Convallaria
majalis. Lily
of the valley, May lily, Muguet
Family Liliaceae
Lily of the valley flowers are used in perfumery. PART USED:Leaves, whole plant TASTE: Sweet at first, then bitter ODOR: Pleasant
TOXICITY: All parts of the plant are toxic, including the red
berries which may be attractive to children.[4] ACTIONS GROUP:The Circulatory System- Herbs for the Heart and Arteries
1. Cardiac tonic.[3] Cardioactive-
digitalis like action (Digitalis purpurea-
Foxglove), but is less cumulative.
2 . Antispasmodic.
3. Diuretic. INDICATIONS
1. Congestive heart failure,[1,2,3]
with dropsy. Cardiac asthma.[1,2]
Arrhythmias.[1,2] Valvular heart
disorders. Edema of cardiac origin.
2. "Clears the mind and strengthens the memory"
3. Swellings CONTRAINDICATIONS- When giving Lily of the valley check the patients
dietary potassium intake, note the low dosage and dispense with particular
care, excessive doses may cause vomiting and diarrhoea. COMBINATIONS
PREPARATIONS:
Dried leaves 0.06-0.2 g.[1]
Infusion 0.06-0.2 in 1.2-4 ml water.
Fluid extract (BPC1934) 0.3-0.6 ml.[3]
1:1 in 25% alcohol 0.6-2 ml.[1,2]
Tincture (BPC1934) 0.3-1.2.[3] 1:8
in 60% alcohol 0.3-1.2 ml or 1:5 in 40% alcohol 0.5-1 ml.[1,2] ORIGIN Europe, North America and Northern Asia. DESCRIPTION Small herb. Leaves broadly lanceolate, up to 15 cm long and
about 5 cm wide, parallel-veined with entire margins. Flower stem carries eight
to twelve small, stalked, bell-shaped white flowers with six stamens. Rhizome;
cylindrical, slender, internodes about 5 cm apart bearing numerous slender rootlets,
pale brown. References
[1] British Herbal Pharmacopoeia 1983
Published by the British Herbal Medicine Association ISBN 0 903032 07 4.
[2] Herbal Materia Medica Course Notes For Diploma of Naturopathy and Diploma
of Herbalism Students by Lydia Mottram.
[3]Potter's New Cyclopaedia of Botanical Drugs and Preparations
R.C. Wren Revised by Elizabeth M. Williamson and Fred J Evans. First published
in Great Britain in 1988 and reprinted in 1989 and 1994 by the C. W. Daniel
Company Limited. 1 Church Path, Saffron Walden Essex. Published 1988 Printed
and bound by Biddles, Guildford ISBN 085207 1973.
[4] New York Times Images
1. en.wikipedia.org
by Llez CC BY-SA 3.0
2. onlineplantnursery.com
3. en.wikipedia.org
Public Domain
Inner Path can not take any responsibility for any adverse effects from
the use of plants. Always seek advice from a professional before using a plant
medicinally.Constituents
Cardioactive glycosides including convallatoxin,
convalloside convallatoxol, and desglucocheirotoxin, lokunjoside, convallamaroside,
glycosides of bipindogenin, sarmentologenin, sarmentosigenin A, rhodexin A,
rhodexoside.[1,2,3,4,5]
Saponin glycoside- convallamarine. Leaves; Flavonoid glycosdes.[6] References
[1]Laufke, R. (1958) Planta Med. 6, 237
[2] Tschesche, R. et al. (1959) Naturwissensch. 46,
109
[3] Bleir, W. et al. (1965) Pharm. Acta Helv. 40,
554
[4] Tschesche, R. in Pharmacognosy and Phytochemistry, Ed. H. Wagner and L.
Horhammer, Pub. Springer-Verlag (1971)
[5] Kipp. B. and Kubelka, W. (1982) Planta Med. 45, 87
[6] Pharmacognosy, 12th Ed. Trease, G. E. and Evans, W. C. Pub. Bailliere
Tindall (1983) UK
Research
The usual form for use is the isolated glycoside convallatoxin.[1]
Convallamaroside has antifungal and antibiotic activity but this effect is not
therapeutically useful since it forms a complex in the body with cholesterol.[1] References
[1] Martindale. The Extra Pharmacopoeia, 27th Ed. Pub. The Pharmaceutical Press
(1977) UK
[2] Bleir, W. et al. (1965) Pharm. Acta Helv. 40,
554
Steroidal Glycosides from Convallaria majalis Whole Plants and Their
Cytotoxic Activity.
