Effet chez le porcelet d'une exposition à un régime co-contaminé en ...
Effet chez le porcelet d'une exposition à un régime co-contaminé en ...
Effet chez le porcelet d'une exposition à un régime co-contaminé en ...
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INTRODUCTION2.2) TCT type A and BTwo reports focused on the interaction betwe<strong>en</strong> type B and type A trichothec<strong>en</strong>es, DON and T-2toxin (Fri<strong>en</strong>d et al., 1992; Kub<strong>en</strong>a et al., 1989b). In swine, except for the highest dose of T-2 toxinthat interact synergistically with DON in the decreased BWG and feed intake, a <strong>le</strong>ss than additiveeffect was observed on these zootechnic parameters following the <strong>co</strong>mbination exposure, ref<strong>le</strong>ctingpredominantly the DON effect (Fri<strong>en</strong>d et al., 1992) (Tab<strong>le</strong> 5). By <strong>co</strong>ntrast, in broi<strong>le</strong>r chicks, most ofthe observed effects (oral <strong>le</strong>sions, total protein, albumin and LDH) were due to T-2 toxin in the<strong>co</strong>mbined treatm<strong>en</strong>t (Kub<strong>en</strong>a et al., 1989b). However, an additive effect was obtained on the bodyweight gain and on the serum cho<strong>le</strong>sterol <strong>co</strong>nc<strong>en</strong>tration (Tab<strong>le</strong> 5). Decreased cho<strong>le</strong>sterol <strong>le</strong>vels <strong>co</strong>uldsuggest inhibition of biosynthesis, with liver involvem<strong>en</strong>t and perhaps a shift of <strong>co</strong>nc<strong>en</strong>tration fromblood to the liver.2.3) TCT type BOne study investigated the interaction betwe<strong>en</strong> the two type B trichothec<strong>en</strong>es, deoxyniva<strong>le</strong>noland niva<strong>le</strong>nol (NIV), using two differ<strong>en</strong>t low doses of both toxins (Gouze et al., 2005) (Tab<strong>le</strong> 5).Although the lowest dose of NIV and the two doses of DON used did not affect the plasmatic <strong>le</strong>vels ofuric acid, wh<strong>en</strong> used in <strong>co</strong>mbination the toxins act in a synergistic manner. Whatever the dose of NIVand DON used, wh<strong>en</strong> the toxins were used in <strong>co</strong>mbination an additive effect was observed for thetotal protein <strong>le</strong>vel.Ingestion of DON or NIV induces IgA nephropathy in mice. Dep<strong>en</strong>ding on the doses of two toxins,wh<strong>en</strong> used in <strong>co</strong>mbination the interaction range from synergistic to additive or <strong>le</strong>ss than additive onIgA synthesis. The hepatic drug metabolism activity was also assessed. Wh<strong>en</strong> mice were exposed toDON and NIV, the toxins showed an antagonistic interaction on the activities of two monooxyg<strong>en</strong>ase(EROD and PROD). By <strong>co</strong>ntrast, for the highest doses of DON and NIV, a synergistic effect wasobserved on the e<strong>le</strong>vated activity of glutathione S-transferase (DCNB as substrates).3) Interaction betwe<strong>en</strong> Deoxyniva<strong>le</strong>nol (DON) and other Fusariotoxins3.1) Interaction betwe<strong>en</strong> DON and Zeara<strong>le</strong>none (ZEA)Three publications investigated the interaction betwe<strong>en</strong> DON and zeara<strong>le</strong>none (ZEA) (Boeira etal., 2000; Forsell et al., 1986; Pestka et al., 1987). Forsell et al. (1986) showed in mice that exposureto the <strong>co</strong>mbined treatm<strong>en</strong>t resulted mainly in antagonistic interaction (Tab<strong>le</strong> 5). The authorobserved an antagonistic effect of ZEA on the DON-induced e<strong>le</strong>vation of serum IgA. Similarly,39