Tafadzwa Mandimika
†‡, Hakan Baykus
†, Yvonne Vissers
§, Prescilla Jeurink

, Jenneke Poortman
†, Cutberto Garza

, Harry Kuiper
† and Ad Peijnenburg
*† RIKILT, Institute of Food Safety, Wageningen University and Research Centre, Post Office Box 230, 6700 AE Wageningen, , Division of Nutritional Sciences, Cornell University, Ithaca, New York 14853, WU Agrotechnology and Food Sciences, Wageningen University and Research Centre, Post Office Box 8129, 6700 EV Wageningen, , WU Cell Biology and Immunology, Wageningen University and Research Centre, Post Office Box 9101, 6700 HB Wageningen, , and Office of the Provost, Boston College, Chestnut Hill, Massachusetts 02467
J. Agric. Food Chem., 2007, 55 (24), pp 10055–10066
DOI: 10.1021/jf0724320
Publication Date (Web): November 1, 2007
Copyright © 2007 American Chemical Society
†
RIKILT, Institute of Food Safety, Wageningen University and Research Centre.
,
,
§
WU Agrotechnology and Food Sciences, Wageningen University and Research Centre.
,
WU Cell Biology and Immunology, Wageningen University and Research Centre.
,
Boston College.
,
* To whom correspondence should be addressed: Toxicology and Effect Monitoring Group, RIKILT, Institute of Food Safety, Wageningen University and Research Centre, Post Office Box 230, 6700 AE Wageningen, The Netherlands. Telephone:
+ 31-317-475462 . Fax:
+ 31-317-417717. E-mail:
ad.peijnenburg@wur.nl.
Abstract
α-Chaconine and α-solanine are naturally occurring toxins. They account for 95% of the total glycoalkaloids in potatoes (Solanum tuberosum L.). At high levels, these glycoalkaloids may be toxic to humans, mainly by disrupting cell membranes of the gastrointestinal tract. Gene-profiling experiments were performed, whereby Caco-2 cells were exposed to equivalent concentrations (10 µM) of pure α-chaconine or α-solanine or glycoalkaloid mixtures of varying α-chaconine/α-solanine ratios for 6 h. In addition, lactate dehydrogenase, cell cycle, and apoptosis analyses experiments were also conducted to further elucidate the effects of glycoalkaloids. The main aims of the study were to determine the transcriptional effects of these glycoalkaloid treatments on Caco-2 cells and to investigate DNA microarray utility in conjunction with conventional toxicology in screening for potential toxicities and their severity. Gene expression and pathway analyses identified changes related to cholesterol biosynthesis, growth signaling, lipid and amino acid metabolism, mitogen-activated protein kinase (MAPK) and NF-κB cascades, cell cycle, and cell death/apoptosis. To varying extents, DNA microarrays discriminated the severity of the effect among the different glycoalkaloid treatments.