PREPARATIONS3X/day
Dried root 0.5-2 g.
Decoction 0.5-2g in 10-40 ml of water or milk.[1]
Fluid extract 1:1 in 45% alcohol 0.5-2 ml.[1,2]
0.3-2 ml.[3] ORIGIN: Mediterranean region. Cultivated in Britain and the USA. DESCRIPTION: Perennial herb
that may grow to 2 m tall. Leaves are divided into wedge-shaped segments, the
stems hollow and erect and the flowers are yellow in umbels during Summer. The
fleshy rhizome has a greyish-brown external surface and bears numerous longitudinally
furrowed rootlets. The bark is thick, spongy, often with small cavities, whitish,
and separated from the wood by a dark line. The wood is yellowish, radiate and
shows glistening oil glands in transverse section. 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. Images
1. en.wikipedia.org
by Raffi Kojian - http://Gardenology.org
CC BY-SA 3.0
2. specialtyproduce.com
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
Volatile oil;containing
phthalides (about 70%), including E- and Z-butylidenephthalide, E-
and Z-ligustilide, senkyunolide, isosenkyunolide, validene-4,5-dihydrophthalide,
butylphthalide.[3,4,5] Volatile oil[1]
containing carvacrol, umbelliferone, angelic acid.[1]
a and b pinene, a-
and b- phellandrine, carvacrol.[1,6]
A bitter principle.[1,2]
Resins.[1,2]
Coumarins; b ergapten, coumarin, psoralen, umbelliferon.[7,8]
F furocoumaroins including psoralen, rutoside, sitosterols.[1]
Benzoic, butyric and isovaleric acids.[6]
b-sitosterol, resins, gums.[6]
The phthalides have sedative and anticonvulsant activity in animals.[9,10]
Lovage extracts and oil are reportedly strongly diuretic in mice and rabbits.[6] 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] Gijbels, M. J. et al. (1982) Planta Med. 44, 207
[4] Gijbels, M. J. et al. (1981) Chromatographia 14
(8), 451
[5] Lawrence, R. M. (1980) Perf. Flav. 5, 29
[6] Encyclopedia of Common Natural Ingredients used in Food Drugs and Cosmetics,
Albert Y. Leung. Pub. John Wiley & Sons Inc. (1980) NY
[7] Albulscu, D. et al. (1975) Farmacia 23, 159
[8] Fischer, F. C. and Svendson, A. B. (1976) Phytochem. 15,
1079
[9] Bjeldanes, L. F. and Kim, I. (1977) J. Org. Chem. 42, 2333
[10] Yu, S. R. and You, S. Q. (1984) Yao Hsueh Hsueh Pao 19
(8), 566
Antimycobacterial polyacetylenes from Levisticum officinale.
Schinkovitz A, Stavri M, Gibbons S, Bucar F. Abstract
No conflicts of interest concerning financial matters or personal relationships
exist between the authors and those who might bias this work. The present work
is in part included the PhD thesis of A. Schinkovitz (University of Graz) but
has not been published elsewhere previously. The dichloromethane extract of
the roots of Levisticum officinale L. (Apiaceae) exhibited significant antimycobacterial
activity against Mycobacterium fortuitum and Mycobacterium aurum in a microtiter
plate dilution assay and was further analysed following a bioassay-guided fractionation
strategy. 3(R)-Falcarinol (3(R)-(-)-1,9-heptadecadien-4,6-diin-3-ol] and 3(R)-8(S)-falcarindiol
[3(R)-8(S)-(+)-1,9-heptadecadien-4,6-diin-3,8-diol] could be identified as the
active components in this extract. The minimal inhibitory concentration (MIC)
of 3(R)-falcarinol against M. fortuitum and M. aurum was 16.4 microM while that
of 3(R)-8(S)-falcarindiol was 30.7 microM against M. fortuitum and 61.4 microm
against M. aurum, respectively. Previously, 3(R),8(R)-dehydrofalcarindiol was
isolated from Artemisia monosperma and surprisingly this polyacetylene exhibited
no antimycobacterial activity at 128 microg/mL. This indicates that the terminal
methyl group is vital for retention of antimycobacterial activity. Reference
antibiotics ethambutol and isoniazid exhibited an activity of 115.5 microM and
14.6 microM against M. fortuitum, and 3.4 microM and 29.2 microM against M.
aurum, respectively.
