Usnea extract

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Usnea 1:2 Herbal Extract in Ethanol and Purified Water

Common Name: Usnea
Botanical Name: Usnea species
Part Used: Thallus
Ratio: 1:2
Percentage of alcohol: 25%
Source: Trade

Ingredients

Ingredient Per 1 ml
Usnea spp. (Usnea) thallus extract
equiv. thallus dry
500 mg
 

Usnea is a lichen. A lichen is not really a plant, but is a symbiotic relationship between a fungus and an algae. The inner part of the lichen, known as the cortex, is a filamentous fungus that looks like a thin white thread and stretches like elastic when it gets wet.

The algae is a photobiont, providing photosynthesis for the lichen, while the fungus is a mycobiont, providing water and minerals. Together, they live as a single entity and produce constituents different from those of either original organism. These constituents possess unique antibacterial and anti-fungal properties to protect the lichen from harmful microorganisms.

Lichens have been used in medicine, pharmacy and industry from antiquity to present day in the treatment of various diseases. Interestingly, the word lichen is derived from the Greek “Leikhen - Leprous” and refers to use of lichens in treating skin diseases due to their peeling-skin appearance.

Antibacterial:

Herbalist and director of the North American Institute of Medical Herbalism, Paul Bergner notes that Usnea is “very effective for topical use in the treatment of resistant bacteria, as a douche and for urinary tract infections” Usnea is regarded to have a strong localised antibacterial action and is generally non-systemic in this regard (2).

Anti-fungal:

Usnea is considered a primary anti-fungal phytomedicine among herbalists and many European anti-fungal creams and balms are made from Usnea species . In preclinical studies, Usnea and its constituents have been found to be active against (5, 8, 9): Candida, Malassezia yeasts, Microsporum gypseum, Trichophyton mentagrophytes, Trichophyton rubrum.

 In one clinical study, an usnic acid combination was also found to be active against Tinea pedis. During shortterm treatment with the association of a copper salt of usnic acid and of undecilenic acid (another anti-fungal compound), 65 patients (sportsmen) with Tinea pedis exhibited a significant improvement in their clinical condition(7,9).

Antioxidant:

This effect was attributed to the herb’s antioxidant potential as all administered doses were found to activate superoxide dismutase (SOD) and glutathione s-transferase (GST) enzymes and protect against oxidative damage in mucosal cells.

Anti-parasitic:

In preclinical studies, Usnea and its constituents have been found to be active against (10, 11, 12): Leishmania spp, Trypanosoma cruzi, Trichomonas vaginalis.The constituent usnic acid also showed leishmanicidal properties both in vitro and in vivo. 

Anti-viral:

Usnic acid has demonstrated anti-viral activity in vitro, exerting its action by inhibiting virus RNA transcription and causing an abolition of viral DNA replication. In preclinical studies, Usnea and its constituents have been found to be active against: Epstein-Barr virus, Herpes simplex virus, Junin virus, Polyomavirus (2,3, 5, 6, 8).

Immunostimulating:

European Usnea preparations have been shown to enhance the resistance to colds and influenza as, besides its strong selective antibacterial activity, Usnea also has the advantage of supporting the natural defences of the body (1, 4).

Caution:  Do not use Usnea internally during pregnancy. Furthermore, safety in lactation has not been established, therefore use is not recommended. Contains alcohol.

REFERENCES: 

1. Hobbs, C. (1990). Usnea: The Herbal Antibiotic. California, United States of America: Botanica

Press.

2. Buhner, S. H. (2012). Herbal Antibiotics: Natural Alternatives for Treating Drug-Resistant

Bacteria, 2nd edn. Massachusetts, United States of America: Storey Publishing.

3. Campanella, L., Delfini, M., Ercole, P., Iacoangeli, A., & Risuleo, G. (2002). Molecular

characterization and action of usnic acid: a drug that inhibits proliferation of mouse

polyomavirus in vitro and whose main target is RNA transcription. Biochimie, 84(4), 329-334.

4. Weiss, R. F. (2001). Weiss’s Herbal Medicine Classic Edition. Stuttgart, Germany: Thieme.

17. Bothwell, J. (2002). UpS List of Herbs and Analogs. Journal of Medicinal Plant Conservation,

8-9.

5. Perry, N. B., Benn, M. H., Brennan, N. J., Burgess, E. J., Ellis, G., Galloway, D. J., Lorimer, S. D.,

& Tangeny, R. S. (1999). Antimicrobial, antiviral and cytotoxic activity of New Zealand lichens.

Lichenologist, 31(6), 627-636.

6. Cansaran, D., Kahya, D., Yurdakulola, E., Atakol, O. (2006). Identification and Quantitation of

Usnic Acid from the Lichen Usnea Species of Anatolia and Antimicrobial Activity, Zeitschrift für

Naturforschung, 61(11-12), 773-776.

7. Cocchietto, M., Skert, N., Nimis, P. L., & Sava, G. (2002). A review on usnic acid, an interesting

natural compound. Naturwissenschaften, 89(4), 137-146.

8. Molnár, K., & Farkas, E. (2010). Current Results on Biological Activities of Lichen Secondary

Metabolites: a Review. Zeitschrift für Naturforschung, 65(3), 157-173.

9. De Battisti, F., Codolo, R., & Nicolato, A. (1991). Attività di una associazione antibattericoantimicotico

sulla sintomatologia della Tinea pedis in un gruppo di sportivi. Chron Derm, 3, 375-380.

10. De Carvalho, E. A., Andrade, P. P., Silva, N. H., Pereira, E. C., & Figueiredo, R. C. (2005). Effect of

usnic acid from the lichen Cladonia substellata on Trypanosoma cruzi in vitro: an ultrastructural

study. Micron, 36(2), 155-161.

11. Fournet, A., Ferreira, M. E., Rojas de Arias, A., Torres de Ortiz, S., Inchausti, A., Yaluff, G.,

Quilhot, W., Fernandez, E., & Hidalgo, M. E. (1997). Activity of compounds isolated from

Chilean lichens against experimental cutaneous leishmaniasis. Comparative Biochemistry and

Physiology Part C: Pharmacology, Toxicology and Endocrinology, 116(1), 51-54.

12. Wu, J., Zhang, M., Ding, D., Tan, T., & Yan, B. (1995). [Effect of Cladonia alpestris on

Trichomonas vaginalis in vitro]. Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi, 13(2), 126-129. [Abstract Only]

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