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In vitro hepatic aflatoxicol production is related to a higher resistance to aflatoxin B1 in poultry
A study was conducted to determine the cytosolic in vitro hepatic enzymatic kinetic parameters V m a x , K M , and intrinsic clearance (CL i n t ) for aflatoxin B 1 (AFB 1 ) reductase [aflatoxicol (AFL) production] and AFL dehydrogenase (AFB 1 production) in four commercial poultry species (chicken,...
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Published in: | Scientific reports 2020-03, Vol.10 (1), Article 5508 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A study was conducted to determine the cytosolic
in vitro
hepatic enzymatic kinetic parameters V
m
a
x
, K
M
, and intrinsic clearance (CL
i
n
t
) for aflatoxin B
1
(AFB
1
) reductase [aflatoxicol (AFL) production] and AFL dehydrogenase (AFB
1
production) in four commercial poultry species (chicken, quail, turkey and duck). Large differences were found in AFB
1
reductase activity, being the chicken the most efficient producer of AFL (highest CL
i
n
t
value). Oxidation of AFL to AFB
1
showed only slight differences among the different poultry species. On average all species produced AFB
1
from AFL at a similar rate, except for the turkey which produced AFB
1
from AFL at a significantly lower rate than chickens and quail, but not ducks. Although the turkey and duck showed differences in AFL oxidation V
m
a
x
and K
M
parameters, their CL
i
n
t
values did not differ significantly. The ratio AFB
1
reductase/AFL dehydrogenase enzyme activity was inversely related to the known
in vivo
sensitivity to AFB
1
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 AFB
1
, these results suggest that AFL production is a detoxication reaction in poultry. Conversion of AFB
1
to AFL prevents the formation of the AFB
1
-8,9-
exo
-epoxide which, upon conversion to AFB
1
-dihydrodiol, is considered to be the metabolite responsible for the acute toxic effects of AFB
1
. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-020-62415-y |