• Tidak ada hasil yang ditemukan

Enhancers and Inhibitors of Iron Absorption

Dalam dokumen Molecular, Genetic, and Nutritional Aspects of (Halaman 190-194)

As already described above, vitamin C (ascorbic acid) is a strong enhancer of dietary iron absorption since it is a ferrireduc- tant. Other organic acids (citric, malic, tartaric, and lactic) can have enhancing effects; generally, acidic gastric secretions are thought to help promote iron absorption, particularly since DMT-1 is a proton-coupled transporter. Other food factors can block nonheme iron absorption, for example, phytic acid. Even small amounts (5–10 mg) inhibit iron absorption by 50% (Food and Nutrition Board, 2001). Polyphenols, which are found in fruit and vegetables, coffee and tea, as well as in wine, are also potent inhibitors of iron uptake. Certain drugs may reduce iron absorption, including antacids and pro- ton pump inhibitors that decrease acid in the stomach. Since metals often share transport pathways, competition between cations can occur, especially between zinc and iron. On the other hand, because copper is required for ferroxidases that promote iron uptake (hephaestin, ceruloplasmin), copper-deficiency anemia can arise (Gulec et al., 2014).

In surveys of the US population, it has been reported that men intake an average of 16–18 mg/day and that women take in about 15 mg/day (Food and Nutrition Board, 2001). Of course, strong dietary influences such as those described above factor into the final amount of iron absorbed, but generally men consume more than the recommended amount of iron while women take in less. Thus, iron-deficiency anemia during pregnancy is of particular concern. Iron supplements are avail- able to prevent and treat iron deficiency but their use should be discussed with a health care provider. An over-the-counter multivitamin/multimineral supplement typically contains about 18 mg of iron, which is above the recommended amount.

Iron fortification programs have been implemented to prevent iron deficiency in many countries, but are controversial due to the extent that high iron can cause oxidative stress and place people who have inherited or acquired overload diseases at risk despite benefit to the population as a whole (Allen, 2002). In the age of personalized care and precision medicine, given the significant health impact of iron it is important for one to know and keep track of their individual iron status since iron deficiency can be reversed through changes in diet and supplementation, while iron overload can be limited through these measures as well.

REFERENCES

Ali-Rahmani, F., Schengrund, C.L., Connor, J.R., 2014. HFE gene variants, iron, and lipids: a novel connection in Alzheimer’s disease. Front. Pharmacol.

5, 165.

Allen, L.H., 2002. Iron supplements: scientific issues concerning efficacy and implications for research and programs. J. Nutr. 132, 813S–819S.

Allen, R.P., Earley, C.J., 2007. The role of iron in restless legs syndrome. Mov. Disord. 22 (Suppl. 18), S440–S448.

Beard, J.L., 2008. Why iron deficiency is important in infant development. J. Nutr. 138, 2534–2536.

Bloomer, S.A., Brown, K.E., Buettner, G.R., Kregel, K.C., 2008. Dysregulation of hepatic iron with aging: implications for heat stress-induced oxidative liver injury. Am. J. Physiol. Regul. Integr. Comp. Physiol. 294, R1165–R1174.

Camaschella, C., 2015. Iron-deficiency anemia. N. Engl. J. Med. 372, 1832–1843.

Constantine, C.C., Anderson, G.J., Vulpe, C.D., McLaren, C.E., Bahlo, M., Yeap, H.L., Gertig, D.M., Osborne, N.J., Bertalli, N.A., Beckman, K.B., Chen, V., Matak, P., McKie, A.T., Delatycki, M.B., Olynyk, J.K., English, D.R., Southey, M.C., Giles, G.G., Hopper, J.L., Allen, K.J., Gurrin, L.C., 2009. A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis. Br. J. Haematol. 147, 140–149.

Danesh, J., Appleby, P., 1999. Coronary heart disease and iron status: meta-analyses of prospective studies. Circulation 99, 852–854.

Distante, S., Robson, K.J., Graham-Campbell, J., Arnaiz-Villena, A., Brissot, P., Worwood, M., 2004. The origin and spread of the HFE-C282Y haemo- chromatosis mutation. Hum. Genet. 115, 269–279.

Donovan, A., Lima, C.A., Pinkus, J.L., Pinkus, G.S., Zon, L.I., Robine, S., Andrews, N.C., 2005. The iron exporter ferroportin/Slc40a1 is essential for iron homeostasis. Cell Metab. 1, 191–200.

Drakesmith, H., Prentice, A.M., 2012. Hepcidin and the iron-infection axis. Science 338, 768–772.

Finberg, K.E., Heeney, M.M., Campagna, D.R., Aydinok, Y., Pearson, H.A., Hartman, K.R., Mayo, M.M., Samuel, S.M., Strouse, J.J., Markianos, K., Andrews, N.C., Fleming, M.D., 2008. Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA). Nat. Genet. 40, 569–571.

