Monday, May 18, 2020

FUMITORY (Fumaria officinalis L. (Fumariaceae))


HERBAL
MEDICINAL
PLANT

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FUMITORY

Fumaria officinalis L. (Fumariaceae)




 



BY

RETTODWIKART THENU





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FUMITORY
(fyew’muh-toe-ry)


Fumaria officinalis L. (Fumariaceae)





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 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

DESCRIPTION
MEDICINAL PARTS: The medicinal parts are the dried herb and the aerial parts of the fresh flowering plant.
FLOWER AND FRUIT: The short pedicled flowers are in erect, dense, terminal racemes opposite the leaves and are 5 to 8 mm long. The outer petals are rounded at the front and are crimson to pink. But like the inner petals they are dark-red to black at the tip and have a green keel. The fruit, which appears in the flowering season, is nut-like, globular, slightly flattened at the side, green and has a dent in the top.
LEAVES, STEM AND ROOT: The plant is 10 to 50 cm high and ^ has a tender, erect, angular, branched, hollow and glabrous stem which, like the leaves, is bluish green. The leaves are alternate and divided into 3-pinnate sections. They are petiolate, double pinnate, soft with petioled palmate or pinnatifid pinna.
CHARACTERISTICS: The herb has a bitter, salty taste.

HABITAT: The plant is indigenous to the Mediterranean region to northern Africa and in all of Europe and Siberia. The herb has been introduced into North and South America.
Fumitory is an annual bush or shrub found in Africa, Europe, the United States, Canada, Asia, and Australia.

PRODUCTION: Common Fumitory herb consists of the dried, above ground parts of Fumaria officinalis, gathered during the flowering season.
NOT TO BE CONFUSED WITH: The very similar species F. vaillanti and F. schleicheri.
OTHER NAMES: Earth Smoke, Hedge Fumitory, Beggary, ^Fumus, Vapor, Wax Dolls,





Figure 1. Fumitory Flower and  Herba



PHARMACOPODIAL AND OTHER MONOGRAPHS
BHC 1992(G6)
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 Nmethylsinactine,( 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)  

COMPOUNDS
Flavonoids: including rutin
Hydroxycinnamic acid derivatives: including caffeoylmalic acid
Isoquinoline alkaloids: some of them include
-Protoberberine-type: including (-)-scoulerine
Protopine-type: including protopine; main alkaloid
Spirobenzylisoquinoline-type: fumaricine, (+)-fumariline
Indenobenzazepine-type: including fumaritine, fumarofine
Organic acids: fumaric acid

USES
Fumitory is taken internally as a laxative, a diuretic, and a treatment for biliary illness. Topically, it may be used to treat various skin disorders such as eczema, psoriasis, acne, and scabies. Fumitory may be used as an eyewash to ease conjunctivitis.
INVESTIGATIONAL USES
Researchers are experimenting with the usefulness of fumitory in the treatment of arrhythmias.
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)

ACTIONS
A review of the literature reveals very few studies supporting the use of fumitory as a diuretic, a laxative, or for treatment of skin disorders. In Germany, fumitory is approved for treatment of colicky pain in the gallbladder or biliary system. Only two studies have evaluated the possible use of fumitory in the treatment of cardiac disorders. The fi rst study, using dogs, evaluated the effi cacy of its alkaloid components in treating temporary disorders of coronary blood fl ow. The injected alkaloids signifi cantly reduced ischemic shifts (Gorbunov et al, 1980). The second study evaluated a number of different plant species grown in Bulgaria. Results showed that fumitory exerted a healing effect on ischemic heart disease, atherosclerosis, and hypertension (Petkov, 1979). Another study (Rao et al, 1998) showed Fumaria indica, a different Fumaria sp. from that used for the preparations that are typically available, to be hepatoprotective. When used for irritable bowel syndrome (IBS), there was no noticeable benefi t over a placebo (Brinkhaus et al, 2005).

PHARMACOLOGICAL ACTIONS
IN VITRO AND ANIMAL STUDIES
In in vivo (rats) studies, preparations of the herb had no effect on normal choloresis but modified bile flow that had been artificially increased or decreased.(10) Antispasmodic activity on smooth muscle has been reported.(11) Extracts inhibited formation of gallbladder calculi in animals.(12) The major alkaloid protopine has antihistaminic,(13) hypotensive, bradycardic and sedative activities in small doses,(14) whereas larger doses cause excitation and convulsions.(14) Bactericidal activity against the Gram-positive organisms Bacillus anthracis and Staphylococcus have been reported.(14)
CLINICAL STUDIES
There is a lack of clinical research assessing the effects of fumitory and rigorous randomised controlled clinical trials are required. Clinical studies involving 105 patients with biliary disorders claimed favourable results.(15) However, the methodological limitations of these studies do not allow the reported effects to be attributed to administration of fumitory.





