: A cause of acneiform eruption. Arch Dermatol 1976; 112: 560.
13Blunden G, Jones RT. Toxic effects of Ascophyllum nodosum as a rabbit food additive. In: Food – Drugs from the Sea Proceedings 1972. Washington: Marine Technology Society, 1972: 267–293.
14Hodge VF et al. Rapid accumulation of plutonium and polonium on giant brown algae. Health Phys 1974; 27: 29–35.
15Norman JA et al. Human intake of arsenic and iodine from seaweedbased food supplements and health foods available in the UK. Food Additives Contaminants 1987; 5: 103–109.
16Halocarbons. Natural pollution by algal seaweeds. Chem Br 1985: 513–514.
17Walkiw O, Douglas DE. Health food supplements prepared from kelp
– a source of elevated urinary arsenic. Can Med Assoc J 1974; 111: 1301–1302.
18Walkiw O, Douglas DE. Health food supplements prepared form kelp – a source of elevated urinary arsenic. Clin Toxicol 1975; 8: 325– 331.
19Jones RT et al. Effects of dietary Ascophyllum nodosum on blood parameters of rats and pigs. Botanica Marina 1979; 22: 393–394.
Fumitory
Summary and Pharmaceutical Comment
Fumitory is characterised by isoquinoline alkaloids which represent the principal active ingredients. Animal studies support some of the traditional uses, but there is a lack of rigorous clinical research assessing the effects of preparations of fumitory. Fumitory should not be used in home-made
F ophthalmic preparations. In view of the active constituents and the lack of safety data, excessive ingestion of fumitory should be avoided.
Species (Family)
Fumaria officinalis L. (Fumariaceae)
Synonym(s)
Common Fumitory, Fumitory
Part(s) Used
Herb
Pharmacopoeial and Other Monographs
BHC 1992(G6)
Figure 1 Selected constituents of fumitory.
BHP 1996(G9)
BP 2007(G84)
Complete German Commission E(G3)
Martindale 35th edition(G85)
Ph Eur 2007(G81)
Legal Category (Licensed Products)
GSL(G37)
Constituents
The following is compiled from several sources, including General References G2 and G6.
Alkaloids Isoquinoline-type. Protopines including protopine (fumarine) as the major alkaloid and cryptopine,(1, 2) protoberberines including aurotensine, stylopine, sinactine and N- methylsinactine,(3) spirobenzylisoquinolines including fumaritine, fumaricine and fumariline,(4, 5) benzophenanthridines including
sanguinarine,(6) and indenobenzazepines including fumaritridine and fumaritrine.(6, 7)
Flavonoids Glycosides of quercetin including isoquercitrin, rutin and quercetrin-3,7-diglucoside-3-arabinoglucoside.(8, 9)
Acids Chlorogenic, caffeic and fumaric acids.(8)
276
Other constituents Bitter principles, mucilage and resin.
Food Use
Fumitory is listed by the Council of Europe as a natural source of food flavouring (category N3). This category indicates that fumitory can be added to foodstuffs in the traditionally accepted manner, although there is insufficient information available for an adequate assessment of potential toxicity.(G16)
Herbal Use
Fumitory is stated to possess weak diuretic and laxative properties and to act as a cholagogue. Traditionally, it has been used to treat cutaneous eruptions, conjunctivitis (as an eye lotion) and, specifically, chronic eczema.(G2, G6, G7, G8, G64)
Dosage
Dosages for oral administration (adults) for traditional uses recommended in standard herbal reference texts are given below.
Figure 2 Fumitory (Fumaria officinalis).
Figure 3 Fumitory – dried drug substance (herb).