Matsuo Y, et al. Abstract
Phytochemical examination of Convallaria majalis (Liliaceae) whole plants yielded
15 steroidal glycosides (1-15), including nine new compounds (4-6, 10-15) with
a lycotetrose unit. The structures of the new compounds were determined using
two-dimensional Nuclear magnetic resonance (NMR) analyses and chemical methods.
The isolated compounds were evaluated for cytotoxicity against HL-60 human promyelocytic
leukemia cells, A549 human lung adenocarcinoma cells, and HSC-4 and HSC-2 human
oral squamous cell carcinoma cell lines. Of these, (25S)-spirost-5-en-3ß-yl
O-ß-d-glucopyranosyl-(1-2)-O-[ß-d-xylopyranosyl-(1-3)]-O-ß-d-glucopyranosyl-(1-4)-ß-d-galactopyranoside
(1) exhibited cytotoxic activity against HL-60, A549, HSC-4, and HSC-2 cells
with IC50 values ranging from 0.96 to 3.15 µM. The corresponding furostanol
glycoside of 1, (25S)-26-[(ß-d-glucopyranosyl)oxy]-22a-hydroxyfurost-5-en-3ß-yl
O-ß-d-glucopyranosyl-(1-2)-O-[ß-d-xylopyranosyl-(1-3)]-O-ß-d-glucopyranosyl-(1-4)-ß-d-galactopyranoside
(8), was cytotoxic to the adherent cell lines of A549, HSC-4, and HSC-2 cells
with IC50 values of 2.97, 11.04, and 8.25 µM, respectively. The spirostanol
lycotetroside (1) caused necrotic cell death in A549 cells in a dose-dependent
manner. Alternatively, the furostanol lycotetroside (8) induced apoptotic cell
death in A549 cells in a time-dependent manner, as was evident by morphological
observations and flow cytometry analyses.
PMID 29112119 PMCID PMC5713327
Int J Mol Sci. 2017. ncbi.nlm.nih.gov
Convallatoxin, the active cardiac glycoside of lily of the valley, minimally
affects the ADVIA Centaur digoxin assay.
Dasgupta A, et al. J Clin Lab Anal. 2018. Abstract
OBJECTIVE: Lily of the valley is a poisonous plant due to the presence of the
cardiac glycoside convallatoxin which is known to interfere with serum digoxin
measurement using the LOCI digoxin assay and other digoxin assays. We evaluated
potential interference of convallatoxin as well as extract of lily of the valley
with the ADVIA Centaur digoxin assay by comparing results obtained using the
LOCI digoxin assay.
MATERIALS AND METHODS: Aliquots of a drug-free serum pool and a digoxin serum
pool were supplemented with nanograms to 1 µg quantities of convallatoxin
or 1.0 and 2.5 µL of lily of the valley extract per milliliter of serum
followed by measurement of digoxin concentrations using the LOCI and ADVIA Centaur
digoxin assays.
RESULTS: Apparent digoxin concentrations were minimal using the ADVIA Centaur
digoxin assay when aliquots of drug-free serum were supplemented with convallatoxin
or extract of lily of the valley but apparent digoxin levels were very high
using the LOCI digoxin assay. Moreover, minimal interference in serum digoxin
measurement using the ADVIA Centaur digoxin assay was observed when aliquots
of serum digoxin pool were further supplemented with lily of the valley extract.
As expected, the LOCI digoxin assay showed significant interference of convallatoxin
in serum digoxin measurement.
CONCLUSIONS: Significant interference of convallatoxin in serum digoxin measurement
using the LOCI digoxin assay could be minimized using the ADVIA Centaur digoxin
assay.
PMID 29855084 PMCID PMC6817247 ncbi.nlm.nih.gov