A Review of Rodent Models of Type 2 Diabetic Skeletal Fragility

被引:149
作者
Fajardo, Roberto J. [1 ]
Karim, Lamya [2 ,3 ]
Calley, Virginia I. [1 ]
Bouxsein, Mary L. [2 ,3 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Dept Orthopaed, San Antonio, TX 78229 USA
[2] Beth Israel Deaconess Med Ctr, Ctr Adv Orthopaed Studies, Boston, MA 02215 USA
[3] Harvard Univ, Sch Med, Boston, MA USA
基金
美国国家卫生研究院;
关键词
DIABETES; FRACTURE RISK; TYPE; 2; ANIMAL MODELS; BONE; HIGH-FAT DIET; BONE-MINERAL DENSITY; LONG-TERM TREATMENT; GOTO-KAKIZAKI RATS; ANIMAL-MODEL; POSTMENOPAUSAL WOMEN; VERTEBRAL FRACTURES; HIP FRACTURE; INSULIN-SECRETION; PSAMMOMYS-OBESUS;
D O I
10.1002/jbmr.2210
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Evidence indicating that adult type 2 diabetes (T2D) is associated with increased fracture risk continues to mount. Unlike osteoporosis, diabetic fractures are associated with obesity and normal to high bone mineral density, two factors that are typically associated with reduced fracture risk. Animal models will likely play a critical role in efforts to identify the underlying mechanisms of skeletal fragility in T2D and to develop preventative treatments. In this review we critically examine the ability of current rodent models of T2D to mimic the skeletal characteristics of human T2D. We report that although there are numerous rodent models of T2D, few have undergone thorough assessments of bone metabolism and strength. Further, we find that many of the available rodent models of T2D have limitations for studies of skeletal fragility in T2D because the onset of diabetes is often prior to skeletal maturation and bone mass is low, in contrast to what is seen in adult humans. There is an urgent need to characterize the skeletal phenotype of existing models of T2D, and to develop new models that more closely mimic the skeletal effects seen in adult-onset T2D in humans. (c) 2014 American Society for Bone and Mineral Research.
引用
收藏
页码:1025 / 1040
页数:16
相关论文
共 201 条
[1]
Age-dependent changes in metabolism, contractile function, and ischemic sensitivity in hearts from db/db mice [J].
Aasum, E ;
Hafstad, AD ;
Severson, DL ;
Larsen, TS .
DIABETES, 2003, 52 (02) :434-441
[2]
IMPACT OF DIABETIC INHERITANCE ON GLUCOSE-TOLERANCE AND INSULIN-SECRETION IN SPONTANEOUSLY DIABETIC GK-WISTAR RATS [J].
ABDELHALIM, SM ;
GUENIFI, A ;
LUTHMAN, H ;
GRILL, V ;
EFENDIC, S ;
OSTENSON, CG .
DIABETES, 1994, 43 (02) :281-288
[3]
Methionine-Restricted C57BL/6J Mice Are Resistant to Diet-Induced Obesity and Insulin Resistance but Have Low Bone Density [J].
Ables, Gene P. ;
Perrone, Carmen E. ;
Orentreich, David ;
Orentreich, Norman .
PLOS ONE, 2012, 7 (12)
[4]
Bone metabolism in male patients with type 2 diabetes [J].
Achemlal, L ;
Tellal, S ;
Rkiouak, F ;
Nouijai, A ;
Bezza, A ;
Derouiche, E ;
Ghafir, D ;
El Maghraoui, A .
CLINICAL RHEUMATOLOGY, 2005, 24 (05) :493-496
[5]
Altered endothelial/pericyte ratio in Goto-Kakizaki rat retina [J].
Agardh, CD ;
Agardh, E ;
Zhang, H ;
Ostenson, CG .
JOURNAL OF DIABETES AND ITS COMPLICATIONS, 1997, 11 (03) :158-162
[6]
Skeletal changes in type-2 diabetic Goto-Kakizaki rats [J].
Ahmad, T ;
Ohlsson, C ;
Sääf, M ;
Östenson, CG ;
Kreicbergs, A .
JOURNAL OF ENDOCRINOLOGY, 2003, 178 (01) :111-116
[7]
Insufficient islet compensation to insulin resistance vs. reduced glucose effectiveness in glucose-intolerant mice [J].
Ahrén, B ;
Pacini, G .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2002, 283 (04) :E738-E744
[8]
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
[9]
AMIR G, 1991, DIABETES RES CLIN EX, V17, P135
[10]
[Anonymous], NAT DIAB FACT SHEET