The use of animal models in diabetes research

Aileen J. F. King*

*Corresponding author for this work

Research output: Contribution to journalLiterature reviewpeer-review

1012 Citations (Scopus)

Abstract

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 .

Original languageEnglish
Pages (from-to)877-894
Number of pages18
JournalBritish Journal of Pharmacology
Volume166
Issue number3
DOIs
Publication statusPublished - Jun 2012

Keywords

  • type 1 diabetes
  • type 2 diabetes
  • 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

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