Figure 2. Dried Fumitory dan Powder Fumitory


ACTIVITIES
 Amphicholeretic (1; BRU; HHB; PHR; PH2); Anesthetic (1; HHB); Antiarrhythmic (1; BRU); Anticholinergic (1; BRU); Antihistaminic (1; CAN); Antiinflammatory (f; MAD; PNC); Antilithic (1; CAN); Antiseptic (1; PNC); Antispasmodic (2; APA; KOM; PH2; SHT); Aphrodisiac (f; MAD); Bradycardic (1; CAN); Cholagogue (f; CAN; SHT); Cholekinetic (SHT); Choleretic (1; PH2; SHT); Depurative (f; HHB; PHR; PH2); Diaphoretic (f; MAD); Diuretic (f; APA; CAN; MAD; PNC); Emetic (f; MAD); Hypertensive (1; HHB); Hypotensive (1; CAN; HHB); Laxative (f; APA; CAN; PNC); Litholytic (f; MAD); Poison (1; HHB); Sedative (1; CAN); Stomachic (f; HHB); Tonic (f; PNC).

INDICATIONS
Acne (f; PNC); Alopecia (f; MAD); Amenorrhea (f; MAD); Arrhythmia (1; BRU); Arthrosis (f; PHR; PH2); Atherosclerosis (f; MAD; PHR; PH2); Bile-Duct Spasm (2; KOM; PH2); Bladder Stone (f; MAD); Cancer (f; JLH; MAD); Cancer, colon (f; JLH); Cancer, gut (f; JLH); Cancer, liver (f; JLH); Cancer, uterus (f; JLH); Cardiopathy (1; APA; BRU); Cholecystosis (2; KOM; MAD; PH2); Colic (1; APA); Conjunctivosis (f; CAN; MAD); Constipation (1; APA; CAN; PH2; PNC); Cramp (2; APA; KOM; PH2; SHT); Cystosis (f; PHR; PH2); Dermatosis (1; APA; CAN; PHR; PH2); Dropsy (f; MAD); Dyskinesia (1; APA); Eczema (f; CAN; HHB; PH2); Enterosis (2; KOM; PH2); Exanthema (f; MAD); Fever (f; MAD); Gas (f; MAD); Gastrosis (2; APA; KOM; PH2); Gout (f; MAD); Halitosis (f; MAD); Headache (1; APA); Hepatosis (2; JLH; MAD; PHR; PH2); High Blood Pressure (1; APA; CAN; HHB); Hypoglycemia (f; PHR; PH2); Infection (f; PHR; PH2); Inflammation (f; MAD; PNC); Insomnia (1; CAN); Itch (f; PH2); Jaundice (f; MAD); Leprosy (f; MAD); Low Blood Pressure (1; HHB); Melancholy (f; MAD); Nausea (1; APA); Nervousness (1; CAN); Ophthalmia (f; MAD); Pain (1; HHB); Psoriasis (1; APA); Rheumatism (f; PHR; PH2); Scabies (f; MAD); Sclerosis (f; JLH); Sore (f; MAD); Sore Throat (f; MAD); Spasm (2; KOM); Splenosis (f; MAD); Stomachache (f; HHB; MAD); Stone (f; MAD); Syphilis (f; MAD); Uterosis (f; JLH); Water Retention (f; APA; CAN; MAD; PNC).

INDICATIONS AND USAGE
Approved by Commission E:
Liver and gallbladder complaints Spastic discomfort in the area of the gallbladder and bile ducts, as well as the gastrointestinal tract.
Unproven Uses: In folk medicine, the herb has been used for skin diseases, constipation, cystitis, arteriosclerosis, rheuma tism, arthritis, as a blood purifier, hypoglycemia and for infections.
Homeopathic Uses: for chronic, itching eczema resulting from liver disease.

PRODUCT AVAILABILITY
Dried herb, extract, tincture
Plant Parts Used: Flowering parts, leaves

DOSAGES
Dosages for oral administration (adults) for traditional uses recommended in standard herbal reference texts are given below.
·         Herb 2–4 g as an infusion three times daily.(G6,G7)
·         Liquid extract 2–4mL (1 : 1 in 25% alcohol) three times daily.(G6, G7)
·         Tincture 1–4mL (1 : 5 in 45% alcohol) three times daily.(G6, G7)

DOSAGES
·         Adult PO dried herb: 6 g/day (Blumenthal, 1998)
·         Adult PO fl uid extract: 2-4 ml (1:1 dilution) in 25% alcohol, tid
·         Adult PO tea: 2-4 g tid
·         Adult PO tincture: 1-4 ml (1:5 dilution) in 45% alcohol, tid
·         Adult topical: apply dried herb prn

DOSAGES
1.25–2 tsp (2–3 g) herb/cup water up to 2 ×/day (APA); 2–3 tsp (2.4–3.6 g) herb/cup tea/day (MAD);
2–4 g herb, or in tea, 3 ×/day (CAN); 6 g herb/day, drink 1 cup warm tea (2–3 g/cup, steeped 20 minutes) 30 minutes before meals (PH2); 6 g/day (APA; KOM; SHT);
2–4 ml liquid herb extract (1:1 in 25% ethanol) 3 ×/day (CAN); 2–4 ml liquid herb extract (PNC);
2–4 g aqueous extract (HHB); 1–4 ml herb tincture (1:5 in 45% ethanol) 3 ×/day (CAN); 3.65 g sap/day (MAD); 2–3 tsp (2.4–3.5 g) expressed juice in hot or cold infusion (PH2).

