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Hydrolysis of ochratoxin A by the microbial activity of digesta in the gastrointestinal tract of rats

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Abstract

This study established the influence of dietary neomycin sulphate on the rate of hydrolysis of ochratoxin A (OA) by digesta from the intestine, and its effect on the excretion of OA and its hydrolyzed metabolite, alpha ochratoxin (Oα), in the urine and feces of the rat. The first in vitro study demonstrated that digesta from the cecum and the large intestine were able to hydrolyze OA whereas digesta from the small intestine and stomach had very low hydrolytic activity against this substrate. Homogenates of the liver had no hydrolytic activity. The second in vivo study demonstrated that digesta from the large intestine and cecum of the neomycin treated rats was much less effective (P<0.001) in promoting the hydrolysis of OA than digesta from the control rats. Neomycin when added directly to the in vitro system, however, did not affect the rate at which OA was hydrolyzed. In a third study, OA was administered in vivo to control and neomycin-treated rats. Rats fed the neomycin containing diet compared to those fed the control diet had a higher concentration (P<0.005) of blood OA, and a greater cumulative excretion of OA plus Oα over the entire 5 day collection period in the feces (P<0.0001) and a corresponding decrease in the cumulative excretion of OA plus Oα in the urine (P<0.0001). Individually, there was a marked increase in cumulative fecal excretion of OA (P<0.05) and a corresponding decrease in excretion of Oα (P<0.05). Individual OA and Oα values in the urine tended to follow an opposite pattern to that seen in the feces but the differences were not significant (P<0.05). Overall, the results demonstrate that an antibiotic such as neomycin when added to the diet greatly reduces the rate of hydrolysis of OA by digesta from the lower sections of the gastrointestinal tract. Neomycin also alters the pattern of excretion of OA and Oα in the feces and possibly the urine in rats fed OA. These results suggest that intestinal microorganisms affect disposition of OA.

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References

  • Chu FS, Chang CC (1971) Sensitivity of chicks to ochratoxins. J Assoc Offic Anal Chem 54:1032–1034

    Google Scholar 

  • Dobbins WO (1968) Drug-induced steatorrhea. Gastroenterology 54:1193–1195

    Google Scholar 

  • Doster RC, Sinnhuber RO, Wales JH (1972) Acute intraperitoneal toxicity of ochratoxin A and B in rainbow trout. Fd Cosmet Toxicol 10:85–92

    Google Scholar 

  • Doster RC, Sinnhuber RO (1972) Comparative rate of hydrolysis of ochratoxin A and B in vitro. Fd Cosmet Toxicol 10:389–394

    Google Scholar 

  • Frohlich AA, Marquardt RR, Bernatsky A (1988) Quantitation of ochratoxin A: Use of reverse phase thin layer chromatography for sample cleanup followed by liquid chromatography or direct fluorescence measurement. J Assoc Offic Anal Chem 71:949–953

    Google Scholar 

  • Kim RS (1975) Studies on the metabolism of some synthetic steroids in rabbits. PhD Thesis, University of Manitoba, Canada

    Google Scholar 

  • Galtier P (1978) Contribution of pharmacokinetic studies to mycotoxicology—ochratoxin A. Vet Sci Commun 1:349–358

    Google Scholar 

  • Galtier P, Charpenteau JL, Alvinerie M, Labouche C (1979) The pharmacokinetic profile of ochratoxin A in the rat after oral and intravenous administration. Drug Metabol Dispos 7:429–434

    Google Scholar 

  • Hansen CE, Dueland S, Drevon CA, Stormer FC (1982) Metabolism of ochratoxin A by primary cultures of rat hepatocytes. Appl Environ Microbiol 43:1267–1271

    Google Scholar 

  • Hult K, Hokby E, Hagglund U, Gatenbeck S, Rutqvist L, Sellyey G (1979) Ochratoxin A in pig blood: Method of analysis and use as a tool for feed studies. Appl Environ Microbiol 38:772–776

    Google Scholar 

  • Kanisawa M, Suzuki S, Kozuka Y, Yamazaki M (1977) Histopathological studies on the toxicity of ochratoxin A in rats. 1. Acute oral toxicity. Toxicol Appl Pharmacol 41:55–64

