4.5 Article

Biodiesel from soybean promotes cell proliferation in vitro

Journal

TOXICOLOGY IN VITRO
Volume 34, Issue -, Pages 283-288

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tiv.2016.05.004

Keywords

Biodiesel; BEAS-2B; Cytotoxicity; Cytokines; Cell proliferation; Metal; Particles; PAH

Categories

Funding

  1. Foundation for the Support of Research in Rio de Janeiro State (FAPERJ)
  2. National Council for Technological and Scientific Development (CNPq)
  3. Brazilian Federal Agency for Support and Evaluation of Graduate Education (PROCAD-CAPES)
  4. National Institute of General Medical Sciences of the National Institutes of Health (NIH) [R25GM061838]
  5. RCMI Grant (National Institute on Minority Health and Health Disparities) from the National Institutes of Health [G12 MD007600]
  6. University of Puerto Rico-Medical Sciences Campus, Deanship of Biomedical Sciences
  7. University of Puerto Rico-Medical Sciences Campus, Department of Biochemistry

Ask authors/readers for more resources

Toxicological responses of exhaust emissions of biodiesel are different due to variation in methods of generation and the tested biological models. A chemical profile was generated using ICP-MS and GC-MS for the biodiesel samples obtained in Brazil. A cytotoxicity assay and cytoldne secretion experiments were evaluated in human bronchial epithelial cells (BEAS-2B). Cells were exposed to polar (acetone) and nonpolar (hexane) extracts from particles obtained from fuel exhaust: fossil diesel (B5), pure soybean biodiesel (B100), soybean biodiesel with additive (B100A) and ethanol additive (EtOH). Biodiesel and its additives exhibited higher organic and inorganic constituents on particles when compared to B5. The biodiesel extracts did not exert any toxic effect at concentrations 10, 25, 50, 75, and 100 mu g mL(-1). In fact quite the opposite, a cell proliferation effect induced by the B100 and B100A extracts is reported. A small increase in concentrations of inflammatory mediators (Interleukin-6, IL-6; and Interleukin-8, IL-8) in the medium of biodiesel-treated cells was observed, however, no statistical difference was found. An interesting finding indicates that the presence of metals in the nonpolar (hexane) fraction of biodiesel fuel (B100) represses cytoldne release in lung cells. This was revealed by the use of the metal chelator. Results suggest that metals associated with biodiesel's organic constituents might play a significant role in molecular mechanisms associated to cellular proliferation and immune responses. Published by Elsevier Ltd.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available