Animal models for assessing the impact of natural products on the aetiology and metabolic pathophysiology of Type 2 diabetes

被引:55
作者
Asrafuzzaman, Md. [1 ]
Cao, Yingnan [2 ]
Afroz, Rizwana [3 ]
Kamato, Danielle [3 ]
Gray, Susan [3 ]
Little, Peter J. [2 ,3 ]
机构
[1] Bangladesh Univ Hlth Sci, ANRAP, Dhaka 1216, Bangladesh
[2] Sun Yat Sen Univ, Xinhua Coll, Dept Pharm, Guangzhou 510520, Guangdong, Peoples R China
[3] Univ Queensland, Sch Pharm, Pharm Australia Ctr Excellence, 20 Cornwall St, Woolloongabba, Qld 4102, Australia
关键词
Animal models; Genetics; Hyperglycaemia; Streptozotocin; HIGH-FAT DIET; PANCREATIC BETA-CELLS; INSULIN-RESISTANCE; MOUSE MODEL; GLUCOSE-TOLERANCE; RECEPTOR; OBESITY; HYPERGLYCEMIA; MICE; RISK;
D O I
10.1016/j.biopha.2017.03.010
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Type 2 diabetes mellitus is a complex and heterogeneous disorder which in its most common manifestation arises from insulin resistance and later insulin insufficiency. Type 2 diabetes is characterised by impaired insulin sensitivity and diagnosed as hyperglycaemia. Because of its cardiovascular consequences, Type 2 diabetes represents one of the world's leading causes of mortality and morbidity. Drug discovery and development are required to produce better ways to prevent, treat and manage diabetes and its complications. Diabetes is a human, not an animal disease, so animals do not get Type 2 diabetes. However there are animal models which are variously suitable for the investigation of new agents for the treatment of Type 2 diabetes. In this Review we have examined the various models that are available for the study of natural products with a focus on models (genetic, nutritional and spontaneous) for the metabolic abnormities of diabetes. These models are also relevant to the investigation of Western medicines for the treatment of diabetes. A suitable experimental model plays an important role in drug discovery for translational studies leading to increased understanding of the molecular basis and management of diabetes. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:1242 / 1251
页数:10
相关论文
共 110 条
[1]   Early neonatal death in mice homozygous for a null allele of the insulin receptor gene [J].
Accili, D ;
Drago, J ;
Lee, EJ ;
Johnson, MD ;
Cool, MH ;
Salvatore, P ;
Asico, LD ;
Jose, PA ;
Taylor, SI ;
Westphal, H .
NATURE GENETICS, 1996, 12 (01) :106-109
[2]   Preventive Effects of Salacia reticulata on Obesity and Metabolic Disorders in TSOD Mice [J].
Akase, Tomoko ;
Shimada, Tsutomu ;
Harasawa, Yukiko ;
Akase, Tomohide ;
Ikeya, Yukinobu ;
Nagai, Eiichi ;
Iizuka, Seiichi ;
Nakagami, Gojiro ;
Iizaka, Shinji ;
Sanada, Hiromi ;
Aburada, Masaki .
EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2011, 2011 :1-10
[3]   Diabetes: a look to the future [J].
Alberti, K. George M. M. ;
Zimmet, Paul Z. .
LANCET DIABETES & ENDOCRINOLOGY, 2014, 2 (01) :E1-E2
[4]  
Alberti KGMM, 1998, DIABETIC MED, V15, P539, DOI 10.1002/(SICI)1096-9136(199807)15:7<539::AID-DIA668>3.0.CO
[5]  
2-S
[6]   The M16 mouse: An outbred animal model of early onset polygenic obesity and diabesity [J].
Allan, MF ;
Eisen, EJ ;
Pomp, D .
OBESITY RESEARCH, 2004, 12 (09) :1397-1407
[7]  
Amer Diabet Assoc, 2013, DIABETES CARE, V36, pS67, DOI [10.2337/dc13-S067, 10.2337/dc11-S062, 10.2337/dc10-S011, 10.2337/dc10-S062, 10.2337/dc12-s064, 10.2337/dc11-S011, 10.2337/dc12-s011, 10.2337/dc14-S081, 10.2337/dc13-S011]
[8]  
Arulmozhi D. K., 2004, Indian Journal of Pharmacology, V36, P217
[9]   MOLECULAR MAPPING OF THE MOUSE DB MUTATION [J].
BAHARY, N ;
LEIBEL, RL ;
JOSEPH, L ;
FRIEDMAN, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (21) :8642-8646
[10]   Body composition, visceral fat, leptin, and insulin resistance in Asian Indian men [J].
Banerji, MA ;
Faridi, N ;
Atluri, R ;
Chaiken, RL ;
Lebovitz, HE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (01) :137-144