The relationship between serum ferritin concentration and tissue non-heme iron or tissue ferritin in dairy cattle.
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Biomedical subjects
Publications and source records attributed to K Furugouri.
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Granulomatous lesions of bovine paratuberculosis contained ferritin, lactoferrin, and a small amount of transferrin, as demonstrated by the immunohistochemical method. Macrophages in the normal bovine ileum did not contain lactoferrin and transferrin; however, ferritin was found in individual macrophages of Peyer's patches. These results may help elucidate the relationship between intracellular growth of Mycobacterium paratuberculosis and the presence of iron-binding proteins in the granulomas.
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Serum ferritin concentration of nursing calves was measured by a two-site immunoradiometric assay to assess developmental changes and to evaluate relationships of serum ferritin with iron-related blood characteristics. Serum ferritin concentration of calves was low at birth and elevated slightly at 3 days of age. From 1 wk of age onward, serum ferritin concentration of untreated calves and calves fed only whole milk for 4 wk decreased and remained low throughout the nursing period. This finding almost coincided with hematological characteristics. However, that nearly normal hematological measures and weight gain persisted and that they did not develop any anemic symptom indicate that serum ferritin concentration is more sensitive than other hematological characteristics to iron depletion. However, serum ferritin concentration of calves administered 130 mg of ferrous fumarate (40 mg iron) daily from 3 to 22 days of age or injected with 4 ml of iron-dextran intramuscularly (400 mg iron) at 3 days and 2 wk of age increased sharply just after treatment and persisted high for 2 to 6 wk of age. However, there was large variation between animals for serum ferritin concentration. Thus, it seems likely that serum ferritin concentration is an index for monitoring prelatent iron deficiency of calves.
Serum ferritin concentration of 40 nursing piglets was measured by a two-site immuno-radiometric assay to assess relationships of serum ferritin to Fe-related blood characteristics and nonheme Fe concentration of the liver. Hemoglobin concentration rapidly decreased after nursing to 55% of the birth level at 2 to 4 wk of age when the piglets exhibited severe symptoms of Fe deficiency. However, an im injection of 1 ml of iron-dextran (100 mg Fe) at 3 d of age restored the hemoglobin level to near the concentration of 10 g/100 ml by 2 wk of age. Serum ferritin concentration was low at birth and 1 d of age, but increased by 3 d of age. From 1 wk of age onward, serum ferritin level of the unsupplemented animals decreased linearly and declined to the lowest level at 3 wk of age. With iron-dextran injection, however, systemic concentration of ferritin peaked at 1 wk of age and decreased linearly to 3 wk of age. Serum ferritin of both groups was almost depleted at 3 to 4 wk of age. Although a single injection of 100 mg Fe from iron-dextran is adequate to maximize weight gain and to maintain normal hemoglobin level, serum ferritin concentration was almost exhausted after 2 wk of age. Serum ferritin concentration of both groups increased gradually from 4 wk of age, followed by a quadratic rise to 8 wk of age. The elevation of serum ferritin of the unsupplemented group after 4 wk of age almost paralleled that of hemoglobin concentration.(ABSTRACT TRUNCATED AT 250 WORDS)
Concentration of ferritin in blood serum of dairy cows was measured by a two-site immunoradiometric assay to assess changes in the iron nutritional status during gestation, parturition, and lactation. Although anemia did not occur in pregnancy of dairy cows, there were slight decreases of red cell counts, hemoglobin, and hematocrit in the early stage of lactation. Ferritin concentration remained relatively constant in late gestation (35 ng/ml), but deviations were considerable. Ferritin rose gradually from 3 days prepartum with a sharp elevation after parturition. At 1 to 2 wk postpartum, it had increased to about twice amounts in late gestation. During the subsequent 8 wk postpartum, it fell gradually and thereafter maintained almost unchanged (40 ng/ml). Both iron in blood serum and total iron-binding capacity declined from 2 wk prepartum to the end of gestation but showed a rise beginning about 2 wk after parturition. Because changes in iron-related proteins just before and after delivery may be results of inflammatory reactions accompanying delivery, ferritin concentration is not a good index for diagnosis of iron deficiency in lactating cows just after parturition.
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Fifty piglets from birth to 14 days of age were used to investigate iron binding substances of neonatal intestinal mucosa, and to evaluate the effects of these substances in neonatal iron absorption. 59Fe-labeled ferric citrate with a molecular weight of 1,500 was injected directly into the ligated duodenum. Approximately 65% of radioiron in the whole homogenate of scraped intestinal mucosa was precipitate by centrifugation for 30 minutes at 10,000 X g. Over 70% of the radioiron of the supernatant applied to Sephadex G-200 column was eluted and separated into three radioiron fractions. These iron binding substances were identified as ferritin, transferrin and a low molecular weight form by elution characteristics on chromatography and by immunological technique. Although ferritin radioactivity was the major fraction of peak 1 (73%), transferrin activity was only 54% of the whole radioiron of peak 2. The sodium dodecyl sulfate (SDS) extract of saline insoluble particles from the mucosa applied to Sepharose 4B column eluted as a single peak near the point corresponded with the ferritin peak. Although the ferritin peak contained a higher percentage of the 59Fe than the transferrin peak at birth, the percentage of ferritin decreased and percentage of transferrin increased with age. A SDS soluble iron binding substance was found in the insoluble particles of mucosa of newborn as well as nursing piglets. Since SDS, as well as saline soluble, iron binding proteins were detected in the newborn intestinal mucosa, neonatal cell membrane and cytoplasma may have an active iron transfer system. Thus, it seems likely that neonatal mucosal cell has two active iron transport mechanisms: endocytosis and transport across the plasma membrane.
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