In vitro anti-inflammatory effects of citrulline on peritoneal macrophages in Zucker diabetic fatty rats

被引:36
作者
Breuillard, Charlotte [1 ]
Bonhomme, Sandra [1 ]
Couderc, Remy [1 ,2 ]
Cynober, Luc [1 ,3 ]
De Bandt, Jean-Pascal [1 ,3 ]
机构
[1] Univ Paris 05, Sorbonne Paris Cite, Fac Pharm, Lab Biol Nutr,EA 4466, Paris, France
[2] Hop Armand Trousseau, AP HP, Serv Biochim, Paris, France
[3] Hop Univ Paris Ctr, Hop Cochin, AP HP, Serv Biochim, Paris, France
关键词
Citrulline; Diabetes; Peritoneal macrophages; Cytokines; NITRIC-OXIDE PRODUCTION; TNF-ALPHA PRODUCTION; L-ARGININE; ENTERAL NUTRITION; SKELETAL-MUSCLE; ADIPOSE-TISSUE; OBESE RATS; INSULIN; AVAILABILITY; ACTIVATION;
D O I
10.1017/S0007114514002086
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
In type 2 diabetes (T2D) macrophage dysfunction increases susceptibility to infection and mortality. This may result from the associated decreased plasma concentration of arginine, an amino acid that plays an important role in immunity. In vitro, increasing arginine availability leads to an improvement in macrophage function; however, arginine supplementation in diabetic obese patients may be detrimental. The aim of the present study was to assess in vitro whether citrulline, an arginine precursor, could replace arginine in the regulation of macrophage function under a condition of diabetes and obesity. Peritoneal macrophages from diabetic obese or lean rats were incubated for 6 h in an arginine-free medium, in the presence of increasing citrulline concentrations (0.1, 0.5, 1 or 2 mmol/l). Cytokine and NO production was determined. Peritoneal macrophages from either lean or diabetic obese rats produced NO, and at higher levels in the cells from lean rats. In diabetic obese rats, TNF-alpha production decreased with increasing citrulline concentrations, but was higher than that in the cells from lean rats. In contrast, IL-6 production increased with increasing citrulline concentrations. The present experiment shows that citrulline is effectively used for NO production and regulates cytokine production in macrophages from diabetic obese rats. This effect warrants in vivo evaluation in T2D-related inflammation.
引用
收藏
页码:120 / 124
页数:5
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