A low protein diet in early life delays the onset of diabetes in the non-obese diabetic mouse

被引:18
作者
Chamson-Reig, Astrid [1 ]
Arany, Edith J. [1 ,2 ]
Summers, Kelly [1 ,3 ]
Hill, David J. [1 ,2 ,4 ,5 ]
机构
[1] St Josephs Hlth Care, Lawson Hlth Res Inst, London, ON N6A 4V2, Canada
[2] Univ Western Ontario, Dept Med, London, ON N6A 5A5, Canada
[3] Univ Western Ontario, Dept Microbiol & Immunol, London, ON N6A 5A5, Canada
[4] Univ Western Ontario, Dept Physiol & Pharmacol, London, ON N6A 5A5, Canada
[5] Univ Western Ontario, Dept Paediat, London, ON N6A 5A5, Canada
关键词
ISLET MORPHOLOGY; NEONATAL-RAT; APOPTOSIS; FETAL; EXPRESSION; TAURINE; SUPPLEMENTATION; PATHOGENESIS; EXPOSURE; CELLS;
D O I
10.1677/JOE-09-0002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dietary insult in early life can affect the development and future function of the endocrine pancreas. We maintained pregnant non-obese diabetic (NOD) mice on a low protein (LP, 8% protein versus control, 20%) diet from conception until the weaning of pups at day 21. Serum insulin and pancreatic insulin content were reduced in LP-fed NOD offspring at 8 weeks, as were serum interferon gamma and pancreatic tumor necrosis factor alpha, while the number of pancreatic islets demonstrating peri-insulitis, and the degree of invasiveness were reduced. To determine if LP caused early morphometric changes in the pancreas, we measured mean islet area at days 3 and 21. Mean islet size did not differ with diet, but by 8 weeks of age LP-fed NOD females exhibited a significantly reduced islet number and mean islet area, and a lower fractional area of pancreas occupied by both alpha- and beta-cells than control-fed mice. The onset of diabetes was delayed in NOD puce of both genders fed LP diet. The mechanism is likely to involve both altered beta-cell morphology and function and changes in cytotoxic cytokines. Journal of Endocrinology (2009) 201, 231-239
引用
收藏
页码:231 / 239
页数:9
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