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Abstract
As part of an effort to improve the safety of plant foods, a need exists to more clearly
delineate the mechanisms of toxicities of glycoalkaloids, which may be present in
Solanum plant species such as potatoes, tomatoes and eggplants. Alpha-chaconine is
a major glycoalkaloid present in potatoes. To assess the possible influence of structure
of pteridine derivatives on toxicity of potato glycoalkaloids, a previous study that
demonstrated the protective effects of folic acid against the Solanum glycoalkaloid
alpha-chaconine-induced toxicity on Xenopus laevis frog embryo cell membranes was
extended to two folate analogues--a synthetic compound widely used as a therapeutic
agent methotrexate, and naturally occurring L-monapterin. Adverse effects on embryos
were evaluated by observing changes in membrane potentials with an electrochromic
dye, di-4-ANEPPS, as a fluorescent probe for the integrity of the membranes. Methotrexate
decreased alpha-chaconine-induced polarization, as did folic acid. This decrease may
result from an alteration of membrane conformations that prevents the binding of the
glycoalkaloid to the membrane receptor sites, and/or from effects on folic acid metabolism.
In contrast, L-monapterin did not significantly reduce the alpha-chaconine-induced
toxicity. The possible significance of these results to food safety is discussed.