    Google Scholar 

  • Krogh P (1987) Ochratoxins in food. In: Krogh P (ed), Mycotoxins in food. Academic Press, NY, pp 97–121

    Google Scholar 

  • Kumagai S, Aibara K (1982) Intestinal absorption and secretion of ochratoxin A in the rat. Toxicol Appl Pharmacol 64:94–102

    Google Scholar 

  • Madhyastha MS, Marquardt RR, Frohlich AA (1992) Effect of dietary cholestyramine in the elimination of ochratoxin in rats. Fd. Chem. Toxicol (in press)

  • Marquardt RR, Ward AT, Misir R (1979) The retention of nutrients by chicks fed rye diets supplemented with amino acids and penicillin. Poult Sci 58:631–640

    Google Scholar 

  • Merck and Co (1986) The Merck veterinary manual, 6th ed. Merck and Co Inc, Rahway, NJ, pp 1519–1525

    Google Scholar 

  • Moroi K, Suzuki S, Kuga T, Yamazaki M, Kanisawa M (1985) Reduction of ochratoxin A toxicity in mice treated with phenylalanine and phenobarbital. Toxicol Lett 25:1–5

    Google Scholar 

  • Nel W, Purchase IFH (1968) The fate of ochratoxin A in rats. J S Afr Chem Inst 21:87–88

    Google Scholar 

  • Pitout MJ (1969) The hydrolysis of ochratoxin A by some proteolytic enzymes. Biochem Pharmacol 18:485–491

    Google Scholar 

  • Rolandelli RH, Koruda MJ, Settle RG, Leskiw MJ, Stein TP, Rombeau JL (1989) The effect of pectin on hepatic lipogenesis in the enterally-fed rat. J Nutr 119:89–93

    Google Scholar 

  • Roth A, Chakor K, Creppy EE, Kane A, Roschenthaler R, Dirheimer G (1988) Evidence for an enterohepatic circulation of ochratoxin A in mice. Toxicology 48:293–308

    Google Scholar 

  • Savage DC (1981) The microbial flora in the gastrointestinal tract. In: Nutrition in health and disease and international development. Alan R Liss Inc, NY, pp 893–908

    Google Scholar 

  • Sreemannarayana O, Frohlich AA, Vitti TG, Marquardt RR, Abramson D (1988) Studies of the tolerance and disposition of ochratoxin A in young calves. J Anim Sci 66:1703–1711

    Google Scholar 

  • Statistical Analysis System Institute Inc (1986) SAS user's guide: Statistics, 1986 ed. SAS Institute Inc, Carey, NC, 584 pp

    Google Scholar 

  • Stormer FC, Storen O, Hansen CE, Pedersen JI, Aasen AJ (1983) Formation of (4R)- and (4S)-4-hydroxyochratoxin A and 10-hydroxyochratoxin A from ochratoxin A by rabbit liver microsomes. Appl Environ Microbiol 45:1183–1187

    Google Scholar 

  • Suzuki S, Satoh T, Yamazaki M (1977) The pharmacokinetics of ochratoxin A in rats. Japan J Pharmacol 27:735–744

    Google Scholar 

  • Vonk HS, Western JRH (1984) Proteinases in mammals. In: Comparative biochemistry and physiology of enzymatic digestion, Academic Press, NY, pp 94–183

    Google Scholar 

  • Xiao H, Marquardt RR, Frohlich AA, Phillips GD, Vitti TG (1991) Effect of a hay and grain diet on the bioavailability of ochratoxin A in the rumen of sheep. J Anim Sci 69:3715–3723

    Google Scholar 

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Madhyastha, M.S., Marquardt, R.R. & Frohlich, A.A. Hydrolysis of ochratoxin A by the microbial activity of digesta in the gastrointestinal tract of rats. Arch. Environ. Contam. Toxicol. 23, 468–472 (1992). https://doi.org/10.1007/BF00203811

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  • DOI: https://doi.org/10.1007/BF00203811

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