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Anamu Extract Concentrate

Also known as: Anamú, Guinea Hen Weed, Garlic Weed, Petiveria alliacea

Overview

Anamu, scientifically known as *Petiveria alliacea*, is a tropical plant native to Central and South America. It is traditionally used for its purported immune-modulating and anti-tumor properties. The plant contains various bioactive compounds, including organosulfur compounds like dibenzyl trisulfide, as well as flavonoids and coumarins. Research on Anamu is primarily preclinical, involving in vitro and in vivo studies, with limited human trials. The available evidence suggests potential anti-tumor and antimicrobial activities, but the quality of evidence is considered low, with a lack of randomized controlled trials or systematic reviews. Further research is needed to validate its efficacy and safety in humans.

Benefits

Anamu extract has demonstrated anti-tumor activity in preclinical studies, showing a 55% reduction in tumor growth in a murine mammary carcinoma model. It has also shown reduced metastasis in murine myeloid leukemia models. Additionally, Anamu exhibits antimicrobial activity, proving effective against *S. aureus* and *P. aeruginosa* in vitro. Secondary benefits include immunomodulation, particularly in leukemia models, and antioxidant/pro-oxidant effects that vary depending on the cell line. However, it's important to note that these benefits are primarily based on preclinical research, and more human studies are needed to confirm these effects.

How it works

Anamu's mechanism of action involves several pathways. It reduces glucose uptake in cancer cells, potentially inhibiting their growth. The extract also modulates oxidative stress, acting as a pro-oxidant in some cancer cells (e.g., B16-F10 melanoma) and as an antioxidant in others. Furthermore, Anamu enhances anti-tumor immune responses, contributing to its potential anti-cancer effects. The organosulfur compounds present in Anamu are believed to play a significant role in these biological activities, influencing cellular metabolism and immune function.

Side effects

Due to the limited human data, the common side effects of Anamu extract are not well-quantified. Traditional use suggests caution during pregnancy due to its potential abortifacient properties. Drug interactions are possible, particularly with drugs metabolized by CYP450 enzymes, given the presence of organosulfur compounds. In vitro studies have shown synergistic effects with doxorubicin in leukemia cells, but this requires careful consideration in clinical settings. Murine studies indicate dose-dependent effects, suggesting that high doses may lead to toxicity. Comprehensive human toxicology data is lacking, necessitating caution in its use.

Dosage

Preclinical studies have used a wide range of concentrations, from 225-2528 μg/mL in vitro to unspecified doses in vivo. Human equivalent dosages have not been established due to the lack of clinical trials. Standardized extracts are not commercially validated, making it difficult to determine appropriate dosages. Given the limited safety data and potential for toxicity, it is crucial to avoid self-medication and to consult with a healthcare professional before using Anamu extract. Until more research is available, its use should be restricted to research contexts.

FAQs

Is there human clinical evidence?

No randomized controlled trials or controlled human trials have been identified in peer-reviewed literature. The current evidence is primarily preclinical.

How long until effects manifest?

Murine models suggest effects may be observed within 2-3 weeks of treatment. However, this may not translate directly to humans.

Is the efficacy cancer-specific?

Evidence suggests some specificity, with effectiveness observed in mammary carcinoma and leukemia models, but not in melanoma models.

Research Sources

  • https://pmc.ncbi.nlm.nih.gov/articles/PMC10706186/ – This preclinical study demonstrated a 55% tumor reduction in a 4T1 breast cancer murine model but showed no effect in a B16-F10 melanoma model. The study highlights the potential of Anamu extract as an anti-cancer agent, but also points to the need for further research to understand its specific mechanisms and efficacy across different cancer types. The lack of clear extract standardization and the use of murine models limit the direct applicability of these findings to human treatment.
  • https://pmc.ncbi.nlm.nih.gov/articles/PMC10302921/ – This in vitro study found that Anamu extract synergistically enhanced the effects of doxorubicin in leukemia cells. The study suggests that Anamu may have potential as an adjunct therapy in leukemia treatment, but the high concentrations used in the study (μg/mL-mg/mL range) warrant caution. Further research is needed to determine whether these effects can be achieved at safe and tolerable doses in vivo.
  • https://www.mdpi.com/1422-0067/24/16/12972 – This preclinical in vivo study showed that Anamu extract reduced tumor burden and metastasis in a leukemia model. The study supports the potential of Anamu as an anti-cancer agent, particularly in leukemia. However, the findings are limited by the use of a single tumor model and the lack of human translation, highlighting the need for further research to validate these effects in humans.
  • https://ashpublications.org/blood/article/142/Supplement%201/5289/499756/A-Systematic-Review-and-Meta-Analysis-to-Evaluate – This systematic review and meta-analysis evaluates the efficacy of various interventions. It provides a framework for assessing the quality and strength of evidence, which is essential for understanding the limitations of current studies on Anamu extract and for guiding future research efforts.
  • https://www.scielo.br/j/bjps/a/Mn7K8b9ksNF6VD8DWtHxJvy/ – This study investigates the antimicrobial properties of Anamu extract. It provides evidence for Anamu's effectiveness against specific bacteria, contributing to the understanding of its broader pharmacological potential. The findings support the traditional use of Anamu for treating infections, but further research is needed to determine its clinical efficacy and safety.

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