Zinc as a Potential Coadjuvant in Therapy for Type 2 Diabetes

Food and Nutrition Bulletin - Tập 34 Số 2 - Trang 215-221 - 2013
Manuel Ruz1, Fernando Carrasco, Pamela Rojas, Juana Codoceo, Jorge Inostroza, Karen Basfi-fer, Alejandra Valencia, Karla Yohannessen Vásquez, José E. Galgani, Álvaro Pérez, G López, Miguel Arredondo, Francisco Pérez‐Bravo
1Department of Nutrition, Faculty of Medicine, University of Chile, Independencia 1027, Correo 7, Santiago, Chile. [email protected]

Tóm tắt

Background Type 2 diabetes is highly prevalent in populations having high rates of overweight and obesity. It is a chronic condition responsible for long-term severe dysfunction of several organs, including the kidneys, heart, blood vessels, and eyes. Although there are a number of pharmacologic products in the market to treat insulin resistance and impaired insulin secretion—the most prominent features of this disease—interventions directed at preserving the integrity and function of β-cells in the long term are less available. The use of some nutrients with important cellular protective roles that may lead to a preservation of β-cells has not been fully tested; among these, zinc may be an interesting candidate. Objective To assess the potential of zinc supplementation as coadjuvant to diabetes therapy. Methods This article reviews the available information on the use of zinc as part of diabetes therapy. Results Cellular and animal models provide information on the insulin mimetic action of zinc, as well as its role as a regulator of oxidative stress, inflammation, apoptosis, and insulin secretion. Zinc supplementation studies in humans are limited, although some positive effects have been reported; mainly, a modest but significant reduction in fasting glucose and a trend to decreased glycated hemoglobin (HbA1c). Conclusions Zinc supplementation may have beneficial effects on glycemic control. Nevertheless, among the studies considered, the vast majority lasted for 6 months or less, suggesting the importance of conducting long-duration studies given the characteristics of type 2 diabetes as a chronic disease.

Từ khóa


Tài liệu tham khảo

10.2337/dc11-S062

10.2337/diacare.27.5.1047

Ministerio de Salud. Gobierno de Chile. Encuesta Nacional de Salud 2009–2010. Available at: http://www.redsalud.gov.cl/portal/url/item/99bbf09a908d3eb8e04001011f014b49.pdf. Accessed 5 April 2013.

10.1016/0002-9343(91)80165-I

Kahn SE, 2001, J Clin Endocrinol Metab, 86, 4047

10.1172/JCI7231

10.1001/jama.287.3.360

10.1016/0002-9343(81)90579-9

10.2337/diab.30.5.435

10.2337/diab.46.11.1725

10.1007/s11892-010-0115-5

10.1007/s10495-009-0339-5

10.1007/978-90-481-3271-3_22

10.1111/j.1463-1326.2009.01115.x

10.2337/diabetes.51.9.2796

10.2337/db08-0043

10.1210/er.2001-0039

10.1196/annals.1331.020

10.1111/j.1475-1313.2008.00595.x

10.1007/s00592-009-0128-1

10.2337/diab.44.11.1249

10.2337/db07-0954

10.1038/414782a

10.1038/ncpendmet0786

10.2337/dc11-S011

Nathan DM, Buse JB, Davidson MB, Ferrannini E, Holman RR, Sherwin R, Zinman B; American Diabetes Association; European Association for Study of Diabetes, 2009, Diabetes Care, 321, 193

10.1002/(SICI)1096-9136(199804)15:4<290::AID-DIA570>3.0.CO;2-M

10.2337/db10-1392

10.1210/en.2002-220405

10.1186/1758-5996-2-70

10.1093/ajcn/76.1.148

10.2337/dc06-0996

10.2174/157339911794940729

10.1038/ejcn.2010.283

10.1016/j.ophtha.2009.06.040

10.2337/diaspect.22.4.214

10.1016/B0-12-227055-X/01308-0

10.3945/an.110.000232

10.1021/bi00476a001

Sunderman FW, 1995, Ann Clin Lab Sci, 25, 134

10.3945/jn.111.140053

10.1126/science.2270485

10.1093/jn/130.5.1447S

10.1089/ars.2010.3111

10.1007/978-1-4471-3879-2_18

King JC, 2006, Modern nutrition in health and disease, 10, 271

10.1097/01.mco.0000247479.87402.5b

10.1172/JCI101000

Ripa S, 1995, Minerva Med, 86, 415

10.1016/0009-8981(81)90457-5

10.1016/0002-9343(83)91205-6

10.1093/jn/114.1.224

10.1159/000108108

Zargar AH, 2002, Saudi Med J, 23, 539

10.1007/BF02021210

10.1177/42.7.8014471

10.1007/BF00275265

10.1016/0306-9877(94)90029-9

10.2337/db06-1454

10.1177/153537020122600107

10.1016/j.taap.2004.05.014

10.1016/j.jnutbio.2009.01.009

10.2337/diabetes.53.9.2330

10.1016/j.numecd.2008.09.004

10.1189/jlb.0307148

10.1073/pnas.0705894104

10.1111/j.1463-1326.2009.01110.x

10.1242/jcs.03164

10.1007/s00125-010-1733-9

10.1038/nrg2178

10.1038/nature05616

10.1089/rej.2007.0613

10.1186/1472-6823-9-7

10.2337/diabetes.52.1.102

10.2337/diabetes.50.9.2040

10.1073/pnas.91.21.9956

10.1177/153537029922200309

10.1007/s10522-005-4907-y

10.1007/s001250050009

Beletate V, 2007, Cochrane Database Syst Rev, CD005525

10.1385/BTER:112:2:109

10.1016/j.jtemb.2012.08.001

10.1186/1758-5996-4-13

10.2337/dc08-1913

10.1016/0002-9343(86)90183-X

Gupta R, 1998, J Assoc Physicians India, 46, 939