The use of animal models in diabetes research

被引:939
作者
King, Aileen J. F. [1 ]
机构
[1] Kings Coll London, Diabet Res Grp, London SE1 1UL, England
关键词
type; 1; diabetes; 2; animal models; LOW-DOSE STREPTOZOTOCIN; BETA-CELL MASS; IMPROVES GLYCEMIC CONTROL; GOTO-KAKIZAKI RATS; ENDOPLASMIC-RETICULUM STRESS; INSULIN-RESISTANCE; PANCREATIC-ISLETS; MOUSE MODEL; GLUCOSE-TOLERANCE; PSAMMOMYS-OBESUS;
D O I
10.1111/j.1476-5381.2012.01911.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Diabetes is a disease characterized by a relative or absolute lack of insulin, leading to hyperglycaemia. There are two main types of diabetes: type 1 diabetes and type 2 diabetes. Type 1 diabetes is due to an autoimmune destruction of the insulin-producing pancreatic beta cells, and type 2 diabetes is caused by insulin resistance coupled by a failure of the beta cell to compensate. Animal models for type 1 diabetes range from animals with spontaneously developing autoimmune diabetes to chemical ablation of the pancreatic beta cells. Type 2 diabetes is modelled in both obese and non-obese animal models with varying degrees of insulin resistance and beta cell failure. This review outlines some of the models currently used in diabetes research. In addition, the use of transgenic and knock-out mouse models is discussed. Ideally, more than one animal model should be used to represent the diversity seen in human diabetic patients. LINKED ARTICLES Animal Models This paper is the latest in a series of publications on the use of animal models in pharmacology research. Readers might be interested in the previous papers. Robinson V (2009). . Holmes AM, Rudd JA, Tattersall FD, Aziz Q, Andrews PLR (2009). . Giacomotto J and Segalat L (2010). McGrath JC, Drummond GB, McLachlan EM, Kilkenny C, Wainwright CL (2010). . Kilkenny C, Browne W, Cuthill IC, Emerson M, Altman DG (2010). . Emerson M (2010). . Berge O-G (2011). . Vickers SP, Jackson HC and Cheetham SC (2011). . Percie du Sert N, Holmes AM, Wallis R, Andrews PLR (2012). . The complete series including future publications, as they occur, can be found at .
引用
收藏
页码:877 / 894
页数:18
相关论文
共 212 条
[61]   Glycemic Control Promotes Pancreatic Beta-Cell Regeneration in Streptozotocin-Induced Diabetic Mice [J].
Grossman, Eric J. ;
Lee, David D. ;
Tao, Jing ;
Wilson, Raphael A. ;
Park, Soo-Young ;
Bell, Graeme I. ;
Chong, Anita S. .
PLOS ONE, 2010, 5 (01)
[62]  
GRUSSNER R, 1993, HORM METAB RES, V25, P199, DOI 10.1055/s-2007-1002076
[63]   INDUCTION OF TYPE-I DIABETES BY KILHAM RAT VIRUS IN DIABETES-RESISTANT BB/WOR RATS [J].
GUBERSKI, DL ;
THOMAS, VA ;
SHEK, WR ;
LIKE, AA ;
HANDLER, ES ;
ROSSINI, AA ;
WALLACE, JE ;
WELSH, RM .
SCIENCE, 1991, 254 (5034) :1010-1013
[64]   Chronic leucine supplementation improves glycemic control in etiologically distinct mouse models of obesity and diabetes mellitus [J].
Guo, Kaiying ;
Yu, Yi-Hao ;
Hou, Jue ;
Zhang, Yiying .
NUTRITION & METABOLISM, 2010, 7
[65]   Minireview: Transcriptional regulation in pancreatic development [J].
Habener, JF ;
Kemp, DM ;
Thomas, MK .
ENDOCRINOLOGY, 2005, 146 (03) :1025-1034
[66]   Physiological response to long-term peripheral and central leptin infusion in lean and obese mice [J].
Halaas, JL ;
Boozer, C ;
BlairWest, J ;
Fidahusein, N ;
Denton, DA ;
Friedman, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (16) :8878-8883
[67]   THE NOD MOUSE [J].
HANAFUSA, T ;
MIYAGAWA, J ;
NAKAJIMA, H ;
TOMITA, K ;
KUWAJIMA, M ;
MATSUZAWA, Y ;
TARUI, S .
DIABETES RESEARCH AND CLINICAL PRACTICE, 1994, 24 :S307-S311
[68]   Transgenic mice with green fluorescent protein-labeled pancreatic β-cells [J].
Hara, M ;
Wang, XY ;
Kawamura, T ;
Bindokas, VP ;
Dizon, RF ;
Alcoser, SY ;
Magnuson, MA ;
Bell, GI .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2003, 284 (01) :E177-E183
[69]   Iodine and tri-iodo-thyronine reduce the incidence of type 1 diabetes mellitus in the autoimmune prone BB rats [J].
Hartoft-Nielsen, Marie-Louise ;
Rasmussen, Aase Krogh ;
Bock, Troels ;
Feldt-Rasmussen, Ulla ;
Kaas, Anne ;
Buschard, Karsten .
AUTOIMMUNITY, 2009, 42 (02) :131-138
[70]   The diabetes-prone NZO/HILt strain. I. Immunophenotypic comparison to the related NZB/BINJ and NZW/LacJ strains [J].
Haskell, BD ;
Flurkey, K ;
Duffy, TM ;
Sargent, EE ;
Leiter, EH .
LABORATORY INVESTIGATION, 2002, 82 (07) :833-842