Cyclopiazonic acid (CPA) and aflatoxin are known sometimes to coexist in nature but little is known of possible biological interaction in mammals that consume mixtures of these two mycotoxins. Guinea pigs were dosed orally with CPA (2.2 mg/kg) or aflatoxin (0.045 mg B1/kg) singly or in combination. Effects of toxin consumption were determined on clinical health, body weight gain, pathological change, and several immunologically related parameters including delayed cutaneous hypersensitivity, antibody response, complement hemolytic titer, intracutaneous mitogen (PHA) and in vitro lymphocyte blastogenesis. In contrast to an earlier study by others, significant synergy between these two toxins was demonstrated in reduced rate of body weight gain, lethality and histologic changes (vacuolization) in hepatocytes. Reductions in complement titer, intradermal PHA, delayed cutaneous hypersensitivity response and in vitro lymphocyte blastogenesis were related to aflatin activity. No effects on antibody formation to Brucella abortus were observed with either toxin or the combination of toxins. Cyclopiazonic acid appeared to restore the suppressive effects of aflatoxin in delayed cutaneous hypersensitivity response and in vitro lymphocyte blastogenesis.
Three-day-old chick embryos (Hamburger-Hamilton stages 18-19) were exposed to a dose of ethyl alcohol (0.32 ml of 50% ethanol) that causes cardiac malformations in 96.6% of the animals. Ethanol was administered into the air sac after 72-80 h of incubation. Samples of albumin at the opposite pole of the egg were drawn 0-50 h after treatment and quantitated for ethanol concentration with capillary gas-liquid chromatography. Ethanol concentrations in the albumin increased significantly (P < 0.05) at 2, 5 and 15 h after injection of ethanol, reached a maximum mean ethanol concentration at 20 h (217.3 +/- 23.5 mg dl-1), decreased significantly at 30 h to 175.4 +/- 27.5 mg dl-1, then increased again and stabilized at 40-50 h. Individual sample concentrations ranged from 0 mg dl-1 (at 0.5-2 h) to 286.5 mg dl-1 at 40 h. Ethanol concentrations in the albumin were comparable to human blood alcohol levels during intoxication (> 150 mg dl-1). Our results suggest that a potent cardioteratogenic dose of ethanol in the chick embryo is reasonable in terms of potential human embryo exposure.
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