[HTML][HTML] Modeling chick to assess diabetes pathogenesis and treatment

SP Datar, RR Bhonde - The review of diabetic studies: RDS, 2011 - ncbi.nlm.nih.gov
SP Datar, RR Bhonde
The review of diabetic studies: RDS, 2011ncbi.nlm.nih.gov
Animal models have been used extensively in diabetes research. Studies on animal models
have contributed to the discovery and purification of insulin, development of new therapeutic
approaches, and progress in fundamental and clinical research. However, conventional
rodent and large animal mammalian models face ethical, practical, or technical limitations.
Therefore, it would be beneficial developing an alternative model for diabetes research
which would overcome these limitations. Amongst other vertebrates, birds are …
Abstract
Animal models have been used extensively in diabetes research. Studies on animal models have contributed to the discovery and purification of insulin, development of new therapeutic approaches, and progress in fundamental and clinical research. However, conventional rodent and large animal mammalian models face ethical, practical, or technical limitations. Therefore, it would be beneficial developing an alternative model for diabetes research which would overcome these limitations. Amongst other vertebrates, birds are phylogenically closer to mammals, and amongst birds, the chick has been used as one of the favored models in developmental biology, toxicology, cancer research, immunology, and drug testing. Chicken eggs are readily available, have a short incubation period and easily accessible embryos. Based on these inimitable advantages, the present review article aims to discuss the suitability of the chick as a model system to study specific aspects of diabetes. The review focuses on the application of i) chick pancreatic islets for screening of antidiabetic agents and for islet banking,(ii) shell-less chick embryo culture as a model to study hyperglycemia-induced malformations observed in mammalian embryos, and (iii) chick chorioallantoic membrane (CAM) to examine glucose-induced endothelial damage leading to inhibition of angiogenesis.
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