Zanthoxylumclava-herculis.-
Southern prickly ash
Z. americanum.- Northern prickly ash,
Xanthoxyllum fraxinium, X. americanumPrickly
ash, American
prickly ash Family: Rutaceae
PART USED: Bark TASTE: Pungent and bitter, causing salivation ODOR:
Slight ACTIONS GROUP: The circulation system - Herbs for the veins & peripheral circulation
1. Antirheumatic.[1,2,3] Circulatory
stimulant.[1] Analgesic.[3]
2. Bitter tonic.[2]
3. Diaphoretic.[1,2,3]
4. Alterative.[2] Antipyretic.[3]
5. Carminative.[1,3] Antidiarrheal.[3]
6. Sialagogue.[1] INDICATIONS
1. Insufficient peripheral circulation.[1,2]
Raynaud’s syndrome.[1,2] Intermittent
claudication.[1,2] Chronic rheumatic
disorders.[1,2] Cramps.[1,2]
Rheumatism.[3] Insufficient circulation.[3]
2. Atonic dyspepsia. Intestinal colic.
3. Nervous headaches. Paralysis of mouth and tongue. Toothache.[3]
4. Chronic gynaecological problems.
5. Liver disorders including hypoactivity.
6. Asthma.
7. Intermittent fevers. Fevers.[3]
8. General stimulant. Tonic.[3] SPECIFIC INDICATIONS: Peripheral circulatory insufficiency, associated
with rheumatic symptoms.[1] COMBINATIONS
- Deficient circulation, use with Myrica cerifera-
Bayberry bark and Zingiber officinalis-
Ginger.
- Rheumatism, use with Guaiacum, Menyanthes
and Capsicum annuum. PREPARATIONS:3X /day
Dried bark 1-3 g,[1,2] or by decoction[1]
1:20.
Fluid extract 1: 1 in 45% alcohol 1-3 ml.[1,3]
Dried berries 0.5-1.5 g.
Tincture 1:5 in 45% alcohol 2-5 ml.[1,2] PART USED:Berries- Dried
full grown. TASTE: Pungent and bitter ODOR: Aromatic ACTIONS and INDICATIONS Similar to the bark, but
more active in promoting circulation.[1] PREPARATIONS
Dried berries 0.5-1.5 g.[1,2,3]
Liquid Extract 1:1 in 45% alcohol 0.5-1.5 ml.[1] ORIGIN: Canada and USA DESCRIPTION Bark: Northern prickly ash bark occurs in curved or
quilled fragments about 1 mm thick, externally brownish grey, faintly furrowed
with whitish patches and flattened spines about 5 mm long.
Southern prickly ash is about 2 mm thick, with conical, corky spines up to 2 cm
long. Fracture short, green in the outer and yellow in the inner part. 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. src.sfasu.edu
2. google.com.au
3. mountainroseherbs.com
4. pennherb.com
5. hobbyfarms.com
6. eattheweeds.com
7. en.wikipedia.org
by A. Barra CC BY-SA 4.0
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. Similar plants
Z. zanthoxyloides, a West African
species, is used for similar purposes, has been externsively investigated chemically
and pharacologically. It has related but different constituents and contains
fagaramide, a potent prostaglandin inhibitor in animal tests. References|
[1] Medicinal Plants of Tropical West Africa, B. Oliver-Bever. Pub. Cambridge
University Press (1986) UK
Bark: Z. clavaherculis: Alkaloids-[1]
Chelerythrine and magnoflorine- both quaternary 1-benzyltetrahydroisoquioline
alkaloids.[1] There
are no coumarins in Z. clavaherculis.[1]
Asarin, a lignan.[5]
Amides; herculin, neoherculin.[6,7,8] Z. americanum: Nitidine and lauriflorine- both benzophenanthridine
alkaloids[1] Coumarins: Xanthyletin,
xanthoxyletin, alloxanthyletin.[5,6] Both species: Alkaloids; g-fagarine,
b-fagarine, magnoflorine, laurifoline, nitidine,
chelerythrine, tambetarine and candicine.[3,4]
Resins. Volatile oil. Berries: Resin.[1,2]
Volatile oil.[1,2] Tannin.[2] References
[1] British Herbal Pharmacopoeia 1983 Published by the British Herbal Medicine
Association ISBN 0 903032 07 4.
[2] 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.
[3] Gottleib, O.R. (1979) J. Ethnopharmacol. 1, 309
[4] Sarath-Kumara, S.J. et al. (1985) J. Sci. Food. Agric. 36 (2),
93
[5] Encyclopedia of Common Natural Ingredients used in Food Drugs and Cosmetics,
Albert Y. Leung. Pub. John Wiley & Sons Inc. (1980) NY
[6] Fish, F. et al. (1975) Lloydia 38, 268
[7] Drogenkunde, 8th Ed. Heinz, A., Hoppe. Pub. W. de Gruyter (1975) Berlin
[8] Fish, F. and Waterman, P.G. (1973) J. Pharm, Pharmac. 25s, 115
Research
Chelerythrine is antimicrobial.[1] References
[1] 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.
Activity of Zanthoxylum clava-herculis extracts against multi-drug
resistant methicillin-resistant Staphylococcus aureus (mdr-MRSA). Gibbons S, Leimkugel J, Oluwatuyi M, Heinrich M. Abstract
In a continuing search for compounds with antibiotic activity against methicillin-resistant
Staphylococcus aureus (MRSA) possessing multidrug ef flux systems, we have
demonstrated activity associated with extracts from Southern prickly ash bark,
Zanthoxylum clava-herculis. Bioassay-guided isolation of an alkaloid extract
led to the characterization of the benzo[c]phenanthridine alkaloid chelerythrine
as the major active principle. This compound exhibited potent activity against
strains of MRSA, which were highly resistant to clinically useful antibiotics
via multidrug ef flux mechanisms.
Copyright 2003 John Wiley & Sons, Ltd.