Quantitative trait loci for lipid metabolism in the study of OLETF x (OLETF x Fischer 344) backcross rats

被引:8
作者
Yamasaki, Y
Watanabe, TK
Okuno, S
Ono, T
Oga, K
Mizoguchi-Miyakita, A
Goto, Y
Shinomiya, H
Momota, H
Miyao, H
Hayashi, I
Asai, T
Suzuki, M
Harada, Y
Hishigaki, H
Wakitani, S
Takagi, T
Nakamura, Y
Tanigami, A
机构
[1] Otsuka Pharmaceut Co Ltd, Otsuka GEN Res Inst, Kawauchi, Tokushima 7710192, Japan
[2] Osaka Minami Natl Hosp, Dept Orthopaed Surg, Osaka, Japan
[3] Univ Tokyo, Inst Med Sci, Ctr Human Genome, Lab Genome Database, Tokyo, Japan
[4] Univ Tokyo, Inst Med Sci, Ctr Human Genome, Mol Med Lab, Tokyo, Japan
关键词
hyperlipidaemia; OLETF rat; quantitative trait loci analysis; type II diabetes;
D O I
10.1046/j.1440-1681.2000.03353.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. The Otsuka Long-Evans Tokushima Fatty (OLETF) rat is a model of type II diabetes with accompanying dyslipidaemia and obesity. 2. To define chromosomal intervals associated with obesity (abdominal fat weight and plasma leptin levels), dyslipidaemia (plasma triglyceride, cholesterol and free fatty acids) and hyperglycaemia (plasma glucose levels), we have performed genome-wide quantitative traits loci (QTL) analyses of 115 male OLETF x (OLETF x Fischer 344) backcross animals at 16 weeks of age. 3. The Diabetes Mellitus OLETF type I (Dmo1) locus on rat chromosome 1 showed statistically significant involvement in elevations of plasma levels of triglycerides (P = 4.87 x 10(-6) at D1Rat90) and total cholesterol (P = 1.16 x 10(-5) at D1Rat306). 4. No other loci produced significant linkage to these observed phenotypes. 5. These analyses have confirmed the importance of Dmo1 in lipid homeostasis at younger ages as well as during overt diabetes, which appears later. Thus, alterations at the Dmo1 locus are a major risk factor for pathogenesis in the strain, a finding that agrees with physiological studies that indicate a role for dyslipidaemia in the type II diabetic syndrome of OLETF rats.
引用
收藏
页码:881 / 886
页数:6
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