Animal Models of Diabetes Mellitus for Islet Transplantation

被引:44
作者
Sakata, Naoaki [1 ]
Yoshimatsu, Gumpei [1 ]
Tsuchiya, Haruyuki [1 ]
Egawa, Shinichi [2 ]
Unno, Michiaki [1 ]
机构
[1] Tohoku Univ, Grad Sch Med, Dept Surg,Div Hepatobiliarypancreat Surg, Aoba Ku, Sendai, Miyagi 9808574, Japan
[2] Tohoku Univ, Int Res Inst Disaster Sci, Div Int Cooperat Disaster Med, Sendai, Miyagi 9808574, Japan
关键词
PANCREATIC FRAGMENT AUTOTRANSPLANTATION; LONG-TERM NORMOGLYCEMIA; BETA-CELL REGENERATION; GLYCATION END-PRODUCTS; PORTAL-VEIN; AUTO-TRANSPLANTATION; INSULIN-RESISTANCE; LEPTIN RECEPTOR; PORCINE ISLETS; VITAMIN-D;
D O I
10.1155/2012/256707
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Due to current improvements in techniques for islet isolation and transplantation and protocols for immunosuppressants, islet transplantation has become an effective treatment for severe diabetes patients. Many diabetic animal models have contributed to such improvements. In this paper, we focus on 3 types of models with different mechanisms for inducing diabetes mellitus (DM): models induced by drugs including streptozotocin (STZ), pancreatomized models, and spontaneous models due to autoimmunity. STZ-induced diabetes is one of the most commonly used experimental diabetic models and is employed using many specimens including rodents, pigs or monkeys. The management of STZ models is well established for islet studies. Pancreatomized models reveal different aspects compared to STZ-induced models in terms of loss of function in the increase and decrease of blood glucose and therefore are useful for evaluating the condition in total pancreatomized patients. Spontaneous models are useful for preclinical studies including the assessment of immunosuppressants because such models involve the same mechanisms as type 1 DM in the clinical setting. In conclusion, islet researchers should select suitable diabetic animal models according to the aim of the study.
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页数:11
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