Scutellarialateriflora.Scullcap,Hoodwort, Helmet flower, Quaker bonnet Family: Labiatae PART USED:Aerial parts.
Gathered during the late flowering period. TASTE: Bitter ODOR: Slight ACTIONS GROUP: The Musculo-Skeletal System- Antispasmodics
1. Antispasmodic.[2,5]
2. Anticonvulsive.[1,2,5] Nervine.[5]
3. Sedative.[1,2,5] INDICATIONS
1. Convulsive disorders including St Vitus' Dance. Delirium tremens. Epilepsy,[1,2]
and especially grand-mal epilepsy.[1,2]
Headaches including migraines and tension headaches. Fearfulness- with mental
confusion and inability to concentrate. Neuralgias. Chorea.[1]
Hysteria.[1,5] Nervous tension states.[1,5]
Rabies.
2. Dysmenorrhea. "Undue sexual desire”
3. Nervous heart conditions.
4. Rheumatic conditions.
5. Urinary incontinence. SPECIFIC INDICATIONS: Grand mal.[1] COMBINATIONS
- Nervous states, use with Hops and Passionflower.
PREPARATIONS:3X /day
Dried herb 1-2 g,[1,2,5] or by
infusion 1:20.[1,2]
Fluid extract 1:1 in 25% alcohol 2-4 ml.[1,2,5]
45% alcohol (Mediherb-S. baicalensis as well). 30% alcohol.
Fluid extract- leaf 1:1 45% alcohol.[4]
Tincture 1:5 in 45% alcohol 1-2 ml.[1,2] MANUFACTURING: Tends to stick to percolating tubes. ORIGIN: North America. DESCRIPTION: Leaves opposite, cordate-lanceolat3e, shortly stalked with
a tapering apex. Flowers blue, with a helmet-shaped upper lip, in axillary racemes.
Hydridization with other species readily occurs and substitution may occur in
commerce. 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] Innerpath
[4] The Pharmaceutical Plant Company Pty Ltd ppcherbs.com.au
[5] 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 Rolf Engstrand
CC BY-SA 3.0
2. amazon.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
Bitter flavonoid glycosides- scutellarin.[1,2,3]
Tannin.[3] Volatile oil and waxes-
mainly C31, C33 and C35 hydrocarbons.
Iridoids; catalpol is present in both S. lateriflora and S. galericulata.[9] S. baicalensis contains the flavonoids baicalin, baicalein, wogonin,
skullcapflavones I and II, and many other flavones.[4,5,6,7] S. galericulata contains wogonin, baicalin, baicalein, apigenin,
scutellarein, eridictyol and luteolin glycosides.[8] 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] Drogenkunde, 8th Ed. Heinz. A., Hoppe. Pub. W. de Gruyter (1975) Berlin
[4] Kimura, Y. et al. (1985) Planta Med. 51, 132
[5] Kimura, Y. et al. (1984) Planta Med. 50, 290
[6] Kubo, M. et al. (1984) Chem. Pharm. Bull. 32 (7), 2724
[7] Takido, M. et al. (1979) Yakugaku Zasshi 99 (4), 443-444
[8] Barberan, F.A.T. (1986) Fitoterapia 57 (2), 67
[9] Kooiman, P. (1972) Acta. Bot. Neeri. 21(4), 417
[10] Yagmai, M. S. and Benson, G.G. (1979) J. Nat. Prod. 42 (2), 229
Research
American Skullcap (Scutellaria lateriflora): a randomised, double-blind
placebo-controlled crossover study of its effects on mood in healthy volunteers. Brock C, Whitehouse J, Tewfik I, Towell T. Abstract
Scutellaria lateriflora, a traditional herbal remedy for stress and anxiety, was
tested on human volunteers for its effects on mood. In a placebo-controlled, double-blind,
crossover study, 43 healthy participants were randomised to a sequence of three
times daily S. lateriflora (350 mg) or placebo, each over two weeks. In this relatively
non-anxious population (81% were mildly anxious or less, i.e. Beck Anxiety Inventory
(BAI) scores=15), there was no significant difference between skullcap and placebo
with BAI (p=0.191). However, there was a significant group effect (p=0.049), suggesting
a carryover effect of skullcap. For Total Mood Disturbance measured by the Profile
of Mood States, there was a highly significant (p=<0.001) decrease from pre-test
scores with skullcap but not placebo (p=0.072). The limitations of carryover effect,
generally low anxiety scores and differences in anxiety levels between groups
at baseline (p=0.022), may have reduced the chances of statistical significance
in this study. However, as S. lateriflora significantly enhanced global mood without
a reduction in energy or cognition, further study assessing its putative anxiolytic
effects in notably anxious subjects with co-morbid depression is warranted.