PMID: 18350523 DOI: 10.1002/ptr.2408 Phytother Res. 2008 May;22(5):681-4. doi:
10.1002/ptr.2408. ncbi.nlm.nih.gov
The activity of Levisticum officinale W.D.J. Koch essential oil against
multidrug-resistant Mycobacterium tuberclosis
Mansour Miran, Mohammad Mehdi Feizabadi, Hossein Kazemian, Jalil Kardan-Yamchi,
Hamid Reza Monsef-Esfahani, and Samad Nejad Ebrahimi Abstract
Background and Objectives:
Essential oils are used for controlling and preventing human diseases and the
application of those can often be quite safe and effective with no side effect.
The essential oils have been found to have antiparasitic, antifungal, antiviral,
antioxidant and especially antibacterial activity including antibacterial activity
against tuberculosis. In this study the chemical composition and anti-TB activity
of essential oil extracted from Levisticum officinale has been evaluated.
Materials and Methods:
The essential oil of L. officinale was obtained by the hydro distillation method
and the oil was analyzed by GC-FID and GC-MS techniques. The antibacterial activity
of essential oil was evaluated through Minimum Inhibitory Concentration (MIC)
assay using micro broth dilution method against multidrug-resistant Maycobacterium
tuberculosis. The molecular modeling of major compounds was evaluated through
molecular docking using Auto Dock Vina against-2-trans-enoyl-ACP reductase (InhA)
as key enzyme in M. tuberclosis cell wall biosynthesis.
Results:
The hydrodistillation on aerial parts of L. officinale yielded 2.5% v/w of essential
oil. The major compounds of essential oil were identified as a-terpinenyl acetate
(52.85%), ß- phellandrene (10.26%) and neocnidilide (10.12%). The essential
oil showed relatively good anti-MDR M. tuberculosis with MIC = 252 µg/ml.
The results of Molecular Docking showed that affinity of major compounds was
comparable to isoniazid.
Conclusion:
The essential oil of aerial parts extracted from L. officinale was relatively
active against MDR M. tuberculosis, and molecular docking showed the major compounds
had high affinity to inhibit 2-trans-enoyl-acyl carrier protein reductase (InhA)
as an important enzyme in M. tuberculosis cell wall biosynthesis.
Iran J Microbiol. 2018 Dec; 10(6): 394–399.
PMCID: PMC6414743
PMID: 30873267 ncbi.nlm.nih.gov
Chemical Composition and antiproliferative activity of essential oil
from the leaves of a medicinal herb, Levisticum officinale, against UMSCC1 head
and neck squamous carcinoma cells.
Sertel S, Eichhorn T, Plinkert PK, Efferth T. Abstract
BACKGROUND:
Oral squamous cell carcinoma (OSCC) is a challenging disease with a high mortality
rate. Natural products represent a valuable source for the development of novel
anticancer drugs. We investigated the cytotoxic potential of essential oil from
the leaves of a medicinal plant, Levisticum officinale (lovage) on head and
neck squamous carcinoma cells (HNSCC).
MATERIALS AND METHODS:
Cytotoxicity of lovage essential oil was investigated on the HNSCC cell line,
UMSCC1. Additionally, we performed pharmacogenomics analyses.
RESULTS:
Lovage essential oil extract had an IC50 value of 292.6 µg/ml. Genes involved
in apoptosis, cancer, cellular growth and cell cycle regulation were the most
prominently affected in microarray analyses. The three pathways to be most significantly
regulated were extracellular signal-regulated kinase 5 (ERK5) signaling, integrin-linked
kinase (ILK) signaling, virus entry via endocytic pathways and p53 signaling.
CONCLUSION:
Levisticum officinale essential oil inhibits human HNSCC cell growth.
PMID: 21273597
Anticancer Res. 2011 Jan;31(1):185-91. ncbi.nlm.nih.gov