Iron is an essential element involved in cellular respiration and oxygen transport. In higher vertebrates, there is no known regulated excretory mechanism for iron, and iron homeostasis is tightly controlled via its uptake. In the case of fish, iron is acquired predominantly from the diet, with the...

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spelling ftciteseerx:oai:CiteSeerX.psu:10.1.1.518.2648 2023-05-15T15:32:54+02:00 The Pennsylvania State University CiteSeerX Archives application/pdf http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.518.2648 http://jeb.biologists.org/content/204/21/3779.full.pdf en eng http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.518.2648 http://jeb.biologists.org/content/204/21/3779.full.pdf Metadata may be used without restrictions as long as the oai identifier remains attached to it. http://jeb.biologists.org/content/204/21/3779.full.pdf text ftciteseerx 2016-01-08T09:58:04Z Iron is an essential element involved in cellular respiration and oxygen transport. In higher vertebrates, there is no known regulated excretory mechanism for iron, and iron homeostasis is tightly controlled via its uptake. In the case of fish, iron is acquired predominantly from the diet, with the contribution from iron uptake from the water via the gills probably being negligible (Roeder and Roeder, 1966; Andersen, 1997). The estimated daily dietary requirement for iron of teleost fish ranges between 30 and 170 mg kg- 1 (Watanabe et al., 1997), and aquacultural practice is to add iron to the feed. Deviations from this supplementation can compromise fish health, and iron-deficient diets result in a reduction in hepatic iron stores and haematocrit (Andersen et al., 1997), whereas iron-rich diets are toxic, causing reduced growth (Desjardins et al., 1987) as well as being linked to an increase in pathogen virulence (Fouz et al., 1994). The mechanisms by which the teleost fish intestine absorbs iron are poorly understood, but bioavailability is influenced by the form in which iron is found in the diet (Andersen et al., 1997). In Atlantic salmon, Fe(III)2O3 is poorly absorbed (Maage and Sreier, 1998), whereas haem iron is more bioavailable than iron(II) sulphate, which in turn is more bioavailable than elemental iron (Andersen et al., 1997). In contrast, mammalian dietary iron uptake processes have been characterised, and there are two distinct forms of iron, haem and non-haem (Fe3+). In the case of non-haem iron, the acidic environment of the stomach solubilises iron from its ingested matrix (Powell et al., 1999), probably in the ferric form (Fe3+), and gastric and small intestine mucins bind this iron and maintain iron solubility at pH values approaching neutrality in the intestine (Whitehead et al., 1996). Ferric iron is reduced either via dietary compounds, such as ascorbate (Raja et al., 1992), or via a membrane-bound ferric reductase (McKie et al., 2001). The microclimate close to the tissue is maintained ... Text Atlantic salmon Unknown
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description Iron is an essential element involved in cellular respiration and oxygen transport. In higher vertebrates, there is no known regulated excretory mechanism for iron, and iron homeostasis is tightly controlled via its uptake. In the case of fish, iron is acquired predominantly from the diet, with the contribution from iron uptake from the water via the gills probably being negligible (Roeder and Roeder, 1966; Andersen, 1997). The estimated daily dietary requirement for iron of teleost fish ranges between 30 and 170 mg kg- 1 (Watanabe et al., 1997), and aquacultural practice is to add iron to the feed. Deviations from this supplementation can compromise fish health, and iron-deficient diets result in a reduction in hepatic iron stores and haematocrit (Andersen et al., 1997), whereas iron-rich diets are toxic, causing reduced growth (Desjardins et al., 1987) as well as being linked to an increase in pathogen virulence (Fouz et al., 1994). The mechanisms by which the teleost fish intestine absorbs iron are poorly understood, but bioavailability is influenced by the form in which iron is found in the diet (Andersen et al., 1997). In Atlantic salmon, Fe(III)2O3 is poorly absorbed (Maage and Sreier, 1998), whereas haem iron is more bioavailable than iron(II) sulphate, which in turn is more bioavailable than elemental iron (Andersen et al., 1997). In contrast, mammalian dietary iron uptake processes have been characterised, and there are two distinct forms of iron, haem and non-haem (Fe3+). In the case of non-haem iron, the acidic environment of the stomach solubilises iron from its ingested matrix (Powell et al., 1999), probably in the ferric form (Fe3+), and gastric and small intestine mucins bind this iron and maintain iron solubility at pH values approaching neutrality in the intestine (Whitehead et al., 1996). Ferric iron is reduced either via dietary compounds, such as ascorbate (Raja et al., 1992), or via a membrane-bound ferric reductase (McKie et al., 2001). The microclimate close to the tissue is maintained ...
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