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Fumitory |
277 |
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Herb |
2–4 g as an infusion three times daily.(G6, G7) |
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Liquid |
extract |
2–4 mL (1 : 1 in 25% alcohol) |
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times |
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daily.(G6, G7) |
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Tincture 1–4 mL (1 : 5 in 45% alcohol) three times daily.(G6, G7) |
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Pharmacological Actions |
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In vitro and animal studies |
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In in vivo (rats) studies, preparations of the herb had no effect on |
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normal choloresis but modified bile flow that had been artificially |
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increased or decreased.(10) Antispasmodic activity on smooth |
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muscle has been reported.(11) Extracts inhibited formation of gall- |
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bladder calculi in animals.(12) The major alkaloid protopine has |
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antihistaminic,(13) hypotensive, bradycardic and sedative activities |
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in small doses,(14) whereas larger doses cause excitation and |
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convulsions.(14) Bactericidal activity against the Gram-positive |
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organisms Bacillus anthracis and Staphylococcus have been |
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reported.(14) |
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Clinical studies |
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There is a lack of clinical research assessing the effects of fumitory |
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and rigorous randomised controlled clinical trials are required. |
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Clinical studies involving 105 patients with biliary disorders |
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claimed favourable results.(15) However, the methodological |
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limitations of these studies do not allow the reported effects to |
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be attributed to administration of fumitory. |
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Side-effects, Toxicity |
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None documented. However, there is a lack of clinical safety and |
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toxicity data for fumitory and further investigation of these |
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aspects is required. |
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Contra-indications, Warnings |
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None documented. |
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Drug interactions |
None documented. However, the potential for |
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preparations of fumitory to interact with other medicines |
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administered concurrently, particularly those with similar or |
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opposing effects, should be considered. |
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Pregnancy and lactation The safety of fumitory during |
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pregnancy and lactation has not been established. In view of |
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lack of pharmacological and toxicity data, the use of fumitory |
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during pregnancy and lactation should be avoided. |
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Preparations |
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Proprietary single-ingredient preparations |
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Austria: Bilobene; Oddibil. Brazil: Oddibil. France: Oddibil. |
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Germany: Bilobene. Hungary: Bilobene. |
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Proprietary multi-ingredient preparations |
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Austria: Hepabene; Oddispasmol. Czech Republic: Hepabene. |
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France: Actibil; Bolcitol; Depuratif Parnel; Depuratum; |
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Schoum. Hungary: Hepabene. Italy: Soluzione |
Schoum. |
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Russia: Hepabene (Гепабене). Spain: Natusor Hepavesical; Odisor; Solucion Schoum. UK: Echinacea; Skin Cleansing.
278 Fumitory
References
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1 |
Sener B. Turkish species of Fumaria L. and their alkaloids. VII |
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Alkaloids from Fumaria officinalis L. and F. cilicica Hansskn. Gazi |
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Univ Eczacilik Fak Derg 1985; 2: 45–49. |
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2 |
Hermansson J, Sandberg F. Alkaloids of Fumaria officinalis. Acta |
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Pharm Suec 1973; 10: 520–522. |
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3 |
Mardirossian ZH et al. Alkaloids of Fumaria officinalis. |
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Phytochemistry 1983; 22: 759–761. |
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4 |
MacLean DB et al. Structure of three minor alkaloids of Fumaria |
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officinalis. Can J Chem 1969; 47: 3593–3599. |
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5 |
Murav'eva DA et al. Isolation of fumaritine from Fumaria officinalis. |
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Khim Farm Zh 1974; 8: 32–34. |
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6 |
Forgacs P et al. Alcaloides des Papavéracées II: Composition chimique |
F |
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de dix-sept espèces de Fumaria. Plantes Med Phytother 1986; 20: 64– |
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81. |
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7 |
Forgacs P et al. Composition chimique des Fumariacées. Alcaloides de |
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quatorze espèces de Fumaria. Plantes Med Phytother 1982; 16: 99–115. |
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8 |
Massa V et al. Sur les pigments phenoliques du Fumaria officinalis L. |
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Trav Soc Pharm Montpellier 1971; 31: 233–236. |
9 Torck M et al. Flavonoids of Fumaria officinalis L. Ann Pharm Fr
1971; 29: 591–596.
10Boucard M, Laubenheimer B. Action du nébulisat de fumeterre sur le débit bilaire du rat. Therapie 1966; 21: 903–911.
11Reynier M et al. Action du nébulisat de fumeterre officinal sur la musculature lisse. Contribution à l'étude du mécanisme de son activité thérapeutique. Trav Soc Pharm Montpellier 1977; 37: 85– 102.
12Lagrange E, Aurousseau M. Effect of spray-dried product of Fumaria officinalis on experimental gall bladder lithiasis in mice. Ann Pharm Fr 1973; 31: 357–362.
13Abdul Habib Dil. Activité anti-histaminique de la fumarine. Therapie 1973; 28: 767–774.
14Preininger V. The pharmacology and toxicology of the papaveraceae alkaloids. In: RHF Manske, ed. The Alkaloids XV. London: Academic Press, 1975: 207–261.
15Fiegel G. Die amphocholoretische Wirkung der Fumaria officinalis. Z Allgemeinmed Landarzt 1971; 34: 1819–1820.