scholarly journals Cytosol is required for the modulation by dietary casein of the hepatic microsomal activation of aflatoxin B1 to mutagenic metabolites detectable in Salmonella

Mutagenesis ◽  
1999 ◽  
Vol 14 (4) ◽  
pp. 365-373 ◽  
Author(s):  
G. M. Woodall
Author(s):  
Mikhail F. Denissenko ◽  
Jeanne Cahill ◽  
Tatiana B. Koudriakova ◽  
Nicholas Gerber ◽  
Gerd P. Pfeifer

1992 ◽  
Vol 13 (2) ◽  
pp. 171-176 ◽  
Author(s):  
Agneta Blanck ◽  
Barbro Lindhe ◽  
Inger Porsch Hällström ◽  
Pia Lindeskog ◽  
Jan-Ake Gustafsson

1986 ◽  
Vol 49 (12) ◽  
pp. 974-976
Author(s):  
MIGUEL D'AQUINO ◽  
SILVIA BEJAR ◽  
ERNESTO BOLLINI

The Bacillus subtilis 1791 rec− assay was used to quantify genotoxic mycotoxins. This assay is based on detection of mycotoxin-produced DNA alterations arising from recombinational deficiency in rec− cells. Aflatoxin B1 showed a linear dose-response relationship when the inhibition halo was taken as a parameter for the evaluation procedure. Assays carried out with or without hepatic microsomal activation exhibited a similar response.


Author(s):  
E.P. Dolgov ◽  
◽  
A.A. Abramov ◽  
E.V. Kuzminova ◽  
E.V. Rogaleva ◽  
...  

The article presents the data on the study of the influence of mycotoxins combination (T-2 toxin at the concentration of 0.095 mg/kg and aflatoxin B1 in the concentration of 0.019 mg/kg) on the body of quails and the results of pharmacocorrection of toxicosis with a complex consisting of beet pulp and lecithin. Structural changes in the intestines of quais at fodder mycotoxicosis are described. The use of antitoxic feed additives in poultry led to a weakening of the action of xenobiotics, which was confirmed by an increase in the safety of poultry and increase in body weight of quails, a decrease in the clinical manifestations of intoxication, as well as in positive changes in the structure of the intestine of the poultry during histological examination.


Aflatoxin M1 is one of mycotoxin derivatives, which is secreted in milk of dairy cattle fed on feed contaminated with Aflatoxin-B1 (AFB1). The current study was designed to prepare a vaccine against AFB1and to evaluate its efficacy in reducing or preventing secretion of AFM1 in milk. Aflatoxin-B1 was prepared, purified and transformed into oxime, then it was fixed on bovine serum albumins. The AFB1-BSA conjugate was adjuvanted with Gold Nano particles then Montanide ISA 206. The prepared vaccine was used for immunization of rabbits by S/c routes as 100 µg/dose and dairy cattle by I/M routes as 500 µg/dose. The vaccinated animals were boosted at 3 weeks post primary immunization. Serum samples were collected and examined for the anti-AFB1 using AGPT. A mean titer of 15.2 AGPU/ml was detected at 2 weeks post primary vaccination then significantly increased till reached to 76.8 AGPU/ml at 6 weeks post Booster vaccination. All vaccinated rabbits were challenged with dose of 0.3 mg AFB1 toxin/Kg. The vaccinated rabbit showed 100% protection and no AFB1 toxin residue was detected in their livers. Milk samples were collected from non-vaccinated and AFB1-immunized dairy cattle then examined with ELISA for quantitation of AFM1 residues before and after vaccination. The results showed that the prepared AFB1 vaccine was safe, potent and able to reduce AFM1 release in milk of vaccinated heifers by 70%. So the vaccination of lactating animals with the AFB1vaccine might represent a valid tool for the prevention of AFM1 contamination of milk and dairy products.


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