Pau D'Arco

"Tabebuia Avellanedae"

Amy Bigus, Deanna Massengill, and Christy Walker

Common Names

General description

Chemical Composition

  1. lapachenole
  2. quercetin
  3. o- and p-hydroxybenzoic acid

History and Folk Use

Use inner bark for variety of conditions

Pharmacology

First active constituent studied was lapachol, but many studies show better results with the whole extract

  1. laxative effect
  2. antimicrobial activity
  3. anti-cancer effect
  4. antiparasitic activity
  5. anti-oxidant effect
  6. anti-fungal activity
  7. analgesic effect
  8. anti-inflammatory activity

Laxative Effect

Anti-oxidant effect

Analgesic effect

Anti-bacterial/Anti-parasitic action

Anti-inflammatory effects

Anti-cancer effects

Anti-viral effects

Clinical Applications

Dosage

Toxicity

  1. nausea (*positive sign herb is working*) - due to accumulation of toxins & wastes
  2. anticoagulant effects (high doses)
  3. loose bowels, diarrhea (high doses)

Review of Literature

Lapachol (2-hydroxy-3-(3-methyl-2-butenyl)-1,4-naphthoquinone) is identified as an active compound isolated from the lapacho tree. Walker 256 rat carcinosarcoma showed sensitivity to lapachol by daily intraperitoneal injection at levels up to those producing limited toxicity. Lapachol exhibited marked effectiveness by oral route of administration with best activity shown with twice a day oral administration on Days 3-6.

Pau d'arco showed clear evidence of differentiation-inducing activity. In vitro studies showed lapachol activity at concentrations similar to that of many anti-cancer drugs. Activity on pau d'arco and lapachol was inhibited by vitamin K1. the structure of lapachol resembles that of vitamin K. Results indicate that the concentrations of lapachol and pau d'arco required for differentiation are considerably less than that required for cytotoxicity. The results also suggest that lapachol interacts with a vitamin-K-dependent reaction involved in the erythroid differentiation program. Targeted vitamin-K-requiring reactions may therefore include the activity of an oncogenic receptor tyrosine kinase.

References

1