Ferulic acid prevents pathological and functional abnormalities of the kidney in Otsuka Long-Evans Tokushima Fatty diabetic rats

被引:42
作者
Fujita, Atsuyo [1 ]
Sasaki, Hideyuki [1 ]
Doi, Asako [1 ]
Okamoto, Kunihisa [1 ]
Matsuno, Shohei [1 ]
Furuta, Hiroto [1 ]
Nishi, Masahiro [1 ]
Nakao, Taisei [1 ]
Tsuno, Takuo
Taniguchi, Hisaji [2 ]
Nanjo, Kishio [1 ]
机构
[1] Wakayama Med Univ, Dept Med 1, Wakayama 6418509, Japan
[2] Wakayama Ind Tech Ctr, Div Chem Technol, Wakayama, Japan
关键词
diabetic nephropathy; ferulic acid; oxidative stress; TGF-beta; 1; mesangium hypertrophy;
D O I
10.1016/j.diabres.2007.08.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We investigated the preventive effects of ferulic acid (FA) and a-tocopherol (AT) on the progression of diabetic nephropathy. Otsuka Long-Evans Tokushima Fatty (OLETF) and Long-Evans Tokushima Otsuka (LETO) rats were used as type 2 diabetes and non-diabetes models, respectively. Two-thirds of the OLETF rats were fed 0.2% FA-containing or 0.5% AT-containing chow. Diabetic nephropathy was assessed based on urinary protein excretion and pathological changes which were scored based on the percentages of extracellular matrix area in the glomerular area. Furthermore, renal messenger RNA (mRNA) expression of intercellular adhesion molecule-1 (ICAM-1), cyclooxygenase-2 (COX-2) and transforming growth factor-beta 1 (TGF-(beta 1) was quantified by real-time polymerase chain reaction. After 12 weeks of FA- or AT-supplementation, urinary protein in untreated- OLETF group was significantly higher than that in LETO group, thus FA-supplementation significantly decreased urinary protein excretion. Pathological scores in FA-supplemented group were significantly lower than those in untreated OLETF group. Supplementation with either FA or AT significantly prevented the elevation of TGF-beta 1 mRNA expression caused by diabetes. Treatment with neither FA nor AT had a significant effect on COX-2 or ICAM-1 mRNA expressions. We have demonstrated the preventative effects of FA on diabetic nephropathy via suppression of TGF-beta 1 upregulation, furthermore FA may be more potent than AT. (c) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:11 / 17
页数:7
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