PMID: 23878109 DOI: 10.1002/ptr.5044 Phytother Res. 2014 May;28(5):692-8.
doi: 10.1002/ptr.5044. Epub 2013 Jul 22. ncbi.nlm.nih.gov
Phytochemical and biological analysis of skullcap (Scutellaria lateriflora
L.): a medicinal plant with anxiolytic properties. Awad R, Arnason JT, Trudeau V, Bergeron C, Budzinski JW, Foster BC, Merali
Z. Abstract
The phytochemistry and biological activity of Scutellaria lateriflora L. (American
skullcap) which has been traditionally used as a sedative and to treat various
nervous disorders such as anxiety was studied. In vivo animal behaviour trials
were performed to test anxiolytic effects in rats orally administered S. laterifolia
extracts. Significant increases in the number of entries into the center of an
"open-field arena"; number of unprotected head dips, number of entries
and the length of time spent on the open arms of the Elevated Plus-Maze were found.
The identification and quantification of the flavonoid, baicalin in a 50% EtOH
extract (40 mg/g) and its aglycone baicalein in a 95% EtOH extract (33 mg/g),
as well as the amino acids GABA in H2O and EtOH extracts (approximately 1.6 mg/g)
and glutamine in a H2O extract (31 mg/g), was performed using HPLC. These compounds
may play a role in anxiolytic activity since baicalin and baicalein are known
to bind to the benzodiazepine site of the GABAA receptor and since GABA is the
main inhibitory neurotransmitter.
PMID: 14692724 DOI: 10.1078/0944-7113-00374 Phytomedicine. 2003 Nov;10(8):640-9.
ncbi.nlm.nih.gov
An investigation into the efficacy of Scutellaria lateriflora in healthy
volunteers. Wolfson P, Hoffmann DL. Abstract
Scutellaria lateriflora is an herbal medicine with long-standing traditional use
as a relaxing nervine. There has been controversy in the literature with regards
to its efficacy, and this study was designed to clarify its effectiveness in reducing
anxiety, one of the phytotherapeutic indications. A double blind, placebo-controlled
study of healthy subjects demonstrated noteworthy anxiolytic effects. The use
of phytomedicines for the treatment of anxiety is reviewed, as is the published
literature on S. lateriflora and its putative toxicity.
PMID: 12652886 Altern Ther Health Med. 2003 Mar-Apr;9(2):74-8. ncbi.nlm.nih.gov
Anti-oxidative and DNA protecting effects of flavonoids-rich Scutellaria
lateriflora. Lohani M, Ahuja M, Buabeid MA, Dean S, Dennis S, Suppiramaniam V, Kemppainen
B, Dhanasekaran M. Abstract
Scutellaria lateriflora (American skullcap), a native plant of North America,
has been used by Americans and Europeans as a nerve tonic for more than 200 years.
In vivo studies have shown anxiolytic activity ofS. lateriflora in animals and
humans. However, the neuroprotective mechanisms ofS. lateriflora are not fully
understood. Oxidative stress plays a vital role in the neurodegenerative and neuropsychiatric
diseases such as anxiety, Alzheimer's disease, depression, and Parkinson's disease.
Bioactive compounds present in various medicinal plants neutralize or scavenge
toxic free radicals and thus suppress oxidative stress. Therefore, the objective
of this study was to investigate the antioxidant effects of S. lateriflora. The
antioxidant potential of aqueous or ethanolic extracts of S. lateriflora was determined
in mouse brain tissue using various biochemical assays. Protective effects of
S. lateriflora against oxidative stress induced DNA fragmentation was determined
using plasmid DNA. The ethanolic and aqueous extracts scavenged the 1,1-diphenyl-2-picrylhydrazyl
(DPPH) radicals. The ethanolic extract reduced tert-butyl peroxide-induced reactive
oxygen species (ROS) and lipid peroxides in the mouse brain homogenates. Furthermore,
the ethanolic extract of S. lateriflora protected hydrogen peroxide-UV induced
cleavage of supercoiled plasmid DNA. In conclusion, S. lateriflora exhibited significant
antioxidant effects. The current findings posit S. lateriflora as one of the potential
experimental herbal drugs that should be screened for its therapeutic potential
against various oxidative stress associated mental disorders.
Nat Prod Commun. 2013 Oct;8(10):1415-8.
ncbi.nlm.nih.gov