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Absorption and metabolism of iron as related to the cotton fur syndrome in mink

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Title Absorption and metabolism of iron as related to the cotton fur syndrome in mink
Names Bailey, David Eugene (creator)
Stout, F. M. (advisor)
Date Issued 1966-06-30 (iso8601)
Note Graduation date: 1967
Abstract "Cotton fur" (CF) in mink (Mustela vison) is characterized
by lack of pigment in the underfur of dark mink and is part of a
syndrome including hypochromic, microcytic anemia and substandard
growth, resulting from an iron deficiency. Such symptoms
are produced by feeding rations containing raw Pacific hake
(Merluccius productus), even though the ration contains adequate
iron.
The research reported herein concerns two phases of the
CF abnormality; first a study using purifed diets to determine if
iron deficiency per se results in failure of pigment formation, and
second, studies of iron metabolism using ⁵⁹Fe as a tracer to
determine why iron is not utilized by mink fed hake-containing
rations.
Standard dark mink kits were fed either a basal iron-deficient
diet or the basal diet with 15 ppm of added iron. Chemical analysis of the diets showed that they contained 4.6 and 19.7 ppm of iron,
respectively. Blood data illustrated that a hypochromic, microcytic
anemia was present in those animals receiving the iron-deficient
diet. After the winter furring cycle, all mink on the deficient diet
exhibited unpigmented underfur and those receiving the adequate
diet had normally pigmented underfur; establishing the necessity of
iron as a chromotrichial nutrient.
In a subsequent trial four groups of mink received purified
diets with 0, 5, 10, and 15 ppm of added iron. Results supported
those of the previous one, with 75 and 33 percent CF incidence in
the 0 and 5 ppm groups respectively, and no CF in either the 10 or
15 ppm groups. Limited data showed that 70 percent of the ⁵⁹Fe
present in mink hair was located in the melanin granule, indicating
that iron may be an integral part of the melanin molecule.
Eight trials involving 37 individual iron balance trials were
conducted using ⁵⁹Fe to provide information on the second objective.
⁵⁹Fe was administered in feed or stomach tubed and iron absorption
was determined from blood and excretory data.
Ferrous citrate-⁵⁹Fe was given in either raw Pacific hake or
sole based rations. From blood data, iron absorption was 1.4
percent for the raw hake-fed mink versus 11.2 percent for mink
receiving sole. Due to uncontrollable fecal ⁵⁹Fe contamination of
urine, plasma radioactivity was used to determine if the iron was being absorbed and excreted in the urine,
To ensure complete ingestion of the tracer dose, mink were
stomach tubed with ⁵⁹Fe in a water filtrate of hake, and controls
received the radioisotope in distilled water. Iron absorption was
greater (16.3%) in presence of raw hake filtrate than with distilled
water (11.6%). Mink fed raw hake containing rations absorbed 7.5
percent and those fed rations of cooked hake absorbed 6.7 percent
of the ⁵⁹Fe given. ⁵⁹FeSO₄ was given in cooked and raw hake
suspensions and iron absorption was 23.2 percent for the cooked
hake and less (12.3%) for raw hake with iron added immediately,
as compared to 15.9 percent for iron allowed to incubate with raw
hake.
⁵⁹Fe-hemoglobin was adminstered in cooked and raw hake
suspensions and absorption of iron was completely stopped in the
mink given raw hake, but only lowered (5.2%) in those given cooked
hake. ⁵⁹FeCl₃ was given with cooked and raw hake suspensions.
Mink receiving cooked hake absorbed 16.6 percent and those receiving
raw hake absorbed only 2.9 percent, suggesting that the
factor present in raw hake specifically interferes with the utilization
of ferric iron.
Form of iron, presence of other feedstuffs, and length of
incubation of added iron were found to influence the utilization of
iron in presence or absence of raw hake. ⁵⁹Fe activity of blood components indicate that in every case where iron utilization is
impaired by the presence of raw hake, interference is at the absorptive
level. Time of feed passage through the gastrointestinal tract
as determined by excretion of radioactive iron for the 37 observations
made was 185±22 minutes with a range of 59-360 minutes.
Genre Thesis/Dissertation
Topic Iron -- Metabolism
Identifier http://hdl.handle.net/1957/47917

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