Zinc, the pancreas, and diabetes: Insights from rodent studies and future directions

被引:165
作者
Taylor, CG [1 ]
机构
[1] Univ Manitoba, Dept Human Nutr Sci, Winnipeg, MB R3T 2N2, Canada
关键词
diabetes; insulin; pancreas; zinc;
D O I
10.1007/s10534-005-3686-x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Molecular and cellular studies have demonstrated several roles for zinc (Zn) in insulin production and the consequent actions of insulin on metabolism. Clinical and epidemiological studies suggest that reduced Zn status is associated with diabetes. Investigations of Zn in rodent models of diabetes have provided a valuable link for understanding the molecular, cellular, clinical and epidemiological observations in the context of inter-organ metabolism and the metabolic disturbances of diabetes. This review highlights some of the current knowledge and future research directions for the role of Zn in the pancreas and diabetes based on rodent studies and experimental manipulations of Zn. Overall, Zn supplementation is effective for preventing or ameliorating diabetes in several rodent models of Type 1 and Type 2 diabetes. Studies with chemically-induced Type 1 diabetes indicate that the protective effects of Zn involve antioxidant mechanisms whether it is Zn alone (as an antioxidant), Zn induction of metallothionein or Zn inhibition of redox-sensitive transcription factors. Further studies are needed to identify the mechanism(s) for Zn protection in Type 2 diabetes, including pancreatic and peripheral effects. Experimental manipulations of Zn status in rodent models of diabetes provide a valuable approach to explore mechanisms for the protective effects of Zn; however, long term clinical studies establishing safety (lack of toxicity) and efficacy are required before any recommendations can be made for people with diabetes.
引用
收藏
页码:305 / 312
页数:8
相关论文
共 61 条
[1]  
Apostolova MD, 1997, J TRACE ELEM MED BIO, V11, P1
[2]   Two SUR1-specific histidine residues mandatory for zinc-induced activation of the rat KATP channel [J].
Bancila, V ;
Cens, T ;
Monnier, D ;
Chanson, F ;
Faure, C ;
Dunant, Y ;
Bloc, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (10) :8793-8799
[3]   Obesity and hyperleptinemia in metallothionein (-I and -II) null mice [J].
Beattie, JH ;
Wood, AM ;
Newman, AM ;
Bremner, I ;
Choo, KHA ;
Michalska, AE ;
Duncan, JS ;
Trayhurn, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (01) :358-363
[4]   ZINC SUPPLEMENTATION ATTENUATES INSULIN SECRETORY ACTIVITY IN PANCREATIC-ISLETS OF THE OB OB MOUSE [J].
BEGINHEICK, N ;
DALPESCOTT, M ;
ROWE, J ;
HEICK, HMC .
DIABETES, 1985, 34 (02) :179-184
[5]   THE PHYSIOLOGICAL-ROLE OF ZINC AS AN ANTIOXIDANT [J].
BRAY, TM ;
BETTGER, WJ .
FREE RADICAL BIOLOGY AND MEDICINE, 1990, 8 (03) :281-291
[6]   Zinc, insulin and diabetes [J].
Chausmer, AB .
JOURNAL OF THE AMERICAN COLLEGE OF NUTRITION, 1998, 17 (02) :109-115
[7]   Overexpression of metallothionein in pancreatic β-cells reduces streptozotocin-induced DNA damage and diabetes [J].
Chen, HN ;
Carlson, EC ;
Pellet, L ;
Moritz, JT ;
Epstein, PN .
DIABETES, 2001, 50 (09) :2040-2046
[8]   Identification and cloning of a β-cell-specific zinc transporter, ZnT-8, localized into insulin secretory granules [J].
Chimienti, F ;
Devergnas, S ;
Favier, A ;
Seve, M .
DIABETES, 2004, 53 (09) :2330-2337
[9]   Survey of mRNAs encoding zinc transporters and other metal complexing proteins in pancreatic islets of rats from birth to adulthood: similar patterns in the Sprague-Dawley and Wistar BB strains [J].
Clifford, KS ;
MacDonald, MJ .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2000, 49 (2-3) :77-85
[10]   Metallothionein is a component of exocrine pancreas secretion: Implications for zinc homeostasis [J].
DeLisle, RC ;
Sarras, MP ;
Hidalgo, J ;
Andrews, GK .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1996, 271 (04) :C1103-C1110