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Cytotoxic effect of Deoxynivalenol on the proliferation of the HepG2 cell line

Efecto citotóxico de Deoxinivalenol sobre la proliferación de la línea celular HepG2



How to Cite
Garzón-González, Harold D., Jaimes-Mendez, N., Rojas-Contreras, L., Salmen-Halabi, S., & Gil-Durán, M. A. (2021). Cytotoxic effect of Deoxynivalenol on the proliferation of the HepG2 cell line. Journal MVZ Cordoba, 26(3), e2080. https://doi.org/10.21897/rmvz.2080

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Harold Duván Garzón-González
Nancy Jaimes-Mendez
Liliana Rojas-Contreras
Siham Salmen-Halabi
Manuel Alejandro Gil-Durán

Harold Duván Garzón-González,

Harold Duván Garzón González

biogar27@gmail.com

Universidad de Pamplona, Facultad de Ciencias Básicas, Departamento de Biología, Grupo de Investigación en Biología Molecular y Genética (BIOMOGEN),  Pamplona, Colombia.


Nancy Jaimes-Mendez,

Nancy Jaimes Méndez

Universidad de Pamplona, Facultad de Ciencias Básicas, Departamento de Biología, Grupo de Investigación en Biología Molecular y Genética (BIOMOGEN),  Pamplona,  Colombia.


Liliana Rojas-Contreras,

Liliana Rojas Contreras

olrojas@unipamplona.edu.co

Universidad de Pamplona, Facultad de Ciencias Básicas, Departamento de Microbiología, Grupo de Investigación en Microbiología y Biotecnología (GIMBIO),  Pamplona, Colombia.

 


Siham Salmen-Halabi,

Siham Salmen Halabi

Salmensiham9@gmail.com

Universidad de Los Andes, Facultad de Medicina, Instituto de Inmunología Clínica (IDIC), Edificio Louis Pasteur, Av 16 de Septiembre Sector Campo de Oro, Mérida, Venezuela


Manuel Alejandro Gil-Durán,

Manuel Alejandro Gil Durán

alejandrogild@gmail.com 

Universidad de Pamplona, Facultad de Ciencias Básicas, Departamento de Matemáticas, Grupo de Investigación en Biología Molecular y Genética (BIOMOGEN), Km 1 Vía Bucaramanga, Ciudad Universitaria, Pamplona, Colombia.


Objetive. To determine the cytotoxic effect and induction of apoptosis of Deoxynivalenol (DON) on the human hepatocarcinoma cell line (HepG2). Materials and methods. The HepG2 cell line was exposed to concentrations of 10, 25, 50 and 75 µM of lyophilized DON for 48 and 72 hours. Subsequently, the cytotoxic activity of DON was evaluated using the MTT assay. Finally, it analyzed the morphological changes of apoptosis in HepG2 cells by transmission electron microscopy, after treatment with 50 μM of DON for 48 hours. Results. DON, affects the metabolic activity and proliferation of HepG2 cells above 10 µM, compared to the control. The IC50 of DON on HepG2 cells, 42.8 µM SD±1.12 and 29.6 µM SD±3.1 at 48 hours and 72 hours of treatment, respectively. The morphological characteristics of apoptosis in HepG2 cells, such as nuclear and cellular fragmentation, invagination of the plasma membrane, and the formation of apoptotic bodies. Conclusions. DON is a cytotoxic agent in HepG2 cells that alters cellular metabolic activity, with a significant antiproliferative effect dependent on concentration and exposure time, and induces apoptotic cell death.


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