2012
DOI: 10.1016/j.foodcont.2012.02.007
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Occurrence of fumonisins in food – An interdisciplinary approach to the problem

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Cited by 75 publications
(44 citation statements)
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“…FB 1 is the most prevalent and toxic among the fumonisins (EFSA, 2005). It is mainly found in maize and maize-based animal feeds (Soriano and Dragacci, 2004;Waskiewicz et al, 2012) and it was present in all rabbit feed samples analysed by Greco et al (2012). Fumonisins inhibit ceramide synthase leading to the accumulation of free sphinganine and sphingosine in the cellular membranes (Riley, 1996).…”
Section: Introductionmentioning
confidence: 99%
“…FB 1 is the most prevalent and toxic among the fumonisins (EFSA, 2005). It is mainly found in maize and maize-based animal feeds (Soriano and Dragacci, 2004;Waskiewicz et al, 2012) and it was present in all rabbit feed samples analysed by Greco et al (2012). Fumonisins inhibit ceramide synthase leading to the accumulation of free sphinganine and sphingosine in the cellular membranes (Riley, 1996).…”
Section: Introductionmentioning
confidence: 99%
“…Consequently, when cereal plants are infected with fungi, there is a risk of the contamination of the grain with mycotoxins and subsequent transfer to feed and food. From a global perspective, three classes of Fusarium mycotoxins are of particular importance in agricultural environments: zearalenone, fumonisins and a range of trichothecenes [13][14][15][16]. Within the trichothecene group, deoxynivalenol (DON) is associated with growth inhibition.…”
Section: Introductionmentioning
confidence: 99%
“…Among these, toxicologically the most important are FB analogues, which are mainly produced by Fusarium verticillioides and F. proliferatum. More new fumonisins (19)(20)(21) have been detected using liquid chromatography/electrospray ionisation ion-trap multistage mass spectrometry (MS) but only three of them [fumonisin B 1 (FB 1 ), B 2 (FB 2 ), and B 3 (FB 3 )] seem to occur more frequently (22). Fumonisins (FBs) are structurally similar to sphinganine and they disrupt sphingolipid metabolism by inhibiting ceramide synthase -a process underlying the mechanism of toxicity and the pathogenesis of fumonisin-related diseases (23).…”
mentioning
confidence: 99%