DOSAGES
Mode of Administration: Comminuted drug and its galenic preparations for internal use.
Preparation: To prepare an infusion, pour boiling water over 2 to 3 gm drug and strain after 20 minutes.
Daily Dosage: 6 gm of drug. Infusions for gallbladder complaints, drink 1 warm cup 30 minutes before meals.
Pressed juice—2 to 3 teaspoons (2.4 to 3.5 gm drug) daily as a cold or hot infusion.
Grated fresh plant—1 teaspoon 3 times daily (about 50% plant material).
Homeopathic Dosage: 5 drops, 1 tablet or 10 globules every 30 to 60 minutes (acute) or 1 to 3 times daily (chronic); parenterally: 1 to 2 ml sc acute: 3 times daily; chronic: once a day (HAB34).
Storage: Protect from light and moisture.


CONTRAINDICATIONS, INTERACTIONS, AND SIDE EFFECTS
Not listed (AHP). None reported (KOM). HH3 says protopine is spasmogenic; I’m more inclined to believe BRU, which calls it antispasmodic.

SIDE-EFFECTS, ADVERSE REACTIONS, TOXICITY
None documented. However, there is a lack of clinical safety and toxicity data for fumitory and further investigation of these aspects is required.
CNS: Seizures (overdose)
CV: Decreased blood pressure, decreased pulse
EENT: Increased intraocular pressure
GI: Nausea, vomiting, anorexia
GU: Acute renal failure
INTEG: Hypersensitivity reactions

CONTRA-INDICATIONS, WARNINGS
None documented.
Drug interactions None documented. However, the potential for preparations of fumitory to interact with other medicines administered concurrently, particularly those with similar or opposing effects, should be considered. Pregnancy and lactation The safety of fumitory during pregnancy and lactation has not been established. In view of lack of pharmacological and toxicity data, the use of fumitory during pregnancy and lactation should be avoided. Until more research is available, fumitory should not be used during pregnancy and breastfeeding. It should not be given to children. Fumitory should not be used by persons with seizure disorders or increased intraocular pressure, and it should not be used by those with hypersensitivity to it.

INTERACTIONS
Drug
Antiarrhythmics, beta-blockers, cardiac glycosides: The actions of fumitory may increase the effects of antiarrhythmics, beta-blockers, cardiac glycosides; do not use concurrently.

CLIENT CONSIDERATIONS
Assess
·         Assess the reason the client is using fumitory.
·         Assess for hypersensitivity reactions. If present, discontinue use of fumitory and administer an antihistamine or other appropriate therapy.
·         Assess the client’s cardiac status, including blood pressure and pulse (character). Watch for decreasing pulse.
·         Assess for other cardiovascular drugs the client may be taking. Fumitory should not be taken concurrently with antiarrhythmics, cardiac glycosides, or betablockers (see Interactions).
Administer
·         Instruct the client to store fumitory products in a cool, dry place, away from heat and moisture.
Teach Client/Family
·         Caution the client not to use fumitory in children or those who are pregnant or breastfeeding until more research is available.

PREPARATIONS
Proprietary single-ingredient preparations
Austria: Bilobene; Oddibil. Brazil: Oddibil. France: Oddibil. Germany: Bilobene. Hungary: Bilobene.
Proprietary multi-ingredient preparations
Austria: Hepabene; Oddispasmol. Czech Republic: Hepabene. France: Actibil; Bolcitol; Depuratif Parnel; Depuratum; Schoum. Hungary: Hepabene. Italy: Soluzione Schoum. Russia: Hepabene (Гепабене). Spain: Natusor Hepavesical; Odisor; Solucion Schoum. UK: Echinacea; Skin Cleansing.



REFERENCE




Barnes, J., Anderson, L. A., and Phillipson, J. D. 2007. Herbal Medicines Third Edition. Pharmaceutical Press. Auckland and London.

Duke, J. A. with Mary Jo Bogenschutz-Godwin, Judi duCellier, Peggy-Ann K. Duke. 2002. Handbook of Medicinal Herbs 2nd Ed. CRC Press LLC. USA.

Gruenwald, J., Brendler, T., Jaenicke, Ch. 2000.  PDR for Herbal Medicines.  Medical Economics Company, Inc. at Montvale, NJ 07645-1742. USA

Linda S-Roth. 2010. Mosby’s Handbook Of Herbs & Natural Supplements, Fourth Edition. Mosby Elsevier. USA









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