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Scutellaria Lateriflora - ingredients and uses.

izo

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hello,

on to the next plant that might have some psychotropic effects. have a standartised 100:1x extract of it here, report about its activity will follow and any reports of experiences with this plant is greatly appreciated.

i start with a short description of its psychoactive effects:

Scutellaria Lateriflora not only led to a reduction in anxiety in the studies, but also improved mood without causing a deterioration in the ability to concentrate.

 
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this is what the encyclopedia from c. rätsch offers an information, not very much that you can find there about this plant:

cutellaria lateriflora L. (Labiatae) - Skullcap, Mad-dog skullcap
Skullcap is a component of supposedly psychoactive smoking mixtures used as a substitute for marijuana (see Cannabis
indica) are offered. The herb was formerly used as a sedative and nerve tonic, and even for
treatment of epilepsy,
Neuralgia and insomnia prescribed. The plant contains the flavonoid scutellarin, which is sedative
and has an anticonvulsant effect (FOSTER and DUKE 1990: 1860. A species described under the name Scutellaria arvense
is said to be psychoactive or hallucinogenic (SCHULTES and HOFMANN 1980: 3670.
 
from the following paper:

2007 - Herbal Medicines in the Treatment of Psychiatric Disorders A Systematic Review

Scutellaria lateriflora (Scullcap). Scullcap is a HM that has traditional use as a sedative in various nervous system disorders in Native American and Eclectic medicine (Felter and Lloyd, 2006 (1898)). To date, two studies have documented anxiolytic activity. In an animal maze-test model, scullcap displayed anxiolytic effects via increasing the number of unprotected head dips and entries into open-field area and arms, with the compounds baicalin and baicalein purported to be involved in this activity via GABA(A) binding (Awad et al., 2003). A double-blind, placebo-controlled cross-over study of healthy adults (n = 19) revealed that scullcap dose-dependently reduced symptoms of anxiety and tension after acute administration compared with control (Wolfson and Hoffmann, 2003).
 
from the following paper:

2013 - Plant-Based Medicines for Anxiety Disorders, Part 2 A Review of Clinical Studies with Supporting Preclinical Evidence

2.16 Skullcap (Scutellaria lateriflora)
The aerial parts of skullcap have been used in European and North American traditional medicine [130, 131] for anticonvulsant, relaxant and nervous system tonic effects [132]. Research has identified diterpenoids, amino acids (GABA and glutamine), essential oil and phenolic compounds in skullcap [132, 133]. A total of 73 bioactive constituents have been identified in the volatile oil, which include mainly sesquiterpenes [134]. Flavones appear to be the main constituents with anxiolytic actions, which include baicalein, baicalin, chrysin and wogonin [131,133]. In vitro research has identified baicalein as a weak benzodiazepine receptor ligand, that has demonstrated anxiolytic and sedative effects that appear to be mediated by interaction at GABAA non-benzodiazepine sites [135]. In addition, baicalin has demonstrated selective partial GABAA receptor antagonism [135], and wogonin has shown anxiolytic effects via interaction with benzodiazapine receptors in the GABA system [136]. Other flavone glycosides have exhibited binding to a 5-HT7 receptor [132]. One in vitro study used a whole plant ethanol extract of skullcap, and found the extract inhibited both glutamic acid decarboxylase and GABA-transaminase, with preferential inhibition of GABA-transaminase that appears to contribute to the anxiolytic activity [36]. Awad et al. [99] studied an acute oral dose of 100 mg of skullcap aqueous extract to rats in the EPM. Results revealed that treated rats spent significantly more time in the open arms compared with placebo, and displayed significantly less risk assessment behaviour in the open field test. One double-bind crossover RCT that investigated the acute anxiolytic effects of skullcap in 19 healthy adults was found [137]. Three different extracts of skullcap (100, 200 and 350 mg) were compared with placebo with a minimum of 2 days separating treatments. Self-assessments of anxiety levels were provided at baseline, 30-, 60-, 90- and 120-min post-dose using an 11-point Likert scale. All three skullcap preparations demonstrated anxiolytic effects on the Acute Psycho-Activity Self-Rating Scale. Although a clinical effect was seen, no statistical data were reported and there were numerous methodological flaws making it impossible to draw conclusions on the anxiolytic effects of skullcap based on this study.
 
and from the following paper:

2008 - Characterization of chemical ingredients and anticonvulsant activity of American skullcap (Scutellaria lateriflora)



American skullcap (the aerial part of Scutellaria lateriflora L.) has been traditionally used by Native Americans and Europeans as a nerve tonic, sedative, and anticonvulsant. However, despite some previous studies, the quality and safety, the bioactive ingredients, and the pharmacological properties of American skullcap are not fully understood. The aims of this study were to characterize the chemical ingredients of American skullcap and to evaluate its anticonvulsant activity. Twelve phenolic compounds including 10 flavonoids and two phenylethanoid glycosides were isolated and identified from American skullcap and used as marker compounds. An HPLC analytic method for analyzing these marker compounds in commercial American skullcap products from different sources was established and validated. The anticonvulsant activity of American skullcap was determined in rat models of acute seizures induced by pilocarpine and pentylenetetrazol. The results from this study indicate that (1) phenolic compounds, especially flavonoids, are the predominant constituents in American skullcap; (2) American skullcap products have similar constituents, but the content and relative proportions of the individual constituents varies widely; and (3) American skullcap has anticonvulsant activity in rodent models of acute seizures.
 
and from the following paper:

2003 - Inhibition of [3H]-LSD Binding to 5-HT7 Receptors by Flavonoids from Scutellaria lateriflora



The hot water and 70% ethanol extracts of dried mad-dog skullcap (Scutellaria lateriflora) both bound to the 5-HT7 receptor, with 87.2 ( 6.2% and 56.7 ( 1.3% inhibition of [3H]-LSD binding to the receptor at 100 íg/mL, respectively. The on-line analysis of a 70% ethanol extract by HPLC-UV/MS resulted in the identification of five flavones (1-5). Fractionation of the ethanol extract resulted in the isolation of three flavone-glucuronides (6-8) and a flavanone-glucuronide (9), including one new compound, lateriflorin (5,6,-dihydroxy-7-glucuronyloxy-2¢-methoxyflavone) (8). The structure of 8 was determined by NMR (1H NMR, 13C NMR, and NOESY experiments) and MS analysis. From the results obtained in the testing of the pure compounds, it is evident that the activity on the 5-HT7 receptor is at least partly due to the presence of flavonoids. Scutellarin and ikonnikoside I showed the highest inhibition of [3H]-LSD binding with IC50 values of 63.4 and 135.1 íM, respectively.
 
relevant papers:

1973 - A New Phenylquinolizidol of Heimia salicifolia.pdf
1985 - THE PHENYL- AND BIPHENYL-QUINOLIZIDINES OF IN-VITRO-GROWNH EIMIA SALICIFOLIA.pdf
1986 - PROSTAGLANDIN SYNTHETASE INHIBITION BY ALKALOIDS OF HEIMIA SALICIFOLIA.pdf
1994 - Heimia SALICIFOLIA a phytochemical and phytopharmacologic review.pdf
2008 - Alkaloids from Heimia salicifolia.pdf
2008 - Identification of sinicuichi alkaloids in human serum after intoxication caused by oral intake of a Heimia salicifolia extract.pdf
2019 - Asymmetric Total Synthesis of Biphenylquinolizidine Alkaloids 4"-O-Demethyllythridine and 14-epi-4"-O-Demethyllythridine.pdf

as said, bioassay of the 100:1x extract will follow.
 
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