Fleming, M.D., 2011. Congenital sideroblastic anemias: iron and heme lost in mitochondrial translation. Hematology 2011, 525–531.

Food and Nutrition Board, I.O.M., 2001. Dietary Reference Intakes for Vitamin A, Vitamin K, Boron, Chromium, Opper, Iodine, Iron, Manganese, Molyb- denum, Nickel, Silicon, Vanadium, and Zinc. National Academy Press, Washington, DC, pp. 290–393.

Ford, E.S., Cogswell, M.E., 1999. Diabetes and serum ferritin concentration among U.S. adults. Diabetes Care 22, 1978–1983.

Galy, B., Ferring-Appel, D., Becker, C., Gretz, N., Grone, H.J., Schumann, K., Hentze, M.W., 2013. Iron regulatory proteins control a mucosal block to intestinal iron absorption. Cell Rep. 3, 844–857.

Ganz, T., Nemeth, E., 2012. Hepcidin and iron homeostasis. Biochim. Biophys. Acta 1823, 1434–1443.

Goodnough, L.T., Schrier, S.L., 2014. Evaluation and management of anemia in the elderly. Am. J. Hematol. 89, 88–96.

Guida, C., Altamura, S., Klein, F.A., Galy, B., Boutros, M., Ulmer, A.J., Hentze, M.W., Muckenthaler, M.U., 2015. A novel inflammatory pathway mediat- ing rapid hepcidin-independent hypoferremia. Blood 125, 2265–2275.

Gulec, S., Anderson, G.J., Collins, J.F., 2014. Mechanistic and regulatory aspects of intestinal iron absorption. Am. J. Physiol. Gastrointest. Liver Physiol.

307, G397–G409.

Gunshin, H., Starr, C.N., Direnzo, C., Fleming, M.D., Jin, J., Greer, E.L., Sellers, V.M., Galica, S.M., Andrews, N.C., 2005. Cybrd1 (duodenal cytochrome b) is not necessary for dietary iron absorption in mice. Blood 106, 2879–2883.

Guralnik, J.M., Eisenstaedt, R.S., Ferrucci, L., Klein, H.G., Woodman, R.C., 2004. Prevalence of anemia in persons 65 years and older in the United States: evidence for a high rate of unexplained anemia. Blood 104, 2263–2268.

Haas, J.D., Brownlie 4th, T., 2001. Iron deficiency and reduced work capacity: a critical review of the research to determine a causal relationship. J. Nutr.

131, 676S–688S, discussion 688S–690S.

Hentze, M.W., Muckenthaler, M.U., Galy, B., Camaschella, C., 2010. Two to tango: regulation of mammalian iron metabolism. Cell 142, 24–38.

Jenkitkasemwong, S., Wang, C.Y., Mackenzie, B., Knutson, M.D., 2012. Physiologic implications of metal-ion transport by ZIP14 and ZIP8. Biometals 25, 643–655.

Kato, I., Dnistrian, A.M., Schwartz, M., Toniolo, P., Koenig, K., Shore, R.E., Zeleniuch-Jacquotte, A., Akhmedkhanov, A., Riboli, E., 1999. Iron intake, body iron stores and colorectal cancer risk in women: a nested case-control study. Int. J. Cancer 80, 693–698.

Kautz, L., Jung, G., Valore, E.V., Rivella, S., Nemeth, E., Ganz, T., 2014. Identification of erythroferrone as an erythroid regulator of iron metabolism.

Nat. Genet. 46, 678–684.

Kim, J., Wessling-Resnick, M., 2014. Iron and mechanisms of emotional behavior. J. Nutr. Biochem. 25, 1101–1107.

Korolnek, T., Hamza, I., 2014. Like iron in the blood of the people: the requirement for heme trafficking in iron metabolism. Front. Pharmacol. 5, 126.

Kuhn, L.C., 2015. Iron regulatory proteins and their role in controlling iron metabolism. Metallomics 7, 232–243.

Lane, D.J., Bae, D.H., Merlot, A.M., Sahni, S., Richardson, D.R., 2015. Duodenal cytochrome b (DCYTB) in iron metabolism: an update on function and regulation. Nutrients 7, 2274–2296.

Lomagno, K.A., Hu, F., Riddell, L.J., Booth, A.O., Szymlek-Gay, E.A., Nowson, C.A., Byrne, L.K., 2014. Increasing iron and zinc in pre-menopausal women and its effects on mood and cognition: a systematic review. Nutrients 6, 5117–5141.

Lozoff, B., Beard, J., Connor, J., Barbara, F., Georgieff, M., Schallert, T., 2006. Long-lasting neural and behavioral effects of iron deficiency in infancy.

Nutr. Rev. 64, S34–S43, discussion S72–S91.

