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Pharmacology of Leonotis Leonurus (Wild Dagga)?
Does anyone have any information on the pharmacology of Leonotis Leonurus? I can't seem to find any significant data on it. Leonurine is one of the alkaloids and it also contains a number of diterpenoids but no indication as to what may be mediating the effects. I suspect there is just very little study done on this plant as there probably isn't any great incentive but perhaps someone may have some information?
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Re: Pharmacology of Leonotis Leonurus (Wild Dagga)?
SWIM has found a little gem relevant to this discussion and has tried to make it a little bit easier to for SWIY to read. The pharmaceutical information is near the bottom.
LEONOTIS LEONURUS HERBA Definition Leonotis herba consists of the dried aerial parts of Leonotis leonurus (L.) R. Br. (Lamiaceae). Synonyms Phlomis leonurus L. Leonotis leonurus (L.) R. Br. var. albiflora Benth. Vernacular names wilde dagga (A), lion's ear, minaret flower (E), unfincafincane (X), lebake (S), umhlalampetu (Sh) DESCRIPTION Macroscopical Shrub 2-5 m tall, branching from a thick woody base; stem pale brown and densely pubescent; leaves simple, opposite, petiolate, coriaceous, 50-100 ´ 10-20 mm, linear, acute at apex and base, serrate in the distal half; upper surface bright green, lower surface densely pubescent; inflorescence of 3-11 compact verticils; calyx 12-16 mm long, 4 mm in diameter, calyx teeth 10, subequal, spreading; corolla tubular, bright orange, 40-49 mm long, covered with orange hairs; fruit a nutlet 5-6 ´ 1.5-2 mm, brown. Microscopical Characteristic features are: the numerous uniseriate, curved, thick-walled, warty, 2-3 celled non-glandular trichomes of leaf and stem, 60-100 m in length, particularly abundant on margin of lamina and main veins of lower leaf surface; the numerous glandular hairs of leaf and stem, with unicellular stalk and 4-celled head (up to 20 m in diameter) and yellow-brown contents; the less numerous glandular trichomes of leaf lamina, with unicellular stalk and 6-8 celled head, thick-walled, head about 40 m in diameter; cells of the lower epidermis with sinuous walls and striated cuticle, lacking stomata; cells of the upper epidermis with sinuous walls and numerous raised anomocytic stomata; single palisade layer; abundant crystal sand in cells of the mesophyll; occasional yellow hairs of the corolla. Crude drug Supplied in bundles comprising young leafy twigs, the leaves having a characteristic aromatic-pungent odour, bright yellow-green colour and rough texture; occasional flowers and fruits are present. Geographical distribution Locally common at forest margins, on rocky hillsides and river banks and in tall grassland of the Eastern and Western Cape Provinces, Kwazulu-Natal and Mpumalanga. QUALITY STANDARDS Identity test Major compounds:Thin layer chromatography on silica gel using as solvent a mixture of toluene:diethyl ether:1.75m acetic acid (1:1:1). Reference compound: thymol (0,1% in chloroform) yellow-mustard (Rf :0,19); yellow-mustard (Rf: 0,38); blue-mauve (Rf: 0,4); thymol (pink): Rf:0,8. Ethanol (70%) extractive value not less than 22% Volatile oil content not less than 0,15% (0,15-0,18%). PURITY TESTS Major chemical constituents 1. Diterpenoid labdane lactones: premarrubiin 0.00933-0.01567%, marrubiin (possibly an artifact derived from premarrubiin during extraction) 2. Tannins, quinones, saponins, alkaloids and triterpene steroids were detected in preliminary tests in our laboratories; iridoids were not detected. MEDICINAL USES Dosage forms Used mainly in the form of an aqueous decoction, orally, per rectum and as a topical application. Internal For the treatment of cough, cold, influenza, chest infections, diabetes, hypertension, eczema, epilepsy, delayed menstruation, intestinal worms, constipation, spider bites and scorpion stings and as an antidote for snakebite. External For the relief of haemorrhoids, eczema, skin rashes and boils. Pharmacology / Bioactivity Molluscicidal activity of 80% ethanolic extracts of dried leaf, stem and fruits of Sudanese plants against Biomphalaria pfeifferi and Bulinus truncatus could not be demonstrated in vitro (concentration 200mg/litre). Anticonvulsant activity of an aqueous extract of dried leaf has been demonstrated in vivo in the mouse (dose: 200.0mg/kg IP) . In an in vitro assay for antiphage activity of aqueous fresh leaf+stem extracts of Greek plants, no activity was demonstrated against Bacteriophages MS2, PHI-CHI-174, T-7, T2, T4 or Bacteriophage-OPS7 . Extracts of shade-dried roots of Ethiopian plants were examined for anti-fertility activity in the rat, both in vitro (uterine stimulant activity) and in vivo (anti-implantation effects). Weak uterine stimulant activity was shown for 95% ethanol extracts but not for aqueous or n-butanol extracts (conc. 2.0%). Anti-implantation activity was shown by both n-butanol nd (%% ethanolic axtracts but not by aqueous extracts (dose: 0,93g/kg intragastrically) . Anti-nematodal activity has been demonstrated in vitro against Caenorhabditis elegans for aqueous and 100% ethanol extracts of the dried aerial parts of South African plants, at concentrations of 1.0mg/ml. A hexane extract proved inactive at a concentration of 2.0mg/ml. The same study found water and ethanol extracts to be inactive in an in vitroassay for anti-amoebic activity. ASSAY Brine shrimp lethality assay preliminary results showed no effect on brine shrimps in the concentrations tested. Antibiotic activity assay No in vitro antimicrobial activity was observed in preliminary assays, in the concentrations used. Last edited by PandorymDMT; 13-07-2009 at 22:43. |
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