Experimental Diabetes Mellitus in Different Animal Models
Animal models have historically played a critical role in the exploration and characterization of disease pathophysiology and target identification and in the evaluation of novel therapeutic agents and treatments in vivo. Diabetes mellitus disease, commonly known as diabetes, is a group of metabolic...
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Series: | Journal of Diabetes Research |
Online Access: | http://dx.doi.org/10.1155/2016/9051426 |
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doaj-edab2e18aa1d419a8047d8ab1ca7dc052020-11-25T00:45:18ZengHindawi LimitedJournal of Diabetes Research2314-67452314-67532016-01-01201610.1155/2016/90514269051426Experimental Diabetes Mellitus in Different Animal ModelsAmin Al-awar0Krisztina Kupai1Médea Veszelka2Gergő Szűcs3Zouhair Attieh4Zsolt Murlasits5Szilvia Török6Anikó Pósa7Csaba Varga8Department of Physiology, Anatomy and Neuroscience, Faculty of Science and Informatics, University of Szeged, Kozep Fasor 52, 6726 Szeged, HungaryDepartment of Physiology, Anatomy and Neuroscience, Faculty of Science and Informatics, University of Szeged, Kozep Fasor 52, 6726 Szeged, HungaryDepartment of Physiology, Anatomy and Neuroscience, Faculty of Science and Informatics, University of Szeged, Kozep Fasor 52, 6726 Szeged, HungaryDepartment of Physiology, Anatomy and Neuroscience, Faculty of Science and Informatics, University of Szeged, Kozep Fasor 52, 6726 Szeged, HungaryDepartment of Laboratory Science and Technology, Faculty of Health Sciences, American University of Science and Technology, Alfred Naccache Avenue, Beirut 1100, LebanonSport Science Program, Qatar University, Doha, QatarDepartment of Physiology, Anatomy and Neuroscience, Faculty of Science and Informatics, University of Szeged, Kozep Fasor 52, 6726 Szeged, HungaryDepartment of Physiology, Anatomy and Neuroscience, Faculty of Science and Informatics, University of Szeged, Kozep Fasor 52, 6726 Szeged, HungaryDepartment of Physiology, Anatomy and Neuroscience, Faculty of Science and Informatics, University of Szeged, Kozep Fasor 52, 6726 Szeged, HungaryAnimal models have historically played a critical role in the exploration and characterization of disease pathophysiology and target identification and in the evaluation of novel therapeutic agents and treatments in vivo. Diabetes mellitus disease, commonly known as diabetes, is a group of metabolic disorders characterized by high blood glucose levels for a prolonged time. To avoid late complications of diabetes and related costs, primary prevention and early treatment are therefore necessary. Due to its chronic symptoms, new treatment strategies need to be developed, because of the limited effectiveness of the current therapies. We overviewed the pathophysiological features of diabetes in relation to its complications in type 1 and type 2 mice along with rat models, including Zucker Diabetic Fatty (ZDF) rats, BB rats, LEW 1AR1/-iddm rats, Goto-Kakizaki rats, chemically induced diabetic models, and Nonobese Diabetic mouse, and Akita mice model. The advantages and disadvantages that these models comprise were also addressed in this review. This paper briefly reviews the wide pathophysiological and molecular mechanisms associated with type 1 and type 2 diabetes, particularly focusing on the challenges associated with the evaluation and predictive validation of these models as ideal animal models for preclinical assessments and discovering new drugs and therapeutic agents for translational application in humans.http://dx.doi.org/10.1155/2016/9051426 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Amin Al-awar Krisztina Kupai Médea Veszelka Gergő Szűcs Zouhair Attieh Zsolt Murlasits Szilvia Török Anikó Pósa Csaba Varga |
spellingShingle |
Amin Al-awar Krisztina Kupai Médea Veszelka Gergő Szűcs Zouhair Attieh Zsolt Murlasits Szilvia Török Anikó Pósa Csaba Varga Experimental Diabetes Mellitus in Different Animal Models Journal of Diabetes Research |
author_facet |
Amin Al-awar Krisztina Kupai Médea Veszelka Gergő Szűcs Zouhair Attieh Zsolt Murlasits Szilvia Török Anikó Pósa Csaba Varga |
author_sort |
Amin Al-awar |
title |
Experimental Diabetes Mellitus in Different Animal Models |
title_short |
Experimental Diabetes Mellitus in Different Animal Models |
title_full |
Experimental Diabetes Mellitus in Different Animal Models |
title_fullStr |
Experimental Diabetes Mellitus in Different Animal Models |
title_full_unstemmed |
Experimental Diabetes Mellitus in Different Animal Models |
title_sort |
experimental diabetes mellitus in different animal models |
publisher |
Hindawi Limited |
series |
Journal of Diabetes Research |
issn |
2314-6745 2314-6753 |
publishDate |
2016-01-01 |
description |
Animal models have historically played a critical role in the exploration and characterization of disease pathophysiology and target identification and in the evaluation of novel therapeutic agents and treatments in vivo. Diabetes mellitus disease, commonly known as diabetes, is a group of metabolic disorders characterized by high blood glucose levels for a prolonged time. To avoid late complications of diabetes and related costs, primary prevention and early treatment are therefore necessary. Due to its chronic symptoms, new treatment strategies need to be developed, because of the limited effectiveness of the current therapies. We overviewed the pathophysiological features of diabetes in relation to its complications in type 1 and type 2 mice along with rat models, including Zucker Diabetic Fatty (ZDF) rats, BB rats, LEW 1AR1/-iddm rats, Goto-Kakizaki rats, chemically induced diabetic models, and Nonobese Diabetic mouse, and Akita mice model. The advantages and disadvantages that these models comprise were also addressed in this review. This paper briefly reviews the wide pathophysiological and molecular mechanisms associated with type 1 and type 2 diabetes, particularly focusing on the challenges associated with the evaluation and predictive validation of these models as ideal animal models for preclinical assessments and discovering new drugs and therapeutic agents for translational application in humans. |
url |
http://dx.doi.org/10.1155/2016/9051426 |
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