Potent Anti-amoebic Effects of Ibogaine, Voacangine and the Root Bark Alkaloid Fraction of Tabernaemontana arborea

Author:

Carrero Julio César1ORCID,Curay-Herrera Violeta2,Chacón-Niño Lysette1,Krengel Felix3,Guzmán-Gutiérrez Silvia-Laura4,Silva-Miranda Mayra4,González-Ramírez Luisa-Carolina5,Bobes Raúl J.1,Espitia Clara1,Reyes-Chilpa Ricardo6,Laclette Juan-Pedro1

Affiliation:

1. Departamento de Inmunología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad de México, México

2. Escuela Profesional de Ciencias Biológicas, Facultad de Ciencias, Universidad de Piura, Piura, Perú

3. Departamento de Ecología y Recursos Naturales, Facultad de Ciencias, Universidad Nacional Autónoma de México, Ciudad de México, México

4. CONACyT-Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad de México, México

5. Grupo de Investigación “Análisis de Muestras Biológicas y Forenses”, Carrera Laboratorio Clínico, Facultad de Ciencias de la Salud, Universidad Nacional de Chimborazo, Riobamba, Ecuador

6. Departamento de Productos Naturales, Instituto de Química, Universidad Nacional Autónoma de México, Ciudad de México, México

Abstract

AbstractPlants of Tabernaemontana species have several pharmacological activities including antimicrobial effects. Amoebiasis continues to be a public health problem, with increasing evidence of resistance to metronidazole. In this study, we assessed the effect of the alkaloid fraction of T. arborea root bark and the alkaloids ibogaine and voacangine on the viability and infectivity of Entamoeba histolytica trophozoites. Cultures were exposed to 0.1 – 10 µg/mL for 24, 48 and 72 h, and viability was then determined using a tetrazolium dye reduction assay and type of cellular death analyzed by flow cytometry. Results showed that the alkaloid fraction, but mainly ibogaine and voacangine alkaloids, exhibited potent dose-dependent anti-amoebic activity at 24 h post-exposure (IC50 4.5 and 8.1 µM, respectively), comparable to metronidazole (IC50 6.8 µM). However, the effect decreased after 48 and 72 h of exposure to concentrations below 10 µg/mL, suggesting that the alkaloids probably were catabolized to less active derivatives by the trophozoites. The treatment of trophozoites with the IC50 s for 24 h induced significant morphological changes in the trophozoites, slight increase in granularity, and death by apoptonecrosis. The capacity of T. arborea alkaloids to inhibit the development of amoebic liver abscesses in hamsters was evaluated. Results showed that even when the treatments reduced the number of amoebic trophozoites in tissue sections of livers, they were unable to limit the formation of abscesses, suggesting their rapid processing to inactive metabolites. This work leaves open the possibility of using Tabernaemontana alkaloids as a new alternative for amoebiasis control.

Funder

Institutional program “Nuevas alternativas para el tratamiento de enfermedades infecciosas”

Programa de Apoyo a Proyectos de Investigación e Innovación Tecnológica

Consejo Nacional de Ciencia y Tecnología

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Analytical Chemistry

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