Mackenzie, H.S., Brenner, B.M., 1995. Fewer nephrons at birth: a missing link in the etiology of essential hypertension? Am. J. Kidney Dis. 26, 91–98.

Mena, N.P., Urrutia, P.J., Lourido, F., Carrasco, C.M., Nunez, M.T., 2015. Mitochondrial iron homeostasis and its dysfunctions in neurodegenerative disorders. Mitochondrion 21, 92–105.

Meynard, D., Babitt, J.L., Lin, H.Y., 2014. The liver: conductor of systemic iron balance. Blood 123, 168–176.

Nemeth, E., Tuttle, M.S., Powelson, J., Vsghn, M.B., Donovan, A., Ward, D.M., Ganz, T., Kaplan, J., 2004. Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization. Science 306, 2090–2093.

Papanikolaou, G., Samuels, M.E., Ludwig, E.H., MacDonald, M.L., Franchini, P.L., Dube, M.P., Andres, L., MacFarlane, J., Sakellaropoulos, N., Politou, M., Nemeth, E., Thompson, J., Risler, J.K., Zaborowska, C., Babakaiff, R., Radomski, C.C., Pape, T.D., Davidas, O., Christakis, J., Brissot, P., Lock- itch, G., Ganz, T., Hayden, M.R., Goldberg, Y.P., 2004. Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis.

Nat. Genet. 36, 77–82.

Pietrangelo, A., 2004. Hereditary hemochromatosis–a new look at an old disease. N. Engl. J. Med. 350, 2383–2397.

Prado, E.L., Dewey, K.G., 2014. Nutrition and brain development in early life. Nutr. Rev. 72, 267–284.

Qiu, A., Jansen, M., Sakaris, A., Min, S.H., Chattopadhyay, S., Tsai, E., Sandoval, C., Zhao, R., Akabas, M.H., Goldman, I.D., 2006. Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption. Cell 127, 917–928.

Quigley, J.G., Yang, Z., Worthington, M.T., Phillips, J.D., Sabo, K.M., Sabath, D.E., Berg, C.L., Sassa, S., Wood, B.L., Abkowitz, J.L., 2004. Identification of a human heme exporter that is essential for erythropoiesis. Cell 118, 757–766.

Rao, R., Georgieff, M.K., 2007. Iron in fetal and neonatal nutrition. Semin. Fetal Neonat. Med. 12, 54–63.

Iron: Basic Nutritional Aspects Chapter | 14 173

Salonen, J.T., Tuomainen, T.P., Salonen, R., Lakka, T.A., Nyyssonen, K., 1998. Donation of blood is associated with reduced risk of myocardial infarction.

The Kuopio Ischaemic heart disease risk factor study. Am. J. Epidemiol. 148, 445–451.

Sazawal, S., Black, R.E., Ramsan, M., Chwaya, H.M., Stoltzfus, R.J., Dutta, A., Dhingra, U., Kabole, I., Deb, S., Othman, M.K., Kabole, F.M., 2006.

Effects of routine prophylactic supplementation with iron and folic acid on admission to hospital and mortality in preschool children in a high malaria transmission setting: community-based, randomised, placebo-controlled trial. Lancet 367, 133–143.

Steinbicker, A.U., Muckenthaler, M.U., 2013. Out of balance–systemic iron homeostasis in iron-related disorders. Nutrients 5, 3034–3061.

van der, A.D., Peeters, P.H., Grobbee, D.E., Marx, J.J., van der Schouw, Y.T., 2005. Dietary haem iron and coronary heart disease in women. Eur. Heart J. 26, 257–262.

Ward, R.J., Dexter, D.T., Crichton, R.R., 2015. Neurodegenerative diseases and therapeutic strategies using iron chelators. J. Trace Elem. Med. Biol. 31, 267–273.

Wessling-Resnick, M., 2010. Iron homeostasis and the inflammatory response. Annu. Rev. Nutr. 30, 105–122.

Worthen, C.A., Enns, C.A., 2014. The role of hepatic transferrin receptor 2 in the regulation of iron homeostasis in the body. Front. Pharmacol. 5, 34.

Xu, W., Barrientos, T., Andrews, N.C., 2013. Iron and copper in mitochondrial diseases. Cell Metab. 17, 319–328.

Zimmermann, M.B., Hurrell, R.F., 2007. Nutritional iron deficiency. Lancet 370, 511–520.

Molecular, Genetic, and Nutritional Aspects of Major and Trace Minerals. http://dx.doi.org/10.1016/B978-0-12-802168-2.00015-4 175

Copyright © 2017 Elsevier Inc. All rights reserved.

Chapter 15

Hepcidin and the Hormonal Control

Dalam dokumen Molecular, Genetic, and Nutritional Aspects of (Halaman 190-194)