Abstract

A study was conducted to determine the cytosolic in vitro hepatic enzymatic kinetic parameters Vmax, KM, and intrinsic clearance (CLint) for aflatoxin B1 (AFB1) reductase [aflatoxicol (AFL) production] and AFL dehydrogenase (AFB1 production) in four commercial poultry species (chicken, quail, turkey and duck). Large differences were found in AFB1 reductase activity, being the chicken the most efficient producer of AFL (highest CLint value). Oxidation of AFL to AFB1 showed only slight differences among the different poultry species. On average all species produced AFB1 from AFL at a similar rate, except for the turkey which produced AFB1 from AFL at a significantly lower rate than chickens and quail, but not ducks. Although the turkey and duck showed differences in AFL oxidation Vmax and KM parameters, their CLint values did not differ significantly. The ratio AFB1 reductase/AFL dehydrogenase enzyme activity was inversely related to the known in vivo sensitivity to AFB1 being highest for the chicken, lowest for the duck and intermediate for turkeys and quail. Since there is no evidence that AFL is a toxic metabolite of AFB1, these results suggest that AFL production is a detoxication reaction in poultry. Conversion of AFB1 to AFL prevents the formation of the AFB1-8,9-exo-epoxide which, upon conversion to AFB1-dihydrodiol, is considered to be the metabolite responsible for the acute toxic effects of AFB1.

Highlights

  • A study was conducted to determine the cytosolic in vitro hepatic enzymatic kinetic parameters Vmax, KM, and intrinsic clearance (CLint) for aflatoxin B1 (AFB1) reductase [aflatoxicol (AFL) production] and AFL dehydrogenase (AFB1 production) in four commercial poultry species

  • Aflatoxicol (AFL) is a metabolite produced by the enzymatic reduction of carbon 1 (C1) in the cyclopentanone ring of aflatoxin B1 (AFB1)

  • AFL oxidation to AFB1 has been reported in primary rat hepatocyte culture[6], whereas AFB1 reduction to AFL has been found in rat erythrocyte cytosol[7]

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Summary

Introduction

A study was conducted to determine the cytosolic in vitro hepatic enzymatic kinetic parameters Vmax, KM, and intrinsic clearance (CLint) for aflatoxin B1 (AFB1) reductase [aflatoxicol (AFL) production] and AFL dehydrogenase (AFB1 production) in four commercial poultry species (chicken, quail, turkey and duck). Lozano and Diaz[16] reported that hepatic cytosolic in vitro reduction rates of AFB1 follow the order turkey > duck > quail > chicken, but did not determine enzymatic parameters such as maximal velocity (Vmax), Michaleis-Menten constant (KM) or intrinsic clearance (CLint). Since it is well-known that different poultry species exhibit different sensitivities to AFB1, the present study was conducted with the aim of investigating possible differences in the enzymatic kinetic parameters KM, Vmax and CLint for AFB1 reduction and AFL oxidation and to relate these differences with the known in vivo susceptibility to AFB1 of each of these four poultry species

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